Ritodrine hydrochloride
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Ritodrine hydrochloride
structure -
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CAS No:
23239-51-2
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Formula:
C17H21NO3.ClH
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Chemical Name:
Ritodrine hydrochloride
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Synonyms:
Benzenemethanol,4-hydroxy-α-[(1R)-1-[[2-(4-hydroxyphenyl)ethyl]amino]ethyl]-,hydrochloride (1:1),(αS)-rel-;Benzyl alcohol,p-hydroxy-α-[1-[(p-hydroxyphenethyl)amino]ethyl]-,hydrochloride,erythro-;Benzenemethanol,4-hydroxy-α-[1-[[2-(4-hydroxyphenyl)ethyl]amino]ethyl]-,hydrochloride,(R*,S*)-;Benzenemethanol,4-hydroxy-α-[(1R)-1-[[2-(4-hydroxyphenyl)ethyl]amino]ethyl]-,hydrochloride,(αS)-rel-;Ritodrine hydrochloride;DU 21220;Yutopar;Pre-Par;(±)-Ritodrine hydrochloride;Miolene;Prempar;Utemerin;Utopar;NSC 291565;52447-11-7
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Categories:
Active Pharmaceutical Ingredients > Hormones and the Endocrine System
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CAS No:
Description
Ritodrine hydrochloride (DU21220 hydrochloride) is a β-2 adrenergic receptor agonist.Target: β-2 Adrenergic ReceptorRitodrine is a tocolytic drug, used to stop premature labor. Ritodrine can significantly prolong a short interval more quickly but with relatively more side effects than magnesium sulphate. Stratified RCTs for different gestational ages and different labour stages should be designed for further study [1]. Ritodrine is a beta-2 adrenergic receptor agonist - a class of medica
Ritodrine hydrochloride is a primary amine.|An adrenergic beta-2 agonist used to control PREMATURE LABOR.
Ritodrine hydrochloride Basic Attributes
323.81
323.128815
245-514-8
DTXSID8045438
G - Genito urinary system and sex hormones
2922504500
Characteristics
72.72000
3.54490
1.213 g/cm3
193-195 °C (decomp)
512.3ºC at 760 mmHg
175.6ºC
-20°C Freezer
166.5 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]
Safety Information
NONH for all modes of transport
3
22
36
DO6524000
Xn
H302
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 41 companies from 3 notifications to the ECHA C&L Inventory.
Drug Information
Drugs that prevent preterm labor and immature birth by suppressing uterine contractions (TOCOLYSIS). Agents used to delay premature uterine activity include magnesium sulfate, beta-mimetics, oxytocin antagonists, calcium channel inhibitors, and adrenergic beta-receptor agonists. The use of intravenous alcohol as a tocolytic is now obsolete. (See all compounds classified as Tocolytic Agents.)|Compounds bind to and activate ADRENERGIC BETA-2 RECEPTORS. (See all compounds classified as Adrenergic beta-2 Receptor Agonists.)|Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)
DU 21220
Ritodrine hydrochloride Use and Manufacturing
Tocolytic
Human Drugs -> FDA Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book) -> Active Ingredients
Computed Properties
Molecular Weight:323.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:323.1288213
Monoisotopic Mass:323.1288213
Topological Polar Surface Area:72.7
Heavy Atom Count:22
Complexity:284
Defined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It acts on the β2 receptors of uterine smooth muscle, thereby inhibiting the contraction frequency and intensity of uterine smooth muscle. It is a drug that can be taken orally, intramuscularly, or intravenously to effectively prolong pregnancy and prevent premature birth.
Registered Holders
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Hainan Wuren Pharmaceutical Co., Ltd.
Active
China
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Suzhou Lixin Pharmaceutical Co., Ltd.
Active
China
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Jumpcan Pharmaceutical Group Co., Ltd.
Active
China
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