STEFFIMYCIN B
STEFFIMYCIN B Basic information
- Product Name:
- STEFFIMYCIN B
- Synonyms:
-
- 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-
- CAS:
- 54526-94-2
- MF:
- C29H32O13
- MW:
- 588.56
- Mol File:
- 54526-94-2.mol
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STEFFIMYCIN B Chemical 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)
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STEFFIMYCIN B Usage And Synthesis
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 BSupplier
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Shenzhen Polymeri Biochemical Technology Co., Ltd.
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BOC Sciences
- Tel
- 16314854226; +16314854226
- inquiry@bocsci.com
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STEFFIMYCIN B(54526-94-2)Related Product Information
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- Steffimycin
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- STEFFIMYCIN B
- 2,5-DIMETHYL-4'-METHOXYBENZOPHENONE
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