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  • Amylase
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α-amylase

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    57
    TargetMol | Inhibitors_Agonists
  • Natural Products
    22
    TargetMol | Natural_Products
  • Recombinant Protein
    8
    TargetMol | Recombinant_Protein
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.
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Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside
pinocembrin-7-o-3-o-galloyl-4-6-hexahydroxydiphenoyl-beta-d-glucoside, Pinocembrin 7-O-(3''-galloyl-4'',6''-(S)-hexahydroxydiphenoyl)-beta-D-glucose
T2S1682205370-59-8
Pinocembrin 7-O-[3''-O-galloyl-4'',6''-hexahydroxydiphenoyl]-β-D-glucoside can moderately inhibit α-amylase activity, with an IC50 value of 0.03 µmol ml.
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TargetMol | Citations Cited
Amylase
Diastase
T11369000-92-4
Amylase (Diastase) is any one of a group of enzymes which catalyses the breakdown of starch into maltose.
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Isoeugenol acetate
Isoeugenyl acetate, Acetisoeugenol, Acetylisoeugenol
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.
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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.
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Tannic acid
Gallotannic acid
T08011401-55-4
Tannic acid (Gallotannic acid) is a novel hERG channel blocker.
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trans-Chalcone
Chalcone, Cinnamophenone, Chalkone
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.
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Ethyl trans-caffeate
Ethyl caffeate, Caffeic Acid Ethyl Ester
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.
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TargetMol | Citations Cited
Inulobiose
TN8319470-58-6
Inulobiose, a difructan disaccharide isolated from Pistacia vera L., demonstrates inhibitory effects on α-glycosidase (α-glycosidase) and α-amylase (α-amylase) activities, with IC50 values of 1.87 and 40.72 mg mL respectively. It is utilized in research related to diabetes and glomerular filtration rate testing.
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(-)-epigallocatechin-3-(3''-o-methyl) gallate
(-)-EGCG-3''-O-ME
TN160883104-87-4
(-)-Epigallocatechin-3-(3''-O-methyl) gallate ((-)-EGCG-3''-O-ME) is a natural product isolated from tea leaves with potent antioxidant, cytotoxic, and antibacterial properties, and it improves the adhesive stability of etching rinsing adhesives to dentin.
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Kaempferol-3,7-di-O-β-glucoside
Kaempferol 3,7-di-O-glucoside
TN436825615-14-9
Kaempferol-3,7-di-O-β-glucoside (Kaempferol 3,7-diglucoside) is a flavonol from Morettia philaena that inhibits α-amylase, α-glucosidase, and acetylcholinesterase. It exhibits neuroprotective activity, slowing amyloid β peptide-induced damage in differentiated neuronal cells SH-SY5Y, and can be used in the study of neurological disorders such as Alzheimer's disease.
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Irilone
Irolone, 5,4'-Dihydroxy-6,7-methylenedioxyisoflavone
TN652441653-81-0
Irilone is a flavonoid with α-amylase inhibitory activity and highly selective inhibition of CYP3A4. In addition, Irilone enhances progesterone receptor (PR) signaling via estrogen receptor (ER) and glucocorticoid receptor (GR) when combined with progesterone.Irilone has potential anti-inflammatory activity and inhibits nitric oxide (NO) production by lipopolysaccharide (LPS)-induced RAW264.7 in mouse macrophages.
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7,4'-Di-O-methylapigenin
4',7-DIMETHOXY-5-HYDROXYFLAVONE
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.
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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.
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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).
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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 22% inhibition against α-amylase at a concentration of 0.556 mg mL [1].
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2,7'-Phloroglucinol-6,6'-bieckol
TN75941621988-60-0
2,7 -Phloroglucinol-6,6'-bieckol serves as an effective oral dual α-amylase α-glucosidase inhibitor, demonstrating IC 50 concentrations of 6.94 μM and 23.35 μM, respectively. This compound is beneficial in mitigating postprandial hyperglycemia among diabetic mice and is applicable in diabetes research [1].
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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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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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Trilobatin
P-Phlorizin
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.
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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).
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Kaempferol 3-O-alpha-L-(2, 3-di-Z-p-coumaroyl) rhamnoside
TN77131197343-21-7
Kaempferol 3-O-alpha-L-(2, 3-di-Z-p-coumaroyl) rhamnoside (compound 42), a flavonol extracted from Platanus Occidentalis, functions as an inhibitor of alpha-amylase and DPP IV [1].
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