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Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester, stereoisomer (121263-19-2)

Identification
Name:Carbonic acid,(1R)-2-[12-[(2R)-2-(benzoyloxy)propyl]-3,10-dihydro-4,9-dihydroxy-2,6,7,11-tetramethoxy-3,10-dioxo-1-perylenyl]-1-methylethyl4-hydroxyphenyl ester, stereoisomer
Synonyms:Perylene,carbonic acid deriv.; Calphostin C; Cladochrome E; PKF 115-584; UCN 1028C
CAS:121263-19-2
Molecular Formula: C44H38 O14
Molecular Weight: 790.76412
InChI: InChI=1S/C44H38O14/c1-20(56-43(50)22-10-8-7-9-11-22)16-25-31-32-26(17-21(2)57-44(51)58-24-14-12-23(45)13-15-24)42(55-6)40(49)34-28(47)19-30(53-4)36(38(32)34)35-29(52-3)18-27(46)33(37(31)35)39(48)41(25)54-5/h7-15,18-21,45,48-49H,16-17H2,1-6H3
Molecular Structure: (C44H38O14) Perylene,carbonic acid deriv.; Calphostin C; Cladochrome E; PKF 115-584; UCN 1028C
Properties
Density:1.48 g/cm3
Refractive index:1.707
Water Solubility:Soluble in DMF: 1 mg/mL
Solubility:Soluble in DMF: 1 mg/mL
Appearance:red to brown powder
Biological Activity: Potent, selective and photo-dependent inhibitor of protein kinase C that targets the regulatory domain (IC 50 = 50 nM). Displays > 1000-fold selectivity over other protein kinases such as cAMP-dependent protein kinase and tyrosine-specific protein kinase. Inhibits cell proliferation of malignant glioma cells in light-treated conditions in vitro (IC 50 ~ 40-60 nM).
Storage Temperature: −20°C
Color: red to brown
Safety Data
 

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