| Identification | Back 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 Properties | Back Directory | [Boiling point ]
799.7±60.0 °C(Predicted) | [density ]
1.405±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMF: soluble | [form ]
solid | [pka]
8.55±0.20(Predicted) | [color ]
Yellow to greenish | [InChIKey]
OMDANBMKOUVKAG-BMGMCLONNA-N | [SMILES]
C12OC(=O)C3=C(C(OC)=CC(C=C)=C3)C=1C=C(OC)C1C(O)=CC=C(C2=1)[C@@H]1O[C@H](C)[C@H](O)[C@@](C)(O)[C@H]1O |&1:26,28,30,32,35,r| |
| Hazard Information | Back 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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Lynnchem
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86-(0)29-85992781 17792393971 |
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http://www.lynnchem.com/ |
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Novachemistry
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https://www.novachemistry.com/ |
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Energy Chemical
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http://www.energy-chemical.com |
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