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Propiomazine

HCID 4940
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
362-29-8
표준 SMILES
CCC(=O)c1ccc2c(c1)N(CC(C)N(C)C)c1ccccc1S2
InChIKey
UVOIBTBFPOZKGP-UHFFFAOYSA-N
분자식
C20H24N2OS
평균 분자량
340.5 g/mol
단동위원소 질량
340.16093457

개요

Propiomazine 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.

이름 및 식별자

우선 이름
Propiomazine
IUPAC
1-[10-[2-(dimethylamino)propyl]phenothiazin-2-yl]propan-1-one
영어명
propiomazine
분자식
C20H24N2OS
분자량
340.48

이름 및 동의어

propiomazine362-29-8PropionylpromethazinePhenoctylPropiomazinaPropiomazinumWy-13591-{10-[2-(dimethylamino)propyl]-10H-phenothiazin-2-yl}propan-1-oneCB 16782-Propionyl-10-(2-(dimethylamino)propyl)phenothiazine3-Propionyl-10-dimethylaminoisopropylphenothiazine10-(2-Dimethylaminopropyl)-2-propionylphenothiazine
이름 더 보기
(±)-Propiomazinepropiomazine USP/EP/BP1-[10-[2-(Dimethylamino)propyl]phenothiazin-2-yl-1-propanone1-[10-[2-(dimethylamino)propyl]phenothiazin-2-yl]propan-1-one1-[10-[2-(Dimethylamino)propyl]-10H-phenothiazin-2-yl]propan-1-one1-{10-[2-(dimethylamino)propyl]-10H-phenothiazin-2-yl}-1-propanone1-Propanone, 1-[10-[2-(dimethylamino)propyl]-10H-phenothiazin-2-yl]-
DorevanPropavanCB-1678DorevaneIndorm10-Dimethylaminoisopropyl-2-propionylphenothiazine242Z0PM79Y1-Propanone, 1-(10-(2-(dimethylamino)propyl)-10H-phenothiazin-2-yl)-

물성

구조 계산 물성

XLogP
4.8
극성 표면적
48.9 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
4
회전 가능 결합 수
5
무거운 원자 수
24
형식 전하
0
복잡도
441

실험 및 물리화학적 성질

LogP · 2건

4.5

4.4

Solubility · 2건

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

Human DrugsPharmaceuticals
Boiling Point235-245 °C @ 0.5 MM HG
Melting Point · 3건

MP: 160-161 °C; CRYSTALS FROM ISOPROPANOL /MALEATE/

MP: 201-206 °C /HYDROCHLORIDE/

MP: 240-242 °C /METHIODIDE/

Physical DescriptionSolid
Other Experimental PropertiesPRACTICALLY ODORLESS; YELLOW POWDER /HYDROCHLORIDE/

물리화학적 성질

끓는 점
0.5 · bp0.5 235-245°
밀도
1.137 · 1.137±0.06 g/cm3(Predicted)
산도 계수 (pKa)
6.6 · pKa 6.6(H2O) (Uncertain)

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 4건

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.

유해성 정보

Hazard Classes and CategoriesAcute Tox. 4 (100%)

독성 정보

Interactions · 4건

...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.

Health EffectsThey cause slurred speech, disorientation and "drunken" behavior. They are physically and psychologically addictive.
Toxicity Summary · 1건

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.

Signs and Symptoms · 1건

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.

화학 및 산업

약리 정보

ATC Code · 2건

N - Nervous system

QN - Nervous system

Protein Binding81%
PharmacodynamicsAlthough propiomazine is a phenothiazine, it is not used as an antipsychotic. It posesses antihistamine effects and is mostly used as a sedative in treating insomnia.
Mechanism of Action · 2건

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/

Metabolism/Metabolites · 2건

Unknown, but most likely hepatic as with other phenothiazines.

Unknown, but most likely hepatic as with other phenothiazines.

Absorption, Distribution and Excretion · 2건

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/

Cellular LocationsMembrane
Metabolite PathwaysPropiomazine H1-Antihistamine Action

용도 및 제조

Uses

관련 반응

0건
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화합물 노트

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이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트

데이터베이스 식별자

CAS
362-29-8
PubChem CID
4940
DTXSID
DTXSID1023520
ChEMBL
CHEMBL1201210
ChEBI
CHEBI:8491
UNII
242Z0PM79Y
EC Number
206-646-1
Nikkaji
J5.699E
Human Toxicity Excerpts · 5건

SEE 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.

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

안전 데이터

유해 물질 데이터
362-29-8(Hazardous Substances Data)
· 2건

MEDICATION

Propiomazine is largely used for its antihistamininc sleep inducing effects in treating insomnia.

Methods of Manufacturing · 2건

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/

Formulations/Preparations · 2건

1678 CB, DOREVANE, INDORM, PROPAVAN. /MALEATE/

LARGON. /HYDROCHLORIDE/

Use ClassificationPharmaceuticals

응용 분야

용도Propiomazine is used in the preparation of analgesics as well as maintaining its own analgesic effects whilst applied to various neurological diseases.

공급사26 곳

北京华美互利生物化工010-56205725 · [email protected]
湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
United Life Science020-82099279 18988968278 · [email protected]
湖北广奥生物科技有限公司027-02702759223056 18162699093 · [email protected]
湖北成海化工有限公司027-59220433 18327245847 · [email protected]
上海复和化学科技有限公司0086-21-67651709 · [email protected]
Wuhan NCE Biomedical Co.,Ltd.4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
南京政琦科技有限公司19853943728 19853943728 · [email protected]
HANGZHOU LEAP CHEM CO., LTD.+86-571-87711850 +86-15355479329 · [email protected]
陕西缔都医药化工有限公司+86-29-81139210 +86-17392587031 · [email protected]
上海源叶生物科技有限公司18916372613 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
上海芮晖化工科技有限公司021-31433387 15618786686 · [email protected]
深圳聚合生化科技有限公司+86-400-002-6226 13028896684 · [email protected]
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.+8618950047208 · [email protected]
陕西萃康医药科技有限公司13186333400 19299362551 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
北京百灵威科技有限公司18210857532 18210857532 · [email protected]
上海传芊化工科技中心15869524721 · [email protected]
Hefei TNJ Chemical Industry Co.,Ltd.+86-0551-65418671 +86-189 4982 3763 · [email protected]
南京世洲生物科技有限公司17301488900 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]
河南伊诺凯新材料有限公司15090072163 · [email protected]
湖北实顺生物科技有限公司027-59223025 15107168801 · [email protected]

추가 설명

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.