SML3377
BG-3
≥98% (HPLC)
别名:
N-(4-Chlorophenyl)-6-ethyl-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7-amine, SID 124738112
SMILES string
CC1=NC2=NC=NN2C(NC3=CC=C(Cl)C=C3)=C1CC
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
BG-3 is a cell penetrant, potent and selective inhibitor of Pax2 (paired-box 2) that inhibits Pax2 transactivation ability. BG-3 inhibit the ability of Pax proteins to recruit PTIP and promote H3K4 methylation at Pax binding sites. BG-3 is not cytotoxic.
cell penetrant, potent and selective inhibitor of Pax2 that inhibits Pax2 transactivation ability
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Shayna T J Bradford et al.
Cell chemical biology, 29(3), 412-422 (2021-11-26)
The Pax family of developmental control genes are frequently deregulated in human disease. In the kidney, Pax2 is expressed in developing nephrons but not in adult proximal and distal tubules, whereas polycystic kidney epithelia or renal cell carcinoma continues to
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