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엡셀렌

Ebselen

HCID 3194
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
60940-34-3
표준 SMILES
O=c1c2ccccc2[se]n1-c1ccccc1
InChIKey
DYEFUKCXAQOFHX-UHFFFAOYSA-N
분자식
C13H9NOSe
평균 분자량
274.181 g/mol
단동위원소 질량
274.98493521

이름 및 식별자

우선 이름
Ebselen
IUPAC
2-Phenyl-1,2-benzoselenazol-3(2H)-one
현지명
엡셀렌
영어명
Ebselen
분자식
C13H9NOSe
분자량
274.18

이름 및 동의어

엡셀렌SPI-10052-PHENYL-1,2-BENZISOSELENAZOL-3(2H)-ONEPZ51DR-3305EBSELENRP-60931CCG-39161NSC 639762Ebselen>Ebselen,99%

데이터베이스 식별자

CAS
60940-34-3
PubChem CID
3194
DTXSID
DTXSID7045150
ChEMBL
CHEMBL51085
ChEBI
CHEBI:77543
UNII
40X2P7DPGH
EC Number
612-054-8
Nikkaji
J22.968G

물성

물리화학적 성질

녹는점
176 · 176-182 °C
끓는 점
402.8 · 402.8±28.0 °C(Predicted)
저장 조건
2 · 2-8°C
용해도
에탄올, 메탄올, 아세톤, 아세토니트릴에 용해됩니다.
산도 계수 (pKa)
-0.4 · -0.40±0.20(Predicted)
물리적 상태
결정성 분말
색상
노란색에서 베이지색
생물학적 소스
rabbit
Merck
14 · 14,3486
안정성
2 · 제공된 대로 구매일로부터 2년 동안 안정적입니다. DMSO 또는 에탄올 용액은 -20°에서 최대 3개월 동안 보관할 수 있습니다.
InChI
InChI=1S/C13H9NOSe/c15-13-11-8-4-5-9-12(11)16-14(13)10-6-2-1-3-7-10/h1-9H
InChIKey
DYEFUKCXAQOFHX-UHFFFAOYSA-N
SMILES
[Se]1C2=C(C=CC=C2)C(=O)N1C1=CC=CC=C1

화학적 성질

yellow to beige crystalline powder

안전 및 규제

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

안전 데이터

wgk
3
rtecs
DE4140750
ridadr
UN 3283 6.1/PG 3
HS 번호
29310099
risk_code
23/25-33-50/53-36/37/38
hazard_code
T,N,Xi
safety_code
20/21-28-45-60-61-28A-36/37-26
포장분류
III
위험 등급
6.1
Hazard Classifications
Acute Tox. 3 InhalationAcute Tox. 3 OralAquatic Acute 1Aquatic Chronic 1STOT RE 2
스토리지 클래스
6.1D - Non-combustible acute toxic Cat.3toxic hazardous materials or hazardous materials causing chronic effects

화학 및 산업

응용 분야 · 3건

개요Ebselen is one of the selenium-containing anti-inflammatory drugs.In 2003, Rocha and co-workers identified diselenides as a new class of antiinflammatory agents.In 2014, Nogueira and co-workers reported the synthesis and anti-inflammatory activity of salicyclic-based diselenides and selenocynates.Recently, Wilhelm and co-workers identified 4-phenylselenyl-7-chloroquinoline 270 as a potent antiinflammatory compound.

용도Ebselen is a lipid-soluble organoselenium compound. Numerous in vivo experiments have demonstrated that ebselen is able to inhibit both vasospasm and tissue damage in cerebral stroke/ischemia animal models (i.e. rat, mice, guinea pig and dog).For example, ebselen has been shown to provide significant protection against ischemic damage in both gray and white matter, and in the ventral posterior nucleus of rodent brains.Additionally, administration of ebselen in gerbils significantly reduces neuronal death induced by ischemia and reperfusion in the hippocampal CA1 region.It has been reported that ebselen inhibits inositol monophosphatase and acts as a safe treatment for bipolar disorder. The optimal GPx-like activity of ebselen was observed at neutral or nearphysiological pH (7.4), and the activity of ebselen was barely detected in acidic medium.During ischemia, brain pH falls rapidly within the first 5 min from 7.0 to 6.2, which is not optimal for ebselen's GPx-like activity.Meanwhile, since ebselen has shown promising activity in the treatment of stroke, it seems that GPx-like activity of ebselen in the brain may not occur.Thus, the enzymatic reduction of ebselen by TrxR might be the main contribution to its antioxidant property during ischemia. Unlike inorganic and aliphatic selenium compounds, ebselen does not liberate the selenium moiety, which remains within the ring structure. Subsequent metabolism involves methylation, glucuronidation and hydroxylation. Additionally, ebselen could also inhibit enzymes such as lipoxygenases, nitric oxide synthases, nitrogen oxides, protein kinase C and H1/K1-ATPase. Besides the relationship with redox systems, another neuroprotective mechanism of ebselen is involved in controlling the expression of gaminobutyric acid shunt enzymes to supply the tricarboxylic acid cycle, and significantly inhibiting acetylcholinesterase activity,demonstrating its engagement in the metabolic system.

일반 설명Ebselen is a sympathomimetic amine.

상·하류 제품 정보

상류 원료

관련 반응

7건
반응 기록 만들기
HRID 568924 반응식
HRID 568924반응물로uspto-grants-1988_03
HRID 568925 반응식
HRID 568925반응물로uspto-grants-1988_03
HRID 568926 반응식
HRID 568926반응물로uspto-grants-1988_03
HRID 568927 반응식
HRID 568927반응물로uspto-grants-1988_03
HRID 568928 반응식
HRID 568928반응물로uspto-grants-1988_03
HRID 2290788 반응식
HRID 2290788반응물로uspto-grants-1986_10
HRID 2290789 반응식
HRID 2290789반응물로uspto-grants-1986_10

화합물 노트

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이 페이지에서기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
Benzoyl chloride, 2-(chloroseleno)-1,3,4,6,7,9,9b-헵타아자페날렌-2,5,8-트리아민아닐린

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추가 설명

정의ChEBI: A benzoselenazole that is 1,2-benzoselenazol-3-one carrying an additional phenyl substituent at position 2. Acts as a mimic of glutathione peroxidase.