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Compile Data Set for Download or QSAR

Found 59 hits Enz. Inhib. hit(s) with Target = 'Luteinizing hormone/Choriogonadotropin receptor'   
Target
(Institution)
LigandTarget
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50256858
PNG
(CHEMBL474041 | Cyclopentyl-carbamic acid [1,1',3',...)
Show SMILES O=C(NC1CCCC1)Oc1cc(cc(c1)-c1ccccc1)-c1ccccc1
Show InChI InChI=1S/C24H23NO2/c26-24(25-22-13-7-8-14-22)27-23-16-20(18-9-3-1-4-10-18)15-21(17-23)19-11-5-2-6-12-19/h1-6,9-12,15-17,22H,7-8,13-14H2,(H,25,26)
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n/an/a 2.30E+3n/an/an/an/an/an/a



Leiden University

Curated by ChEMBL


Assay Description
Displacement of [3H]Org43553 from human luteinizing hormone receptor expressed in CHOK1 cells


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206401
PNG
(CHEMBL246321 | N-((S)-1-amino-3-(4-hydroxyphenyl)-...)
Show SMILES CC(C)(C)c1ccc(cc1)-n1nc(cc1CCCCC(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O)-c1cccnc1
Show InChI InChI=1S/C32H37N5O3/c1-32(2,3)24-12-14-25(15-13-24)37-26(20-28(36-37)23-7-6-18-34-21-23)8-4-5-9-30(39)35-29(31(33)40)19-22-10-16-27(38)17-11-22/h6-7,10-18,20-21,29,38H,4-5,8-9,19H2,1-3H3,(H2,33,40)(H,35,39)/t29-/m0/s1
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311n/an/an/an/an/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Displacement of [125I]-hCG from LH receptor


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50189773
PNG
(CHEMBL211129 | N-tert-butyl-5-amino-4-(2-fluoro-3-...)
Show SMILES COc1cccc(c1F)-c1nc(SC)nc2sc(C(=O)NC(C)(C)C)c(N)c12
Show InChI InChI=1S/C19H21FN4O2S2/c1-19(2,3)24-16(25)15-13(21)11-14(22-18(27-5)23-17(11)28-15)9-7-6-8-10(26-4)12(9)20/h6-8H,21H2,1-5H3,(H,24,25)
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n/an/an/an/a 1.50E+3n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at LHCGR expressed in HEK293 EM cells measured by intracellular cAMP accumulation


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50189777
PNG
(CHEMBL212815 | N-tert-butyl-5-amino-4-(3-fluorophe...)
Show SMILES CSc1nc(-c2cccc(F)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C18H19FN4OS2/c1-18(2,3)23-15(24)14-12(20)11-13(9-6-5-7-10(19)8-9)21-17(25-4)22-16(11)26-14/h5-8H,20H2,1-4H3,(H,23,24)
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n/an/an/an/a 1.20E+3n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at LHCGR expressed in HEK293 EM cells measured by intracellular cAMP accumulation


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50189774
PNG
(CHEMBL378091 | N-tert-butyl-5-amino-4-(3-hydroxyph...)
Show SMILES CSc1nc(-c2cccc(O)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C18H20N4O2S2/c1-18(2,3)22-15(24)14-12(19)11-13(9-6-5-7-10(23)8-9)20-17(25-4)21-16(11)26-14/h5-8,23H,19H2,1-4H3,(H,22,24)
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n/an/an/an/a 1.90E+3n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at LHCGR expressed in HEK293 EM cells measured by intracellular cAMP accumulation


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50189778
PNG
(CHEMBL211405 | N-tert-butyl-5-amino-4-(3-methoxyph...)
Show SMILES COc1cccc(c1)-c1nc(SC)nc2sc(C(=O)NC(C)(C)C)c(N)c12
Show InChI InChI=1S/C19H22N4O2S2/c1-19(2,3)23-16(24)15-13(20)12-14(10-7-6-8-11(9-10)25-4)21-18(26-5)22-17(12)27-15/h6-9H,20H2,1-5H3,(H,23,24)
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n/an/an/an/a 300n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at LHCGR expressed in HEK293 EM cells measured by intracellular cAMP accumulation


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50189779
PNG
(CHEMBL377399 | N-tert-butyl-5-amino-4-(3-methoxyph...)
Show SMILES COc1cccc(c1)-c1nc(SC)nc2sc(C(=O)N(C)C(C)(C)C)c(N)c12
Show InChI InChI=1S/C20H24N4O2S2/c1-20(2,3)24(4)18(25)16-14(21)13-15(11-8-7-9-12(10-11)26-5)22-19(27-6)23-17(13)28-16/h7-10H,21H2,1-6H3
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n/an/an/an/a 800n/an/an/an/a



National Institute of Diabetes and Digestive and Kidney Diseases

Curated by ChEMBL


Assay Description
Agonist activity at LHCGR expressed in HEK293 EM cells measured by intracellular cAMP accumulation


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335477
PNG
((S)-4-(3-(2-((1-(2-(2-(2-(2-(4-((4-(1-acetyl-6-bip...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCOCCn4cc(COc5ccc(cc5)[C@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C67H76N14O8S2/c1-43(82)81-55-26-23-50(71-61(84)46-19-17-45(18-20-46)44-13-10-9-11-14-44)36-54(55)67(7,42-66(81,5)6)48-21-24-53(25-22-48)89-41-52-40-80(78-76-52)28-30-87-32-34-88-33-31-86-29-27-79-39-51(75-77-79)37-70-56(83)38-69-49-16-12-15-47(35-49)59-57-58(68)60(62(85)74-65(2,3)4)91-63(57)73-64(72-59)90-8/h9-26,35-36,39-40,69H,27-34,37-38,41-42,68H2,1-8H3,(H,70,83)(H,71,84)(H,74,85)/t67-/m0/s1
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n/an/an/an/a 57n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335478
PNG
((S)-4-(3-(2-((1-(14-(4-((4-(1-acetyl-6-biphenyl-4-...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCOCCOCCn4cc(COc5ccc(cc5)[C@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C69H80N14O9S2/c1-45(84)83-57-26-23-52(73-63(86)48-19-17-47(18-20-48)46-13-10-9-11-14-46)38-56(57)69(7,44-68(83,5)6)50-21-24-55(25-22-50)92-43-54-42-82(80-78-54)28-30-89-32-34-91-36-35-90-33-31-88-29-27-81-41-53(77-79-81)39-72-58(85)40-71-51-16-12-15-49(37-51)61-59-60(70)62(64(87)76-67(2,3)4)94-65(59)75-66(74-61)93-8/h9-26,37-38,41-42,71H,27-36,39-40,43-44,70H2,1-8H3,(H,72,85)(H,73,86)(H,76,87)/t69-/m0/s1
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n/an/an/an/a 39n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335467
PNG
(5-amino-N-tert-butyl-2-(methylthio)-4-(3-(2-oxo-2-...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCC#C)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C23H26N6O2S2/c1-6-10-25-15(30)12-26-14-9-7-8-13(11-14)18-16-17(24)19(20(31)29-23(2,3)4)33-21(16)28-22(27-18)32-5/h1,7-9,11,26H,10,12,24H2,2-5H3,(H,25,30)(H,29,31)
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n/an/an/an/a 1n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335468
PNG
((R)-4-(3-(2-((1-(2-(4-((4-(1-acetyl-6-biphenyl-4-y...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCn4cc(COc5ccc(cc5)[C@@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C61H64N14O5S2/c1-37(76)75-49-26-23-44(65-55(78)40-19-17-39(18-20-40)38-13-10-9-11-14-38)30-48(49)61(7,36-60(75,5)6)42-21-24-47(25-22-42)80-35-46-34-74(72-70-46)28-27-73-33-45(69-71-73)31-64-50(77)32-63-43-16-12-15-41(29-43)53-51-52(62)54(56(79)68-59(2,3)4)82-57(51)67-58(66-53)81-8/h9-26,29-30,33-34,63H,27-28,31-32,35-36,62H2,1-8H3,(H,64,77)(H,65,78)(H,68,79)/t61-/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335469
PNG
((R)-4-(3-(2-((1-(2-(2-(4-((4-(1-acetyl-6-biphenyl-...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCn4cc(COc5ccc(cc5)[C@@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C63H68N14O6S2/c1-39(78)77-51-26-23-46(67-57(80)42-19-17-41(18-20-42)40-13-10-9-11-14-40)32-50(51)63(7,38-62(77,5)6)44-21-24-49(25-22-44)83-37-48-36-76(74-72-48)28-30-82-29-27-75-35-47(71-73-75)33-66-52(79)34-65-45-16-12-15-43(31-45)55-53-54(64)56(58(81)70-61(2,3)4)85-59(53)69-60(68-55)84-8/h9-26,31-32,35-36,65H,27-30,33-34,37-38,64H2,1-8H3,(H,66,79)(H,67,80)(H,70,81)/t63-/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335470
PNG
((R)-4-(3-(2-((1-(2-(2-(2-(4-((4-(1-acetyl-6-biphen...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCn4cc(COc5ccc(cc5)[C@@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C65H72N14O7S2/c1-41(80)79-53-26-23-48(69-59(82)44-19-17-43(18-20-44)42-13-10-9-11-14-42)34-52(53)65(7,40-64(79,5)6)46-21-24-51(25-22-46)86-39-50-38-78(76-74-50)28-30-85-32-31-84-29-27-77-37-49(73-75-77)35-68-54(81)36-67-47-16-12-15-45(33-47)57-55-56(66)58(60(83)72-63(2,3)4)88-61(55)71-62(70-57)87-8/h9-26,33-34,37-38,67H,27-32,35-36,39-40,66H2,1-8H3,(H,68,81)(H,69,82)(H,72,83)/t65-/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335471
PNG
((R)-4-(3-(2-((1-(2-(2-(2-(2-(4-((4-(1-acetyl-6-bip...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCOCCn4cc(COc5ccc(cc5)[C@@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C67H76N14O8S2/c1-43(82)81-55-26-23-50(71-61(84)46-19-17-45(18-20-46)44-13-10-9-11-14-44)36-54(55)67(7,42-66(81,5)6)48-21-24-53(25-22-48)89-41-52-40-80(78-76-52)28-30-87-32-34-88-33-31-86-29-27-79-39-51(75-77-79)37-70-56(83)38-69-49-16-12-15-47(35-49)59-57-58(68)60(62(85)74-65(2,3)4)91-63(57)73-64(72-59)90-8/h9-26,35-36,39-40,69H,27-34,37-38,41-42,68H2,1-8H3,(H,70,83)(H,71,84)(H,74,85)/t67-/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335472
PNG
((R)-4-(3-(2-((1-(14-(4-((4-(1-acetyl-6-biphenyl-4-...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCOCCOCCn4cc(COc5ccc(cc5)[C@@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C69H80N14O9S2/c1-45(84)83-57-26-23-52(73-63(86)48-19-17-47(18-20-48)46-13-10-9-11-14-46)38-56(57)69(7,44-68(83,5)6)50-21-24-55(25-22-50)92-43-54-42-82(80-78-54)28-30-89-32-34-91-36-35-90-33-31-88-29-27-81-41-53(77-79-81)39-72-58(85)40-71-51-16-12-15-49(37-51)61-59-60(70)62(64(87)76-67(2,3)4)94-65(59)75-66(74-61)93-8/h9-26,37-38,41-42,71H,27-36,39-40,43-44,70H2,1-8H3,(H,72,85)(H,73,86)(H,76,87)/t69-/m1/s1
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335473
PNG
(5-amino-4-(3-(2-((1-(2-(2-(2-azidoethoxy)ethoxy)et...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCN=[N+]=[N-])nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C29H38N12O4S2/c1-29(2,3)37-26(43)25-23(30)22-24(35-28(46-4)36-27(22)47-25)18-6-5-7-19(14-18)32-16-21(42)33-15-20-17-41(40-38-20)9-11-45-13-12-44-10-8-34-39-31/h5-7,14,17,32H,8-13,15-16,30H2,1-4H3,(H,33,42)(H,37,43)
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TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335474
PNG
((S)-4-(3-(2-((1-(2-(4-((4-(1-acetyl-6-biphenyl-4-y...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCn4cc(COc5ccc(cc5)[C@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C61H64N14O5S2/c1-37(76)75-49-26-23-44(65-55(78)40-19-17-39(18-20-40)38-13-10-9-11-14-38)30-48(49)61(7,36-60(75,5)6)42-21-24-47(25-22-42)80-35-46-34-74(72-70-46)28-27-73-33-45(69-71-73)31-64-50(77)32-63-43-16-12-15-41(29-43)53-51-52(62)54(56(79)68-59(2,3)4)82-57(51)67-58(66-53)81-8/h9-26,29-30,33-34,63H,27-28,31-32,35-36,62H2,1-8H3,(H,64,77)(H,65,78)(H,68,79)/t61-/m0/s1
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n/an/an/an/a 24n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335475
PNG
((S)-4-(3-(2-((1-(2-(2-(4-((4-(1-acetyl-6-biphenyl-...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCn4cc(COc5ccc(cc5)[C@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C63H68N14O6S2/c1-39(78)77-51-26-23-46(67-57(80)42-19-17-41(18-20-42)40-13-10-9-11-14-40)32-50(51)63(7,38-62(77,5)6)44-21-24-49(25-22-44)83-37-48-36-76(74-72-48)28-30-82-29-27-75-35-47(71-73-75)33-66-52(79)34-65-45-16-12-15-43(31-45)55-53-54(64)56(58(81)70-61(2,3)4)85-59(53)69-60(68-55)84-8/h9-26,31-32,35-36,65H,27-30,33-34,37-38,64H2,1-8H3,(H,66,79)(H,67,80)(H,70,81)/t63-/m0/s1
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n/an/an/an/a 80n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50335476
PNG
((S)-4-(3-(2-((1-(2-(2-(2-(4-((4-(1-acetyl-6-biphen...)
Show SMILES CSc1nc(-c2cccc(NCC(=O)NCc3cn(CCOCCOCCn4cc(COc5ccc(cc5)[C@]5(C)CC(C)(C)N(C(C)=O)c6ccc(NC(=O)c7ccc(cc7)-c7ccccc7)cc56)nn4)nn3)c2)c2c(N)c(sc2n1)C(=O)NC(C)(C)C
Show InChI InChI=1S/C65H72N14O7S2/c1-41(80)79-53-26-23-48(69-59(82)44-19-17-43(18-20-44)42-13-10-9-11-14-42)34-52(53)65(7,40-64(79,5)6)46-21-24-51(25-22-46)86-39-50-38-78(76-74-50)28-30-85-32-31-84-29-27-77-37-49(73-75-77)35-68-54(81)36-67-47-16-12-15-45(33-47)57-55-56(66)58(60(83)72-63(2,3)4)88-61(55)71-62(70-57)87-8/h9-26,33-34,37-38,67H,27-32,35-36,39-40,66H2,1-8H3,(H,68,81)(H,69,82)(H,72,83)/t65-/m0/s1
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n/an/an/an/a 75n/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO-K1 cells assessed as stimulation of luciferase activity by CRE-driven luciferase reporter gene...


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50452578
PNG
(CHEMBL2369793)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)\C=C\c1ccc(OC)cc1
Show InChI InChI=1S/C52H69N11O10/c1-5-55-50(71)44-13-9-25-63(44)51(72)39(12-8-24-56-52(53)54)59-46(67)40(26-31(2)3)60-48(69)42(28-34-29-57-38-11-7-6-10-37(34)38)62-47(68)41(27-33-14-19-35(65)20-15-33)61-49(70)43(30-64)58-45(66)23-18-32-16-21-36(73-4)22-17-32/h6-7,10-11,14-23,29,31,39-44,57,64-65H,5,8-9,12-13,24-28,30H2,1-4H3,(H,55,71)(H,58,66)(H,59,67)(H,60,69)(H,61,70)(H,62,68)(H4,53,54,56)/b23-18+/t39-,40-,41-,42+,43-,44-/m0/s1
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n/an/an/a 347n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405762
PNG
(CHEMBL2369798)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1ccc2ccccc2c1
Show InChI InChI=1S/C54H69N11O9/c1-4-57-52(73)46-16-10-24-65(46)53(74)41(15-9-23-58-54(55)56)61-48(69)42(25-32(2)3)62-50(71)44(29-37-30-59-40-14-8-7-13-39(37)40)64-49(70)43(27-33-18-21-38(67)22-19-33)63-51(72)45(31-66)60-47(68)28-34-17-20-35-11-5-6-12-36(35)26-34/h5-8,11-14,17-22,26,30,32,41-46,59,66-67H,4,9-10,15-16,23-25,27-29,31H2,1-3H3,(H,57,73)(H,60,68)(H,61,69)(H,62,71)(H,63,72)(H,64,70)(H4,55,56,58)/t41-,42-,43-,44+,45-,46-/m0/s1
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n/an/an/a 15.8n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405763
PNG
(CHEMBL412573)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)COc1cccc2ccccc12
Show InChI InChI=1S/C54H69N11O10/c1-4-57-52(73)45-18-11-25-65(45)53(74)40(17-10-24-58-54(55)56)61-48(69)41(26-32(2)3)62-50(71)43(28-35-29-59-39-16-8-7-14-37(35)39)64-49(70)42(27-33-20-22-36(67)23-21-33)63-51(72)44(30-66)60-47(68)31-75-46-19-9-13-34-12-5-6-15-38(34)46/h5-9,12-16,19-23,29,32,40-45,59,66-67H,4,10-11,17-18,24-28,30-31H2,1-3H3,(H,57,73)(H,60,68)(H,61,69)(H,62,71)(H,63,72)(H,64,70)(H4,55,56,58)/t40-,41-,42-,43+,44-,45?/m0/s1
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n/an/an/a 12.9n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405764
PNG
(CHEMBL264298)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C61H75N11O9/c1-4-64-59(79)53-24-14-30-72(53)60(80)48(23-13-29-65-61(62)63)68-55(75)49(31-38(2)3)69-57(77)51(33-43-35-66-47-22-11-10-21-46(43)47)71-56(76)50(32-39-25-27-44(73)28-26-39)70-58(78)52(37-81-36-40-15-6-5-7-16-40)67-54(74)34-42-19-12-18-41-17-8-9-20-45(41)42/h5-12,15-22,25-28,35,38,48-53,66,73H,4,13-14,23-24,29-34,36-37H2,1-3H3,(H,64,79)(H,67,74)(H,68,75)(H,69,77)(H,70,78)(H,71,76)(H4,62,63,65)/t48-,49-,50-,51+,52-,53?/m0/s1
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n/an/an/a 3.02n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405765
PNG
(CHEMBL2369791)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)c1c[nH]c2ccccc12
Show InChI InChI=1S/C46H67N11O9/c1-6-49-44(65)38-14-10-20-57(38)45(66)33(13-9-19-50-46(47)48)52-40(61)34(21-26(2)3)53-41(62)35(22-27(4)5)54-42(63)36(23-28-15-17-29(59)18-16-28)55-43(64)37(25-58)56-39(60)31-24-51-32-12-8-7-11-30(31)32/h7-8,11-12,15-18,24,26-27,33-38,51,58-59H,6,9-10,13-14,19-23,25H2,1-5H3,(H,49,65)(H,52,61)(H,53,62)(H,54,63)(H,55,64)(H,56,60)(H4,47,48,50)/t33-,34-,35+,36-,37-,38-/m0/s1
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n/an/an/a 191n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo luteinising hormone inhibiting potency in rats is expressed as negative logarithm of the concentration (antagonist)


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405766
PNG
(CHEMBL386525)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)CCc1cccc2ccccc12
Show InChI InChI=1S/C62H77N11O9/c1-4-65-60(80)54-24-14-32-73(54)61(81)49(23-13-31-66-62(63)64)69-56(76)50(33-39(2)3)70-58(78)52(35-44-36-67-48-22-11-10-21-47(44)48)72-57(77)51(34-40-25-28-45(74)29-26-40)71-59(79)53(38-82-37-41-15-6-5-7-16-41)68-55(75)30-27-43-19-12-18-42-17-8-9-20-46(42)43/h5-12,15-22,25-26,28-29,36,39,49-54,67,74H,4,13-14,23-24,27,30-35,37-38H2,1-3H3,(H,65,80)(H,68,75)(H,69,76)(H,70,78)(H,71,79)(H,72,77)(H4,63,64,66)/t49-,50-,51-,52+,53-,54?/m0/s1
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n/an/an/a 79.4n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405767
PNG
(CHEMBL265413)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CC12CC3CC(CC(C3)C1)C2
Show InChI InChI=1S/C54H77N11O9/c1-4-57-51(73)45-12-8-18-65(45)52(74)40(11-7-17-58-53(55)56)61-47(69)41(19-31(2)3)62-49(71)43(24-36-29-59-39-10-6-5-9-38(36)39)64-48(70)42(23-32-13-15-37(67)16-14-32)63-50(72)44(30-66)60-46(68)28-54-25-33-20-34(26-54)22-35(21-33)27-54/h5-6,9-10,13-16,29,31,33-35,40-45,59,66-67H,4,7-8,11-12,17-28,30H2,1-3H3,(H,57,73)(H,60,68)(H,61,69)(H,62,71)(H,63,72)(H,64,70)(H4,55,56,58)/t33?,34?,35?,40-,41-,42-,43+,44-,45?,54?/m0/s1
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n/an/an/a 3.16n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405768
PNG
(CHEMBL2369790)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1c[nH]c2ccccc12
Show InChI InChI=1S/C47H69N11O9/c1-6-50-45(66)39-14-10-20-58(39)46(67)34(13-9-19-51-47(48)49)54-41(62)35(21-27(2)3)55-42(63)36(22-28(4)5)56-43(64)37(23-29-15-17-31(60)18-16-29)57-44(65)38(26-59)53-40(61)24-30-25-52-33-12-8-7-11-32(30)33/h7-8,11-12,15-18,25,27-28,34-39,52,59-60H,6,9-10,13-14,19-24,26H2,1-5H3,(H,50,66)(H,53,61)(H,54,62)(H,55,63)(H,56,64)(H,57,65)(H4,48,49,51)/t34-,35-,36+,37-,38-,39-/m0/s1
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n/an/an/a 2.75E+3n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo luteinising hormone inhibiting potency in rats is expressed as negative logarithm of the concentration (antagonist)


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405769
PNG
(CHEMBL275694)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1cccc2ccccc12
Show InChI InChI=1S/C55H71N11O9/c1-4-58-53(74)47-19-11-27-66(47)54(75)42(18-10-26-59-55(56)57)62-49(70)43(28-33(2)3)63-51(72)45(30-37-31-60-41-17-8-7-16-40(37)41)65-50(71)44(29-34-20-23-38(68)24-21-34)64-52(73)46(32-67)61-48(69)25-22-36-14-9-13-35-12-5-6-15-39(35)36/h5-9,12-17,20-21,23-24,31,33,42-47,60,67-68H,4,10-11,18-19,22,25-30,32H2,1-3H3,(H,58,74)(H,61,69)(H,62,70)(H,63,72)(H,64,73)(H,65,71)(H4,56,57,59)/t42-,43-,44-,45+,46-,47?/m0/s1
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n/an/an/a 1.82n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405770
PNG
(CHEMBL216617)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1cccc2ccccc12
Show InChI InChI=1S/C57H72N10O9/c1-4-60-55(75)49-19-11-29-67(49)56(76)44(18-10-28-61-57(58)59)63-51(71)45(30-35(2)3)64-53(73)47(33-37-20-23-38-12-5-6-14-41(38)31-37)65-52(72)46(32-36-21-25-42(69)26-22-36)66-54(74)48(34-68)62-50(70)27-24-40-16-9-15-39-13-7-8-17-43(39)40/h5-9,12-17,20-23,25-26,31,35,44-49,68-69H,4,10-11,18-19,24,27-30,32-34H2,1-3H3,(H,60,75)(H,62,70)(H,63,71)(H,64,73)(H,65,72)(H,66,74)(H4,58,59,61)/t44-,45-,46-,47+,48-,49?/m0/s1
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n/an/an/a 0.562n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
Luteinising hormone inhibiting potency in rats is expressed as negative logarithm of the concentration (antagonist)


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405771
PNG
(CHEMBL2369810)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)\C=C\c1cccc2ccccc12
Show InChI InChI=1S/C50H70N10O9/c1-6-53-48(68)42-17-11-25-60(42)49(69)37(16-10-24-54-50(51)52)56-44(64)38(26-30(2)3)57-45(65)39(27-31(4)5)58-46(66)40(28-32-18-21-35(62)22-19-32)59-47(67)41(29-61)55-43(63)23-20-34-14-9-13-33-12-7-8-15-36(33)34/h7-9,12-15,18-23,30-31,37-42,61-62H,6,10-11,16-17,24-29H2,1-5H3,(H,53,68)(H,55,63)(H,56,64)(H,57,65)(H,58,66)(H,59,67)(H4,51,52,54)/b23-20+/t37-,38-,39+,40-,41-,42-/m0/s1
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n/an/an/a 204n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo luteinising hormone inhibiting potency in rats is expressed as negative logarithm of the concentration (antagonist)


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405773
PNG
(CHEMBL2369813)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1cccc2ccccc12
Show InChI InChI=1S/C50H72N10O9/c1-6-53-48(68)42-17-11-25-60(42)49(69)37(16-10-24-54-50(51)52)56-44(64)38(26-30(2)3)57-45(65)39(27-31(4)5)58-46(66)40(28-32-18-21-35(62)22-19-32)59-47(67)41(29-61)55-43(63)23-20-34-14-9-13-33-12-7-8-15-36(33)34/h7-9,12-15,18-19,21-22,30-31,37-42,61-62H,6,10-11,16-17,20,23-29H2,1-5H3,(H,53,68)(H,55,63)(H,56,64)(H,57,65)(H,58,66)(H,59,67)(H4,51,52,54)/t37-,38-,39+,40-,41-,42-/m0/s1
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n/an/an/a 251n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405774
PNG
(CHEMBL2369800)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C52H68N10O9/c1-4-55-50(70)44-20-12-26-62(44)51(71)39(19-11-25-56-52(53)54)58-46(66)40(27-32(2)3)59-47(67)41(28-33-13-6-5-7-14-33)60-48(68)42(29-34-21-23-37(64)24-22-34)61-49(69)43(31-63)57-45(65)30-36-17-10-16-35-15-8-9-18-38(35)36/h5-10,13-18,21-24,32,39-44,63-64H,4,11-12,19-20,25-31H2,1-3H3,(H,55,70)(H,57,65)(H,58,66)(H,59,67)(H,60,68)(H,61,69)(H4,53,54,56)/t39-,40-,41+,42-,43-,44-/m0/s1
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n/an/an/a 14.8n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405775
PNG
(CHEMBL2369806)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1c[nH]c2ccccc12
Show InChI InChI=1S/C51H69N11O9/c1-4-54-49(70)43-17-11-25-62(43)50(71)38(16-10-24-55-51(52)53)58-45(66)39(26-31(2)3)59-46(67)40(27-32-12-6-5-7-13-32)60-47(68)41(28-33-18-21-35(64)22-19-33)61-48(69)42(30-63)57-44(65)23-20-34-29-56-37-15-9-8-14-36(34)37/h5-9,12-15,18-19,21-22,29,31,38-43,56,63-64H,4,10-11,16-17,20,23-28,30H2,1-3H3,(H,54,70)(H,57,65)(H,58,66)(H,59,67)(H,60,68)(H,61,69)(H4,52,53,55)/t38-,39-,40+,41-,42-,43-/m0/s1
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n/an/an/a 851n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405772
PNG
(CHEMBL2369787)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)\C=C/c1ccc(OC)cc1
Show InChI InChI=1S/C52H69N11O10/c1-5-55-50(71)44-13-9-25-63(44)51(72)39(12-8-24-56-52(53)54)59-46(67)40(26-31(2)3)60-48(69)42(28-34-29-57-38-11-7-6-10-37(34)38)62-47(68)41(27-33-14-19-35(65)20-15-33)61-49(70)43(30-64)58-45(66)23-18-32-16-21-36(73-4)22-17-32/h6-7,10-11,14-23,29,31,39-44,57,64-65H,5,8-9,12-13,24-28,30H2,1-4H3,(H,55,71)(H,58,66)(H,59,67)(H,60,69)(H,61,70)(H,62,68)(H4,53,54,56)/b23-18-/t39-,40-,41-,42+,43-,44-/m0/s1
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n/an/an/a 347n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405777
PNG
(CHEMBL274609)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C63H76N10O9/c1-4-66-61(80)55-24-14-32-73(55)62(81)50(23-13-31-67-63(64)65)69-57(76)51(33-40(2)3)70-59(78)53(36-43-25-28-44-17-8-9-19-46(44)34-43)71-58(77)52(35-41-26-29-48(74)30-27-41)72-60(79)54(39-82-38-42-15-6-5-7-16-42)68-56(75)37-47-21-12-20-45-18-10-11-22-49(45)47/h5-12,15-22,25-30,34,40,50-55,74H,4,13-14,23-24,31-33,35-39H2,1-3H3,(H,66,80)(H,68,75)(H,69,76)(H,70,78)(H,71,77)(H,72,79)(H4,64,65,67)/t50-,51-,52-,53+,54-,55?/m0/s1
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n/an/an/a 3.63n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405778
PNG
(CHEMBL2369799)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C52H74N10O9/c1-4-55-50(70)44-20-12-26-62(44)51(71)39(19-11-25-56-52(53)54)58-46(66)40(27-32(2)3)59-47(67)41(28-33-13-6-5-7-14-33)60-48(68)42(29-34-21-23-37(64)24-22-34)61-49(69)43(31-63)57-45(65)30-36-17-10-16-35-15-8-9-18-38(35)36/h8-10,15-18,21-24,32-33,39-44,63-64H,4-7,11-14,19-20,25-31H2,1-3H3,(H,55,70)(H,57,65)(H,58,66)(H,59,67)(H,60,68)(H,61,69)(H4,53,54,56)/t39-,40-,41+,42-,43-,44-/m0/s1
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n/an/an/a 832n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405779
PNG
(CHEMBL411175)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C56H76N10O9/c1-6-59-54(73)48-22-14-28-66(48)55(74)43(21-13-27-60-56(57)58)62-50(69)44(29-35(2)3)63-51(70)45(30-36(4)5)64-52(71)46(31-37-23-25-41(67)26-24-37)65-53(72)47(34-75-33-38-15-8-7-9-16-38)61-49(68)32-40-19-12-18-39-17-10-11-20-42(39)40/h7-12,15-20,23-26,35-36,43-48,67H,6,13-14,21-22,27-34H2,1-5H3,(H,59,73)(H,61,68)(H,62,69)(H,63,70)(H,64,71)(H,65,72)(H4,57,58,60)/t43-,44-,45+,46-,47-,48?/m0/s1
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n/an/an/a 32.4n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405780
PNG
(CHEMBL2369809)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)\C=C\c1cccnc1
Show InChI InChI=1S/C45H67N11O9/c1-6-49-43(64)37-12-9-21-56(37)44(65)32(11-8-20-50-45(46)47)52-39(60)33(22-27(2)3)53-40(61)34(23-28(4)5)54-41(62)35(24-29-13-16-31(58)17-14-29)55-42(63)36(26-57)51-38(59)18-15-30-10-7-19-48-25-30/h7,10,13-19,25,27-28,32-37,57-58H,6,8-9,11-12,20-24,26H2,1-5H3,(H,49,64)(H,51,59)(H,52,60)(H,53,61)(H,54,62)(H,55,63)(H4,46,47,50)/b18-15+/t32-,33-,34+,35-,36-,37-/m0/s1
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n/an/an/a 1.91E+3n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo luteinising hormone inhibiting potency in rats is expressed as negative logarithm of the concentration (antagonist)


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405782
PNG
(CHEMBL413887)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCCc1c[nH]c2ccccc12
Show InChI InChI=1S/C56H73N11O9/c1-4-59-54(75)48-18-11-27-67(48)55(76)43(17-10-26-60-56(57)58)63-50(71)44(28-34(2)3)64-52(73)46(31-36-20-23-37-12-5-6-13-38(37)29-36)65-51(72)45(30-35-21-24-40(69)25-22-35)66-53(74)47(33-68)62-49(70)19-9-14-39-32-61-42-16-8-7-15-41(39)42/h5-8,12-13,15-16,20-25,29,32,34,43-48,61,68-69H,4,9-11,14,17-19,26-28,30-31,33H2,1-3H3,(H,59,75)(H,62,70)(H,63,71)(H,64,73)(H,65,72)(H,66,74)(H4,57,58,60)/t43-,44-,45-,46+,47-,48?/m0/s1
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n/an/an/a 8.51n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405783
PNG
(CHEMBL2369807)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C54H69N11O9/c1-4-57-52(73)46-19-11-25-65(46)53(74)41(18-10-24-58-54(55)56)61-48(69)42(26-32(2)3)62-50(71)44(28-36-30-59-40-17-8-7-16-39(36)40)64-49(70)43(27-33-20-22-37(67)23-21-33)63-51(72)45(31-66)60-47(68)29-35-14-9-13-34-12-5-6-15-38(34)35/h5-9,12-17,20-23,30,32,41-46,59,66-67H,4,10-11,18-19,24-29,31H2,1-3H3,(H,57,73)(H,60,68)(H,61,69)(H,62,71)(H,63,72)(H,64,70)(H4,55,56,58)/t41-,42-,43-,44+,45-,46-/m0/s1
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n/an/an/a 6.61n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405784
PNG
(CHEMBL415109)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](COCc1ccccc1)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C59H74N10O9/c1-4-62-57(76)51-25-15-31-69(51)58(77)46(24-14-30-63-59(60)61)65-53(72)47(32-38(2)3)66-54(73)48(33-39-16-7-5-8-17-39)67-55(74)49(34-40-26-28-44(70)29-27-40)68-56(75)50(37-78-36-41-18-9-6-10-19-41)64-52(71)35-43-22-13-21-42-20-11-12-23-45(42)43/h5-13,16-23,26-29,38,46-51,70H,4,14-15,24-25,30-37H2,1-3H3,(H,62,76)(H,64,71)(H,65,72)(H,66,73)(H,67,74)(H,68,75)(H4,60,61,63)/t46-,47-,48+,49-,50-,51?/m0/s1
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n/an/an/a 10.5n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405785
PNG
(CHEMBL275709)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)Cc1cccc2ccccc12
Show InChI InChI=1S/C56H70N10O9/c1-4-59-54(74)48-19-11-27-66(48)55(75)43(18-10-26-60-56(57)58)62-50(70)44(28-34(2)3)63-52(72)46(31-36-20-23-37-12-5-6-14-39(37)29-36)64-51(71)45(30-35-21-24-41(68)25-22-35)65-53(73)47(33-67)61-49(69)32-40-16-9-15-38-13-7-8-17-42(38)40/h5-9,12-17,20-25,29,34,43-48,67-68H,4,10-11,18-19,26-28,30-33H2,1-3H3,(H,59,74)(H,61,69)(H,62,70)(H,63,72)(H,64,71)(H,65,73)(H4,57,58,60)/t43-,44-,45-,46+,47-,48?/m0/s1
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n/an/an/a 6.31n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405786
PNG
(CHEMBL429543)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1c[nH]c2ccccc12
Show InChI InChI=1S/C55H71N11O9/c1-4-58-53(74)47-16-10-26-66(47)54(75)42(15-9-25-59-55(56)57)62-49(70)43(27-33(2)3)63-51(72)45(30-35-17-20-36-11-5-6-12-37(36)28-35)64-50(71)44(29-34-18-22-39(68)23-19-34)65-52(73)46(32-67)61-48(69)24-21-38-31-60-41-14-8-7-13-40(38)41/h5-8,11-14,17-20,22-23,28,31,33,42-47,60,67-68H,4,9-10,15-16,21,24-27,29-30,32H2,1-3H3,(H,58,74)(H,61,69)(H,62,70)(H,63,72)(H,64,71)(H,65,73)(H4,56,57,59)/t42-,43-,44-,45+,46-,47?/m0/s1
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n/an/an/a 25.1n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405787
PNG
(CHEMBL2369808)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC1CCCCC1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1c[nH]c2ccccc12
Show InChI InChI=1S/C51H75N11O9/c1-4-54-49(70)43-17-11-25-62(43)50(71)38(16-10-24-55-51(52)53)58-45(66)39(26-31(2)3)59-46(67)40(27-32-12-6-5-7-13-32)60-47(68)41(28-33-18-21-35(64)22-19-33)61-48(69)42(30-63)57-44(65)23-20-34-29-56-37-15-9-8-14-36(34)37/h8-9,14-15,18-19,21-22,29,31-32,38-43,56,63-64H,4-7,10-13,16-17,20,23-28,30H2,1-3H3,(H,54,70)(H,57,65)(H,58,66)(H,59,67)(H,60,68)(H,61,69)(H4,52,53,55)/t38-,39-,40+,41-,42-,43-/m0/s1
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n/an/an/a 363n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Rattus norvegicus)
BDBM50405789
PNG
(CHEMBL412984)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(C)=O)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](C)C(N)=O
Show InChI InChI=1S/C69H92Cl2N18O13/c1-37(2)30-51(60(95)83-50(13-8-28-78-69(75)76)67(102)89-29-9-14-57(89)66(101)80-38(3)58(72)93)84-59(94)49(12-7-27-77-68(73)74)82-62(97)53(33-42-19-25-46(92)26-20-42)86-65(100)56(36-90)88-64(99)55(34-43-35-79-48-11-6-5-10-47(43)48)87-63(98)54(32-41-17-23-45(71)24-18-41)85-61(96)52(81-39(4)91)31-40-15-21-44(70)22-16-40/h5-6,10-11,15-26,35,37-38,49-57,79,90,92H,7-9,12-14,27-34,36H2,1-4H3,(H2,72,93)(H,80,101)(H,81,91)(H,82,97)(H,83,95)(H,84,94)(H,85,96)(H,86,100)(H,87,98)(H,88,99)(H4,73,74,77)(H4,75,76,78)/t38-,49-,50-,51+,52-,53+,54-,55-,56+,57-/m1/s1
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n/an/an/a 0.363n/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vivo inhibition of leutenising hormone in rats.


J Med Chem 32: 2340-4 (1989)

More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206403
PNG
(CHEMBL269261 | N-((S)-1-amino-3-(4-tert-butoxyphen...)
Show SMILES CC(C)(C)Oc1ccc(C[C@H](NC(=O)CCCCNc2cc(nn2-c2ccc(cc2)C(C)(C)C)-c2cccnc2)C(N)=O)cc1
Show InChI InChI=1S/C36H46N6O3/c1-35(2,3)27-14-16-28(17-15-27)42-32(23-30(41-42)26-10-9-20-38-24-26)39-21-8-7-11-33(43)40-31(34(37)44)22-25-12-18-29(19-13-25)45-36(4,5)6/h9-10,12-20,23-24,31,39H,7-8,11,21-22H2,1-6H3,(H2,37,44)(H,40,43)/t31-/m0/s1
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n/an/an/an/a 1.21E+4n/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO cells assessed as production of cAMP after 60 mins by SPA


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206404
PNG
((S)-N-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-y...)
Show SMILES CC(C)(C)c1ccc(cc1)-n1nc(cc1NCCCC(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O)-c1ccncc1
Show InChI InChI=1S/C31H36N6O3/c1-31(2,3)23-8-10-24(11-9-23)37-28(20-26(36-37)22-14-17-33-18-15-22)34-16-4-5-29(39)35-27(30(32)40)19-21-6-12-25(38)13-7-21/h6-15,17-18,20,27,34,38H,4-5,16,19H2,1-3H3,(H2,32,40)(H,35,39)/t27-/m0/s1
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n/an/an/an/a>1.00E+5n/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO cells assessed as production of cAMP after 60 mins by SPA


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206400
PNG
(CHEMBL247945 | N-((S)-1-amino-3-(4-hydroxyphenyl)-...)
Show SMILES CC(C)(C)c1ccc(cc1)-n1nc(cc1-c1cccc(c1)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O)-c1cc2ccccc2cn1
Show InChI InChI=1S/C38H35N5O3/c1-38(2,3)29-13-15-30(16-14-29)43-35(22-33(42-43)32-21-25-7-4-5-8-28(25)23-40-32)26-9-6-10-27(20-26)37(46)41-34(36(39)45)19-24-11-17-31(44)18-12-24/h4-18,20-23,34,44H,19H2,1-3H3,(H2,39,45)(H,41,46)/t34-/m0/s1
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n/an/an/an/a 500n/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO cells assessed as production of cAMP after 60 mins by SPA


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206405
PNG
((S)-N-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-y...)
Show SMILES CC(C)(C)c1ccc(cc1)-n1nc(CCCCC(=O)N[C@@H](Cc2ccc(O)cc2)C(N)=O)cc1-c1ccncc1
Show InChI InChI=1S/C32H37N5O3/c1-32(2,3)24-10-12-26(13-11-24)37-29(23-16-18-34-19-17-23)21-25(36-37)6-4-5-7-30(39)35-28(31(33)40)20-22-8-14-27(38)15-9-22/h8-19,21,28,38H,4-7,20H2,1-3H3,(H2,33,40)(H,35,39)/t28-/m0/s1
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n/an/an/an/a 2.30E+3n/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO cells assessed as production of cAMP after 60 mins by SPA


Citation and Details
More data for this
Ligand-Target Pair
Luteinizing hormone/Choriogonadotropin receptor


(Homo sapiens)
BDBM50206398
PNG
(CHEMBL429108 | N-(4-hydroxyphenethyl)-5-(1-(4-tert...)
Show SMILES CC(C)(C)c1ccc(cc1)-n1nc(cc1CCCCC(=O)NCCc1ccc(O)cc1)-c1cccnc1
Show InChI InChI=1S/C31H36N4O2/c1-31(2,3)25-12-14-26(15-13-25)35-27(21-29(34-35)24-7-6-19-32-22-24)8-4-5-9-30(37)33-20-18-23-10-16-28(36)17-11-23/h6-7,10-17,19,21-22,36H,4-5,8-9,18,20H2,1-3H3,(H,33,37)
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n/an/an/an/a 80n/an/an/an/a



Merck Serono Geneva Research Center

Curated by ChEMBL


Assay Description
Agonist activity at human LH receptor expressed in CHO cells assessed as production of cAMP after 60 mins by SPA


Citation and Details
More data for this
Ligand-Target Pair
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