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BDBM50400168 CHEMBL2179025

SMILES: OCCNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1

InChI Key: InChIKey=RISVWPNEPKGDDF-CPAHRSPMSA-N

Data: 2 IC50

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 2 hits for monomerid = 50400168   
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))
BDBM50400168
PNG
(CHEMBL2179025)
Show SMILES OCCNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1 |r,wU:11.10,wD:18.19,TLB:19:18:11:15.14.13,10:11:21.17.18:15.14.13,10:11:13:21.18.20,THB:19:18:11.16.15:13,20:18:11:15.14.13,20:14:11:21.17.18,17:16:13:21.18.20,17:18:11.16.15:13,(2.28,-22.72,;3.61,-23.49,;3.61,-25.03,;4.95,-25.8,;6.28,-25.04,;6.28,-23.49,;7.61,-22.72,;8.95,-23.48,;10.28,-22.71,;10.27,-21.17,;11.61,-23.47,;12.95,-22.7,;12.94,-20.95,;11.9,-19.88,;12.56,-18.61,;12.58,-20.05,;13.75,-21.37,;15.16,-20.81,;15.02,-19.18,;16.55,-19.2,;13.97,-18.06,;14.24,-20.4,;8.95,-25.03,;7.61,-25.81,;10.29,-25.8,;10.45,-27.33,;11.96,-27.65,;12.73,-26.31,;11.69,-25.17,)|
Show InChI InChI=1S/C22H32N4O3/c27-6-5-23-21-24-12-17(19(26-21)14-3-1-2-4-14)20(28)25-18-15-7-13-8-16(18)11-22(29,9-13)10-15/h12-16,18,27,29H,1-11H2,(H,25,28)(H,23,24,26)/t13?,15?,16?,18-,22-
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PC cid
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n/an/a 12n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of human 11beta-HSD1 by HTRF assay


J Med Chem 55: 10652-61 (2012)


Article DOI: 10.1021/jm3013163
BindingDB Entry DOI: 10.7270/Q2BG2Q4S
More data for this
Ligand-Target Pair
11-beta-hydroxysteroid dehydrogenase 1


(Mus musculus (mouse))
BDBM50400168
PNG
(CHEMBL2179025)
Show SMILES OCCNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1 |r,wU:11.10,wD:18.19,TLB:19:18:11:15.14.13,10:11:21.17.18:15.14.13,10:11:13:21.18.20,THB:19:18:11.16.15:13,20:18:11:15.14.13,20:14:11:21.17.18,17:16:13:21.18.20,17:18:11.16.15:13,(2.28,-22.72,;3.61,-23.49,;3.61,-25.03,;4.95,-25.8,;6.28,-25.04,;6.28,-23.49,;7.61,-22.72,;8.95,-23.48,;10.28,-22.71,;10.27,-21.17,;11.61,-23.47,;12.95,-22.7,;12.94,-20.95,;11.9,-19.88,;12.56,-18.61,;12.58,-20.05,;13.75,-21.37,;15.16,-20.81,;15.02,-19.18,;16.55,-19.2,;13.97,-18.06,;14.24,-20.4,;8.95,-25.03,;7.61,-25.81,;10.29,-25.8,;10.45,-27.33,;11.96,-27.65,;12.73,-26.31,;11.69,-25.17,)|
Show InChI InChI=1S/C22H32N4O3/c27-6-5-23-21-24-12-17(19(26-21)14-3-1-2-4-14)20(28)25-18-15-7-13-8-16(18)11-22(29,9-13)10-15/h12-16,18,27,29H,1-11H2,(H,25,28)(H,23,24,26)/t13?,15?,16?,18-,22-
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 179n/an/an/an/an/an/a



AstraZeneca

Curated by ChEMBL


Assay Description
Inhibition of mouse 11beta-HSD1 by HTRF assay


J Med Chem 55: 10652-61 (2012)


Article DOI: 10.1021/jm3013163
BindingDB Entry DOI: 10.7270/Q2BG2Q4S
More data for this
Ligand-Target Pair