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STEFFIMYCIN B

CAS No.
54526-94-2
Chemical Name:
STEFFIMYCIN B
Synonyms
u40615;Nsc 204855;STEFFIMYCIN B;Steffimycin 4'-methyl ether;5,7-trihydroxy-3,9-dimethoxy-2-methyl-l)oxy)-4-dihydro-2;1,6,11(2h)-naphthacenetrione,4-((6-deoxy-2,4-di-o-methyl-alpha-l-mannopyranosy;4-(2-O,4-O-Dimethyl-α-L-rhamnopyranosyloxy)-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-1,6,11(2H)-naphthacenetrione;4-[(2-O,4-O-Dimethyl-6-deoxy-α-L-mannopyranosyl)oxy]-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-1,6,11(2H)-naphthacenetrione;1,6,11(2H)-Naphthacenetrione, 4-((6-deoxy-2,4-di-o-methyl-alpha-L-mannopyranosyl)oxy)-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-;1,6,11(2H)-Naphthacenetrione, 4-[(6-deoxy-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-, (2S,3S,4R)-
CBNumber:
CB4410845
Molecular Formula:
C29H32O13
Molecular Weight:
588.56
MDL Number:
MFCD01713106
MOL File:
54526-94-2.mol
MSDS File:
SDS
Last updated:2023-05-21 10:59:17

STEFFIMYCIN B Properties

Boiling point 801.2±65.0 °C(Predicted)
Density 1.52±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble
form A lyophilisate
pka 5.09±0.70(Predicted)

STEFFIMYCIN B price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 28087 Steffimycin B 54526-94-2 1mg $303 2024-03-01 Buy
Cayman Chemical 28087 Steffimycin B 54526-94-2 5mg $983 2024-03-01 Buy
Usbiological S7972-84 Steffimycin B 54526-94-2 1mg $482 2021-12-16 Buy
American Custom Chemicals Corporation API0013139 STEFFIMYCIN B 95.00% 54526-94-2 1MG $487.2 2021-12-16 Buy
Product number Packaging Price Buy
28087 1mg $303 Buy
28087 5mg $983 Buy
S7972-84 1mg $482 Buy
API0013139 1MG $487.2 Buy

STEFFIMYCIN B Chemical Properties,Uses,Production

Uses

Steffimycin B is an anthracycline metabolite isolated from a Streptomyces sp., with antibacterial and antineoplastic properties. Crystallographic studies of binding to DNA suggest that it has a higher CpG base sequence specificity over the TpA step, similar to that of daunorubicin and nogalamycin. A close analogue was shown to be active against ras oncogene-expressed cells.

STEFFIMYCIN B Preparation Products And Raw materials

Raw materials

Preparation Products

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STEFFIMYCIN B 1,6,11(2h)-naphthacenetrione,4-((6-deoxy-2,4-di-o-methyl-alpha-l-mannopyranosy 5,7-trihydroxy-3,9-dimethoxy-2-methyl-l)oxy)-4-dihydro-2 u40615 4-(2-O,4-O-Dimethyl-α-L-rhamnopyranosyloxy)-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-1,6,11(2H)-naphthacenetrione 4-[(2-O,4-O-Dimethyl-6-deoxy-α-L-mannopyranosyl)oxy]-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-1,6,11(2H)-naphthacenetrione Steffimycin 4'-methyl ether 1,6,11(2H)-Naphthacenetrione, 4-((6-deoxy-2,4-di-o-methyl-alpha-L-mannopyranosyl)oxy)-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl- Nsc 204855 1,6,11(2H)-Naphthacenetrione, 4-[(6-deoxy-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-3,4-dihydro-2,5,7-trihydroxy-3,9-dimethoxy-2-methyl-, (2S,3S,4R)- 54526-94-2