| Weight | 287.359 g/mol |
|---|---|
| Formula | C17H21NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
ritodrine (26652-09-5)
PrePar · Yutopar · Ritodrine Hydrochloride
Score:
#1330 in Physics
,
#3088 in Biology
,
#3859 in Chemistry
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- Treatment of preterm labor with the beta-adrenergic agonist ritodrine [2] (The New England Journal of Medicine, 1992)
- Nifedipine and ritodrine in the management of preterm labor: A randomized multicenter trial (Obstetrics & Gynecology, 1997)
- Double-blind, randomized, controlled trial of atosiban and ritodrine in the treatment of preterm labor: A multicenter effectiveness and safety study (American Journal of Obstetrics and Gynecology, 2000)
- Results of Double-blind, Multicentre Study with Ritodrine in Premature Labour (BMJ, 1971)
- A comparison of tocolysis with nifedipine or ritodrine: Analysis of efficacy and maternal, fetal, and neonatal outcome (American Journal of Obstetrics and Gynecology, 1990)
- Randomized comparative trial of indomethacin and ritodrine for the long-term treatment of preterm labor. (American Journal of Obstetrics and Gynecology, 1991)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - PrePar
- Yutopar
- Ritodrine Hydrochloride
- Pre Par
- DU21220
- Pre-Par
- DU-21220
- DU 21220
-
SMILESCC(C(C1=CC=C(C=C1)O)O)NCCC2=CC=C(C=C2)O
-
InChIKeyIOVGROKTTNBUGK-UHFFFAOYSA-N
- Pubchem - ritodrine
- Wikipedia - ritodrine
Ritodrine (trade name Yutopar) is a tocolytic drug used to stop premature labor. This drug has been removed from the US market, according to FDA Orange Book. It was available in oral tablets or as an injection and was typically used as the hydrochloride salt, ritodrine hydrochloride.
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Synthesis
Reactant
+
4-CHLOROPHENOL
(Grignard alcohol)
tyramine
+
Reactant
(Alkylation of primary amines)
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