Chlorflavonin
Chlorflavonin Basic information
- Product Name:
- Chlorflavonin
- Synonyms:
-
- Chlorflavonin
- 2-(3-Chloro-2-hydroxyphenyl)-5-hydroxy-3,7,8-trimethoxy-4H-1-benzopyran-4-one
- 3'-Chloro-2',5-dihydroxy-3,7,8-trimethoxyflavone
- 4H-1-Benzopyran-4-one, 2-(3-chloro-2-hydroxyphenyl)-5-hydroxy-3,7,8-trimethoxy-
- Chlorflavonin >=98% (HPLC)
- CAS:
- 23363-64-6
- MF:
- C18H15ClO7
- MW:
- 378.76
- Mol File:
- 23363-64-6.mol
Chlorflavonin Chemical Properties
- Boiling point:
- 612.7±55.0 °C(Predicted)
- Density
- 1.52±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- DMSO: 2mg/mL, clear
- pka
- 6.61±0.40(Predicted)
- form
- powder
- color
- white to beige
Chlorflavonin Usage And Synthesis
Definition
ChEBI: A dihydroxyflavone that is flavone substituted by a chloro group at position 3', hydroxy groups at positions 5 and 2' and methoxy groups at positions 3, 7 band 8 respectively.
Biological Activity
Originally isolated from Aspergillus candidus Link, Chlorflavonin is a non-cytotoxic (up to 100 μM; MRC-5 and THP-1) antibiotic with antifungal activity against certain species of mold fungi (MIC = 0.08 μg/mL against A. amstelodami, A. fumigalus, A. ochraceous; Paecilomyces variotii MIC = 2.5 μg/mL, Botrytis cinerea MIC = 5 μg/mL). Chlorflavonin also exhibits antibiotic activity against M. tuberculosis (MIC90 = 1.56 μM) by targeting acetohydroxyacid synthase (AHAS) catalytic subunit ilvB1. Chlorflavonin is superior to streptomycin against M. tuberculosis inside infected macrophages, synergizes with isoniazid and delamanid, leading to a complete sterilization in liquid cultures.
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