6'-BETA-HYDROXY-LOVASTATIN
Compound with spectra: 1 NMR
| SpectraBase Compound ID | Ad18zgJ4Jzl |
|---|---|
| InChI | InChI=1S/C24H36O6/c1-5-14(2)23(27)30-20-13-24(4,28)12-16-7-6-15(3)19(22(16)20)9-8-18-10-17(25)11-21(26)29-18/h6-7,12,14-15,17-20,22,25,28H,5,8-11,13H2,1-4H3/t14-,15-,17+,18+,19-,20-,22-,24+/m0/s1 |
| InChIKey | FUCXPWLYQFERRA-QOPMPQMQSA-N |
| Mol Weight | 420.5 g/mol |
| Molecular Formula | C24H36O6 |
| Exact Mass | 420.251189 g/mol |
| Enantiomer InChIKey | FUCXPWLYQFERRA-BDRHRPTRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
ZAKDJVVJTNQRTN-OOQIBZCKSA-N
(1-R*,2-E,4-R*,6-E,8-S*,10-S*,11-S*,12-R*)-10,18-DIACETOXY-8-HYDROXY-2,6-DOLABELLADIENE
VIGUIESTIN,DESACETYL=TAGITININ E-A
4-B-H,5-A-H,11-B-H-EUDESM-2-EN-12,6-B-OLIDE,2-OXO
ACANTHOSPERMOLIDE,9-A,15-DIHYDROXY-8-B-METHYLBUTYRYLOXY-14-OXO
11-B-H-ELEMA-1,3-DIEN-12,6-A-OLIDE,8-A,15-DIHYDROXY
No Name
3-O-ACETOXY-GERMACRA-4(15)-EN-6,12-OLIDE
5-alpha-H,11-beta-H-EUDESM-4(15)-EN-12,6-beta-OLIDE,3-beta-ACETOXY
GERMACRANOLIDE FROM TANACETUM ANNUUM;COMPOUND 3
| Title | Journal or Book | Year |
|---|---|---|
| Generation of Human Chiral Metabolites of Simvastatin and Lovastatin by Bacterial CYP102A1 Mutants | Drug Metabolism and Disposition | 2010 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.