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
[H][C@@]12CCC3=C(CC[C@]4(C)[C@H](CC[C@@]34C)[C@H](C)CCCC(C)C)[C@@]1(C)CC[C@H](O)C2(C)C
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 |
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Hypoxia stimulates degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase through accumulation of lanosterol and hypoxia-inducible factor-mediated induction of insigs. | 2007 Sep 14 |
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Effectors of rapid homeostatic responses of endoplasmic reticulum cholesterol and 3-hydroxy-3-methylglutaryl-CoA reductase. | 2008 Jan 18 |
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Trypanosoma cruzi CYP51 inhibitor derived from a Mycobacterium tuberculosis screen hit. | 2009 |
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Code System | Code | Type | Description | ||
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79-62-9
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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9H273A8B2X
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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DTXSID101000181
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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440560
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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C015316
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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Dihydrolanosterol
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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28113
Created by
admin on Sat Dec 16 01:32:38 GMT 2023 , Edited by admin on Sat Dec 16 01:32:38 GMT 2023
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PRIMARY |
SUBSTANCE RECORD