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bullatacin

CAS No.
102989-24-2
Chemical Name:
bullatacin
Synonyms
bullatacin;(+)-Asimicin;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)-
CBNumber:
CB41349878
Molecular Formula:
C37H66O7
Molecular Weight:
622.92
MDL Number:
MFCD03427326
MOL File:
102989-24-2.mol
MSDS File:
SDS
Last updated:2025-04-18 09:52:15

bullatacin 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)
pka 14.46±0.20(Predicted)

bullatacin price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation PXT0001875 ASIMICIN 95.00% 102989-24-2 5MG $503.39 2021-12-16 Buy
Product number Packaging Price Buy
PXT0001875 5MG $503.39 Buy

bullatacin Chemical Properties, Uses, Production

Uses

Asimicin (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 Research

Bullatacin 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

Raw materials

Preparation Products

Global Suppliers ( 6)
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc. +1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Jinan ponder chemical co. LTD 0531-0000 thinklifescience@163.com China 19684 58
Aktin Chemicals, Inc. 028-85159085 18080455027 info@aktin.com China 2069 58
Shanghai Moqi Biological Technology Co., LTD 13341702378 190129269@qq.com China 9999 58
TargetMol Chemicals Inc. 15002134094 marketing@targetmol.cn China 29874 58
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21533 55
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 102989-24-2