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14 similar compounds to monomer 50180268

Compile data set for download or QSAR
Wt: 516.6
BDBM50215034
Wt: 154.2
BDBM36265
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Wt: 154.2
BDBM36266
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Wt: 114.1
BDBM36189
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Wt: 114.1
BDBM36190
Purchase
Wt: 114.1
BDBM36191
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Wt: 196.3
BDBM50003030
Wt: 428.7
BDBM50247109
Wt: 156.2
BDBM50318482
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Wt: 498.3
BDBM50154288
Wt: 437.4
BDBM50154290
Wt: 494.5
BDBM50180270
Wt: 318.4
BDBM50245994
Wt: 336.4
BDBM50245995

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 22 hits for monomerid = 50215034,36265,36266,36189,36190,36191,50003030,50247109,50318482,50154288,50154290,50180270,50245994,50245995   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
D(3) dopamine receptor


(Homo sapiens (Human))
BDBM50215034
PNG
(CHEMBL433552)
Show SMILES COc1ccc(cc1-c1ccc(CN2CCCCCC2c2ccccc2)[nH]1)S(=O)(=O)Oc1ccccc1
Show InChI InChI=1S/C30H32N2O4S/c1-35-30-19-17-26(37(33,34)36-25-13-7-3-8-14-25)21-27(30)28-18-16-24(31-28)22-32-20-10-4-9-15-29(32)23-11-5-2-6-12-23/h2-3,5-8,11-14,16-19,21,29,31H,4,9-10,15,20,22H2,1H3
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10n/an/an/an/an/an/an/an/a


TBA

Assay Description
Ability to displace [125I]-sulpiride from human Dopamine receptor D3, expressed in CHO cells


Citation and Details

BindingDB Entry DOI: 10.7270/Q26112HR
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM36190
PNG
((+/-)-cis-2-methylcyclohexanol)
Show SMILES C[C@H]1CCCC[C@H]1O
Show InChI InChI=1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3/t6-,7+/m0/s1
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340n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 2 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
D(2) dopamine receptor


(Homo sapiens (Human))
BDBM50215034
PNG
(CHEMBL433552)
Show SMILES COc1ccc(cc1-c1ccc(CN2CCCCCC2c2ccccc2)[nH]1)S(=O)(=O)Oc1ccccc1
Show InChI InChI=1S/C30H32N2O4S/c1-35-30-19-17-26(37(33,34)36-25-13-7-3-8-14-25)21-27(30)28-18-16-24(31-28)22-32-20-10-4-9-15-29(32)23-11-5-2-6-12-23/h2-3,5-8,11-14,16-19,21,29,31H,4,9-10,15,20,22H2,1H3
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1.00E+3n/an/an/an/an/an/an/an/a


TBA

Assay Description
Ability to displace [125I]sulpiride from human Dopamine receptor D2, expressed in CHO cells


Citation and Details

BindingDB Entry DOI: 10.7270/Q26112HR
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM36190
PNG
((+/-)-cis-2-methylcyclohexanol)
Show SMILES C[C@H]1CCCC[C@H]1O
Show InChI InChI=1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3/t6-,7+/m0/s1
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7.56E+3n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 1 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM36190
PNG
((+/-)-cis-2-methylcyclohexanol)
Show SMILES C[C@H]1CCCC[C@H]1O
Show InChI InChI=1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3/t6-,7+/m0/s1
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8.43E+3n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 4 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Carbonic anhydrase 6 (CA-VI)


(Homo sapiens (Human))
BDBM36190
PNG
((+/-)-cis-2-methylcyclohexanol)
Show SMILES C[C@H]1CCCC[C@H]1O
Show InChI InChI=1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3/t6-,7+/m0/s1
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4.02E+5n/an/an/an/an/an/an/an/a



Artvin£oruh University

Curated by ChEMBL


Assay Description
Inhibition of human carbonic anhydrase 6 esterase activity using 4-nitrophenylacetate as substrate


Bioorg Med Chem Lett 22: 1352-7 (2012)


Article DOI: 10.1016/j.bmcl.2011.12.069
BindingDB Entry DOI: 10.7270/Q2WH2QF4
More data for this
Ligand-Target Pair
Transient receptor potential M8 protein (TRPM8)


(Rattus norvegicus (Rat))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/an/a 7.50E+4n/an/an/an/a



University of Salerno

Curated by ChEMBL


Assay Description
Agonist activity at rat TRPM8 expressed in HEK293 cells assessed as increase in current amplitude at +80 mV holding potential by whole cell patch-cla...


J Med Chem 59: 2179-91 (2016)


Article DOI: 10.1021/acs.jmedchem.5b01914
BindingDB Entry DOI: 10.7270/Q2B85B1Z
More data for this
Ligand-Target Pair
cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A


(Homo sapiens (Human))
BDBM50180270
PNG
(CHEMBL3815110)
Show SMILES Cn1c(CCCCOc2cn(CC3CC3)nc(-c3ccnn3-c3ccccc3)c2=O)nc2ccccc12
Show InChI InChI=1S/C29H30N6O2/c1-33-24-12-6-5-11-23(24)31-27(33)13-7-8-18-37-26-20-34(19-21-14-15-21)32-28(29(26)36)25-16-17-30-35(25)22-9-3-2-4-10-22/h2-6,9-12,16-17,20-21H,7-8,13-15,18-19H2,1H3
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n/an/a 760n/an/an/an/an/an/a



Takeda Pharmaceutical Company Limited

Curated by ChEMBL


Assay Description
Inhibition of human full length PDE10A2 expressed in African green monkey COS7 cells using [3H]cGMP as substrate preincubated for 30 mins followed by...


Bioorg Med Chem 24: 3447-55 (2016)


Article DOI: 10.1016/j.bmc.2016.05.049
BindingDB Entry DOI: 10.7270/Q2H9974G
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily M member 8 (TRPM8)


(Homo sapiens (Human))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/an/a 3.00E+3n/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of human TRPM8 (unknown origin) expressed in HEK293 cells assessed as inhibition of WS12-induced Ca2+ elevation by FLIPR assay


Bioorg Med Chem Lett 23: 6118-22 (2013)


Article DOI: 10.1016/j.bmcl.2013.09.016
BindingDB Entry DOI: 10.7270/Q2125V4N
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily A member 1


(Homo sapiens (Human))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/an/a 2.84E+4n/an/an/an/a



Ferrara University

Curated by ChEMBL


Assay Description
Activation of TRPA1 channel


J Med Chem 53: 5085-107 (2010)


Article DOI: 10.1021/jm100062h
BindingDB Entry DOI: 10.7270/Q2416Z02
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily A member 1


(Mus musculus)
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/an/a 5.60E+4n/an/an/an/a



Ferrara University

Curated by ChEMBL


Assay Description
Antagonist activity at mouse TRPA1 channel expressed in CHO cells assessed as blockade of agonist-induced whole cell conductance by electrophysiology


J Med Chem 53: 5085-107 (2010)


Article DOI: 10.1021/jm100062h
BindingDB Entry DOI: 10.7270/Q2416Z02
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily M member 8 (TRPM8)


(Homo sapiens (Human))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/a 9.20E+4n/an/an/an/an/an/a



KU Leuven

Curated by ChEMBL


Assay Description
Displacement of [3H]menthol from human TRPM8 expressed in HEK293 cell membranes by scintillation counting


Nat Chem Biol 3: 174-82 (2007)


Article DOI: 10.1038/nchembio862
BindingDB Entry DOI: 10.7270/Q2057G4K
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily M member 8 (TRPM8)


(Homo sapiens (Human))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/a 1.44E+4n/an/an/an/an/a



KU Leuven

Curated by ChEMBL


Assay Description
Binding affinity to human TRPM8 expressed in HEK293 cell membranes


Nat Chem Biol 3: 174-82 (2007)


Article DOI: 10.1038/nchembio862
BindingDB Entry DOI: 10.7270/Q2057G4K
More data for this
Ligand-Target Pair
Transient receptor potential cation channel subfamily M member 8 (TRPM8)


(Homo sapiens (Human))
BDBM50318482
PNG
((-)-menthol | CHEMBL470670 | MENTHOL | l-menthol)
Show SMILES CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O
Show InChI InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)6-10(9)11/h7-11H,4-6H2,1-3H3/t8-,9+,10-/m1/s1
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n/an/an/an/a 2.90E+4n/an/an/an/a



KU Leuven

Curated by ChEMBL


Assay Description
Activity at human TRPM8 expressed in HEK293 cells assessed as compound concentration causing leftward shift of voltage for half maximal activation


Nat Chem Biol 3: 174-82 (2007)


Article DOI: 10.1038/nchembio862
BindingDB Entry DOI: 10.7270/Q2057G4K
More data for this
Ligand-Target Pair
Protein arginine N-methyltransferase 1


(Rattus norvegicus)
BDBM50245994
PNG
(CHEMBL4105514)
Show SMILES CN(C)CCNC(=O)c1ccccc1Sc1ccccc1F
Show InChI InChI=1S/C17H19FN2OS/c1-20(2)12-11-19-17(21)13-7-3-5-9-15(13)22-16-10-6-4-8-14(16)18/h3-10H,11-12H2,1-2H3,(H,19,21)
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n/an/a>2.00E+5n/an/an/an/an/an/a



Zhejiang Sci-Tech University

Curated by ChEMBL


Assay Description
Inhibition of rat His-tagged PRMT1 (11 to 353 residues) expressed in Escherichia coli BL21(DE3) using biotinylated H4 peptide (1 to 21 residues) as s...


J Med Chem 60: 8888-8905 (2017)


Article DOI: 10.1021/acs.jmedchem.7b01134
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50154290
PNG
(CHEMBL3775285)
Show SMILES Fc1cccc(Nc2ncnc3cc4OCC(=O)N(CCCN5CCOCC5)c4cc23)c1
Show InChI InChI=1S/C23H24FN5O3/c24-16-3-1-4-17(11-16)27-23-18-12-20-21(13-19(18)25-15-26-23)32-14-22(30)29(20)6-2-5-28-7-9-31-10-8-28/h1,3-4,11-13,15H,2,5-10,14H2,(H,25,26,27)
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n/an/a 245n/an/an/an/an/an/a



Beijing University of Technology

Curated by ChEMBL


Assay Description
Inhibition of wildtype EGFR (unknown origin) preincubated for 30 mins followed by addition of 2x ATP-substrate mixture measured after 1 hr by Kinase ...


Bioorg Med Chem Lett 26: 1571-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.02.009
BindingDB Entry DOI: 10.7270/Q20G3N1W
More data for this
Ligand-Target Pair
Epidermal growth factor receptor


(Homo sapiens (Human))
BDBM50154288
PNG
(CHEMBL3774906)
Show SMILES Brc1cccc(Nc2ncnc3cc4OCC(=O)N(CCCN5CCOCC5)c4cc23)c1
Show InChI InChI=1S/C23H24BrN5O3/c24-16-3-1-4-17(11-16)27-23-18-12-20-21(13-19(18)25-15-26-23)32-14-22(30)29(20)6-2-5-28-7-9-31-10-8-28/h1,3-4,11-13,15H,2,5-10,14H2,(H,25,26,27)
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n/an/a 90n/an/an/an/an/an/a



Beijing University of Technology

Curated by ChEMBL


Assay Description
Inhibition of wildtype EGFR (unknown origin) preincubated for 30 mins followed by addition of 2x ATP-substrate mixture measured after 1 hr by Kinase ...


Bioorg Med Chem Lett 26: 1571-5 (2016)


Article DOI: 10.1016/j.bmcl.2016.02.009
BindingDB Entry DOI: 10.7270/Q20G3N1W
More data for this
Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 2


(Homo sapiens (Human))
BDBM50247109
PNG
((3S,4aR,6aR,6bR,8aR,12aS,12bR,14aR,14bR)-4,4,6a,6b...)
Show SMILES CC1(C)CC[C@]2(C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1
Show InChI InChI=1S/C30H52O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h20-24,31H,9-19H2,1-8H3/t20-,21+,22+,23-,24+,27-,28+,29-,30-/m1/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of TCPTP (unknown origin) by pNPP assay


Bioorg Med Chem 16: 8697-705 (2008)


Article DOI: 10.1016/j.bmc.2008.07.080
BindingDB Entry DOI: 10.7270/Q2HX1CH7
More data for this
Ligand-Target Pair
Protein-tyrosine phosphatase 1B


(Homo sapiens (Human))
BDBM50247109
PNG
((3S,4aR,6aR,6bR,8aR,12aS,12bR,14aR,14bR)-4,4,6a,6b...)
Show SMILES CC1(C)CC[C@]2(C)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1
Show InChI InChI=1S/C30H52O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h20-24,31H,9-19H2,1-8H3/t20-,21+,22+,23-,24+,27-,28+,29-,30-/m1/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



Chinese Academy of Sciences

Curated by ChEMBL


Assay Description
Inhibition of PTP1B (unknown origin) by pNPP assay


Bioorg Med Chem 16: 8697-705 (2008)


Article DOI: 10.1016/j.bmc.2008.07.080
BindingDB Entry DOI: 10.7270/Q2HX1CH7
More data for this
Ligand-Target Pair
Protein arginine N-methyltransferase 1


(Rattus norvegicus)
BDBM50245995
PNG
(CHEMBL4078812)
Show SMILES CN(C)CCNCc1ccccc1Sc1cccc2ccccc12
Show InChI InChI=1S/C21H24N2S/c1-23(2)15-14-22-16-18-9-4-6-12-20(18)24-21-13-7-10-17-8-3-5-11-19(17)21/h3-13,22H,14-16H2,1-2H3
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UniChem

Patents


Similars

Article
PubMed
n/an/a 3.40E+4n/an/an/an/an/an/a



Zhejiang Sci-Tech University

Curated by ChEMBL


Assay Description
Inhibition of rat His-tagged PRMT1 (11 to 353 residues) expressed in Escherichia coli BL21(DE3) using biotinylated H4 peptide (1 to 21 residues) as s...


J Med Chem 60: 8888-8905 (2017)


Article DOI: 10.1021/acs.jmedchem.7b01134
More data for this
Ligand-Target Pair
Lanosterol synthase


(Rattus norvegicus)
BDBM50003030
PNG
((2S,4aS,8aR)-1,1,4a-Trimethyl-decahydro-naphthalen...)
Show SMILES CC1(C)[C@@H](O)CC[C@]2(C)CCCC[C@@H]12
Show InChI InChI=1S/C13H24O/c1-12(2)10-6-4-5-8-13(10,3)9-7-11(12)14/h10-11,14H,4-9H2,1-3H3/t10-,11-,13-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 9.00E+3n/an/an/an/an/an/a



Marion Merrell Dow Research Institute

Curated by ChEMBL


Assay Description
Inhibitory activity against Oxidosqualene-lanosterol cyclase enzyme obtained from rat liver


J Med Chem 35: 3581-3 (1992)


Article DOI: 10.1021/jm00097a017
BindingDB Entry DOI: 10.7270/Q24T6H9N
More data for this
Ligand-Target Pair
Lanosterol synthase


(Rattus norvegicus)
BDBM50003030
PNG
((2S,4aS,8aR)-1,1,4a-Trimethyl-decahydro-naphthalen...)
Show SMILES CC1(C)[C@@H](O)CC[C@]2(C)CCCC[C@@H]12
Show InChI InChI=1S/C13H24O/c1-12(2)10-6-4-5-8-13(10,3)9-7-11(12)14/h10-11,14H,4-9H2,1-3H3/t10-,11-,13-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>2.50E+4n/an/an/an/an/an/a



Laboratoires Fournier SCA

Curated by ChEMBL


Assay Description
Inhibitory activity against Oxidosqualene-lanosterol cyclase from Rat liver microsomes


J Med Chem 39: 2302-12 (1996)


Article DOI: 10.1021/jm9504621
BindingDB Entry DOI: 10.7270/Q28G8JTB
More data for this
Ligand-Target Pair

Activity Spreadsheet -- ITC Data from BindingDB

Found 17 hits for monomerid = 50215034,36265,36266,36189,36190,36191,50003030,50247109,50318482,50154288,50154290,50180270,50245994,50245995
Cell (A)Syringe (B)Cell
Links
Syringe
Links
Cell + Syr
Links
ΔG°
kcal/mole
-TΔS°
kcal/mole
ΔH°
kcal/mole
log KpHTemp
°C
BDBM11
JPEG
BDBM36189
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
CHEBI
PC cid
PC sid
-4.17-1.89-2.293.066.9025



NIST





J Phys Chem B 101: 87-100 (1997)

BDBM11
JPEG
BDBM36190
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
CHEBI
PC cid
PC sid
-4.08-1.71-2.372.996.9025



NIST





J Phys Chem B 101: 87-100 (1997)

BDBM11
JPEG
BDBM36191
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
CHEBI
PC cid
PC sid
-3.91-1.84-2.072.876.9025



NIST





J Phys Chem B 101: 87-100 (1997)

BDBM36271
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.99-2.46-4.525.137.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36271
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.75-1.37-5.384.957.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36272
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.71-0.919-5.794.927.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36272
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.77-1.41-5.364.967.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM11
JPEG
BDBM36265
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-5.82-0.840-4.984.277.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM11
JPEG
BDBM36266
JPEG
CHEBI
KEGG
MMDB
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-5.86-0.320-5.534.307.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36267
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.20-1.58-4.614.557.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36267
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.15-1.62-4.534.517.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36268
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.29-1.46-4.834.617.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36268
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.35-0.961-5.394.667.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36269
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.85-2.82-4.045.037.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36269
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.39-0.897-5.494.707.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36270
JPEG
BDBM36265
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.73-1.01-5.734.947.2025



Nankai University





J Org Chem 69: 173-80 (2004)

BDBM36270
JPEG
BDBM36266
JPEG
PC cid
PC sid
CHEBI
KEGG
PC cid
PC sid
-6.77-1.50-5.284.977.2025



Nankai University





J Org Chem 69: 173-80 (2004)