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Results for "

a-amyrin

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    10
    TargetMol | Inhibitors_Agonists
  • Natural Products
    9
    TargetMol | Natural_Products
  • Isotope Products
    1
    TargetMol | Isotope_Products
Alpha-Amyrin
alpha-Amyrenol, α-Amyrin, alpha-Amyrine, Viminalol
TN1372638-95-9
Alpha-Amyrin (alpha-Amyrine) is an inhibitor of trypsin and chymotrypsin with antineoplastic effects. alpha-Amyrin can be used in studies about acting as a hepatomodulatory.
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3-Epi-beta-amyrin
T1244136811-63-8
3-Epi-beta-amyrin is a useful organic compound for research related to life sciences. The catalog number is T124413 and the CAS number is 6811-63-8.
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3-Epi-alpha-amyrin
T1245915937-48-4
3-Epi-alpha-amyrin is a useful organic compound for research related to life sciences. The catalog number is T124591 and the CAS number is 5937-48-4.
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11-oxo-alpha-amyrin
Neoilexonol
TN72282118-90-3
11-oxo-alpha-amyrin (Neoilexonol) is a triterpene compound extracted from Leonurus japonicus (Lamiaceae) and is a natural compound .
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beta-Amyrin acetate
TN14381616-93-9
beta-Amyrin acetate inhibits HMG-CoA Reductase (HMGCR) and sEH activity with IC50 of 3.4 μM. beta-Amyrin acetate has anti-inflammatory, antifungal, antioxidant, and anti-hyperlipidemic activities.
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delta-Amyrin acetate
TN381651361-60-5
β-Amyrin acetate and β-Amyrin acetate have antidyslipidemic activity.
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α-Amyrin acetate
α-​Amyrin acetate
T14192863-76-3
α-Amyrin acetate is a natural product( triterpeno), with anti-inflammatory activity, antispasmodic profile and the relaxant effect.
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7-10 days
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Friedelinol
NSC 407041, Friedelan-3-ol, Friedelan-3alpha-ol, epi-Friedelinol, Epifriedelanol
T198805085-72-3
Friedelinol is a pentacyclic trierpene plant as the free acid or the aglycone for many saponins. Friedelinol can rearrange to the isomer, ursolic acid, or be oxidized to taraxasterol and amyrin.
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α-Amyrin palmitate
alpha-Amyrin palmitate
TN338322255-10-3
alpha-Amyrin palmitate is antiarthritic in the adjuvant model of arthritis in rats. alpha-Amyrin palmitate is a potent non-competitive inhibitor of chymotrypsin (Ki=6 microM), it also shows weak cytotoxicity against the A2780 human ovarian cancer cell line.
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