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Compile Data Set for Download or QSAR

Found 1464 hits with Last Name = 'patel' and Initial = 'p'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
SSTR5


(RAT)
BDBM85009
PNG
(H2N-4-NO2-Phe-c[Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr-Nh2)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34-,36-,37-,38+,39-,40+,41+,42+/m0/s1
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0.100n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR3


(RAT)
BDBM50019568
PNG
(Ala-Gly-c(Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-...)
Show SMILES C[C@@H](O)[C@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CSSC[C@H](NC(=O)[C@H](CO)NC1=O)C(O)=O)NC(=O)CNC(=O)[C@H](C)N)[C@@H](C)O
Show InChI InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50+,51-,52+,53-,54-,55+,56-,57-,58+,59-,62+,63+/m0/s1
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0.100n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM85011
PNG
(AcNH-4-NO2-Phe-c[Cys-Tyr-D-Trp-Lys-Thr-Cys]-Tyr-NH...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](Cc1ccc(cc1)[N+]([O-])=O)NC(C)=O
Show InChI InChI=1S/C52H68N12O13S2/c1-27(2)43-52(75)61-42(51(74)63-44(28(3)65)45(54)68)26-79-78-25-41(60-47(70)38(56-29(4)66)21-30-12-16-33(17-13-30)64(76)77)50(73)58-39(22-31-14-18-34(67)19-15-31)48(71)59-40(23-32-24-55-36-10-6-5-9-35(32)36)49(72)57-37(46(69)62-43)11-7-8-20-53/h5-6,9-10,12-19,24,27-28,37-44,55,65,67H,7-8,11,20-23,25-26,53H2,1-4H3,(H2,54,68)(H,56,66)(H,57,72)(H,58,73)(H,59,71)(H,60,70)(H,61,75)(H,62,69)(H,63,74)/t28-,37-,38+,39-,40+,41-,42+,43+,44+/m0/s1
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0.100n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR1


(RAT)
BDBM50019568
PNG
(Ala-Gly-c(Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-...)
Show SMILES C[C@@H](O)[C@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CSSC[C@H](NC(=O)[C@H](CO)NC1=O)C(O)=O)NC(=O)CNC(=O)[C@H](C)N)[C@@H](C)O
Show InChI InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50+,51-,52+,53-,54-,55+,56-,57-,58+,59-,62+,63+/m0/s1
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0.200n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM50019568
PNG
(Ala-Gly-c(Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-...)
Show SMILES C[C@@H](O)[C@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CSSC[C@H](NC(=O)[C@H](CO)NC1=O)C(O)=O)NC(=O)CNC(=O)[C@H](C)N)[C@@H](C)O
Show InChI InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50+,51-,52+,53-,54-,55+,56-,57-,58+,59-,62+,63+/m0/s1
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0.200n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM85009
PNG
(H2N-4-NO2-Phe-c[Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr-Nh2)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34-,36-,37-,38+,39-,40+,41+,42+/m0/s1
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0.200n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM85012
PNG
(AcNH-4-NO2-Phe-c[D-Cys-Tyr-D-Trp-Lys-Thr-Cys]-Tyr-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](Cc1ccc(cc1)[N+]([O-])=O)NC(C)=O
Show InChI InChI=1S/C52H68N12O13S2/c1-27(2)43-52(75)61-42(51(74)63-44(28(3)65)45(54)68)26-79-78-25-41(60-47(70)38(56-29(4)66)21-30-12-16-33(17-13-30)64(76)77)50(73)58-39(22-31-14-18-34(67)19-15-31)48(71)59-40(23-32-24-55-36-10-6-5-9-35(32)36)49(72)57-37(46(69)62-43)11-7-8-20-53/h5-6,9-10,12-19,24,27-28,37-44,55,65,67H,7-8,11,20-23,25-26,53H2,1-4H3,(H2,54,68)(H,56,66)(H,57,72)(H,58,73)(H,59,71)(H,60,70)(H,61,75)(H,62,69)(H,63,74)/t28-,37-,38+,39-,40+,41+,42+,43+,44+/m0/s1
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0.300n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR5


(RAT)
BDBM85009
PNG
(H2N-4-NO2-Phe-c[Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr-Nh2)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34-,36-,37-,38+,39-,40+,41+,42+/m0/s1
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0.420n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534464
PNG
(CHEMBL4483714)
Show SMILES CCc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C28H29NO/c1-2-21-11-12-22(26-8-4-3-7-25(21)26)19-24-20-23(27-9-5-6-10-28(24)27)13-14-29-15-17-30-18-16-29/h3-12,19-20H,2,13-18H2,1H3/b24-19+
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0.790n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534464
PNG
(CHEMBL4483714)
Show SMILES CCc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C28H29NO/c1-2-21-11-12-22(26-8-4-3-7-25(21)26)19-24-20-23(27-9-5-6-10-28(24)27)13-14-29-15-17-30-18-16-29/h3-12,19-20H,2,13-18H2,1H3/b24-19+
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0.859n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534476
PNG
(CHEMBL4443660)
Show SMILES CCCc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C29H31NO/c1-2-7-22-12-13-23(27-9-4-3-8-26(22)27)20-25-21-24(28-10-5-6-11-29(25)28)14-15-30-16-18-31-19-17-30/h3-6,8-13,20-21H,2,7,14-19H2,1H3/b25-20+
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1n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50392592
PNG
(CHEMBL2153381)
Show SMILES CCN(CC)CC(=O)NS(=C)(=O)c1ccc(cc1)C(=O)Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Show InChI InChI=1S/C26H27Cl2N5O4S/c1-4-33(5-2)16-24(34)32-38(3,37)20-10-6-17(7-11-20)25(35)30-22-12-8-18(27)14-21(22)26(36)31-23-13-9-19(28)15-29-23/h6-15H,3-5,16H2,1-2H3,(H,30,35)(H,29,31,36)(H,32,34,37)
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1.10n/an/an/an/an/an/an/an/a



Zydus Research Centre

Curated by ChEMBL


Assay Description
Inhibition of F10a assessed as S-2765 substrate hydrolysis by microplate reader analysis


Eur J Med Chem 58: 136-52 (2012)


Article DOI: 10.1016/j.ejmech.2012.10.005
BindingDB Entry DOI: 10.7270/Q2571D4Q
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534476
PNG
(CHEMBL4443660)
Show SMILES CCCc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C29H31NO/c1-2-7-22-12-13-23(27-9-4-3-8-26(22)27)20-25-21-24(28-10-5-6-11-29(25)28)14-15-30-16-18-31-19-17-30/h3-6,8-13,20-21H,2,7,14-19H2,1H3/b25-20+
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1.20n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Coagulation factor X


(Homo sapiens (Human))
BDBM50392589
PNG
(CHEMBL2153377)
Show SMILES CCN=CC(=O)N=S(C)(=O)c1ccc(cc1)C(=O)Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Show InChI InChI=1S/C24H23Cl2N5O4S/c1-3-27-14-22(32)31-36(2,35)18-8-4-15(5-9-18)23(33)29-20-10-6-16(25)12-19(20)24(34)30-21-11-7-17(26)13-28-21/h4-14,36H,3H2,1-2H3,(H,29,33)(H,28,30,34)(H,31,32,35)
PDB
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1.5n/an/an/an/an/an/an/an/a



Zydus Research Centre

Curated by ChEMBL


Assay Description
Inhibition of F10a assessed as S-2765 substrate hydrolysis by microplate reader analysis


Eur J Med Chem 58: 136-52 (2012)


Article DOI: 10.1016/j.ejmech.2012.10.005
BindingDB Entry DOI: 10.7270/Q2571D4Q
More data for this
Ligand-Target Pair
SSTR5


(RAT)
BDBM85011
PNG
(AcNH-4-NO2-Phe-c[Cys-Tyr-D-Trp-Lys-Thr-Cys]-Tyr-NH...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](Cc1ccc(cc1)[N+]([O-])=O)NC(C)=O
Show InChI InChI=1S/C52H68N12O13S2/c1-27(2)43-52(75)61-42(51(74)63-44(28(3)65)45(54)68)26-79-78-25-41(60-47(70)38(56-29(4)66)21-30-12-16-33(17-13-30)64(76)77)50(73)58-39(22-31-14-18-34(67)19-15-31)48(71)59-40(23-32-24-55-36-10-6-5-9-35(32)36)49(72)57-37(46(69)62-43)11-7-8-20-53/h5-6,9-10,12-19,24,27-28,37-44,55,65,67H,7-8,11,20-23,25-26,53H2,1-4H3,(H2,54,68)(H,56,66)(H,57,72)(H,58,73)(H,59,71)(H,60,70)(H,61,75)(H,62,69)(H,63,74)/t28-,37-,38+,39-,40+,41-,42+,43+,44+/m0/s1
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2.20n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50212395
PNG
(CHEMBL123515)
Show SMILES COc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C27H27NO2/c1-29-27-11-10-20(24-7-4-5-9-26(24)27)18-22-19-21(23-6-2-3-8-25(22)23)12-13-28-14-16-30-17-15-28/h2-11,18-19H,12-17H2,1H3/b22-18+
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2.40n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534485
PNG
(CHEMBL4435655)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2ccc(F)cc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-14-26-16-22(20-13-12-18(25)15-23(20)26)24(27)21-11-7-9-17-8-4-5-10-19(17)21/h4-5,7-13,15-16H,2-3,6,14H2,1H3
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2.40n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
SSTR5


(RAT)
BDBM85012
PNG
(AcNH-4-NO2-Phe-c[D-Cys-Tyr-D-Trp-Lys-Thr-Cys]-Tyr-...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](Cc1ccc(cc1)[N+]([O-])=O)NC(C)=O
Show InChI InChI=1S/C52H68N12O13S2/c1-27(2)43-52(75)61-42(51(74)63-44(28(3)65)45(54)68)26-79-78-25-41(60-47(70)38(56-29(4)66)21-30-12-16-33(17-13-30)64(76)77)50(73)58-39(22-31-14-18-34(67)19-15-31)48(71)59-40(23-32-24-55-36-10-6-5-9-35(32)36)49(72)57-37(46(69)62-43)11-7-8-20-53/h5-6,9-10,12-19,24,27-28,37-44,55,65,67H,7-8,11,20-23,25-26,53H2,1-4H3,(H2,54,68)(H,56,66)(H,57,72)(H,58,73)(H,59,71)(H,60,70)(H,61,75)(H,62,69)(H,63,74)/t28-,37-,38+,39-,40+,41+,42+,43+,44+/m0/s1
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2.5n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534457
PNG
(CHEMBL4444832)
Show SMILES CCCc1ccc(C(=O)c2cn(CCCCCF)c3cccc(F)c23)c2ccccc12
Show InChI InChI=1S/C27H27F2NO/c1-2-9-19-14-15-22(21-11-5-4-10-20(19)21)27(31)23-18-30(17-7-3-6-16-28)25-13-8-12-24(29)26(23)25/h4-5,8,10-15,18H,2-3,6-7,9,16-17H2,1H3
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2.60n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534481
PNG
(CHEMBL4516360)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(F)c12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-15-26-16-21(19-12-8-14-22(25)23(19)26)24(27)20-13-7-10-17-9-4-5-11-18(17)20/h4-5,7-14,16H,2-3,6,15H2,1H3
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2.70n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50068669
PNG
(4-(2-{2-Methyl-3-[1-naphthalen-1-yl-meth-(Z)-ylide...)
Show SMILES CC1=C(CCN2CCOCC2)c2ccccc2\C1=C\c1cccc2ccccc12
Show InChI InChI=1S/C27H27NO/c1-20-23(13-14-28-15-17-29-18-16-28)25-11-4-5-12-26(25)27(20)19-22-9-6-8-21-7-2-3-10-24(21)22/h2-12,19H,13-18H2,1H3/b27-19+
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2.80n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534481
PNG
(CHEMBL4516360)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(F)c12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-15-26-16-21(19-12-8-14-22(25)23(19)26)24(27)20-13-7-10-17-9-4-5-11-18(17)20/h4-5,7-14,16H,2-3,6,15H2,1H3
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3.60n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50212395
PNG
(CHEMBL123515)
Show SMILES COc1ccc(\C=C2/C=C(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C27H27NO2/c1-29-27-11-10-20(24-7-4-5-9-26(24)27)18-22-19-21(23-6-2-3-8-25(22)23)12-13-28-14-16-30-17-15-28/h2-11,18-19H,12-17H2,1H3/b22-18+
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4.10n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534463
PNG
(CHEMBL4550629)
Show SMILES C(CC1=C\C(=C/c2ccc3CCc4cccc2c34)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C28H27NO/c1-2-6-26-24(19-23(25(26)5-1)12-13-29-14-16-30-17-15-29)18-22-11-10-21-9-8-20-4-3-7-27(22)28(20)21/h1-7,10-11,18-19H,8-9,12-17H2/b24-18+
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4.20n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50353747
PNG
(CHEMBL561013 | JWH-018)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12
Show InChI InChI=1S/C24H23NO/c1-2-3-8-16-25-17-22(20-13-6-7-15-23(20)25)24(26)21-14-9-11-18-10-4-5-12-19(18)21/h4-7,9-15,17H,2-3,8,16H2,1H3
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4.30n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534498
PNG
(CHEMBL4474739)
Show SMILES FCCCCCn1cc(C(=O)c2cccc3ccccc23)c2c(F)cccc12
Show InChI InChI=1S/C24H21F2NO/c25-14-4-1-5-15-27-16-20(23-21(26)12-7-13-22(23)27)24(28)19-11-6-9-17-8-2-3-10-18(17)19/h2-3,6-13,16H,1,4-5,14-15H2
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4.40n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50068666
PNG
(4-(2-{3-[1-Naphthalen-1-yl-meth-(E)-ylidene]-3H-in...)
Show SMILES C(CC1=C\C(=C/c2cccc3ccccc23)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C26H25NO/c1-2-9-24-20(6-1)7-5-8-21(24)18-23-19-22(25-10-3-4-11-26(23)25)12-13-27-14-16-28-17-15-27/h1-11,18-19H,12-17H2/b23-18+
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4.70n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
SSTR5


(RAT)
BDBM50019568
PNG
(Ala-Gly-c(Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-...)
Show SMILES C[C@@H](O)[C@H]1NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CSSC[C@H](NC(=O)[C@H](CO)NC1=O)C(O)=O)NC(=O)CNC(=O)[C@H](C)N)[C@@H](C)O
Show InChI InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50+,51-,52+,53-,54-,55+,56-,57-,58+,59-,62+,63+/m0/s1
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5n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50068666
PNG
(4-(2-{3-[1-Naphthalen-1-yl-meth-(E)-ylidene]-3H-in...)
Show SMILES C(CC1=C\C(=C/c2cccc3ccccc23)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C26H25NO/c1-2-9-24-20(6-1)7-5-8-21(24)18-23-19-22(25-10-3-4-11-26(23)25)12-13-27-14-16-28-17-15-27/h1-11,18-19H,12-17H2/b23-18+
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5.60n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534467
PNG
(CHEMBL4549096)
Show SMILES CCCCCn1cc(C(=O)c2ccc(C(=O)CC)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C27H27NO2/c1-3-5-10-17-28-18-24(21-13-8-9-14-25(21)28)27(30)23-16-15-22(26(29)4-2)19-11-6-7-12-20(19)23/h6-9,11-16,18H,3-5,10,17H2,1-2H3
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5.70n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534497
PNG
(CHEMBL4438072)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2c(F)cccc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-15-26-16-20(23-21(25)13-8-14-22(23)26)24(27)19-12-7-10-17-9-4-5-11-18(17)19/h4-5,7-14,16H,2-3,6,15H2,1H3
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6.5n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534480
PNG
(CHEMBL4519883)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2cc(F)ccc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-14-26-16-22(21-15-18(25)12-13-23(21)26)24(27)20-11-7-9-17-8-4-5-10-19(17)20/h4-5,7-13,15-16H,2-3,6,14H2,1H3
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9.90n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM85013
PNG
(H2N-4-NO2-Phe-c[D-Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr-N...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34-,36-,37-,38+,39+,40+,41+,42+/m0/s1
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12.9n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534463
PNG
(CHEMBL4550629)
Show SMILES C(CC1=C\C(=C/c2ccc3CCc4cccc2c34)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C28H27NO/c1-2-6-26-24(19-23(25(26)5-1)12-13-29-14-16-30-17-15-29)18-22-11-10-21-9-8-20-4-3-7-27(22)28(20)21/h1-7,10-11,18-19H,8-9,12-17H2/b24-18+
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16n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534485
PNG
(CHEMBL4435655)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2ccc(F)cc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-14-26-16-22(20-13-12-18(25)15-23(20)26)24(27)21-11-7-9-17-8-4-5-10-19(17)21/h4-5,7-13,15-16H,2-3,6,14H2,1H3
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16n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534462
PNG
(CHEMBL4452573)
Show SMILES CCCCCC1=C\C(=C/c2cccc3ccccc23)c2ccccc12
Show InChI InChI=1S/C25H24/c1-2-3-4-11-21-18-22(25-16-8-7-15-24(21)25)17-20-13-9-12-19-10-5-6-14-23(19)20/h5-10,12-18H,2-4,11H2,1H3/b22-17+
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17n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
SSTR2


(RAT)
BDBM85010
PNG
(H2N-4-NO2-D-Phe-c[D-Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34+,36-,37-,38+,39+,40+,41+,42+/m0/s1
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17.3n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
SSTR5


(RAT)
BDBM85013
PNG
(H2N-4-NO2-Phe-c[D-Cys-Tyr-D-Trp-Lys-Val-Cys]-Tyr-N...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@@H](CSSC[C@@H](NC1=O)C(=O)N[C@H]([C@H](C)O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(cc1)[N+]([O-])=O
Show InChI InChI=1S/C50H66N12O12S2/c1-26(2)41-50(72)59-40(49(71)61-42(27(3)63)43(53)65)25-76-75-24-39(58-44(66)34(52)20-28-11-15-31(16-12-28)62(73)74)48(70)56-37(21-29-13-17-32(64)18-14-29)46(68)57-38(22-30-23-54-35-9-5-4-8-33(30)35)47(69)55-36(45(67)60-41)10-6-7-19-51/h4-5,8-9,11-18,23,26-27,34,36-42,54,63-64H,6-7,10,19-22,24-25,51-52H2,1-3H3,(H2,53,65)(H,55,69)(H,56,70)(H,57,68)(H,58,66)(H,59,72)(H,60,67)(H,61,71)/t27-,34-,36-,37-,38+,39+,40+,41+,42+/m0/s1
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18.1n/an/an/an/an/an/an/an/a



Cyenamid Agricultural Research Center

Curated by PDSP Ki Database




Mol Pharmacol 50: 709-15 (1996)


BindingDB Entry DOI: 10.7270/Q2QZ28HK
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50032565
PNG
((4-Methyl-naphthalen-1-yl)-[1-(2-morpholin-4-yl-et...)
Show SMILES Cc1ccc(C(=O)c2cn(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C26H26N2O2/c1-19-10-11-23(21-7-3-2-6-20(19)21)26(29)24-18-28(25-9-5-4-8-22(24)25)13-12-27-14-16-30-17-15-27/h2-11,18H,12-17H2,1H3
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20n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534482
PNG
(CHEMBL4469157)
Show SMILES CCCCCn1cc(C(=O)c2ccc(C(=O)OC)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C26H25NO3/c1-3-4-9-16-27-17-23(20-12-7-8-13-24(20)27)25(28)21-14-15-22(26(29)30-2)19-11-6-5-10-18(19)21/h5-8,10-15,17H,3-4,9,16H2,1-2H3
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20n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534475
PNG
(CHEMBL4473031)
Show SMILES C(CC1=C\C(=C/c2cccc3ccc4ccccc4c23)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C30H27NO/c1-2-11-29-22(6-1)12-13-23-7-5-8-25(30(23)29)21-26-20-24(27-9-3-4-10-28(26)27)14-15-31-16-18-32-19-17-31/h1-13,20-21H,14-19H2/b26-21+
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23n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534461
PNG
(CHEMBL4577001)
Show SMILES C(CC1=C\C(=C/c2ccnc3ccccc23)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C25H24N2O/c1-2-6-23-21(17-19-9-11-26-25-8-4-3-7-24(19)25)18-20(22(23)5-1)10-12-27-13-15-28-16-14-27/h1-9,11,17-18H,10,12-16H2/b21-17+
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23n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534497
PNG
(CHEMBL4438072)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2c(F)cccc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-15-26-16-20(23-21(25)13-8-14-22(23)26)24(27)19-12-7-10-17-9-4-5-11-18(17)19/h4-5,7-14,16H,2-3,6,15H2,1H3
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36n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM21278
PNG
(5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl...)
Show SMILES Cc1c(nn(c1-c1ccc(Cl)cc1)-c1ccc(Cl)cc1Cl)C(=O)NN1CCCCC1
Show InChI InChI=1S/C22H21Cl3N4O/c1-14-20(22(30)27-28-11-3-2-4-12-28)26-29(19-10-9-17(24)13-18(19)25)21(14)15-5-7-16(23)8-6-15/h5-10,13H,2-4,11-12H2,1H3,(H,27,30)
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47n/an/an/an/an/an/an/an/a



Zydus Research Centre

Curated by ChEMBL


Assay Description
Displacement of [3H]CP55940 from human recombinant CB1 receptor expressed in HEK293 cells


J Med Chem 50: 5951-66 (2007)


Article DOI: 10.1021/jm061490u
BindingDB Entry DOI: 10.7270/Q2Q81CTK
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534487
PNG
(CHEMBL4459965)
Show SMILES COC(=O)c1ccc(C(=O)c2cn(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C27H26N2O4/c1-32-27(31)23-11-10-22(19-6-2-3-7-20(19)23)26(30)24-18-29(25-9-5-4-8-21(24)25)13-12-28-14-16-33-17-15-28/h2-11,18H,12-17H2,1H3
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52n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 2


(Homo sapiens (Human))
BDBM50534480
PNG
(CHEMBL4519883)
Show SMILES CCCCCn1cc(C(=O)c2cccc3ccccc23)c2cc(F)ccc12
Show InChI InChI=1S/C24H22FNO/c1-2-3-6-14-26-16-22(21-15-18(25)12-13-23(21)26)24(27)20-11-7-9-17-8-4-5-10-19(17)20/h4-5,7-13,15-16H,2-3,6,14H2,1H3
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65n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB2 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50009854
PNG
(CHEMBL13078 | [1-(2-Morpholin-4-yl-ethyl)-1H-indol...)
Show SMILES O=C(c1cn(CCN2CCOCC2)c2ccccc12)c1cccc2ccccc12
Show InChI InChI=1S/C25H24N2O2/c28-25(22-10-5-7-19-6-1-2-8-20(19)22)23-18-27(24-11-4-3-9-21(23)24)13-12-26-14-16-29-17-15-26/h1-11,18H,12-17H2
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82n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534494
PNG
(CHEMBL4574099)
Show SMILES C(CC1=C\C(=C/c2ccccc2-c2ccccc2)c2ccccc12)N1CCOCC1
Show InChI InChI=1S/C28H27NO/c1-2-8-22(9-3-1)26-11-5-4-10-23(26)20-25-21-24(27-12-6-7-13-28(25)27)14-15-29-16-18-30-19-17-29/h1-13,20-21H,14-19H2/b25-20+
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83n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50032599
PNG
((4-Methoxy-naphthalen-1-yl)-[1-(2-morpholin-4-yl-e...)
Show SMILES COc1ccc(C(=O)c2cn(CCN3CCOCC3)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C26H26N2O3/c1-30-25-11-10-22(19-6-2-3-8-21(19)25)26(29)23-18-28(24-9-5-4-7-20(23)24)13-12-27-14-16-31-17-15-27/h2-11,18H,12-17H2,1H3
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88n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
Cannabinoid receptor 1


(Homo sapiens (Human))
BDBM50534458
PNG
(CHEMBL4475213)
Show SMILES CCCCCn1cc(C(=O)c2ccc(C(N)=O)c3ccccc23)c2ccccc12
Show InChI InChI=1S/C25H24N2O2/c1-2-3-8-15-27-16-22(19-11-6-7-12-23(19)27)24(28)20-13-14-21(25(26)29)18-10-5-4-9-17(18)20/h4-7,9-14,16H,2-3,8,15H2,1H3,(H2,26,29)
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97n/an/an/an/an/an/an/an/a



Research Triangle Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-CP55940 from human CB1 receptor


J Med Chem 59: 7525-43 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00516
More data for this
Ligand-Target Pair
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