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Merck
모든 사진(1)

주요 문서

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SML2701

Sigma-Aldrich

CBA

≥98% (HPLC)

동의어(들):

4-Chloro-2-[[2-(2-chlorophenoxy)acetyl]amino]benzoic acid

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C15H11Cl2NO4
CAS Number:
351424-20-9
Molecular Weight:
340.16
MDL number:
MFCD01930120
UNSPSC 코드:
12352200
NACRES:
NA.77

Quality Level

100

분석

≥98% (HPLC)

양식

powder

색상

white to beige

solubility

DMSO: 2 mg/mL, clear

저장 온도

2-8°C

SMILES string

Clc1c(cccc1)OCC(=O)Nc2c(ccc(c2)Cl)C(=O)O

InChI

1S/C15H11Cl2NO4/c16-9-5-6-10(15(20)21)12(7-9)18-14(19)8-22-13-4-2-1-3-11(13)17/h1-7H,8H2,(H,18,19)(H,20,21)

InChI key

CVQCJPCMPGKEDH-UHFFFAOYSA-N

생화학적/생리학적 작용

CBA (Compound 5; 4-Chloro-2-[[2-(2-chlorophenoxy)acetyl]amino]benzoic acid) is a cell penetrant, potent and selective TRPM4 (Transient receptor potential melastatin member 4) inhibitor that shows not significant activity against TRPM5, TRPM7, TRPM8, TRPV1, TRPV3, TRPV6. It rescues functional expression of mutant A432T TRPM4 in cells. CBA (Compound 5) exhibits neuroprotective activity against glutamate-induced neurodegeneration.
cell penetrant, potent and selective TRPM4 (Transient receptor potential melastatin member 4) inhibitor

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Beatrice Bianchi et al.
Molecular brain, 11(1), 41-41 (2018-07-13)
Transient receptor potential melastatin member 4 (TRPM4), a Ca2+-activated nonselective cation channel, has been found to mediate cell membrane depolarization in immune response, insulin secretion, cardiovascular diseases, and cancer. In murine experimental autoimmune encephalomyelitis (EAE), TRPM4 deletion and administration of
Lijo Cherian Ozhathil et al.
British journal of pharmacology, 175(12), 2504-2519 (2018-03-27)
TRPM4 is a calcium-activated non-selective cation channel expressed in many tissues and implicated in several diseases, and has not yet been validated as a therapeutic target due to the lack of potent and selective inhibitors. We sought to discover a

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