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BDBM50400160 CHEMBL2179442

SMILES: CC(C)Oc1nc(N[C@@H]2CCOC2)ncc1C(=O)N[C@H]1C2CC3CC1C[C@](O)(C3)C2

InChI Key: InChIKey=GQBVRCDDSNTLFU-POHYLCFZSA-N

Data: 2 IC50

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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50400160   
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))
BDBM50400160
PNG
(CHEMBL2179442)
Show SMILES CC(C)Oc1nc(N[C@@H]2CCOC2)ncc1C(=O)N[C@H]1C2CC3CC1C[C@](O)(C3)C2 |r,wU:19.20,wD:26.29,8.7,TLB:27:26:19:23.22.21,18:19:29.25.26:23.22.21,18:19:21:29.26.28,THB:27:26:19.24.23:21,28:26:19:23.22.21,28:22:19:29.25.26,25:24:21:29.26.28,25:26:19.24.23:21,(11.53,-55.4,;10.19,-54.63,;8.86,-55.4,;10.19,-53.09,;8.86,-52.32,;7.52,-53.09,;6.19,-52.32,;4.85,-53.09,;3.52,-52.32,;2.11,-52.94,;1.08,-51.8,;1.85,-50.46,;3.36,-50.79,;6.19,-50.78,;7.52,-50.01,;8.85,-50.77,;10.18,-50,;10.18,-48.46,;11.52,-50.76,;12.85,-49.99,;12.84,-48.24,;11.81,-47.17,;12.46,-45.9,;12.48,-47.34,;13.65,-48.66,;15.06,-48.1,;14.92,-46.47,;16.45,-46.48,;13.88,-45.35,;14.14,-47.69,)|
Show InChI InChI=1S/C22H32N4O4/c1-12(2)30-20-17(10-23-21(26-20)24-16-3-4-29-11-16)19(27)25-18-14-5-13-6-15(18)9-22(28,7-13)8-14/h10,12-16,18,28H,3-9,11H2,1-2H3,(H,25,27)(H,23,24,26)/t13?,14?,15?,16-,18-,22-/m1/s1
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Similars

Article
PubMed
n/an/a 11n/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))
BDBM50400160
PNG
(CHEMBL2179442)
Show SMILES CC(C)Oc1nc(N[C@@H]2CCOC2)ncc1C(=O)N[C@H]1C2CC3CC1C[C@](O)(C3)C2 |r,wU:19.20,wD:26.29,8.7,TLB:27:26:19:23.22.21,18:19:29.25.26:23.22.21,18:19:21:29.26.28,THB:27:26:19.24.23:21,28:26:19:23.22.21,28:22:19:29.25.26,25:24:21:29.26.28,25:26:19.24.23:21,(11.53,-55.4,;10.19,-54.63,;8.86,-55.4,;10.19,-53.09,;8.86,-52.32,;7.52,-53.09,;6.19,-52.32,;4.85,-53.09,;3.52,-52.32,;2.11,-52.94,;1.08,-51.8,;1.85,-50.46,;3.36,-50.79,;6.19,-50.78,;7.52,-50.01,;8.85,-50.77,;10.18,-50,;10.18,-48.46,;11.52,-50.76,;12.85,-49.99,;12.84,-48.24,;11.81,-47.17,;12.46,-45.9,;12.48,-47.34,;13.65,-48.66,;15.06,-48.1,;14.92,-46.47,;16.45,-46.48,;13.88,-45.35,;14.14,-47.69,)|
Show InChI InChI=1S/C22H32N4O4/c1-12(2)30-20-17(10-23-21(26-20)24-16-3-4-29-11-16)19(27)25-18-14-5-13-6-15(18)9-22(28,7-13)8-14/h10,12-16,18,28H,3-9,11H2,1-2H3,(H,25,27)(H,23,24,26)/t13?,14?,15?,16-,18-,22-/m1/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 21n/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