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TargetSqualene monooxygenase
LigandBDBM20688
Substrate/Competitorn/a
Meas. Tech.ChEMBL_201941 (CHEMBL809128)
IC50>10000±n/a nM
Citation Gotteland, JPBrunel, IGendre, FDésiré, JDelhon, AJunquéro, DOms, PHalazy, S (Aryloxy)methylsilane derivatives as new cholesterol biosynthesis inhibitors: synthesis and hypocholesterolemic activity of a new class of squalene epoxidase inhibitors. J Med Chem38:3207-16 (1995) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Squalene monooxygenase
Name:Squalene monooxygenase
Synonyms:ERG1 | ERG1_HUMAN | SE | SQLE | Squalene epoxidase
Type:PROTEIN
Mol. Mass.:63936.94
Organism:Homo sapiens (Human)
Description:ChEMBL_201924
Residue:574
Sequence:
MWTFLGIATFTYFYKKFGDFITLANREVLLCVLVFLSLGLVLSYRCRHRNGGLLGRQQSG
SQFALFSDILSGLPFIGFFWAKSPPESENKEQLEARRRRKGTNISETSLIGTAACTSTSS
QNDPEVIIVGAGVLGSALAAVLSRDGRKVTVIERDLKEPDRIVGEFLQPGGYHVLKDLGL
GDTVEGLDAQVVNGYMIHDQESKSEVQIPYPLSENNQVQSGRAFHHGRFIMSLRKAAMAE
PNAKFIEGVVLQLLEEDDVVMGVQYKDKETGDIKELHAPLTVVADGLFSKFRKSLVSNKV
SVSSHFVGFLMKNAPQFKANHAELILANPSPVLIYQISSSETRVLVDIRGEMPRNLREYM
VEKIYPQIPDHLKEPFLEATDNSHLRSMPASFLPPSSVKKRGVLLLGDAYNMRHPLTGGG
MTVAFKDIKLWRKLLKGIPDLYDDAAIFEAKKSFYWARKTSHSFVVNILAQALYELFSAT
DDSLHQLRKACFLYFKLGGECVAGPVGLLSVLSPNPLVLIGHFFAVAIYAVYFCFKSEPW
ITKPRALLSSGAVLYKACSVIFPLIYSEMKYMVH
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM20688
n/a
NameBDBM20688
Synonyms:(3R,5R)-7-[(1S,2S,6S,8S,8aR)-6-hydroxy-2-methyl-8-{[(2S)-2-methylbutanoyl]oxy}-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoic acid | CHEMBL1144 | Pravastatin
TypeSmall organic molecule
Emp. Form.C23H36O7
Mol. Mass.424.5277
SMILES[H][C@]12[C@H](C[C@H](O)C=C1C=C[C@H](C)[C@@H]2CC[C@@H](O)C[C@@H](O)CC(O)=O)OC(=O)[C@@H](C)CC |r,c:6,9|
Structure
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