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595-33-5 分子结构
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(2R,10R,14R,15S)-14-acetyl-2,8,15-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl acetate

ChemBase编号:119829
分子式:C24H32O4
平均质量:384.50848
单一同位素质量:384.2300595
SMILES和InChIs

SMILES:
C12=CC(=O)CC[C@@]1(C1[C@@H](C=C2C)C2[C@@]([C@@](CC2)(OC(=O)C)C(=O)C)(CC1)C)C
Canonical SMILES:
O=C1CC[C@]2(C(=C1)C(=C[C@@H]1C2CC[C@]2(C1CC[C@]2(OC(=O)C)C(=O)C)C)C)C
InChI:
InChI=1S/C24H32O4/c1-14-12-18-19(22(4)9-6-17(27)13-21(14)22)7-10-23(5)20(18)8-11-24(23,15(2)25)28-16(3)26/h12-13,18-20H,6-11H2,1-5H3/t18-,19?,20?,22-,23+,24+/m1/s1
InChIKey:
RQZAXGRLVPAYTJ-UFZHOBIOSA-N

引用这个纪录

CBID:119829 http://www.chembase.cn/molecule-119829.html

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名称和登记号

名称和登记号

名称 登记号
IUPAC标准名
(2R,10R,14R,15S)-14-acetyl-2,8,15-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl acetate
IUPAC传统名
(2R,10R,14R,15S)-14-acetyl-2,8,15-trimethyl-5-oxotetracyclo[8.7.0.02,7.011,15]heptadeca-6,8-dien-14-yl acetate
别名
(8R,10R,13S,17R)-17-acetyl-6,10,13-trimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate
Megestrol Acetate
CAS号
595-33-5
PubChem SID
162107935
PubChem CID
17571578

数据来源

数据来源

所有数据来源 商品来源 非商品来源
数据来源 数据ID
PubChem 17571578 external link

理论计算性质

理论计算性质

JChem
Acid pKa 17.826162  质子受体
质子供体 LogD (pH = 5.5) 3.7237444 
LogD (pH = 7.4) 3.7237444  Log P 3.7237444 
摩尔折射率 108.6554 cm3 极化性 42.444622 Å3
极化表面积 60.44 Å2 可自由旋转的化学键
里宾斯基五规则 true 

分子性质

分子性质

药理学性质 产品相关信息 生物活性(PubChem)
生物活性机理
Also has direct cytotoxic effects on breast cancer cells in tissue culture and suppresses luteinising hormone release from the pituitary expand 查看数据来源
The biochemical mechanism of progestin antitumour activity is not well but may involve interaction with progesterone and glucocorticoid receptors, androgenic properties expand 查看数据来源
The precise mechanism by which megestrol acetate produces effects in anorexia and cachexia is unknown at the present time expand 查看数据来源
应用领域
against carcinoma of the breast and endometrium expand 查看数据来源
Antineoplastic agent expand 查看数据来源
Oral contraceptive expand 查看数据来源

详细说明

详细说明

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Ringold, M.J. et al., J.A.C.S., 1959, 81, 3712, (synth)
  • Ellis, B. et al., J.C.S., 1960, 2828, (synth)
  • Elce, J.S. et al., Biochem. J., 1967, 104, 58P
  • Cooper, J.M. et al., Steroids, 1968, 11, 133
  • Annen, K. et al., Annalen, 1983, 712, (deriv)
  • Ni, Y. et al., CA, 1984, 101, 23805, (deriv)
  • Guo, Z. et al., CA, 1985, 103, 54356, (deriv)
  • Negwer, M., Organic-Chemical Drugs and their Synonyms, 6th edn., Akademie-Verlag, 1987, 7162, (synonyms)
  • Martindale, The Extra Pharmacopoeia, 30th edn., Pharmaceutical Press, 1993, 1187
  • Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, VTF000
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专利

专利

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互联网资源

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