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Bevantolol

HCID 2372
노트반응
기본 정보개요이름 및 식별자물성화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
59170-23-9
표준 SMILES
COc1ccc(CCNCC(O)COc2cccc(C)c2)cc1OC
InChIKey
HXLAFSUPPDYFEO-UHFFFAOYSA-N
분자식
C20H27NO4
평균 분자량
345.4 g/mol
단동위원소 질량
345.19400834

개요

Bevantolol is a propanolamine that is 3-aminopropane-1,2-diol in which the hydrogen of the primary hydroxy group is substituted by 3-methylphenyl and one of the hydrogens attached to the nitrogen is substituted by 2-(3,4-dimethoxyphenyl)ethyl. A beta1 adrenoceptor antagonist, it has been shown to be as effective as other beta-blockers for the treatment of angina pectoris and hypertension. It has a role as a beta-adrenergic antagonist, an antihypertensive agent, an anti-arrhythmia drug and a calcium channel blocker.

이름 및 식별자

우선 이름
Bevantolol
IUPAC
1-[2-(3,4-dimethoxyphenyl)ethylamino]-3-(3-methylphenoxy)propan-2-ol
영어명
Bevantolol
분자식
C20H27NO4
분자량
345.43

이름 및 동의어

Bevantolol59170-23-9Bevantololum1-(3,4-Dimethoxyphenethylamino)-3-(m-tolyloxy)-2-propanol(+-)-bevantolol1-((2-(3,4-Dimethoxyphenyl)ethyl)amino)-3-(3-methylphenoxy)-2-propanolNSC-13234834ZXW6ZV211-{[2-(3,4-dimethoxyphenyl)ethyl]amino}-3-(3-methylphenoxy)propan-2-ol1-(3,4-dimethoxyphenethylamino)-3-m-tolyloxy-propan-2-olCHEBI:238698DTXSID70860597
이름 더 보기
Bevanolol.NSC 132348DL-BevantololBevantolol USP/EP/BP1-((3,4-DiMethoxyphenethyl)aMino)-3-(M-tolyloxy)propan-2-ol1-[(3,4-Dimethoxyphenethyl)amino]-3-(m-tolyloxy)-2-propanol1-(3,4-Dimethoxyphenethylamino)-3-(3-methylphenoxy)-2-propanol2-Propanol, 1-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-3-(3-methylphenoxy)-
1-[2-(3,4-Dimethoxy-phenyl)-ethylamino]-3-m-tolyloxy-propan-2-olCI-7751-(2-(3,4-Dimethoxy-phenyl)-ethylamino)-3-m-tolyloxy-propan-2-ol1-((2-(3,4-dimethoxyphenyl)ethyl)amino)-3-(3-methylphenoxy)propan-2-olRefChem:119574C07AB06DTXCID80197265Bevantololum [INN-Latin]

데이터베이스 식별자

CAS
59170-23-9
PubChem CID
2372
DTXSID
DTXSID70860597
ChEMBL
CHEMBL314010
ChEBI
CHEBI:238698
UNII
34ZXW6ZV21
Nikkaji
J12.450H

물성

구조 계산 물성

XLogP
3
극성 표면적
60 Ų
수소 결합 공여자 수
2
수소 결합 수용자 수
5
회전 가능 결합 수
10
무거운 원자 수
25
형식 전하
0
복잡도
355

실험 및 물리화학적 성질

LogP · 2건

3.00

3.0

Solubility1.37e-02 g/L
Melting Point · 2건

137-138 °C

137 - 138 °C

Physical DescriptionSolid

물리화학적 성질

저장 조건
2 · 2-8°C

화학 및 산업

약리 정보

ATC Code · 2건

C - Cardiovascular system

QC - Cardiovascular system

PharmacodynamicsBevantolol is a beta-1 adrenoceptor antagonist that has been shown to be as effective as other beta blockers for the treatment of angina pectoris and hypertension.
Mechanism of Action · 1건

Animal experiments confirm both agonist and antagonist effects on alpha-receptors, in addition to antagonist activity at beta-1 receptors. By binding and antagonizing beta-1 receptors Bevantolol inhibits the normal normal epinephrine-mediated sympathetic actions such as increased heart rate. This has the effect of decreasing preload and blood pressure.

MeSH Pharmacological ClassificationDrugs that bind to and block the activation of ADRENERGIC BETA-1 RECEPTORS.
Cellular LocationsMembrane
Metabolite PathwaysBevantolol Action Pathway

상·하류 제품 정보

상류 원료

염산m-크레졸에피클로로하이드린

공급사11 곳

杭州摩库生物医药科技有限公司+86-057181025280; +8617767106207 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
绵阳万迪诺医药科技有限公司15681201579 15861805752 · [email protected]
上海陶术生物科技股份有限公司13564774135 · [email protected]
江苏艾康生物医药研发有限公司025-58859352 13913916777 · [email protected]
湖北摩科化学有限公司18627753421; 18627756402 · [email protected]
ANHUI WITOP BIOTECH CO., LTD+8618071025641 · [email protected]
TargetMol中国(陶术生物)4008200310 15002144251 · [email protected]
Alchem Pharmtech,Inc.8485655694 · [email protected]
南京宁吉通医药生物科技有限公司0-19710401727 19710401727 · [email protected]
Dideu Industries Group Limited+86-29-81148696 +86-15129568250 · [email protected]

관련 반응

2건
반응 기록 만들기
HRID 104220 반응식
HRID 104220생성물로Training data from https://doi.org/10.1039/C8SC04228D (2/10)
HRID 1769826 반응식
HRID 1769826생성물로uspto-grants-1995_01

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