Adipogen/Fridamycin A/BVT-0469-M005/5 mg

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More Information Product Details Synonyms Product Type Properties Formula MW CAS Source/Host Chemicals Purity Chemicals Appearance Solubility Identity Declaration InChi Key Shipping and Handling Shipping Short Term Storage Long Term Storage Handling Advice Use/Stability Documents MSDS Product Specification Sheet Datasheet
Vineomycinone B2
Chemical
C25H26O10
486.5
30270-05-4
Isolated from Streptomyces parvulus.
≥97% (HPLC, NMR)
Yellow to orange solid.
Soluble in DMSO. Sparingly soluble in methanol or acetone.
Determined by 1H-NMR and MS.
Manufactured by BioViotica.
LKLNNJGYAYDANM-VRSSYPSJSA-N
AMBIENT
+4°C
-20°C
Protect from light.
Stable for at least 1 year after receipt when stored at -20°C.Store solutions at -20°C in the dark.
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  • C-glycosidic angucyclinone derivative.
  • Antibiotic.
  • Antitumor agent.
  • Antibacterial agent.
  • Isomer of fridamycin B (Prod. No. BVT-0470).
Product References
  • The structure of vineomycin B2: N. Imamura, et al.; J. Antibiot. 34, 1517 (1981)
  • Fridamycine, Anthracyclin-analoge Antibiotica: P. Knicke; Ph. D. Thesis Univ. Goettingen (1984)
  • Angucycline group antibiotics: J. Rohr & R. Thiericke; Nat. Prod. Rep. 9, 103 (1992)
  • Synthetic anthracyclines from anthraquinones: R. Cambie, et al.; Austr. J. Chem. 45, 483 (1992)
  • C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycine B2 methyl ester: C.-L. Chen, et al.; JACS 128, 13696 (2006)
  • Convergent de novo synthesis of vineomycinione B2 methyl ester: Q. Chen, et al.; Chem. Comm. 49, 6806 (2013)
  • Total Synthesis of vineomycin B2: S. Kusumi, et al.; JACS 135, 15909 (2013)
  • Angucycline antibiotics and its derivatives from marine-derived actinomycete streptomyces sp. A6H: Z. Hu, et al.; Nat. Prod. Res. (Epub ahead of print) (2016)
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