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Target11-beta-hydroxysteroid dehydrogenase 1
LigandBDBM50382818
Substrate/Competitorn/a
Meas. Tech.ChEMBL_815020 (CHEMBL2027041)
EC50 4±n/a nM
Citation Zhang, LChen, JNing, MZou, QLeng, YShen, J Synthesis and evaluation of piperidine urea derivatives as efficacious 11ß-hydroxysteroid dehydrogenase type 1 inhibitors in diabetic ob/ob mice. Bioorg Med Chem Lett22:2748-52 (2012) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
11-beta-hydroxysteroid dehydrogenase 1
Name:11-beta-hydroxysteroid dehydrogenase 1
Synonyms:11-DH | 11-beta-HSD1 | 11-beta-Hydroxysteroid Dehydrogenase 1 (11-beta-HSD1) | 11-beta-hydroxysteroid dehydrogenase | 11-beta-hydroxysteroid dehydrogenase 1 (11HSD1) | Corticosteroid 11-beta-dehydrogenase isozyme 1 | Corticosteroid 11-beta-dehydrogenase isozyme 1 (11-beta-HSD-1) | Corticosteroid 11-beta-dehydrogenase isozyme 1 (11-beta-HSD1) | Corticosteroid 11-beta-dehydrogenase isozyme 1 (11beta-HSD1) | DHI1_HUMAN | HSD11 | HSD11B1 | HSD11L | SDR26C1
Type:Enzyme
Mol. Mass.:32409.16
Organism:Homo sapiens (Human)
Description:P28845
Residue:292
Sequence:
MAFMKKYLLPILGLFMAYYYYSANEEFRPEMLQGKKVIVTGASKGIGREMAYHLAKMGAH
VVVTARSKETLQKVVSHCLELGAASAHYIAGTMEDMTFAEQFVAQAGKLMGGLDMLILNH
ITNTSLNLFHDDIHHVRKSMEVNFLSYVVLTVAALPMLKQSNGSIVVVSSLAGKVAYPMV
AAYSASKFALDGFFSSIRKEYSVSRVNVSITLCVLGLIDTETAMKAVSGIVHMQAAPKEE
CALEIIKGGALRQEEVYYDSSLWTTLLIRNPCRKILEFLYSTSYNMDRFINK
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  Blast E-value cutoff:
BDBM50382818
n/a
NameBDBM50382818
Synonyms:CHEMBL2023430
TypeSmall organic molecule
Emp. Form.C26H28ClN3O4S
Mol. Mass.514.036
SMILESCN(C1C2CC3CC(C2)CC1C3)C(=O)c1cccc(CN2C(=O)Nc3ccc(Cl)cc3S2(=O)=O)c1 |TLB:1:2:4:8.6.7,THB:6:5:2:8.7.9,6:7:4.5.11:2,9:7:4:11.10.2,9:10:4:8.6.7,(31.33,-9.37,;31.33,-7.83,;32.66,-7.06,;34.07,-7.53,;34.89,-9.07,;34.97,-7.52,;35.96,-6.36,;35.08,-5,;34.96,-6.43,;33.63,-4.49,;32.64,-5.64,;33.47,-7.02,;29.99,-7.06,;29.99,-5.52,;28.66,-7.83,;28.67,-9.38,;27.33,-10.15,;26,-9.37,;26.01,-7.84,;24.67,-7.06,;23.34,-7.83,;23.34,-9.38,;24.67,-10.15,;22,-10.14,;20.66,-9.37,;19.34,-10.15,;18,-9.38,;18,-7.83,;16.67,-7.06,;19.33,-7.06,;20.67,-7.83,;22,-7.05,;21.22,-5.71,;22.76,-5.71,;27.34,-7.07,)|
Structure
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