863-76-3

α-Amyrin acetate Chemical Structure
863-76-3

Chemical Structure

α-Amyrin acetate

  • CAS No.: 863-76-3
  • Formula:C32H52O2
  • Molecular Weight:468.75

IUPAC Name: (3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl acetate

InChIKey: UDXDFWBZZQHDRO-NSTYLNEOSA-N

SMILES: C[C@]12[C@]3(C([C@@]4([H])[C@](C)(CC[C@@H](C)[C@@H]4C)CC3)=CC[C@]1([H])[C@@]5([C@@](C(C)([C@@H](OC(C)=O)CC5)C)([H])CC2)C)C

Biological Activity: α-Amyrin acetate is a pentacyclic triterpenoid compound with oral activity. α-Amyrin acetate can inhibit cancer cells proliferation and induce apoptosis. α-Amyrin acetate can reduce blood glucose level. α-Amyrin acetate can be used for the researches of cancer and metabolic disease, such as breast cancer and diabetes[1][2].

Cat. No. Product Name Purity Description Pricing
HY-N2842
α-Amyrin acetate 99.93% α-Amyrin acetate is a pentacyclic triterpenoid compound with oral activity. α-Amyrin acetate can inhibit cancer cells proliferation and induce apoptosis. α-Amyrin acetate can reduce blood glucose level. α-Amyrin acetate can be used for the researches of cancer and metabolic disease, such as breast cancer and diabetes.
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HY-N10600
3β-Acetoxyurs-12-en-11-one 99.34% 3β-Acetoxyurs-12-en-11-one is a ursane triterpenoid with antimicrobial activity, can be isolated from the stem bark of Morus mesozygia and the leaves of Ficus hirta Vahl (Moraceae).
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HY-N12159
Uvaol diacetate Uvaol diacetate (Compound 5) is a triterpenoid derived from the leaves of Nerium oleunder L. and is an analog of Uvaol (HY-N1109). Uvaol has protective effects against DNA damage and can also induce apoptosis in cancer cells.
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HY-N18959
Ψ-Taraxasterol acetate Ψ-Taraxasterol acetate is a pentacyclic triterpene acetate that can be isolated from the kernel of Vitellaria paradoxa (shea tree).
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HY-N2075
3-Acetyl-beta-boswellic acid 99.05% 3-Acetyl-beta-boswellic acid is a boswellic acid isolated from Boswellia serrata gum resin.
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HY-N2513
β-Boswellic acid 99.89% β-Boswellic acid is isolated from the gum resin of Boswellia serrata with anticancer, antioxidant activity, anti-inflammatory activity and anti-arthritic pain.β-Boswellic acid is an orally active nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells with IC50 values ranging from 0.6 to 7.1 μM. β-Boswellic acid is promising for research of diabetes, inflammatory and arthritic diseases.
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HY-N2815
Ursolic acid acetate 98.0% Ursolic acid acetate (Acetylursolic acid) is a triterpenoid compound and an inhibitor of Plasmodium falciparum heat shock protein 90 (PfHsp90) with a KD of 8.16 μM. Ursolic acid acetate is cytotoxic to KB cells, with an IC50 value of 8.4 μM. Ursolic acid acetate can be used in tumor and antimalarial research.
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HY-N2843
α-Amyrin palmitate 98.0% α-Amyrin palmitate is isolated from Santalum album (sandalwood). α-Amyrin palmitate can be used for the study of arthritis in vivo.
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HY-N2918
Bauerenol acetate Bauerenol acetate is a Triterpenoids product that can be isolated from the herb of Solidago altissima.
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HY-N2923
β-Amyrin acetate 99.98% β-Amyrin acetate is a triterpenoid with potent anti-inflammatory, antifungal, anti-diabetic, anti-hyperlipidemic activities. β-Amyrin acetate can inhibit HMG-CoA reductase activity by locating in the hydrophobic binding cleft of HMG CoA reductase.
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HY-N8423R
α-Amyrin (Standard) ≥98% α-Amyrin (Standard) is a pentacyclic triterpenoid compound with oral activity. α-Amyrin (Standard) activates the ERK and GSK-3β signaling pathways. α-Amyrin (Standard) can inhibit cancer cells proliferation and induce apoptosis. α-Amyrin (Standard) shows anti-bacterial and anti-inflammation activity. α-Amyrin (Standard) can reduce blood glucose level. α-Amyrin (Standard) can be used for the researches of cancer, infection, inflammation, metabolic disease and neurological disease, such as breast cancer, Streptococcus oralis infection, skin inflammation and diabetes.
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References