362-29-8CCC(=O)c1ccc2c(c1)N(CC(C)N(C)C)c1ccccc1S2UVOIBTBFPOZKGP-UHFFFAOYSA-NPropiomazine is a member of the class of phenothiazines that is 10H-phenothiazine substituted by a 2-(dimethylamino)propyl group at nitrogen atom and a propanoyl group at position 2. It has a role as a sedative, a phenothiazine antipsychotic drug, a histamine antagonist, a serotonergic antagonist, a dopaminergic antagonist and a muscarinic antagonist. It is a member of phenothiazines, a tertiary amino compound and an aromatic ketone. It derives from a hydride of a 10H-phenothiazine.
4.5
4.4
SLOWLY OXIDIZED WHEN MOISTENED OR IN AQUEOUS SOLN ON PROLONGED EXPOSURE TO AIR &/OR LIGHT; 1 G SOL IN 4.5 ML WATER; FREELY SOL IN ALCOHOL; INSOL IN BENZENE /HYDROCHLORIDE/
7.03e-03 g/L
MP: 160-161 °C; CRYSTALS FROM ISOPROPANOL /MALEATE/
MP: 201-206 °C /HYDROCHLORIDE/
MP: 240-242 °C /METHIODIDE/
안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.
Warning
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P270, P272, P273, P280, P301+P317, P302+P352, P321, P330, P333+P317, P362+P364, P391, and P501 (click each P-code to see the statement)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
...ENHANCES EFFECT OF CNS DEPRESSANTS: HENCE, DOSE OF BARBITURATES GIVEN CONCOMITANTLY SHOULD BE REDUCED 1/2, DOSES OF MEPERIDINE & MORPHINE SHOULD BE REDUCED 1/4 TO 1/2. /HYDROCHLORIDE/
...ENHANCES ACTION OF...ANALGESICS & ANESTHETICS. /HYDROCHLORIDE/
.../REPORTED/ TO PROTECT EXPTL ANIMALS AGAINST HEPATOTOXIC EFFECTS OF CARBON TETRACHLORIDE...
PHYSOSTIGMINE WAS GIVEN TO 17 PT INLABOR PREVIOUSLY GIVEN SCOPOLAMINE ALONE OR MEPERIDINE & PROPIOMAZINE IN COMBINATION, TO ASCERTAIN ITS EFFECT ON REVERSING THE LOSS OF FETAL HEART RATE VARIABILITY. WITH MEPERIDINE & PROPIOMAZINE COMBINATION, REVERSION OCCURRED IN 10 PT.
Propiomazine is an antagonist at types 1, 2, and 4 dopamine receptors, serotonin (5-HT) receptor types 2A and 2C, muscarinic receptors 1 through 5, alpha(1)-receptors, and histamine H1-receptors. Its main use as a sedative is due to its antihistamine effect.
Rare, serious side effects include convulsions (seizures); difficult or unusually fast breathing; fast or irregular heartbeat or pulse; fever (high); high or low blood pressure; loss of bladder control; muscle stiffness (severe); unusual increase in sweating; unusually pale skin; and unusual tiredness or weakness.
N - Nervous system
QN - Nervous system
Propiomazine acts as an antagonist of dopamine 1, 2, and 4 receptors, serotonin (5-HT) receptor types 2A and 2C, muscarinic receptors 1 through 5, alpha(1)-receptors, and histamine H1-receptors. Its main use as a sedative is due to its antihistamine effect.
...ALSO HAS AN ANTIEMETIC ACTION. /HYDROCHLORIDE/
Unknown, but most likely hepatic as with other phenothiazines.
Unknown, but most likely hepatic as with other phenothiazines.
APPROX HALF OF METABOLITES OF COMMONLY USED PHENOTHIAZINES ARE FOUND IN URINE & REST IN FECES. ULTIMATE SOJOURN OF PHENOTHIAZINE DRUGS IN BODY IS EXCEEDINGLY LONG. 6 MO AFTER DISCONTINUATION OF THESE DRUGS, VARIOUS METABOLITES ARE DETECTABLE IN URINE. /PHENOTHIAZINES/
PHENOTHIAZINE TRANQUILIZERS CROSS PLACENTA RAPIDLY, & THEY HAVE BEEN MEASURED FOR MANY YR IN URINE & TISSUES OF NEONATES OF TREATED MOTHERS, BUT VERY LOW BLOOD LEVELS OF MOTHERS & FETUSES HAVE BEEN MEASURED ONLY RECENTLY... /PHENOTHIAZINES/
현재 필터 조건에 해당하는 반응 기록이 없습니다.
불러오는 중…
362-29-8DTXSID1023520CHEMBL1201210CHEBI:8491SEE PROMETHAZINE. ...CASE IS REPORTED OF 2-YR-OLD CHILD WHO INGESTED 250 MG WITH RESULTING CONFUSION, CONVULSIONS, & STUPOR, BUT EVENTUAL RECOVERY. /PROMETHAZINE/
PHENOTHIAZINES INHIBIT EJACULATION WITHOUT INTERFERING WITH ERECTION. /PHENOTHIAZINES/
MOST DANGEROUS EFFECTS OF PHENOTHIAZINES ARE THOSE RESULTING FROM HYPERSENSITIVITY REACTIONS, PARTICULARLY BLOOD DYSCRASIAS. THERAPEUTIC DOSES... MAY CAUSE FAINTNESS, PALPITATION, NASAL STUFFINESS, DRY MOUTH, & SOME SLIGHT CONSTIPATION. PT MAY COMPLAIN OF BEING COLD, DROWSY, OR WEAK. /PHENOTHIAZINES/
MOST TROUBLESOME SIDE EFFECT IS ORTHOSTATIC HYPOTENSION, WHICH MAY RESULT IN SYNCOPE. ... THERE IS GENERAL AGREEMENT THAT JAUNDICE FOLLOWING PHENOTHIAZINE ADMIN IS HYPERSENSITIVITY REACTION. ... LEUKOCYTOSIS, LEUKOPENIA, & EOSINOPHILIA OCCUR WITH PHENOTHIAZINE MEDICATION. /PHENOTHIAZINES/
For more Human Toxicity Excerpts (Complete) data for PROPIOMAZINE (8 total), please visit the HSDB record page.
MEDICATION
Propiomazine is largely used for its antihistamininc sleep inducing effects in treating insomnia.
SCHMITT ET AL, BULL SOC CHIM FRANCE 1957, 1474; SCHMITT, FRENCH PATENT ADDN 71,342 (ADDN TO FRENCH PATENT 1,176,919 TO CLI N-BYLA).
1-(PHENOTHIAZIN-2-YL)-1-PROPANONE IS CONDENSED WITH 2-(DIMETHYLAMINO)PROPYL CHLORIDE WITH THE AID OF A DEHYDROCHLORINATING AGENT SUCH AS SODAMIDE. THE PROPIOMAZINE THUS FORMED IS DISSOLVED IN A SUITABLE ORG SOLVENT & REACTED WITH AN EQUIMOLAR PORTION OF HYDROGEN CHLORIDE TO YIELD THE SALT. /HYDROCHLORIDE/
1678 CB, DOREVANE, INDORM, PROPAVAN. /MALEATE/
LARGON. /HYDROCHLORIDE/
용도Propiomazine is used in the preparation of analgesics as well as maintaining its own analgesic effects whilst applied to various neurological diseases.
정의ChEBI: A member of the class of phenothiazines that is 10H-phenothiazine substituted by a 2-(dimethylamino)propyl group at nitrogen atom and a propanoyl group at position 2.