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Details

Stereochemistry UNKNOWN
Molecular Formula C19H23NO.ClH
Molecular Weight 317.853
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CINNAMEDRINE HYDROCHLORIDE

SMILES

Cl.CC(C(O)C1=CC=CC=C1)N(C)C\C=C\C2=CC=CC=C2

InChI

InChIKey=RSBLYYMNHJDITE-NBYYMMLRSA-N
InChI=1S/C19H23NO.ClH/c1-16(19(21)18-13-7-4-8-14-18)20(2)15-9-12-17-10-5-3-6-11-17;/h3-14,16,19,21H,15H2,1-2H3;1H/b12-9+;

HIDE SMILES / InChI
Cinnamedrine is an active ingredient of midol (a combination of cinnamedrine hydrochloride, aspirin, phenacetin, and caffeine) used to relieve dysmenorrhea. Midol was an over-the-counter drug, which was discontinued due to a marketing decision.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
midol

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

Midol (a combination of cinnamedrine hydrochloride, aspirin, phenacetin, and caffeine) - two tablets every four hours, with a maximum eight tablets per day.
Route of Administration: Oral
In Vitro Use Guide
It was examined influence of cinnamedrine on the smooth muscle relaxing properties using rat uterus. Cinnamedrine exhibited dose-related spasmolytic activity in the isolated spontaneously contracting rat uterus and in uterine tissue pretreated with oxytocin to augment spasms. The IC50's for cinnamedrine was 36.2 microM; the IC50's after oxytocin pretreatment was 25.7 microM for cinnamedrine.
Name Type Language
CINNAMEDRINE HYDROCHLORIDE
MART.   VANDF   WHO-DD  
Common Name English
Cinnamedrine hydrochloride [WHO-DD]
Common Name English
CINNAMEDRINE HYDROCHLORIDE [MART.]
Common Name English
CINNAMEDRINE HYDROCHLORIDE [VANDF]
Common Name English
CINNAMEDRINE HCL
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C87053
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C87469
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID90944848
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
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RXCUI
314557
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
244-830-3
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY
FDA UNII
T4B6SPQ0UF
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY
SMS_ID
100000176129
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
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PUBCHEM
6434842
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY
CAS
22194-13-4
Created by admin on Fri Dec 15 15:48:56 GMT 2023 , Edited by admin on Fri Dec 15 15:48:56 GMT 2023
PRIMARY