Reaction Details |
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Target | Lanosterol synthase ERG7 |
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Ligand | BDBM50433365 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_956105 (CHEMBL2379169) |
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IC50 | >20000±n/a nM |
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Citation | Lange, S; Keller, M; Müller, C; Oliaro-Bosso, S; Balliano, G; Bracher, F Aminopropylindenes derived from Grundmann's ketone as a novel chemotype of oxidosqualene cyclase inhibitors. Eur J Med Chem63:758-64 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Lanosterol synthase ERG7 |
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Name: | Lanosterol synthase ERG7 |
Synonyms: | ERG7 | ERG7_YEAST | Lanosterol synthase |
Type: | PROTEIN |
Mol. Mass.: | 83460.43 |
Organism: | Saccharomyces cerevisiae |
Description: | ChEMBL_956105 |
Residue: | 731 |
Sequence: | MTEFYSDTIGLPKTDPRLWRLRTDELGRESWEYLTPQQAANDPPSTFTQWLLQDPKFPQP
HPERNKHSPDFSAFDACHNGASFFKLLQEPDSGIFPCQYKGPMFMTIGYVAVNYIAGIEI
PEHERIELIRYIVNTAHPVDGGWGLHSVDKSTVFGTVLNYVILRLLGLPKDHPVCAKARS
TLLRLGGAIGSPHWGKIWLSALNLYKWEGVNPAPPETWLLPYSLPMHPGRWWVHTRGVYI
PVSYLSLVKFSCPMTPLLEELRNEIYTKPFDKINFSKNRNTVCGVDLYYPHSTTLNIANS
LVVFYEKYLRNRFIYSLSKKKVYDLIKTELQNTDSLCIAPVNQAFCALVTLIEEGVDSEA
FQRLQYRFKDALFHGPQGMTIMGTNGVQTWDCAFAIQYFFVAGLAERPEFYNTIVSAYKF
LCHAQFDTECVPGSYRDKRKGAWGFSTKTQGYTVADCTAEAIKAIIMVKNSPVFSEVHHM
ISSERLFEGIDVLLNLQNIGSFEYGSFATYEKIKAPLAMETLNPAEVFGNIMVEYPYVEC
TDSSVLGLTYFHKYFDYRKEEIRTRIRIAIEFIKKSQLPDGSWYGSWGICFTYAGMFALE
ALHTVGETYENSSTVRKGCDFLVSKQMKDGGWGESMKSSELHSYVDSEKSLVVQTAWALI
ALLFAEYPNKEVIDRGIDLLKNRQEESGEWKFESVEGVFNHSCAIEYPSYRFLFPIKALG
MYSRAYETHTL
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BDBM50433365 |
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n/a |
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Name | BDBM50433365 |
Synonyms: | CHEMBL2377450 |
Type | Small organic molecule |
Emp. Form. | C22H41N |
Mol. Mass. | 319.5676 |
SMILES | CNCCCC1=C2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CCC1 |r,c:5| |
Structure |
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