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58551-69-2 分子结构
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(5E)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-3-methyloct-1-en-1-yl]cyclopentyl]hept-5-enoic acid

ChemBase编号:312
分子式:C21H36O5
平均质量:368.50754
单一同位素质量:368.25627425
SMILES和InChIs

SMILES:
O[C@@H]1[C@@H]([C@H]([C@H](O)C1)/C=C/C(O)(CCCCC)C)C/C=C/CCCC(=O)O
Canonical SMILES:
CCCCCC(/C=C/[C@H]1[C@H](O)C[C@@H]([C@@H]1C/C=C/CCCC(=O)O)O)(O)C
InChI:
InChI=1S/C21H36O5/c1-3-4-9-13-21(2,26)14-12-17-16(18(22)15-19(17)23)10-7-5-6-8-11-20(24)25/h5,7,12,14,16-19,22-23,26H,3-4,6,8-11,13,15H2,1-2H3,(H,24,25)/b7-5+,14-12+/t16-,17-,18+,19-,21+/m1/s1
InChIKey:
DLJKPYFALUEJCK-MRVZPHNRSA-N

引用这个纪录

CBID:312 http://www.chembase.cn/molecule-312.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
(5E)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxy-3-methyloct-1-en-1-yl]cyclopentyl]hept-5-enoic acid
IUPAC传统名
tham
商标名
Carboprost
Hemabate
Tham
别名
Carboprost Tromethamine
CAS号
58551-69-2
PubChem SID
160963775
PubChem CID
5284525

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 DB00429 external link
PubChem 5284525 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 4.3552947  质子受体
质子供体 LogD (pH = 5.5) 1.7186534 
LogD (pH = 7.4) -0.030425675  Log P 2.8916311 
摩尔折射率 105.1089 cm3 极化性 40.570885 Å3
极化表面积 97.99 Å2 可自由旋转的化学键 12 
里宾斯基五规则 true 
Log P 4.29  LOG S -3.72 
溶解度 7.08e-02 g/l 

分子性质

分子性质

理化性质 生物活性(PubChem)
溶解度
Carboprost tromethamine dissolves readily in water at room temperature at a concentration greater than 75 mg/mL. expand 查看数据来源
疏水性(logP)
3.3 expand 查看数据来源

详细说明

详细说明

DrugBank DrugBank
DrugBank -  DB00429 external link
Item Information
Drug Groups approved
Description A nonsteroidal abortifacient agent that is effective in both the first and second trimesters of pregnancy. [PubChem]
Indication For aborting pregnancy between the 13th and 20th weeks of gestation as calculated from the first day of the last normal menstrual period and in the following conditions related to second trimester abortion: 1. Failure of expulsion of the fetus during the course of treatment by another method; 2. Premature rupture of membranes in intrauterine methods with loss of drug and insufficient or absent uterine activity; 3. Requirement of a repeat intrauterine instillation of drug for expulsion of the fetus; 4. Inadvertent or spontaneous rupture of membranes in the presence of a previable fetus and absence of adequate activity for expulsion. Also for the treatment of postpartum hemorrhage due to uterine atony which has not responded to conventional methods of management.
Pharmacology Carboprost tromethamine administered intramuscularly stimulates in the gravid uterus myometrial contractions similar to labor contractions at the end of a full term pregnancy. Whether or not these contractions result from a direct effect of carboprost on the myome-trium has not been determined. Nonetheless, they evacuate the products of conception from the uterus in most cases. Postpartum, the resultant myometrial contractions provide hemostasis at the site of placentation. Carboprost tromethamine also stimulates the smooth muscle of the human gastrointestinal tract. This activity may produce the vomiting or diarrhea or both that is common when carbo-prost tromethamine is used to terminate pregnancy and for use postpartum. In laboratory animals and also in humans carboprost tromethamine can elevate body temperature. With the clinical doses of carboprost trometh-amine used for the termination of pregnancy, and for use postpartum, some patients do experience transient temperature increases. In laboratory animals and in humans large doses of carboprost tromethamine can raise blood pressure, probably by contracting the vascular smooth muscle. With the doses of carboprost tromethamine used for terminating pregnancy, this effect has not been clinically significant. In laboratory animals and also in humans carboprost tromethamine can elevate body temperature. With the clinical doses of carboprost tromethamine used for the termination of pregnancy, some patients do experience temperature increases. In some patients, carboprost tromethamine may cause transient bronchoconstriction.
Toxicity Symptoms of overdose include irritation, nausea, vomiting, diarrhea, coughing, dyspnea, asthma, hypertension, flushing, and pyrexia.
Affected Organisms
Humans and other mammals
Biotransformation Metabolized in the lungs and liver. Metabolites are excreted in urine.
External Links
RxList
Drugs.com

参考文献

参考文献

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专利

专利

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