ChemicalBook--->CAS DataBase List--->82196-88-1

82196-88-1

82196-88-1 Structure

82196-88-1 Structure
IdentificationBack Directory
[Name]

CHRYSOMYCIN A
[CAS]

82196-88-1
[Synonyms]

NSC 613946
A,ChrysoMycin
Chrysomycin V
Virenomycin V
(+)-Virenomycin V
CHRYSOMYCIN A USP/EP/BP
ChrysoMycin V, VirenoMycin V, Albacarcin V
8-ethenyl-1-hydroxy-10,12-dimethoxy-4-(3,4,5-trihydroxy-4,6-dimethyloxan-2-yl)naphtho[1,2-c]isochromen-6-one
4-(6-Deoxy-3-C-methyl-beta-gulopyranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one
6H-Benzo[d]naphtho[1,2-b]pyran-6-one,4-(6-deoxy-3-C-methyl-b-gulopyranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-(9CI)
(+)-4-(6-Deoxy-3-C-methyl-β-D-gulo-hexopyranosyl)-8-ethenyl-1-hydroxy-10,12-dimethoxy-6H-benzo[d]naphtho[1,2-b]pyran-6-one
[Molecular Formula]

C28H28O9
[MDL Number]

MFCD07370133
[MOL File]

82196-88-1.mol
[Molecular Weight]

508.52
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMF: soluble
[form ]

solid
[color ]

Yellow to greenish
Safety DataBack Directory
[Symbol(GHS) ]


GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H302+H312-H319-H351
[Precautionary statements ]

P201-P202-P264-P270-P280-P301+P312-P330-P302+P352-P305+P351+P338-P308+P313-P321-P362+P364-P337+P313-P405-P501
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Chrysomycin A is a potent antibacterial, antifungal and antiviral compound.
[Uses]

Chrysomycin A is the major analogue in a complex of C-glycoside antitumor actives isolated from Streptomyces. Chrysomycin A, with a vinyl group in the 8-position, is the most potent analogue of the complex, and is thought to act as an inhibitor of the catalytic activity of human topoisomerase II. Chrysomycin A has a potent antibacterial, antifungal, antiviral and antitumor profile. More recent research on related metabolites, the gilvocarcins, suggests that chrysomycins may act as photoactivated cross-linkers of DNA to histones.
[Uses]

Chrysomycin A is the major analogue in a complex of C-glycoside antitumour actives isolated from Streptomyces. Chrysomycin A, with a vinyl group in the 8-position, is the most potent analogue of the complex, and is thought to act as an inhibitor of the catalytic activity of human topoisomerase II. Chrysomyin A has a potent antibacterial, antifungal, antiviral and antitumour profile. More recent research on related metabolites, the gilvocarcins, suggests that chrysomycins may act as photoactivated, crosslinkers of DNA to histones.
[Definition]

ChEBI: Chrysomycin a is a glycoside.
[storage]

Store at -20°C
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