您当前所在的位置:首页 > 产品中心 > 产品信息
Dinoprostone_分子结构_CAS_363-24-6)
点击图片或这里关闭

Dinoprostone

产品号 DB00917 公司名称 DrugBank
CAS号 363-24-6 公司网站 http://www.ualberta.ca/
分子式 C20H32O5 电 话 (780) 492-3111
分子量 352.46508 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 793

产品价格信息

请登录

产品别名

标题
Dinoprostone
IUPAC标准名
(5Z)-7-[(1R,2R,3R)-3-hydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-5-oxocyclopentyl]hept-5-enoic acid
IUPAC传统名
dinoprostone
商标名
Prostarmon E
Prepidil
Prostin E2
Cervidil
Prostin E
Propess
别名
Dinoprostone Prostaglandin E2
PGE2
Prostaglandin E2

产品登记号

CAS号 363-24-6
PubChem SID 46505549
PubChem CID 5280360

产品性质

疏水性(logP) 2.8
溶解度 58.1 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups approved
Description Dinoprostone is a naturally occurring prostaglandin E2 (PGE2). It has important effects in labour. It also stimulates osteoblasts to release factors which stimualtes bone resorption by osteoclasts. As a prescription drug it is used as a vaginal suppository, to prepare the cervix for labour and to induce labour.
Indication For the termination of pregnancy during the second trimester (from the 12th through the 20th gestational week as calculated from the first day of the last normal menstrual period), as well as for evacuation of the uterine contents in the management of missed abortion or intrauterine fetal death up to 28 weeks of gestational age as calculated from the first day of the last normal menstrual period. Also used in the management of nonmetastatic gestational trophoblastic disease (benign hydatidiform mole). Other indications include improving the cervical inducibility (cervical "ripening") in pregnant women at or near term with a medical or obstetrical need for labor induction, and the management of postpartum hemorrhage.
Pharmacology Dinoprostone is equivalent to prostaglandin E2 (PGE2). It stimulates labor and delivery by stimulating the uterine, and thus terminates pregnancy. Dinoprostone is also capable of stimulating the smooth muscle of the gastrointestinal tract of man. This activity may be responsible for the vomiting and/or diarrhea that is not uncommon when dinoprostone is used to terminate pregnancy.
Toxicity Oral, mouse: LD50 = 750 mg/kg; Oral, rat: LD50 = 500 mg/kg.
Affected Organisms
Humans and other mammals
Biotransformation Rapid metabolism of dinoprostone occurs primarily in the local tissues; any systemic absorption of the medication is cleared mainly in the maternal lungs and, secondarily, at sites such as the liver and kidneys.
Absorption Absorbed at a rate of 0.3 mg per hour over 12 hours while the vaginal system is in place.
Half Life Less than 5 minutes.
Protein Binding 73%, to albumin
Elimination The major route of elimination of the products of PGE2 metabolism is the kidneys.
External Links
Wikipedia
RxList
Drugs.com

参考文献