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160967774 分子结构
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(1R,3S,5Z)-5-{2-[(1R,3aR,4Z,7aR)-1-[(2R)-6-hydroxy-6-methylhept-4-yn-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol

ChemBase编号:4342
分子式:C27H40O3
平均质量:412.6047
单一同位素质量:412.29774514
SMILES和InChIs

SMILES:
O[C@H]1C[C@@H](C(=C)/C(=C\C=C/2\CCC[C@]3([C@@H]2CC[C@@H]3[C@H](C)CC#CC(C)(C)O)C)/C1)O
Canonical SMILES:
O[C@H]1C[C@H](O)C(=C)/C(=C\C=C/2\CCC[C@]3([C@@H]2CC[C@@H]3[C@@H](CC#CC(O)(C)C)C)C)/C1
InChI:
InChI=1S/C27H40O3/c1-18(8-6-14-26(3,4)30)23-12-13-24-20(9-7-15-27(23,24)5)10-11-21-16-22(28)17-25(29)19(21)2/h10-11,18,22-25,28-30H,2,7-9,12-13,15-17H2,1,3-5H3/b20-10-,21-11-/t18-,22-,23-,24-,25+,27-/m1/s1
InChIKey:
BUDPDEVHCQIFNU-PUBYVPDWSA-N

引用这个纪录

CBID:4342 http://www.chembase.cn/molecule-4342.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
(1R,3S,5Z)-5-{2-[(1R,3aR,4Z,7aR)-1-[(2R)-6-hydroxy-6-methylhept-4-yn-2-yl]-7a-methyl-octahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol
IUPAC传统名
(1R,3S,5Z)-5-{2-[(1R,3aR,4Z,7aR)-1-[(2R)-6-hydroxy-6-methylhept-4-yn-2-yl]-7a-methyl-hexahydro-1H-inden-4-ylidene]ethylidene}-4-methylidenecyclohexane-1,3-diol
别名
TX522
19-nor-14-epi-23-yne-1,25 dihydroxyvitamin D3
PubChem SID
160967774
46504586
PubChem CID
46937021

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
DrugBank DB04796 external link
PubChem 46937021 external link
数据来源 数据ID 价格

理论计算性质

理论计算性质

JChem ALOGPS 2.1
Acid pKa 14.333249  质子受体
质子供体 LogD (pH = 5.5) 4.0913553 
LogD (pH = 7.4) 4.091355  Log P 4.0913553 
摩尔折射率 125.7399 cm3 极化性 48.31969 Å3
极化表面积 60.69 Å2 可自由旋转的化学键
里宾斯基五规则 true 
Log P 5.15  LOG S -5.2 
溶解度 2.58e-03 g/l 

分子性质

分子性质

生物活性(PubChem)

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB04796 external link
Item Information
Drug Groups experimental
Indication Investigated for use/treatment in prostate cancer, psoriasis and hyperparathyroidism.
References
Wong MS, Delansorne R, Man RY, Vanhoutte PM: Vitamin D derivatives acutely reduces endothelium-dependent contractions in the aorta of the spontaneously hypertensive rat. Am J Physiol Heart Circ Physiol. 2008 May 16;. [Pubmed]
Eelen G, Verlinden L, Van Camp M, Claessens F, De Clercq P, Vandewalle M, Bouillon R, Verstuyf A: Altered Vitamin D receptor-coactivator interactions reflect superagonism of Vitamin D analogs. J Steroid Biochem Mol Biol. 2005 Oct;97(1-2):65-8. Epub 2005 Jul 20. [Pubmed]
Company Website [Link]

参考文献

参考文献

供应商提供 Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • Wong MS, Delansorne R, Man RY, Vanhoutte PM: Vitamin D derivatives acutely reduces endothelium-dependent contractions in the aorta of the spontaneously hypertensive rat. Am J Physiol Heart Circ Physiol. 2008 May 16;. Pubmed
  • Eelen G, Verlinden L, Van Camp M, Claessens F, De Clercq P, Vandewalle M, Bouillon R, Verstuyf A: Altered Vitamin D receptor-coactivator interactions reflect superagonism of Vitamin D analogs. J Steroid Biochem Mol Biol. 2005 Oct;97(1-2):65-8. Epub 2005 Jul 20. Pubmed
  • Company Website Link
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专利

专利

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