BioViotica

Antibiotic L-696,474

CHF 155.00
In stock
BVT-0331-C500500 µgCHF 155.00
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Product Details
Synonyms 18-Dehydroxycytochalasin H
Product Type Chemical
Properties
Formula

C30H39NO4

MW 477.6
CAS 141994-72-1
Source/Host Chemicals Isolated from Hypoxylon fragiforme.
Purity Chemicals ≥98% (HPLC; NMR)
Appearance White powder.
Solubility Soluble in DMSO methanol or dichlormethane.
Identity Determined by 1H-NMR.
Declaration Manufactured by BioViotica.
InChi Key JVHIPYJQMFNCEK-ZPSJVCBQSA-N
Smiles [H][C@@]1(CC2=CC=CC=C2)NC(=O)[C@]23[C@@]1([H])[C@H](C)C(=C)[C@@H](O)[C@]2([H])\C=C\C[C@H](C)C[C@H](C)\C=C\C3([H])OC(C)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description
  • Natural cytochalasin derivative.
  • Antiviral. Inhibitor of HIV-1 protease.
  • Antifungal activity.
Product References
  1. L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease: I. The producing organism and its fermentation: A.W. Dombrowski, et al.; J. Antibiot. 45, 671 (1992)
  2. L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease: II. Isolation and structure: J. Ondeyka, et al.; J. Antibiot. 45, 679 (1992)
  3. L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease: III. Biological activity: R.B. Lingham, et al.; J. Antibiot. 45, 686 (1992)
  4. Microbial transformation of L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease: T.S. Chen, et al.; J. Nat. Prod. 56, 755 (1993)
  5. An enantioselective, modular, and general route to the cytochalasins: Synthesis of L-696,474 and cytochalasin B: A.M. Haidle & A.G. Myers; PNAS 101, 12048 (2004)
  6. Fungicidal activity of L-696,474 and cytochalasin D from the ascomycete Daldinia concentria against plant pathogenic fungi: L. Du-Qiang, et al.; Acta Phytophyl. Sinica 34, 113 (2007)
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