Drug Information
Drug General Information | Top | |||
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Drug ID |
D0Z9PB
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Former ID |
DNC013648
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Drug Name |
Trisnorsqualene alcohol
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Synonyms |
trisnorsqualene alcohol; CHEMBL47899; Trinorsqualene alcohol; SCHEMBL2587286; SCHEMBL2587282; BDBM50015507; 4,8,13,17,21-Pentamethyl-docosa-4,8,12,16,20-pentaen-1-ol
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C27H46O
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Canonical SMILES |
CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCCO)C)C)C
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InChI |
1S/C27H46O/c1-23(2)13-9-16-26(5)19-10-17-24(3)14-7-8-15-25(4)18-11-20-27(6)21-12-22-28/h13-15,19-20,28H,7-12,16-18,21-22H2,1-6H3/b24-14+,25-15+,26-19+,27-20+
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InChIKey |
WAMKRSMPERYEBH-OGDZRKEVSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Squalene monooxygenase (SQLE) | Target Info | Inhibitor | [1] |
KEGG Pathway | Steroid biosynthesis | |||
Sesquiterpenoid and triterpenoid biosynthesis | ||||
Metabolic pathways | ||||
Biosynthesis of secondary metabolites | ||||
Biosynthesis of antibiotics | ||||
Pathwhiz Pathway | Steroid Biosynthesis | |||
Reactome | Cholesterol biosynthesis | |||
Activation of gene expression by SREBF (SREBP) |
References | Top | |||
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REF 1 | Ellagitannins and hexahydroxydiphenoyl esters as inhibitors of vertebrate squalene epoxidase. J Nat Prod. 2001 Aug;64(8):1010-4. |
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