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(+/-)-블비스타틴

1-Phenyl-1,2,3,4-tetrahydro-4-hydroxypyrrolo(2.3-b)-7-methylquinolin-4-one

HCID 3476986
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
674289-55-5
표준 SMILES
Cc1ccc2c(c1)C(=O)C1(O)CCN(c3ccccc3)C1=N2
InChIKey
LZAXPYOBKSJSEX-UHFFFAOYSA-N
분자식
C18H16N2O2
평균 분자량
292.338 g/mol
단동위원소 질량
292.12117775

이름 및 식별자

우선 이름
1-Phenyl-1,2,3,4-tetrahydro-4-hydroxypyrrolo(2.3-b)-7-methylquinolin-4-one
IUPAC
3a-Hydroxy-6-methyl-1-phenyl-1,2,3,3a-tetrahydro-4H-pyrrolo[2,3-b]quinolin-4-one
현지명
(+/-)-블비스타틴
영어명
(+/-)-BLEBBISTATIN
분자식
C18H16N2O2
분자량
292.33

이름 및 동의어

(+/-)-블비스타틴(±)Bebbistatin(+/-)-BLEBBISTATIN(R)-(+)-BLEBBISTATINBlebbistatin, 10 mM in DMSOE1249 (+/-)-Blebbi- Calbiochem(±)-Blebbistatin (DMSO Solution)Blebbistatin,Inhibitor,Myosin,inhibit(±)-Blebbistatin, inhibitor of myosin II(±)-Blebbistatin, inhibitor of myosin II3a-hydroxy-6-methyl-1-phenyl-2,3-dihydropyrrolo[2,3-b]quinolin-4-one

데이터베이스 식별자

CAS
674289-55-5
PubChem CID
3476986
DTXSID
DTXSID501017342
ChEMBL
CHEMBL1328324
ChEBI
CHEBI:75379
UNII
20WC4J7CQ6
Nikkaji
J1.888.295G

물성

물리화학적 성질

녹는점
210 · 210-212°C
끓는 점
507.3 · 507.3±60.0 °C(Predicted)
밀도
1.31 · 1.31±0.1 g/cm3(Predicted)
저장 조건
20 °C · −20°C
용해도
클로로포름(약간 용해됨), 디클로로메탄, DMSO, 에틸아세테이트, 메탄올에 용해됨
산도 계수 (pKa)
11.15 · 11.15±0.20(Predicted)
물리적 상태
밝은 노란색 고체.
색상
노란색
InChI
InChI=1S/C18H16N2O2/c1-12-7-8-15-14(11-12)16(21)18(22)9-10-20(17(18)19-15)13-5-3-2-4-6-13/h2-8,11,22H,9-10H2,1H3
InChIKey
LZAXPYOBKSJSEX-UHFFFAOYSA-N
SMILES
N1C2=C(C=C(C)C=C2)C(=O)C2(O)CCN(C3=CC=CC=C3)C=12

화학적 성질

Bright Yellow Solid

안전 및 규제

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

안전 데이터

wgk
WGK 2
risk_code
20/21/22-36/37/38
hazard_code
Xn
safety_code
26-36/37
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 2건

개요(±)-Blebbistatin is a racemic mixture of (–)-blebbistatin and (+)-blebbistatin , the active and inactive forms, respectively. (–)-Blebbistatin is a selective cell-permeable inhibitor of non-muscle myosin II ATPases. (–)-Blebbistatin rapidly and reversibly inhibits Mg-ATPase activity and in vitro motility of non-muscle myosin IIA and IIB for several species (IC50s = 0.5-5 μM), while poorly inhibiting smooth muscle myosin (IC50 = 8 μM). Through these effects, (–)-blebbistatin blocks apoptosis-related bleb formation, directed cell migration, and cytokinesis in vertebrate cells. However, prolonged exposure to blue light (450-490 nm) results in degradation of blebbistatin to an inactive product via cytotoxic intermediates, which may be problematic for its use in fluorescent live cell imaging applications. (S)-nitro-Blebbistatin and (R)-nitro-blebbistatin are more stable forms of (–)-blebbistatin and (+)-blebbistatin, respectively. The addition of a nitro group stabilizes the molecules to circumvent their degradation by prolonged blue light exposure. (S)-nitro-Blebbistatin and (R)-nitro-blebbistatin have the same stereochemistry of the active and inactive enantiomers, respectively.

용도Blebbistatin blocked myosin II-dependent cell processes. It blocks cell blebbing rapidly and reversibly. Also rapidly disrupted directed cell migration and cytokinesis in vertebrate cell. It blocks both blebbing and cytokinesis at 50-100μM. (±)-1-Phenyl-1,2,3,4-tetrahydro-4-hydroxypyrrolo[2,3-b]-7-methylquinolin-4-one Selective inhibitor of nonmuscle myosin II; inhibits contraction of the cleavage furrow without disrupting mitosis or contractile ring assembly. Rapidly and reversibly blocks cell blebbing, and disrupts directed cell migration and cytokinesis in vertebrate cells.

공급사56 곳

艾吉析科技(上海)有限公司17717235263 · [email protected]
杭州品高化工有限公司0571-87658025 · [email protected]
上海优宁维生物科技股份有限公司15921930842 15921930842 · [email protected]
上海毕得医药科技股份有限公司400-1647117 13681763483 · [email protected]

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추가 설명 · 1건

정의ChEBI: A pyrroloquinoline that is 1,2,3,3a-tetrahydro-H-pyrrolo[2,3-b]quinolin-4-one substituted by a hydroxy group at position 3a, a methyl group at position 6 and a phenyl group at position 1. It acts as an inhibitor of ATPase ac ivity of non-muscle myosin II.