(5S,9S,10S,14Z,17S)-9-[(tert-butyldimethylsilyl)oxy]-5-(2-hydroxyethyl)-2,2,3,3,6,6,8,10,14,19,19,20,20-tridecamethyl-17-[(1E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-4,18-dioxa-3,19-disilahenicos-14-en-7-one

• ChemBase编号: 179025
• 分子式: C45H87NO5SSi3
• 平均质量: 838.49748
• 单一同位素质量: 837.56127548
• SMILES: C(=C\C[C@@H](/C(=C/c1csc(n1)C)/C)O[Si](C(C)(C)C)(C)C)(\CCC[C@@H]([C@@H](C(C(=O)C([C@H](CCO)O[Si](C(C)(C)C)(C)C)(C)C)C)O[Si](C(C)(C)C)(C)C)C)/C
• Canonical SMILES: OCC[C@@H](C(C(=O)C([C@H]([C@H](CCC/C(=C\C[C@@H](/C(=C/c1csc(n1)C)/C)O[Si](C(C)(C)C)(C)C)/C)C)O[Si](C(C)(C)C)(C)C)C)(C)C)O[Si](C(C)(C)C)(C)C
• InChI: InChI=1S/C45H87NO5SSi3/c1-32(26-27-38(49-53(17,18)42(6,7)8)34(3)30-37-31-52-36(5)46-37)24-23-25-33(2)40(51-55(21,22)44(12,13)14)35(4)41(48)45(15,16)39(28-29-47)50-54(19,20)43(9,10)11/h26,30-31,33,35,38-40,47H,23-25,27-29H2,1-22H3/b32-26-,34-30+/t33-,35?,38-,39-,40-/m0/s1
• InChIKey: LOAKRBOMRITVRR-OSLNQJGMSA-N

名称和登记号

名称

• IUPAC标准名: (5S,9S,10S,14Z,17S)-9-[(tert-butyldimethylsilyl)oxy]-5-(2-hydroxyethyl)-2,2,3,3,6,6,8,10,14,19,19,20,20-tridecamethyl-17-[(1E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-4,18-dioxa-3,19-disilahenicos-14-en-7-one
• IUPAC传统名: (5S,9S,10S,14Z,17S)-9-[(tert-butyldimethylsilyl)oxy]-5-(2-hydroxyethyl)-2,2,3,3,6,6,8,10,14,19,19,20,20-tridecamethyl-17-[(1E)-1-(2-methyl-1,3-thiazol-4-yl)prop-1-en-2-yl]-4,18-dioxa-3,19-disilahenicos-14-en-7-one
• 别名: (3S,6R,7S,8S,12Z,15S,16E)-3,7,15-Tris-{[tert-butyl(dimethyl)silyl]oxy}-1-hydroxy-4,4,6,8,12,16-hexamethyl-17-(2-methyl-1,3-thiazol-4-yl)heptadeca-12,16-dien-5-one

登记号

• CAS号: 193146-53-1
• PubChem SID: 164234935
• PubChem CID: 71752742

理论计算性质

• Acid pKa: 15.889901
• 质子受体: 6
• 质子供体: 1
• LogD (pH = 5.5): 12.587277
• LogD (pH = 7.4): 12.587991
• Log P: 12.588
• 摩尔折射率: 229.4533 cm^3
• 极化性: 96.52479 Å^3
• 极化表面积: 77.88 Å^2
• 可自由旋转的化学键: 24
• 里宾斯基五规则: false

分子性质

理化性质

• 溶解度: Acetone; Dichloromethane; Ethanol; Ethyl Acetate; Methanol
• 外观: Colourless Oil

详细说明

Toronto Research Chemicals - T876625

An intermediate in the synthesis of Epothilones. Epothilones are polyketide natural products that inhibit cancer cells by a mechanism similar to paclitaxel, and also are effective against paclitaxel-resistant tumours. Epothilone D is in phase I clinical

参考文献

• Hoee, G., et al.: Pure Appl. Chem., 71, 11, 2019 (1999)
• Giannakakou, P., et al.: Proc. Natl. Acad. Sci. USA, 97, 2904 (2000)