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sodium (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-[(2H7)propan-2-yl](5,7-2H2)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoate
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ChemBase ID:
169308
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Molecular Formular:
C24H25FNNaO4
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Molecular Mass:
433.4477732
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Monoisotopic Mass:
433.16653079
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SMILES and InChIs
SMILES:
c1cccc2c1c(c(n2C(C)C)/C=C/[C@H](C[C@H](CC(=O)[O-])O)O)c1ccc(cc1)F.[Na+]
Canonical SMILES:
[O-]C(=O)C[C@@H](C[C@@H](/C=C/c1c(c2ccc(cc2)F)c2c(n1C(C)C)cccc2)O)O.[Na+]
InChI:
InChI=1S/C24H26FNO4.Na/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30;/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30);/q;+1/p-1/b12-11+;/t18-,19-;/m1./s1
InChIKey:
ZGGHKIMDNBDHJB-NRFPMOEYSA-M
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Cite this record
CBID:169308 http://www.chembase.cn/molecule-169308.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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sodium (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-[(2H7)propan-2-yl](5,7-2H2)-1H-indol-2-yl]-3,5-dihydroxyhept-6-enoate
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IUPAC Traditional name
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sodium (3R,5S,6E)-7-[3-(4-fluorophenyl)-1-[(2H7)propan-2-yl](5,7-2H2)indol-2-yl]-3,5-dihydroxyhept-6-enoate
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Synonyms
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(3R,5S,6E)-rel-7-[3-(4-Fluorophenyl)-1-(1-methylethyl-deuterated)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic Acid Sodium Salt
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Fluindostatin-D8
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XU 62-320-D8
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Lescol-D8
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Lipaxan-D8
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Primexin-D8
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Fluvastatin-D8 (Major) Sodium Salt
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CAS Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
Data Source
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Data ID
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Price
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TRC
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CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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4.55701
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H Acceptors
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4
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H Donor
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2
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LogD (pH = 5.5)
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2.837187
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LogD (pH = 7.4)
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1.0636245
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Log P
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3.8259492
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Molar Refractivity
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125.6924 cm3
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Polarizability
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46.024704 Å3
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Polar Surface Area
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85.52 Å2
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Rotatable Bonds
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8
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
TRC
Toronto Research Chemicals -
F601252
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A synthetic HMG-CoA reductase inhibitor. Antilipemic.A representative lot was: 1% of d6, 28% of d7, 37% of d8, 21% of d9, 10% of d10, and 2% of d11 |
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google Books
- • Yuan, J., et al.: Atherosclerosis, 87, 147 (1991)
- • Tse, F.L.S., et al.: J. Clin. Pharmacol., 32, 630 (1991)
- • Dain, J.G., et al.: Drug Metab. Disposit., 21, 567 (1991)
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PATENTS
PATENTS
PubChem Patent
Google Patent