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Results for "

α-amylase

" in TargetMol Product Catalog
  • Inhibitor Products
    37
    TargetMol | Activity
  • Natural Products
    17
    TargetMol | inventory
  • Recombinant Protein
    7
    TargetMol | natural
α-Amylase
T196159000-90-2
α-Amylase, a hydrolase enzyme, catalyzes the hydrolysis of internal α-1,4-glycosidic linkages in starch, producing glucose and maltose.
  • $42
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Amylase
T11369000-92-4
Amylase (Diastase) is any one of a group of enzymes which catalyses the breakdown of starch into maltose.
  • $40
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Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside
T2S1682205370-59-8
Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside can moderately inhibit α-amylase activity, with the IC50 value of 0.03 umol/ml.
  • $47
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Kaempferol-3,7-di-O-β-glucoside
TN436825615-14-9
Kaempferol-3,7-di-O-β-glucoside (Kaempferol 3,7-diglucoside) is a flavonol from Morettia philaena, It can inhibit α-amylase, α-glucosidase and Acetylcholinesterase. Kaempferol-3, 7-di-o-β-Glucoside has neuroprotective activity and can slow down differentiated neuronal cells SH-SY5Y from Amyloid β peptide-induced damage. Kaempferol-3, 7-di-o-β-Glucoside can be used to study neurological disorders like Alzheimer's disease.
  • $178
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TargetMol | Inhibitor Sale
Ethyl trans-caffeate
T3S001366648-50-8
1. Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) has anti-inflammatory activity. 2. Ethyl trans-caffeate may as a promising natural compound for future application in chronic liver disease. 3. Ethyl trans-caffeate is a potent chemopreventive compound against skin carcinogenesis caused by solar UV exposure. 4. Ethyl trans-caffeate is the high-resolution structures of representative inhibitors in complex with human pancreatic α-amylase. 5. Ethyl trans-caffeate strongly inhibits neoplastic transformation of JB6 Cl41 cells without toxicity. PI3K, ERK1/2, and p38 kinase activities were suppressed by direct binding with HOEC in vitro.
  • $50
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Irilone
TN652441653-81-0
Irilone has immunomodulatory, and α-amylase inhibitory activities, it exhibits the selective inhibition toward CYP3 A4 rather than other major human CYPs. Irilone exhibited prominent antioxidant activities with the IC50 value of 10.46μM. Irilone potentiat
  • $678
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Ficusonolide
T392191800503-81-4
Ficusonolide exhibits significant antidiabetic activity through its interactions with dipeptidyl peptidase-IV (DPP-IV), protein tyrosine phosphatase 1B (PTP-1B), α-glucosidase, and α-amylase.
  • $1,520
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Isoeugenol acetate
T2S049193-29-8
1. Isoeugenol acetate (Acetylisoeugenol) shows good antifungal activities against R. solani and F. oxysporum. 2. Isoeugenol acetate is a mild sensitizer in vivo.
  • $30
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Fucoidan
T75449072-19-9
Fucoidan is found in various species of brown seaweed and algae,with anticancer, antiviral, neuroprotective, immune-modulating.
  • $46
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Quercetin 3-(6″-caffeoylsophoroside)
T799391032595-77-9
Quercetin 3-(6″-caffeoylsophoroside) is an orally active compound exhibiting α-amylase inhibitory activity, with an IC50 value of 73.66 μg/mL, and demonstrates antidiabetic effects through the reduction of oxidative stress. It is found in the hydro-methanolic extract of Cardamine hirsuta Linn and is utilized in diabetes mellitus research [1].
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Trilobatin
T2S07314192-90-9
Trilobatin (P-Phlorizin) has anti-oxidant effect, can increase superoxide dismutase (SOD) activity.Trilobatin has anti-inflammatory effect, it potentially inhibits the lipopolysaccharide (LPS)-induced inflammatory response by suppressing the NF-κB signaling pathway.Trilobatin shows a strong inhibitory activity against α-glucosidase and a moderate inhibitory activity against α-amylase for management of postprandial hyperglycemia with less side effect.
  • $58
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Ellipyrone A
T75492
Ellipyrone A, a γ-pyrone-based macrocyclic polyketide, demonstrates inhibitory activity against dipeptidyl peptidase-4 (IC 50 = 0.35 mM). Additionally, this compound exhibits anti-glycolytic effects on α-glucosidase (IC 50 = 0.74 mM) and α-amylase (IC 50 = 0.59 mM) [1].
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Isookanin
TN17881036-49-3
Isookanin shows strong diphenyl(2,4,6-trinitrophenyl)iminoazanium (DPPH) radical-scavenging activity with the IC50 value of 7.9 ± 0.53 μM. Isookanin is a potent inhibitor of α-amylase (IC50=0.447 mg ml).
  • $50
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7,4'-Di-O-methylapigenin
T56905128-44-9
7,4'-Di-O-methylapigenin (4',7-DIMETHOXY-5-HYDROXYFLAVONE) can inhibit α-glucosidase and α-amylase enzymes and enhance 2-NBDG uptake in L6 cells, it has hypolipidemic effect on mouse pre-adipocyte (3T3L1) cell lines.
  • $39
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Erythrocentaurin
TN401050276-98-7
Erythrocentaurin has antibacterial activity; it also exhibits a concentration-dependent α-amylase inhibition (IC(50) 1.67 ± 0.28 mg/mL).
  • $320
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8,3′,4′-Trihydroxyflavone-7-O-β-D-glucopyranoside
T75701925701-05-9
8,3′,4′-Trihydroxyflavone-7-O-β-D-glucopyranoside (Compound 3), a natural product isolated from Bidens bipinnata, exhibits a 22% inhibition against α-amylase at a concentration of 0.556 mg/mL [1].
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trans-Chalcone
T3322614-47-1
trans-Chalcone (Chalkone) is an aromatic ketone that forms the central core for a variety of important biological compounds, which are known collectively as chalcones.
  • $30
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