빈다릿

Bindarit

HCID 71354

기본 정보

CAS
130641-38-2
표준 SMILES
CC(C)(OCc1nn(Cc2ccccc2)c2ccccc12)C(=O)O
InChIKey
MTHORRSSURHQPZ-UHFFFAOYSA-N
분자식
C19H20N2O3
평균 분자량
324.4 g/mol
단동위원소 질량
324.1473925

이름 및 식별자

우선 이름
Bindarit
IUPAC
2-[(1-benzylindazol-3-yl)methoxy]-2-methylpropanoic acid
현지명
빈다릿
영어명
Bindarit
분자식
C19H20N2O3
분자량
324.37

이름 및 동의어

Bindarit130641-38-22-((1-Benzyl-1H-indazol-3-yl)methoxy)-2-methylpropanoic acid2-[(1-benzyl-1h-indazol-3-yl)methoxy]-2-methylpropanoic acidAF 2838AF-28382-[(1-benzylindazol-3-yl)methoxy]-2-methylpropanoic acidJQ11LH711MDTXSID301566602-((1-Benzyl-1H-indazol-3-yl)methoxy)-2-methylpropionic acidbindaritum2-((1-benzylindazol-3-yl)methoxy)-2-methylpropanoic acid
이름 더 보기
빈다릿CS-1989indaritBindarit (AF2838)Bindarit, 10 mM in DMSOBindarit, CCL2, CCL7 and CCL8 inhibitor
RefChem:917198DTXCID30791512-((1-benzyl-3-indazolyl)methoxy)-2-methylpropionic acid2-((-1-benzyl-indazol-3-yl)methoxy)-2-methylpropionic acidAF2838Propanoic acid, 2-methyl-2-[[1-(phenylmethyl)-1H-indazol-3-yl]methoxy]-MFCD00866723Propanoic acid, 2-methyl-2-((1-(phenylmethyl)-1H-indazol-3-yl)methoxy)-

데이터베이스 식별자

CAS
130641-38-2
PubChem CID
71354
DTXSID
DTXSID30156660
ChEMBL
CHEMBL2107549
UNII
JQ11LH711M
Nikkaji
J561.826F

물성

구조 계산 물성

XLogP
3
극성 표면적
64.4 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
4
회전 가능 결합 수
6
무거운 원자 수
24

물리화학적 성질

끓는 점
542.9 · 542.9±40.0 °C(Predicted)
밀도
1.18 · 1.18±0.1 g/cm3 (20 ºC 760 Torr)
저장 조건
2 · 2-8°C
용해도
47 · DMSO:47.0(Max Conc. mg/mL);144.89(Max Conc. mM)
물리적 상태
결정성 고체
산도 계수 (pKa)
3.59 · 3.59±0.10(Predicted)

안전 및 규제

안전 데이터

wgk
WGK 3
스토리지 클래스
11 - Combustible Solids

화학 및 산업

응용 분야 · 2건

개요Bindarit is an inhibitor of monocyte chemoattractant protein (MCP) production that is selective for MCP-1/CCL2, MPC-3/CCL7, and MCP-2/CCL8 over other chemokines. It inhibits LPS- or C. albicans-induced production of MCP-1/CCL2 in isolated human monocytes (IC50s = 172 and 403 μM, respectively). Bindarit downregulates NF-κB signaling and prevents p65 and p65/p50-mediated MCP-1/CCL2 promoter activation in RAW264.7 cells. It delays the onset of proteinuria and prolongs survival in a mouse model of experimental lupus nephritis when administered at a dose of 50 mg/kg. It prevents LPS-induced increases in MCP-1/CCL2 expression in mouse brain and spinal cord when administered at a dose of 200 mg/kg and reduces the incidence and severity of experimental autoimmune encephalomyelitis (EAE) in mice. Bindarit is also a noncompetitive inhibitor of monocarboxylate transporter 4 (MCT4; Ki = 30.2 μM for the human transporter) that is selective for MCT4 over MCT1.

용도Bindarit shows anti-inflammatory activity due to a selective inhibition of a subfamily of inflammatory chemokines. Bindarit is a also protein antidenaturant agent. Bindarit modulates the NFkB pathway and has been shown to reduce secondary phase of adjuvant arthritis in rats.

공급사100 곳

阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
郑州阿尔法化工有限公司+86-18530059196 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
武汉英诺医药科技有限公司+86-027-59232304 15387063101 · [email protected]

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6건

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