Ki Summary

Reaction Details

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Target

11-beta-hydroxysteroid dehydrogenase type 2

Ligand

BDBM50197401

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_453208 (CHEMBL902362)

IC50

>100000±n/a nM

Citation

Sorensen, B; Winn, M; Rohde, J; Shuai, Q; Wang, J; Fung, S; Monzon, K; Chiou, W; Stolarik, D; Imade, H; Pan, L; Deng, X; Chovan, L; Longenecker, K; Judge, R; Qin, W; Brune, M; Camp, H; Frevert, EU; Jacobson, P; Link, JT Adamantane sulfone and sulfonamide 11-beta-HSD1 Inhibitors. Bioorg Med Chem Lett17:527-32 (2007) [PubMed] Article

More Info.:

Get all data from this article, Assay Method

11-beta-hydroxysteroid dehydrogenase type 2

Name:

11-beta-hydroxysteroid dehydrogenase type 2

Synonyms:

Type:

Enzyme

Mol. Mass.:

42201.46

Organism:

Mus musculus (mouse)

Description:

Purified recombinant mouse 11beta-HSD2.

Residue:

386

Sequence:

MERWPWPSGGAWLLVAARALLQLLRSDLRLGRPLLAALALLAALDWLCQRLLPPPAALVV
LAGAGWIALSRLARPPRLPVATRAVLITGCDTGFGKETAKKLDAMGFTVLATVLDLNSPG
ALELRDLCSPRLKLLQMDLTKAEDISRVLEITKAHTASTGLWGLVNNAGLNIVVADVELS
PVATFRKCMEVNFFGALELTKGLLPLLRHSRGRIVTVGSPAGDMPYPCLAAYGTSKAAIA
LLMDTFGCELLPWGIKVSIIKPGCFKTDAVTNVNLWEKRKQLLLANIPRELLQAYGEDYI
EHVHGQFLNSLRMALPDLSPVVDAIIDALLAAQPRSRYYPGRGLGLMYFIHHYLPEGLRR
CFLQNFFINHLLPRALRPGQHGPAPA

BDBM50197401

n/a

Name

BDBM50197401

Synonyms:

2-methyl-2-phenoxy-N-(5-sulfamoyl-adamantan-2-yl)-propionamide | CHEMBL241719

Type

Small organic molecule

Emp. Form.

C20H28N2O4S

Mol. Mass.

392.512

SMILES

CC(C)(Oc1ccccc1)C(=O)N[C@H]1C2CC3CC1C[C@](C3)(C2)S(N)(=O)=O |w:16.23,14.25,18.18,wU:13.13,wD:20.26,TLB:13:14:21:17.18.19,12:13:21.16.17:19,THB:15:16:19:22.14.13,15:14:21.16.17:19,13:18:21:22.15.14,TEB:17:18:22:21.16.15,(1.42,4.21,;2.23,2.91,;3.05,1.6,;3.56,3.69,;4.9,2.93,;4.91,1.39,;6.24,.63,;7.57,1.41,;7.56,2.96,;6.22,3.71,;.95,2.06,;1.04,.52,;-.43,2.74,;-1.71,1.89,;-1.72,.36,;-2.74,-.92,;-4.14,-.35,;-4.15,1.24,;-3.11,2.47,;-4.46,1.99,;-4.45,.51,;-5.64,-.77,;-3.12,.02,;-5.94,.92,;-7.44,1.32,;-5.54,2.4,;-6.35,-.57,)|

Structure