CHAETOGLOBOSIN A
CHAETOGLOBOSIN A Basic information
- Product Name:
- CHAETOGLOBOSIN A
- Synonyms:
-
- CHAETOGLOBOSINB
- CHAETOGLOBOSINM
- CHAETOGLOBOSINE
- CHAETOGLOBOSINL
- (13)cytochalasa-13,17,21-triene-1,20,23-trione,6,7-epoxy-19-hydroxy-10-(1h-ind
- 18-dimethyl-,(7s,13e,16s,17e,19r,21e)-ol-3-yl)-1
- chaetoglobosins
- CHAETOGLOBOSIN
- CAS:
- 50335-03-0
- MF:
- C32H36N2O5
- MW:
- 528.64
- Product Categories:
-
- Antibiotic
- Mol File:
- 50335-03-0.mol
CHAETOGLOBOSIN A Chemical Properties
- Melting point:
- 188°C
- Boiling point:
- 608.81°C (rough estimate)
- Density
- 1.1705 (rough estimate)
- refractive index
- 1.5800 (estimate)
- storage temp.
- -20°C
- solubility
- DMSO: soluble10mg/mL
- form
- solid
- pka
- 17.32±0.30(Predicted)
- color
- Yellow
- Stability:
- Stable for 1 year as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month.
CHAETOGLOBOSIN A Usage And Synthesis
Description
Chaetoglobosin A (50335-03-0) is a cytochalasin analog which targets filamentous actin. Displays cytotoxic effects against human colorectal HCT116 cells, IC50=3.15 μM.1 Preferentially induces apoptosis in chronic lymphocytic leukemia cells via targeting the cytoskeleton.2 Enhances the fibrinolytic activity of vascular endothelial cells.3
Occurrence
A complex macrocyclic alkaloid, this base has been isolated from Diplodia rnacrospora. Chaetoglobosin A possesses the property of inhibiting growth in wheat coleoptiles.
Uses
Chaetoglobosin A is a mycotoxic cytochalasan compound.
Definition
ChEBI: A cytochalasan alkaloid isolated from Chaetomium globosum and Calonectria morganii.
storage
+4°C
References
1) Li et al. (2014), Chaetoglobosins from Chaetomium globosum, an endophytic fungus in Ginkgo biloba, and their phytotoxic and cytotoxic activities; J. Agric. Food Chem., 62 3734 2) Knudsen et al. (2014), Chaetoglobosin A preferentially induces apoptosis in chronic lymphocytic leukemia cells by targeting the cytoskeleton; Leukemia, 28 1289 3) Shinohara et al. (2000), Enhancement of fibrinolytic activity of vascular endothelial cells by chaetoglobosin A, crinipellin B, geodin and triticone B; J. Antibiot. (Tokyo), 53 262
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