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Merck
CN

SML2109

Sigma-Aldrich

ST034307

≥98% (HPLC)

别名:

6-Chloro-2-(trichloromethyl)-4H-1-benzopyran-4-one, 6-Chloro-2-(trichloromethyl)chromen-4-one

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关于此项目

经验公式(希尔记法):
C10H4Cl4O2
化学文摘社编号:
分子量:
297.95
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77
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方案

≥98% (HPLC)

表单

powder

颜色

faint green to dark gray

溶解性

DMSO: 2 mg/mL, clear (warmed)

储存温度

−20°C

SMILES字符串

ClC(Cl)(Cl)C1=CC(C2=CC(Cl)=CC=C2O1)=O

InChI

1S/C10H4Cl4O2/c11-5-1-2-8-6(3-5)7(15)4-9(16-8)10(12,13)14/h1-4H

InChI key

NTDHYMSVCBGQJF-UHFFFAOYSA-N

生化/生理作用

ST034307 is a selective inhibitor of adenylyl cyclase 1 (AC1) with analgesic activity. Adenylyl cyclase 1 has been shown to be a potential target for treating pain and reducing the dependency on opioids, but it has been difficult to inhibit AC1 selectively without also inhibiting other isoforms vital to physiological functions. ST034307 is selective for AC1 over all eight other adenylyl cyclase isoforms. It inhibited AC1 and reduced cAMP, while leaving AC8 unaffected and was shown to reduce pain in a mouse inflammatory pain model.
Selective inhibitor of adenylyl cyclase 1 (AC1) with analgesic activity

储存分类代码

11 - Combustible Solids

WGK

WGK 3

法规信息

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分析证书(COA)

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Tarsis F Brust et al.
Science signaling, 10(467) (2017-02-23)
Adenylyl cyclase 1 (AC1) belongs to a group of adenylyl cyclases (ACs) that are stimulated by calcium in a calmodulin-dependent manner. Studies with AC1 knockout mice suggest that inhibitors of AC1 may be useful for treating pain and opioid dependence.
Xiang Li et al.
Microbiology (Reading, England), 170(6) (2024-06-25)
Bacterial infection is a dynamic process resulting in a heterogenous population of infected and uninfected cells. These cells respond differently based on their bacterial load and duration of infection. In the case of infection of macrophages with Crohn's disease (CD)

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