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BDBM50248211 CHEMBL526305::N-cyclopropyl-N-((1s,4R)-4-cyclopropyl-4-hydroxycyclohexyl)-4-((S)-1,1,1-trifluoro-2-hydroxypropan-2-yl)benzamide::N-cyclopropyl-N-(cis-4-cyclopropyl-4-hydroxycyclohexyl)-4-[(1S)-2,2,2-trifluoro-1-hydroxy-1-methylethyl]benzamide

SMILES: C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F

InChI Key: InChIKey=SWXZIRVTPISJMP-SESVDKBCSA-N

Data: 8 IC50

PDB links: 1 PDB ID matches this monomer.

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50248211   
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
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 52n/an/an/an/an/an/a



Amgen Inc

Curated by ChEMBL


Assay Description
Inhibition of human recombinant full length 11beta-HSD1 expressed in HEK293 cells assessed as inhibition of conversion of [3H]cortisone to [3H]cortis...


Bioorg Med Chem Lett 21: 405-10 (2010)


Article DOI: 10.1016/j.bmcl.2010.10.129
BindingDB Entry DOI: 10.7270/Q2K937SB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 121n/an/an/an/an/an/a



Amgen Inc

Curated by ChEMBL


Assay Description
Inhibition of human recombinant full length 11beta-HSD1 expressed in HEK293 cells assessed as inhibition of conversion of [3H]cortisone to [3H]cortis...


Bioorg Med Chem Lett 21: 405-10 (2010)


Article DOI: 10.1016/j.bmcl.2010.10.129
BindingDB Entry DOI: 10.7270/Q2K937SB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 50n/an/an/an/an/an/a



Amgen Inc

Curated by ChEMBL


Assay Description
Inhibition of human recombinant full length 11beta-HSD1 expressed in human adipocytes assessed as inhibition of conversion of [3H]cortisone to [3H]co...


Bioorg Med Chem Lett 21: 405-10 (2010)


Article DOI: 10.1016/j.bmcl.2010.10.129
BindingDB Entry DOI: 10.7270/Q2K937SB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-Hydroxysteroid Dehydrogenase 1 (11-beta-HSD1)


(Rattus norvegicus (rat))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 244n/an/an/an/an/an/a



Amgen, Inc.

Curated by ChEMBL


Assay Description
Inhibition of rat 11beta-HSD1


Bioorg Med Chem Lett 19: 1446-50 (2009)


Article DOI: 10.1016/j.bmcl.2009.01.026
BindingDB Entry DOI: 10.7270/Q2TD9Z8S
More data for this
Ligand-Target Pair
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 14n/an/an/an/an/an/a



Amgen, Inc.

Curated by ChEMBL


Assay Description
Inhibition of FLAG-tagged full length human 11beta-HSD1 expressed in baculovirus-infected Trichoplusia ni Hi5 cells assessed as reduction of [3H]cort...


Bioorg Med Chem Lett 19: 1446-50 (2009)


Article DOI: 10.1016/j.bmcl.2009.01.026
BindingDB Entry DOI: 10.7270/Q2TD9Z8S
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 52n/an/an/an/an/an/a



Amgen, Inc.

Curated by ChEMBL


Assay Description
Inhibition of full length human recombinant 11beta-HSD1 expressed in HEK293 cells in absence of NADPH


Bioorg Med Chem Lett 19: 1446-50 (2009)


Article DOI: 10.1016/j.bmcl.2009.01.026
BindingDB Entry DOI: 10.7270/Q2TD9Z8S
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 121n/an/an/an/an/an/a



Amgen, Inc.

Curated by ChEMBL


Assay Description
Inhibition of full length human recombinant 11beta-HSD1 expressed in HEK293 cells in presence of 3% human serum albumin


Bioorg Med Chem Lett 19: 1446-50 (2009)


Article DOI: 10.1016/j.bmcl.2009.01.026
BindingDB Entry DOI: 10.7270/Q2TD9Z8S
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
11-beta-hydroxysteroid dehydrogenase 1


(Homo sapiens (Human))
BDBM50248211
PNG
(CHEMBL526305 | N-cyclopropyl-N-((1s,4R)-4-cyclopro...)
Show SMILES C[C@](O)(c1ccc(cc1)C(=O)N(C1CC1)[C@H]1CC[C@@](O)(CC1)C1CC1)C(F)(F)F |r,wU:1.2,15.16,18.20,wD:1.1,(8.96,-18.52,;9.72,-17.18,;10.49,-15.85,;11.06,-17.95,;11.06,-19.5,;12.39,-20.27,;13.73,-19.49,;13.72,-17.94,;12.39,-17.18,;15.06,-20.26,;15.06,-21.8,;16.39,-19.49,;16.39,-17.95,;17.16,-16.62,;15.62,-16.62,;17.73,-20.26,;19.05,-19.49,;20.39,-20.26,;20.39,-21.81,;21.72,-21.02,;19.05,-22.57,;17.72,-21.8,;21.72,-22.58,;22.49,-23.91,;23.26,-22.57,;8.38,-16.41,;7.05,-15.64,;7.62,-17.75,;9.15,-15.08,)|
Show InChI InChI=1S/C22H28F3NO3/c1-20(28,22(23,24)25)15-4-2-14(3-5-15)19(27)26(17-8-9-17)18-10-12-21(29,13-11-18)16-6-7-16/h2-5,16-18,28-29H,6-13H2,1H3/t18-,20-,21+/m0/s1
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n/an/a 14n/an/an/an/an/an/a



Amgen Inc

Curated by ChEMBL


Assay Description
Inhibition of human full length 11beta-HSD1 assessed as inhibition of conversion of [3H]cortisone to [3H]cortisol by scintillation proximity assay


Bioorg Med Chem Lett 21: 405-10 (2010)


Article DOI: 10.1016/j.bmcl.2010.10.129
BindingDB Entry DOI: 10.7270/Q2K937SB
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)