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Details

Stereochemistry RACEMIC
Molecular Formula C13H19N2O3
Molecular Weight 251.3016
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of RIMAZOLIUM

SMILES

CCOC(=O)C1=C[N+](C)=C2CCCC(C)N2C1=O

InChI

InChIKey=JOWRFSPJFXLGGY-UHFFFAOYSA-N
InChI=1S/C13H19N2O3/c1-4-18-13(17)10-8-14(3)11-7-5-6-9(2)15(11)12(10)16/h8-9H,4-7H2,1-3H3/q+1

HIDE SMILES / InChI
1,6-Dimethyl-3-carbethoxy-4-oxo-6,7,8,9-tetrahydro-homopyrimidazol (rimazolium, MZ-144) is an analgesic (non-narcotic). It proved to be effective in all the analgesic assays used (independently of the nociceptive stimulus applied) (hot plate, tail flick, writhing tests, Randall-Selitto test, tail clip, surgical pain) differing in this respect from the nonsteroidal antiinflammatory analgetics. Rimazolium lacks the capacity of producing opiate-like physiological dependence. Also rimazolium fails to show any indication of narcotic-like abuse liability by any of clinical assessments. Rimazolium is registered in Hungary under the brand name Probon. In Hungary among analgesics Probon is the first of choice especially in case of chronic pain accompanying chronic respiratory tract diseases.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Effect of rimazolium (Probon) on biotransformation reactions in the rat].
1982 Nov
Analgesic profile of rimazolium as compared to different classes of pain killers.
1988 Apr
Patents

Sample Use Guides

LD50 in rats (mg/kg): 220 i.v.; 720 i.p.; 790 s.c.; 1600 orally
Route of Administration: Other
In Vitro Use Guide
Rimazolium inhibits ethylmorphine-N-demethylation and ethoxycoumarin-O-deethylation by rat liver homogenate when added in vitro in dependence on reaction differently, but marked effects are observed with high concentrations only (10(-3) mol).
Name Type Language
RIMAZOLIUM
WHO-DD  
Common Name English
Rimazolium [WHO-DD]
Common Name English
3-(ETHOXYCARBONYL)-6,7,8,9-TETRAHYDRO-1,6-DIMETHYL-4-OXO-4H-PYRIDO91,2-A)PYRIMIDINIUM
Common Name English
RIMAZOLIUM ION
Common Name English
RIMAZOLIUM CATION
Common Name English
Classification Tree Code System Code
WHO-ATC N02BG02
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
NCI_THESAURUS C257
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
WHO-VATC QN02BG02
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
Code System Code Type Description
SMS_ID
100000078663
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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MESH
C100296
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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FDA UNII
967Y95129A
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EPA CompTox
DTXSID20865436
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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NCI_THESAURUS
C84138
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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DRUG BANK
DB13289
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EVMPD
SUB15142MIG
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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DRUG CENTRAL
4032
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ECHA (EC/EINECS)
252-644-9
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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PUBCHEM
71940
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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WIKIPEDIA
Rimazolium
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CAS
35615-72-6
Created by admin on Fri Dec 15 16:13:55 GMT 2023 , Edited by admin on Fri Dec 15 16:13:55 GMT 2023
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