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Debrisoquine

HCID 2966
노트반응
기본 정보이름 및 식별자물성화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
1131-64-2
표준 SMILES
N=C(N)N1CCc2ccccc2C1
InChIKey
JWPGJSVJDAJRLW-UHFFFAOYSA-N
분자식
C10H13N3
평균 분자량
175.23 g/mol
단동위원소 질량
175.11094743

이름 및 식별자

우선 이름
Debrisoquine
IUPAC
3,4-dihydro-1H-isoquinoline-2-carboximidamide
영어명
debrisoquine
분자식
C10H13N3
분자량
175.23

이름 및 동의어

DebrisoquineDebrisoquin1131-64-2DebrisochinumDebrisoquinaDebrisoquinum2(1H)-Isoquinolinecarboximidamide, 3,4-dihydro-1,2,3,4-tetrahydroisoquinoline-2-carboximidamide3,4-dihydro-1H-isoquinoline-2-carboximidamideX31CDK040EDTXSID7022885CHEBI:34665
이름 더 보기
ebrisoquinDebrisochinDebrisoquine Monomer3,4-Dihydro-2(1H)-isoquinolinecarbimidamide3,4-DIHYDRO-1H-ISOQUINOLINE-2-CARBOXAMIDINE3,4-Dihydro-2(1H)-isoquinolinecarboximidamide
RefChem:388913DTXCID202885C02CC04214-470-1IsocaramidineTendor3,4-dihydroisoquinoline-2(1H)-carboximidamide3,4-Dihydro-2(1H)-isoquinolinecarboxamidine

데이터베이스 식별자

CAS
1131-64-2
PubChem CID
2966
DTXSID
DTXSID7022885
ChEMBL
CHEMBL169901
ChEBI
CHEBI:34665
UNII
X31CDK040E
EC Number
214-470-1
Nikkaji
J7.269I

물성

구조 계산 물성

XLogP
0.8
극성 표면적
53.1 Ų
수소 결합 공여자 수
2
수소 결합 수용자 수
1
회전 가능 결합 수
1
무거운 원자 수
13
형식 전하
0
복잡도
202

실험 및 물리화학적 성질

LogP · 2건

0.75

0.75

Melting Point · 2건

278-280 °C

278 - 280 °C

Physical DescriptionSolid

물리화학적 성질

녹는점
278 · 278-280 °C
끓는 점
309.8 · 309.8±52.0 °C(Predicted)
밀도
1.24 · 1.24±0.1 g/cm3(Predicted)
산도 계수 (pKa)
11.9 · pKa 11.9 (Uncertain)

화학 및 산업

약리 정보

ATC Code · 2건

C - Cardiovascular system;C02 - Antihypertensives;C02C - Antiadrenergic agents, peripherally acting;C02CC - Guanidine derivatives;C02CC04 - Debrisoquine

QC - Cardiovascular system;QC02 - Antihypertensives;QC02C - Antiadrenergic agents, peripherally acting;QC02CC - Guanidine derivatives;QC02CC04 - Debrisoquine

Pharmacodynamics · 1건

Debrisoquin is an adrenergic neuron-blocking drug similar in effects to guanethidine. It is a substrate for a polymorphic cytochrome P-450 enzyme. Persons with certain isoforms of this enzyme are unable to properly metabolize this and many other clinically important drugs. They are commonly referred to as having a debrisoquin 4-hydroxylase polymorphism.

Mechanism of Action · 1건

Debrisoquin acts at the sympathetic neuroeffector junction by inhibiting or interfering with the release and/or distribution of norepinephrine, rather than acting at the effector cell by inhibiting the association of norepinephrine with its receptors. It is taken up by norepinephrine transporters. It becomes concentrated in NE transmitter vesicles, replacing NE in these vesicles. This leads to a gradual depletion of NE stores in the nerve endings. Once inside the terminal it blocks the release of noradrenaline in response to arrival of an action potential. In contrast to ganglionic blocking agents, debrisoquin suppresses equally the responses mediated by alpha-and beta-adrenergic receptors but does not produce parasympathetic blockade. Since sympathetic blockade results in modest decreases in peripheral resistance and cardiac output, debrisoquin lowers blood pressure in the supine position. It further reduces blood pressure by decreasing the degree of vasoconstriction that normally results from reflex sympathetic nervous activity upon assumption of the upright posture, thus reducing venous return and cardiac output more.

Metabolism/Metabolites · 2건

Hepatic.

Debrisoquine has known human metabolites that include 4-Hydroxydebrisoquine.

MeSH Pharmacological Classification · 3건

Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS.

관련 반응

2건
반응 기록 만들기
HRID 542286 반응식
HRID 542286생성물로uspto-grants-1987_04
HRID 2231166 반응식
HRID 2231166생성물로uspto-grants-1988_11

화합물 노트

불러오는 중…

이 페이지에서기본 정보이름 및 식별자물성화학 및 산업관련 반응화합물 노트

Drugs that inhibit the actions of the sympathetic nervous system by any mechanism. The most common of these are the ADRENERGIC ANTAGONISTS and drugs that deplete norepinephrine or reduce the release of transmitters from adrenergic postganglionic terminals (see ADRENERGIC AGENTS). Drugs that act in the central nervous system to reduce sympathetic activity (e.g., centrally acting alpha-2 adrenergic agonists, see ADRENERGIC ALPHA-AGONISTS) are included here.

Drugs that act on adrenergic receptors or affect the life cycle of adrenergic transmitters. Included here are adrenergic agonists and antagonists and agents that affect the synthesis, storage, uptake, metabolism, or release of adrenergic transmitters.

Cellular LocationsCytoplasm;Extracellular

응용 분야

용도Antihypertensive.

상·하류 제품 정보

상류 원료

7-메톡시-1,2,3,4-테트라히드로-이소퀴놀린염화물

공급사13 곳

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