Details
Stereochemistry | MIXED |
Molecular Formula | C19H26N2O5S |
Molecular Weight | 394.485 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(CCNC(C)C(O)C2=CC=C(O)C(NS(C)(=O)=O)=C2)C=C1
InChI
InChIKey=REDZESHOHKCYCT-UHFFFAOYSA-N
InChI=1S/C19H26N2O5S/c1-13(20-11-10-14-4-7-16(26-2)8-5-14)19(23)15-6-9-18(22)17(12-15)21-27(3,24)25/h4-9,12-13,19-23H,10-11H2,1-3H3
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22185153
Curator's Comment: refernce retrieved from https://link.springer.com/book/10.1007/978-1-4757-2085-3#about
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Sulfonanilides. II. Analogs of Catecholamines. | 1967 May 1 |
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Inhibition of human premature labor by mesuprine hydrochloride. | 1971 Jan |
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Effect of mesuprine hydrochloride upon nonpregnant uterine contractility and the cardiovascular system. | 1971 Sep 15 |
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Mesovarial leiomyomas in rats in a chronic toxicity study of mesuprine hydrochloride. | 1972 Dec |
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The effect of mesuprine HC1 on selected smooth muscles. | 1972 Mar |
Patents
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100000081190
Created by
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DTXSID60864089
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C174707
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SUB08796MIG
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7541-30-2
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CHEMBL2111039
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24171
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2629
Created by
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MEO9P8EX05
Created by
admin on Fri Dec 15 15:16:56 UTC 2023 , Edited by admin on Fri Dec 15 15:16:56 UTC 2023
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ACTIVE MOIETY