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bullatacin

bullatacin Suppliers list
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: Jinan ponder chemical co. LTD  
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Company Name: Aktin Chemicals, Inc.  
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Company Name: Shanghai Moqi Biological Technology Co., LTD  
Tel: 13341702378
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Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
bullatacin Basic information
Product Name:bullatacin
Synonyms:bullatacin;2(5H)-Furanone, 3-[(2R,13R)-2,13-dihydroxy-13-[(2R,2'R,5R,5'R)-octahydro-5'-[(1R)-1-hydroxyundecyl][2,2'-bifuran]-5-yl]tridecyl]-5-methyl-, (5S)-;(+)-Asimicin
CAS:102989-24-2
MF:C37H66O7
MW:622.92
EINECS:
Product Categories:
Mol File:102989-24-2.mol
bullatacin Structure
bullatacin Chemical Properties
Melting point 45-48 °C(Solv: methanol (67-56-1); water (7732-18-5))
Boiling point 745.5±40.0 °C(Predicted)
density 1.054±0.06 g/cm3(Predicted)
pka14.46±0.20(Predicted)
Safety Information
MSDS Information
bullatacin Usage And Synthesis
UsesAsimicin (Bullatacin) is antitumor acetogenin that can be isolated from the bark and seeds of the pawpaw tree, Asimina trilobal Dunal. Asimicin inhibits mitochondrial respiration through the inhibition of complex I. Asimicin shows toxicity to Aphis gossypii, mosquito larvae and mammalian[1][2][3][4].
Anticancer ResearchBullatacin is a bis(tetrahydrofuranoid) fatty acid lactone found in some fruits fromAnnonaceae family. It is a member of acetogenin class of phytochemicals. It fightsagainst the MDR phenotype of human mammary adenocarcinoma. It has showsantitumor properties by induction of chromatin migration and tumor cellcondensation followed by apoptosis (Oberlies et al. 1997; Desai et al. 2008).
References[1] Kawamata T, et al. Convergent Total Synthesis of Asimicin via Decarbonylative Radical Dimerization. Chemistry. 2018 Dec 17;24(71):18907-18912. DOI:10.1002/chem.201805317
[2] Zhao GX, et al. Asimin, asiminacin, and asiminecin: novel highly cytotoxic asimicin isomers from Asimina triloba. J Med Chem. 1994 Jun 24;37(13):1971-6. DOI:10.1021/jm00039a009
[3] Ligang Zhou, et al. Secondary Metabolites with Antinematodal Activity from Higher Plants. Studies in Natural Products Chemistry. Volume 37, 2012, Pages 67-114.
[4] E. David Morgan and Ian D. Wilson. Insect Hormones and Insect Chemical Ecology. Comprehensive Natural Products Chemistry. Volume 8, 1999, Pages 263-375.
bullatacin Preparation Products And Raw materials
Tag:bullatacin(102989-24-2) Related Product Information
1-Triacontene Heptacosanoic acid methyl ester Hentriacontanoic acid Methyl melissate Triacontanoic acid Octacosanoic acid 1-Triacontanol METHYL NONACOSANOATE METHYL HEXACOSANOATE TRICOSANOIC ACID ETHYL ESTER TRIACONTANOIC ACID ETHYL ESTER HEXACOSANOIC ACID METHYL HENTRIACONTANOATE LIGNOCERIC ACID ETHYL ESTER bullatacin METHYL OCTACOSANOATE