71968-02-0
Chemical Structure
Aspochalasin D
- CAS No.: 71968-02-0
- Formula:C24H35NO4
- Molecular Weight:401.54
IUPAC Name: (3S,3aR,4S,6aS,7E,11R,12S,13E,15aS)-11,12-dihydroxy-3-isobutyl-4,5,8-trimethyl-3,3a,4,6a,9,10,11,12-octahydro-1H-cycloundeca[d]isoindole-1,15(2H)-dione
InChIKey: GCIKKGSNXSCKCP-WBEGXGIOSA-N
SMILES: O=C1N[C@@H](CC(C)C)[C@]2([H])[C@H](C)C(C)=C[C@@](/C=C(C)/CC[C@@H](O)[C@@H](O)/C=C/3)([H])[C@]12C3=O
Biological Activity: Aspochalasin D is a co-metabolite originally isolated from A. microcysticus with aspochalasins A, B, and C, that is initially thought to be inactive. It has antibacterial activity against Gram-positive and Gram-negative bacteria at a concentration of 1 mg/ml.2 Aspochalasin D is more cytotoxic, via apoptosis, to Ba/F3-V12 cells in an IL-3-free medium than in an IL-3-containing medium (IC50s=0.49 and 1.9 μg/mL, respectively).
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Aspochalasin D | 98.24% | Aspochalasin D is a co-metabolite originally isolated from A. microcysticus with aspochalasins A, B, and C, that is initially thought to be inactive. It has antibacterial activity against Gram-positive and Gram-negative bacteria at a concentration of 1 mg/ml.2 Aspochalasin D is more cytotoxic, via apoptosis, to Ba/F3-V12 cells in an IL-3-free medium than in an IL-3-containing medium (IC50s=0.49 and 1.9 μg/mL, respectively). | ||||||||||||||||||||
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