Name: | 1-Naphthaleneheptanoicacid, 1,2,6,7,8,8a-hexahydro-b,d-dihydroxy-2,6-dimethyl-8-(2-methyl-1-oxobutoxy)-,sodium salt (1:1), (bR,dR,1S,2S,6R,8S,8aR)- |
Synonyms: | 1-Naphthaleneheptanoicacid, 1,2,6,7,8,8a-hexahydro-b,d-dihydroxy-2,6-dimethyl-8-(2-methyl-1-oxobutoxy)-,monosodium salt, [1S-[1a(bS*,dS*),2a,6b,8b(R*),8aa]]-;1-Naphthaleneheptanoic acid, 1,2,6,7,8,8a-hexahydro-b,d-dihydroxy-2,6-dimethyl-8-[(2S)-2-methyl-1-oxobutoxy]-,monosodium salt, (bR,dR,1S,2S,6R,8S,8aR)- (9CI);Lovastatin sodium salt;MB 530B;MSD 803, sodium salt;Monacolin K sodium salt;Sodium mevinolinate; |
InChI: | InChI=1/C24H38O6.Na/c1-5-15(3)24(29)30-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-18(25)12-19(26)13-22(27)28;/h6-7,10,14-16,18-21,23,25-26H,5,8-9,11-13H2,1-4H3,(H,27,28);/q;+1/p-1/t14-,15-,16-,18+,19+,20-,21-,23-;/m0./s1 |
Specification: |
The Lovastatin sodium salt with cas registry number of 75225-50-2, is also called MSD 803, sodium salt; Monacolin K sodium salt. The Lovastatin sodium salt belongs to the following product categories: (1)Intermediates & Fine Chemicals; (2)Metabolites; (3)Pharmaceuticals.
Physical properties of Lovastatin sodium salt: (1)H bond acceptors: 5; (2)#H bond donors: 1; (3)#Freely Rotating Bonds: 8; (4)Polar Surface Area: 72.83 Å2.
You can still convert the following datas into molecular structure: (1)SMILES:[Na+].C[C@@H](CC)C(=O)O[C@H]2C[C@@H](C)\C=C3\C=C/[C@H](C)[C@H](CC[C@@H]1C[C@@H](O)CC(=O)O1)[C@@H]23; (2)InChI:InChI=1/C24H36O5.Na/c1-5-15(3)24(27)29-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-19-12-18(25)13-22(26)28-19;/h6-7,10,14-16,18-21,23,25H,5,8-9,11-13H2,1-4H3;/q;+1/t14-,15-,16-,18+,19+,20-,21-,23-;/m0./s1; (3)InChIKey:GEQITETYWSTZHP-AXHZAXLDBK; (4)Std. InChI:InChI=1S/C24H36O5.Na/c1-5-15(3)24(27)29-21-11-14(2)10-17-7-6-16(4)20(23(17)21)9-8-19-12-18(25)13-22(26)28-19;/h6-7,10,14-16,18-21,23,25H,5,8-9,11-13H2,1-4H3;/q;+1/t14-,15-,16-,18+,19+,20-,21-,23-;/m0./s1; (5)Std. InChIKey:GEQITETYWSTZHP-AXHZAXLDSA-N.
|