炔雌醇环戊醚结构式
|
常用名 | 炔雌醇环戊醚 | 英文名 | Quinestrol |
|---|---|---|---|---|
| CAS号 | 152-43-2 | 分子量 | 364.520 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 502.5±50.0 °C at 760 mmHg | |
| 分子式 | C25H32O2 | 熔点 | 107 - 108ºC | |
| MSDS | 中文版 美版 | 闪点 | 218.8±24.4 °C | |
| 符号 |
GHS07, GHS08 |
信号词 | Danger |
炔雌醇环戊醚用途【用途一】 用作雌激素类药 |
| 中文名 | 炔雌醇环戊醚 |
|---|---|
| 英文名 | quinestrol |
| 中文别名 | 炔雌醚 |
| 英文别名 | 更多 |
| 密度 | 1.2±0.1 g/cm3 |
|---|---|
| 沸点 | 502.5±50.0 °C at 760 mmHg |
| 熔点 | 107 - 108ºC |
| 分子式 | C25H32O2 |
| 分子量 | 364.520 |
| 闪点 | 218.8±24.4 °C |
| 精确质量 | 364.240234 |
| PSA | 29.46000 |
| LogP | 6.67 |
| InChIKey | PWZUUYSISTUNDW-VAFBSOEGSA-N |
| SMILES | C#CC1(O)CCC2C3CCc4cc(OC5CCCC5)ccc4C3CCC21C |
| 外观性状 | 晶体 |
| 蒸汽压 | 0.0±1.4 mmHg at 25°C |
| 折射率 | 1.596 |
| 储存条件 | 室温 |
| 水溶解性 | 可溶于:二噁烷 |
| 分子结构 | 1、 摩尔折射率:107.56 2、 摩尔体积(cm3/mol):315.9 3、 等张比容(90.2K):844.6 4、 表面张力(dyne/cm):51.0 5、 极化率(10-24cm3):42.64 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):无 2.氢键供体数量:1 3.氢键受体数量:2 4.可旋转化学键数量:3 5.互变异构体数量:无 6.拓扑分子极性表面积29.5 7.重原子数量:27 8.表面电荷:0 9.复杂度:613 10.同位素原子数量:0 11.确定原子立构中心数量:5 12.不确定原子立构中心数量:0 13.确定化学键立构中心数量:0 14.不确定化学键立构中心数量:0 15.共价键单元数量:1 |
| 符号 |
GHS07, GHS08 |
|---|---|
| 信号词 | Danger |
| 危害声明 | H302-H312-H332-H350-H360 |
| 警示性声明 | P201-P280-P308 + P313 |
| 个人防护装备 | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| 危害码 (欧洲) | T:Toxic; |
| 风险声明 (欧洲) | R46;R61;R20/21/22 |
| 安全声明 (欧洲) | S53-S22-S36/37/39-S45 |
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 3 |
| RTECS号 | RC8948000 |
|
~%
炔雌醇环戊醚 152-43-2 |
| 文献:Steroids, , vol. 2, p. 387 - 392 |
|
~%
炔雌醇环戊醚 152-43-2 |
| 文献:Gazzetta Chimica Italiana, , vol. 93, p. 1503 - 1519 |
| 炔雌醇环戊醚上游产品 3 | |
|---|---|
| 炔雌醇环戊醚下游产品 0 | |
|
The bioaccumulation and biotransformation of synthetic estrogen quinestrol in crucian carp.
Aquat. Toxicol. 155 , 84-90, (2014) The occurrence and fate of endocrine disrupting chemicals (EDCs) in aquatic species have attracted close attention during the last decades. In this study, the bioaccumulation and biotransformation of ... |
|
|
Photodegradation of quinestrol in waters and the transformation products by UV irradiation.
Chemosphere 89(11) , 1419-25, (2012) Quinestrol is synthetic estrogen used in contraceptive and hormone replacement therapy and occasionally for treating breast cancer and prostate cancer. It can make its way into the environment through... |
|
|
Effects of quinestrol on reproductive hormone expression, secretion, and receptor levels in female Mongolian gerbils (Meriones unguiculatus).
Theriogenology 77(6) , 1223-31, (2012) Quinestrol, a synthetic estrogen with marked estrogenic effects and prolonged activity, has potential as a contraceptive for Mongolian gerbils. The objective of this study was to describe the effects ... |
|
实验名称:Primary qHTS assay for inhibitors of alpha-synuclein gene (SNCA) expression
来源:NCGC
External Id:SNCA-p-activity-luciferase
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:Cytochrome P450 Family 1 Subfamily A Member 2 (CYP1A2) small molecule antagonists: lu...
来源:824
External Id:CYP273
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
|
|
实验名称:qHTS Assay for Small Molecule Inhibitors of the Human hERG Channel Activity
来源:NCGC
External Id:HERG01
|
|
实验名称:uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay
来源:Burnham Center for Chemical Genomics
靶标:cystic fibrosis transmembrane conductance regulator [Homo sapiens]
External Id:SBCCG-A764-CF-PAF-Primary-Assay
|
|
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ant...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_ANT_FLUO8_1536_1X%INH PRUN
|
|
实验名称:Primary qHTS for inhibitors of NSP2Pro chikungunya virus (CHIKV)
来源:NCGC
External Id:APP-Toga-CHIKV-nsp2-p
|
| 3-(Cyclopentyloxy)-19-nor-17a-pregna-1,3,5(10)-trien-20-yn-17-ol |
| 17a-Ethinylestradiol 3-Cyclopentyl Ether |
| MFCD00079189 |
| Quinestrol |
| (8R,9S,13S,14S,17R)-3-cyclopentyloxy-17-ethynyl-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-ol |
| 17α-Ethynylestradiol 3-Cyclopentyl Ether |
| (17α)-3-(Cyclopentyloxy)-19-norpregna-1(10),2,4-trien-20-yn-17-ol |
| EINECS 205-803-1 |