Lysolipin I

CHF 120.00
In stock
BVT-0037-C500500 µgCHF 120.00
BVT-0037-M0011 mgCHF 205.00
BVT-0037-M0055 mgCHF 610.00
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Product Details
Product Type Chemical


MW 597.9
CAS 59113-57-4
Source/Host Chemicals Isolated from Streptomyces violaceoniger.
Purity Chemicals ≥98% (HPLC)
Appearance Yellow needles.
Solubility Soluble in methylene chloride, DMSO or chloroform.
Identity Determined by 1H-NMR.
Declaration Manufactured by BioViotica.
Smiles [H][C@]12OCOC3=C4OC5=C(OC)C(Cl)=CC=C5C(=O)C4=C(O)C(C4=C(O)C5=C(C=C4[C@@H]1OC)[C@@H](O)[C@@H](OC)N(C)C5=O)=C23
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light.
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
After reconstitution protect from light at -20°C.
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
  • Antibiotic.
  • Glycopeptide synthesis inhibitor.
  • Antibacterial, antifungal and anticoccidial.
  • Cytotoxic.
Product References
  1. Lysolipin I, ein neuer Hemmstoff der bakteriellen Zellwandsynthese.: H. Drautz, et al.; Path. Microbiol. 42, 236 (1975)
  2. Metabolic products of microorganisms, 149. Lysolipin I, a new antibiotic from streptomyces violaceoniger: H. Drautz, et al.; Arch. Microbiol. 106, 175 (1975)
  3. Structure of cervinomycin, a novel xantone antibiotic active against anaerobe and mycoplasma.: A. Nakagawa, et al.; J Antibiot 40, 301 (1987)
  4. Biosynthetic studies on the xanthone antibiotics lysolipins X and I: H. Bockholt, et al.; J. Org. Chem. 59, 2064 (1994)
  5. Experiments on the total synthesis of Lysolipin I. Part II. Michael addition of 1,3-cyclohexanedione to quinone acetals: R.O. Duthaler & U.H.U. Wegmann; Helv. Chim. Acta 67, 1755 (2004)
  6. Isolation of the lysolipin gene cluster of streptomyces Tandae Tu 4042: P. Lopez, et al.; Gene 461, 5 (2010)
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