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Liquidambaric acid

  Cat. No.:  DC23068   Featured
Chemical Structure
4481-62-3
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More than 5000 active chemicals with high quality for research!
Field of application
Betulonic acid has anti-cancer , anti-HIV,hepatoprotective and anti-inflammatory activities, it has antiviral activity against herpes simplex virus, it also suppresses ECHO 6 virus reproduction.
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 4481-62-3
Chemical Name: Betulonicacid
Synonyms: Betulonic acid;Betulinonic acid;Liquidambaric acid;LiquidaMba;(+)-Betulonic Acid;3-oxolup-20(29)-en-28-oic acid;Betunolic acid;[ "3-Oxolup-20(29)-en-28-oic acid" ];Betulonicacid;BCP18477;(3As,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7
SMILES: O([H])C([C@]12C([H])([H])C([H])([H])C([H])(C(=C([H])[H])C([H])([H])[H])[C@]1([H])[C@@]1([H])C([H])([H])C([H])([H])[C@]3([H])[C@@]4(C([H])([H])[H])C([H])([H])C([H])([H])C(C(C([H])([H])[H])(C([H])([H])[H])[C@]4([H])C([H])([H])C([H])([H])[C@@]3(C([H])([H])[H])[C@]1(C([H])([H])[H])C([H])([H])C2([H])[H])=O)=O
Formula: C30H46O3
M.Wt: 454.6844
Purity: >98%, Standard References Grade
Sotrage: 4°C for 1 year, -20°C for more than 2 years
Description: Betulonic acid belongs to the pentacyclic triterpenic derivative class, has antitumor activities.
In Vivo: The animals are treated with betulonic acid amide (50 mg/kg in Tween aqueous solution) and heptral (6 mg/kg) as hepatoprotective compounds. It is found that betulonic acid amide stimulats the regenerative response in hepatocytes under conditions of combined toxic exposure and promots recovery of their qualitative and quantitative characteristics. [2]
In Vitro: BEA-NP is found over three-times more permeable than that solubilized by DMSO in Caco-2 cell monocultures.[1]
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
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DC37901 PD-173212 PD-173212 is a small molecule N-type calcium channel blocker.
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DC37321 AI3-15902 AI3-15902 is a biochemical.
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DC36443 DC-Chol DC-Chol is a cationic cholesterol derivative. DC-Chol, as a component of lipoplexes with DOPE, has been used for transfection of mRNA into A549 cells without affecting cell viability. Incubation of DC-chol/DOPE liposomes or lipoplexes with human whole blood has no effect on neutrophil elastase or β-thromboglobulin levels or the number of platelets and red and white blood cells, indicating hemocompatibility. DC-Chol has also been widely used in the synthesis of liposomes for the delivery of siRNA, DNA, and chemotherapeutic agents into cells and mice.
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