Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy-

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Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy- Basic information
Product Name:Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy-
Synonyms:Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy-;Azalamellarin N
CAS:1809535-57-6
MF:C28H22N2O7
MW:498.48
EINECS:
Product Categories:
Mol File:1809535-57-6.mol
Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy- Structure
Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy- Chemical Properties
density 1.49±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)
pka8.72±0.20(predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy- Usage And Synthesis
UsesAzalamellarin N is an inhibitor of pyroptosis and has different inhibitory effects on different pyroptosis inducers. Azalamellarin N inhibits pyroptosis by targeting molecules that act upstream of NLRP3 inflammasome activation, rather than directly targeting components of the NLRP3 inflammasome. Inhibitory potency against different pyroptosis inducers: Nigericin (HY-127019) > R837 (HY-B0180)[1].
References[1] Takouda J, et al. Identification of Azalamellarin N as a Pyroptosis Inhibitor. Biol Pharm Bull. 2024;47(1):28-36. DOI:10.1248/bpb.b23-00569
Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy- Preparation Products And Raw materials
Tag:Benz[7,8]indolizino[3,2-c]quinolin-6(5H)-one, 3,11-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,12-dimethoxy-(1809535-57-6) Related Product Information
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