(2S,10S,11S,13S,14R,15S)-14-hydroxy-14-(2-hydroxyacetyl)-2,13,15-trimethyl-18-oxapentacyclo[8.8.0.01,17.02,7.011,15]octadeca-3,6-dien-5-one

• ChemBase编号: 162006
• 分子式: C22H28O5
• 平均质量: 372.45472
• 单一同位素质量: 372.193674
• SMILES: C1=C[C@]2(C(=CC1=O)CC[C@@H]1C32C(C[C@]2([C@H]1C[C@@H]([C@@]2(C(=O)CO)O)C)C)O3)C
• Canonical SMILES: OCC(=O)[C@@]1(O)[C@@H](C)C[C@@H]2[C@]1(C)CC1OC31[C@H]2CCC1=CC(=O)C=C[C@]31C
• InChI: InChI=1S/C22H28O5/c1-12-8-16-15-5-4-13-9-14(24)6-7-19(13,2)22(15)18(27-22)10-20(16,3)21(12,26)17(25)11-23/h6-7,9,12,15-16,18,23,26H,4-5,8,10-11H2,1-3H3/t12-,15-,16-,18?,19-,20-,21-,22?/m0/s1
• InChIKey: GBDXNHBVYAMODG-ARBQUQLTSA-N

名称和登记号

名称

• IUPAC标准名: (2S,10S,11S,13S,14R,15S)-14-hydroxy-14-(2-hydroxyacetyl)-2,13,15-trimethyl-18-oxapentacyclo[8.8.0.0^1,^1^7.0^2,^7.0^1^1,^1^5]octadeca-3,6-dien-5-one
• IUPAC传统名: (2S,10S,11S,13S,14R,15S)-14-hydroxy-14-(2-hydroxyacetyl)-2,13,15-trimethyl-18-oxapentacyclo[8.8.0.0^1,^1^7.0^2,^7.0^1^1,^1^5]octadeca-3,6-dien-5-one
• 别名: (9β,11β,16β)-9,11-Epoxy-17,21-dihydroxy-16-methylpregna-1,4-diene-3,20-dione; 9β,11β-Epoxy-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione; Betamethasone 9,11-Epoxide; Betamethasone 9-11-Epoxide; 9β,11β-Epoxy-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione

登记号

• CAS号: 981-34-0
• PubChem SID: 162256141
• PubChem CID: 45039145

理论计算性质

• Acid pKa: 12.450934
• 质子受体: 5
• 质子供体: 2
• LogD (pH = 5.5): 1.9521815
• LogD (pH = 7.4): 1.9521776
• Log P: 1.9521815
• 摩尔折射率: 100.6749 cm^3
• 极化性: 39.224995 Å^3
• 极化表面积: 87.13 Å^2
• 可自由旋转的化学键: 2
• 里宾斯基五规则: true

分子性质

理化性质

• 溶解度: Methanol; Sparingly soluble in Chloroform
• 外观: Off-White Solid
• 熔点: 240-245°C

安全信息

• 保存条件: Refrigerator

详细说明

Toronto Research Chemicals - E589175

A metabolite of Mometasone furoate. Low solubility in most solvent.

Toronto Research Chemicals - B327035

Metabolite of Beclometasone (131000)

参考文献

• Caron, J., et al.: J. Pharm. Sci., 73, 1703 (1984)
• Jobe, A., et al.: Am. J. Obstet. Gynecol., 190, 878 (1984)
• Nygaard, L., et al.: J. Pharm. Biomed. Anal., 34, 265 (2004)
• Foe, K., et al.: Drug Metab. Disposition, 26, 132 (1998)
• Xiong, Y., et al.: J. Pharm. Biomed. Anal., 49, 646 (1998)