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TargetLanosterol synthase
LigandBDBM50433365
Substrate/Competitorn/a
Meas. Tech.ChEMBL_956104 (CHEMBL2379168)
IC50>20000±n/a nM
Citation Lange, SKeller, MMüller, COliaro-Bosso, SBalliano, GBracher, F Aminopropylindenes derived from Grundmann's ketone as a novel chemotype of oxidosqualene cyclase inhibitors. Eur J Med Chem63:758-64 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lanosterol synthase
Name:Lanosterol synthase
Synonyms:2,3-epoxysqualene--lanosterol cyclase | ERG7 | ERG7_PNECA | OSC | Oxidosqualene--lanosterol cyclase
Type:PROTEIN
Mol. Mass.:83314.91
Organism:Pneumocystis carinii
Description:ChEMBL_956104
Residue:719
Sequence:
MIYGYTEKELEKTDPDGWRLIVEDTGRQRWKYLKTEEERRERPQTYMEKYFLGKNMDLPE
QPAAKTPIESARKGFSFYKHLQTSDGNWACEYGGVMFLLPGLIIAMYISKIEFPDEMRIE
VIRYLVNHANPEDGGWGIHIEGKSTVFGTALNYVVLRILGLGPDHPVTMKARIRLNELGG
AIGCPQWGKFWLAVLNCYGWEGINPILPEFWMLPEWLPIHPSRWWVHTRAVYLPMGYIYG
EKFTAPVDPLIESLREELYTQPYSSINFSKHRNTTSPVDVYVPHTRFLRVINSILTFYHT
IFRFSWIKDMASKYAYKLIEYENKNTDFLCIGPVNFSIHILAVYWKEGPDSYAFKSHKER
MADFLWISKKGMMMNGTNGVQLWDTSFAVQALVESGLAEDPEFKDHMIKALDFLDKCQIQ
KNCDDQQKCYRHRRKGAWPFSTRQQGYTVSDCTAEALKAVLLLQNLKSFPKRVSYDRLKD
SVDVILSLQNKDGGFASYELIRGPSWLEFINPAEVFGDIMIEHSYPECTTAAVTALCYFR
SLCSHYRGPEINKSVKNAIQFIKESQRPDGSWYESWAICFTYATMFALESLSCVKDFYEN
SFHSRRACDFLVNKQEEDGGWSEGYQSCTDGIWTRHPTGSQVVQTAWACIGLMYANYPDE
TPIKRGINLIMSRQQPNGEWKQEAIEGVFNKNCMISYPNYKFNFTIKALGMYSKRYGNI
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50433365
n/a
NameBDBM50433365
Synonyms:CHEMBL2377450
TypeSmall organic molecule
Emp. Form.C22H41N
Mol. Mass.319.5676
SMILESCNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5|
Structure
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