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Midazolam Maleate

HCID 5384200
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
59467-94-6
표준 SMILES
Cc1ncc2n1-c1ccc(Cl)cc1C(c1ccccc1F)=NC2.O=C(O)/C=C\C(=O)O
InChIKey
XYGVIBXOJOOCFR-BTJKTKAUSA-N
분자식
C22H17ClFN3O4
평균 분자량
441.8 g/mol
단동위원소 질량
441.0891619

개요

See also: Midazolam (has active moiety); Midazolam Hydrochloride (related); Benperidol (annotation moved to).

이름 및 식별자

우선 이름
Midazolam Maleate
IUPAC
(Z)-but-2-enedioic acid;8-chloro-6-(2-fluorophenyl)-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine
영어명
Midazolam maleate salt
분자식
C22H17ClFN3O4
분자량
441.84

이름 및 동의어

Midazolam maleate59467-94-6Midazolam (as maleate)Ro 21-3981/001NSC-313452Ro-213981-003Ro-21-3981/00177520S18SE4H-Imidazo(1,5-a)(1,4)benzodiazepine, 8-chloro-6-(2-fluorophenyl)-1-methyl-, (Z)-2-butenedioate (1:1)RefChem:158831261-775-0Dormicum maleate
이름 더 보기
dormicummidazolammaleateRo-21-3981ro21-3981/001dormicummaleateMidazolam maleate salt USP/EP/BPmidazolam maleate--dea schedule iv itemDL-A-LYSOPHOSPHATIDYLCHOLINE-*GAMMA-O-HE XADECYL
Midazolam maleate saltMidazolam maleate [USAN]VersedMidazolam maleate (USAN)[13C6]-Midazolam maleate salt59467-94-6 (unlabeled)8-Chloro-6-(o-fluorophenyl)-1-methyl-4H-imidazo(1,5-a)(1,4)benzodiazepine maleate (1:1)EINECS 261-775-0

데이터베이스 식별자

CAS
59467-94-6
PubChem CID
5384200

물성

구조 계산 물성

극성 표면적
105 Ų
수소 결합 공여자 수
2
수소 결합 수용자 수
7
회전 가능 결합 수
3
무거운 원자 수
31
형식 전하
0
복잡도
590

물리화학적 성질

녹는점
114 · 114-117° (solvated)
저장 조건
2 · 2-8°C
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
고체
색상
흰색에서 황백색까지
안정성
흡습성

안전 및 규제

GHS 분류

GHS Classification · 4건

Warning

H302 (46.4%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 97 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Regulatory Information · 2건

REACH registered substance: 8-chloro-6-(2-fluorophenyl)-1-methyl-4H-imidazo[1,5-a][1,4]benzodiazepine monomaleate (EC: 261-775-0)

4H-Imidazo1,5-a1,4benzodiazepine, 8-chloro-6-(2-fluorophenyl)-1-methyl-, (2Z)-2-butenedioate (1:1): Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.

Hazard Classes and CategoriesAcute Tox. 4 (46.4%)

안전 데이터

wgk
3
rtecs
NI2922200
ridadr
3249
독성
LD50 in male mice (mg/kg): 760 orally; 86 i.v. (Pieri)
risk_code
22
hazard_code
Xn
safety_code
36
포장분류
III
위험 등급
6.1(b)

화학 및 산업

약리 정보

MeSH Pharmacological Classification · 5건

Agents that are administered in association with anesthetics to increase effectiveness, improve delivery, or decrease required dosage.

Drugs used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.

Agents that alleviate ANXIETY, tension, and ANXIETY DISORDERS, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions. ADRENERGIC BETA-ANTAGONISTS are commonly used in the symptomatic treatment of anxiety but are not included here.

Ultrashort-acting anesthetics that are used for induction. Loss of consciousness is rapid and induction is pleasant, but there is no muscle relaxation and reflexes frequently are not reduced adequately. Repeated administration results in accumulation and prolongs the recovery time. Since these agents have little if any analgesic activity, they are seldom used alone except in brief minor procedures. (From AMA Drug Evaluations Annual, 1994, p174)

Substances that do not act as agonists or antagonists but do affect the GAMMA-AMINOBUTYRIC ACID receptor-ionophore complex. GABA-A receptors (RECEPTORS, GABA-A) appear to have at least three allosteric sites at which modulators act: a site at which BENZODIAZEPINES act by increasing the opening frequency of GAMMA-AMINOBUTYRIC ACID-activated chloride channels; a site at which BARBITURATES act to prolong the duration of channel opening; and a site at which some steroids may act. GENERAL ANESTHETICS probably act at least partly by potentiating GABAergic responses, but they are not included here.

응용 분야

용도Sedative; ligand GABA receptor benzodiazepine modulatory site

상·하류 제품 정보

상류 원료

5-(2-클로로에틸)-2,3-디히드로벤조푸란

관련 반응

3건
반응 기록 만들기
HRID 502497 반응식
HRID 502497생성물로uspto-grants-2010_08
HRID 502498 반응식
HRID 502498생성물로uspto-grants-2010_08
HRID 1042554 반응식
HRID 1042554생성물로uspto-grants-2013_10

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
ChEMBL
CHEMBL2106922
UNII
77520S18SE
EC Number
261-775-0