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CHRYSOMYCIN B

CHRYSOMYCIN B Structure
CAS No.
83852-56-6
Chemical Name:
CHRYSOMYCIN B
Synonyms
B,ChrysoMycin;CHRYSOMYCIN B USP/EP/BP;ChrysoMycin M, VirenoMycin M, Albacarcin M;6H-Benzo[d]naphtho[1,2-b]pyran-6-one, 4-(6-deoxy-3-C-methyl-β-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-;4-(6-Deoxy-3-C-methyl-beta-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-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)-1-hydroxy-10,12-dimethoxy-8-methyl- (9CI)
CBNumber:
CB3503294
Molecular Formula:
C27H28O9
Molecular Weight:
496.51
MOL File:
83852-56-6.mol
MSDS File:
SDS
Modify Date:
2023/6/30 15:45:59

CHRYSOMYCIN B Properties

Boiling point 784.0±60.0 °C(Predicted)
Density 1.410
storage temp. 2-8°C
solubility DMF: soluble
pka 8.59±0.20(Predicted)
form solid
color Yellow to greenish

SAFETY

Risk and Safety Statements

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
NFPA 704
0
2 0

CHRYSOMYCIN B Chemical Properties,Uses,Production

Description

Chrysomycin B is an antibiotic isolated from a strain of Streptomyces. It differs from its analog chrysomycin A by having a methyl, rather than vinyl, group in the 8-position of the chromophore. Like its analog, chrysomycin B suppresses the growth of transplantable tumors in mice, an effect that may be related to its ability to bind DNA. It also causes DNA damage in the human lung adenocarcinoma A549 cell line and inhibits topoisomerase II. Chrysomycin B is structurally very similar to gilvocarcin V, which promotes DNA cross-linking with histone 3 and GRP78 when photoactivated by near-UV light.

Uses

Chrysomycin B is a minor analogue in a complex of C-glycoside antitumour actives isolated from Streptomyces. Chrysomycin B, containing a methyl group in the 8-position, is less active than its vinyl analogue (Chrysomycin A), albeit still a potent antitumour active and an inhibitor of the catalytic activity of human topoisomerase II. More recent research on related metabolites, the gilvocarcins, suggests that chrysomycins may act as photoactivated crosslinkers of DNA to histones.

CHRYSOMYCIN B Preparation Products And Raw materials

Raw materials

Preparation Products

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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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Alta Scientific Co., Ltd. 022-6537-8550 15522853686 China 4515 55 Inquiry
6H-Benzo[d]naphtho[1,2-b]pyran-6-one,4-(6-deoxy-3-C-methyl-b-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl- (9CI) ChrysoMycin M, VirenoMycin M, Albacarcin M 4-(6-Deoxy-3-C-methyl-beta-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl-6H-benzo[d]naphtho[1,2-b]pyran-6-one B,ChrysoMycin 6H-Benzo[d]naphtho[1,2-b]pyran-6-one, 4-(6-deoxy-3-C-methyl-β-gulopyranosyl)-1-hydroxy-10,12-dimethoxy-8-methyl- CHRYSOMYCIN B USP/EP/BP 83852-56-6 A - KAntibiotics Antibacterial Antibiotics A to Antibiotics A-FAntibiotics Antibiotics by Application Antineoplastic and Immunosuppressive AntibioticsAntibiotics Inhibits an EnzymeEnzyme Inhibitors by Enzyme Mechanism of Action R to Spectrum of Activity Topoisomerase II