54526-94-2

Steffimycin B Chemical Structure
54526-94-2

Chemical Structure

Steffimycin B

Synonym(s): NSC 204855; U 40615

  • CAS No.: 54526-94-2
  • Formula:C29H32O13
  • Molecular Weight:588.56

IUPAC Name: (2S,3S,4R)-2,5,7-trihydroxy-4-(((2S,3R,4R,5R,6S)-4-hydroxy-3,5-dimethoxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-3,9-dimethoxy-2-methyl-3,4-dihydrotetracene-1,6,11(2H)-trione

InChIKey: VHJWDTPKSIFZBV-IDORXPLKSA-N

SMILES: OC1=C(C(C2=C3O)=O)C(C(C2=CC(OC)=C3)=O)=CC(C4=O)=C1[C@H]([C@@H]([C@](O)4C)OC)O[C@H](O[C@H]5C)[C@@H]([C@@H]([C@H]5OC)O)OC

Biological Activity: Steffimycin B is an anthracycline bacterial metabolite originally isolated from Streptomyces. It binds to DNA, preferentially intercalating at sites containing cytosine and guanine.2 Steffimycin B is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s=3.5, 6.75, 3.28, and 10.5 μM, respectively). It is active against M. tuberculosis (MIC=5.2 nM), B. cereus (MIC=1.56 μg/mL), and P. falciparum (IC50=2.19 μM).

Cat. No. Product Name Purity Description Pricing
HY-N8470
Steffimycin B Steffimycin B is an anthracycline bacterial metabolite originally isolated from Streptomyces. It binds to DNA, preferentially intercalating at sites containing cytosine and guanine.2 Steffimycin B is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s=3.5, 6.75, 3.28, and 10.5 μM, respectively). It is active against M. tuberculosis (MIC=5.2 nM), B. cereus (MIC=1.56 μg/mL), and P. falciparum (IC50=2.19 μM).
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