Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C30H52O |
| Molecular Weight | 428.7333 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)CCC[C@@H](C)[C@H]1CC[C@@]2(C)C3=C(CC[C@]12C)[C@@]4(C)CC[C@H](O)C(C)(C)[C@@H]4CC3
InChI
InChIKey=MBZYKEVPFYHDOH-BQNIITSRSA-N
InChI=1S/C30H52O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h20-22,25-26,31H,9-19H2,1-8H3/t21-,22-,25+,26+,28-,29-,30+/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Trypanosoma cruzi CYP51 inhibitor derived from a Mycobacterium tuberculosis screen hit. | 2009 |
|
| Effectors of rapid homeostatic responses of endoplasmic reticulum cholesterol and 3-hydroxy-3-methylglutaryl-CoA reductase. | 2008-01-18 |
|
| Hypoxia stimulates degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase through accumulation of lanosterol and hypoxia-inducible factor-mediated induction of insigs. | 2007-09-14 |
|
| Cholesterol-lowering properties of Ganoderma lucidum in vitro, ex vivo, and in hamsters and minipigs. | 2004-02-18 |
|
| The role of cytochrome P450 in the regulation of cholesterol biosynthesis. | 2002-12 |
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| Code System | Code | Type | Description | ||
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79-62-9
Created by
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9H273A8B2X
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DTXSID101000181
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440560
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C015316
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Dihydrolanosterol
Created by
admin on Mon Mar 31 20:53:50 GMT 2025 , Edited by admin on Mon Mar 31 20:53:50 GMT 2025
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28113
Created by
admin on Mon Mar 31 20:53:50 GMT 2025 , Edited by admin on Mon Mar 31 20:53:50 GMT 2025
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PRIMARY |
SUBSTANCE RECORD