Glucosidase

Glucosidase inhibitors block enzymes that cleave glucose units from oligosaccharides, disaccharides and glycoproteins. Intestinal α-glucosidases break down dietary carbohydrates, so their inhibitors are used to study postprandial glucose uptake. Acarbose, a pseudo-oligosaccharide, and miglitol, an iminosugar, are standard inhibitors of these enzymes. In the endoplasmic reticulum, glucosidases I and II trim glucose residues from newly attached N-linked glycans. Trimming and later reglucosylation control glycoprotein binding to the chaperone calnexin, as reported in 1995. Deoxynojirimycin and celgosivir inhibit these processing glucosidases and are used in glycoprotein folding and virology research. Miglustat hydrochloride, an N-alkylated iminosugar, also inhibits glucosylceramide synthase in glycosphingolipid research.

Items 1-25 of 194

  • Miglustat hydrochloride
    Cat. No.
    A12797

    Miglustat hydrochloride

    Synonyms: NB-DNJ

    Miglustat hydrochloride is an orally active α-glucosidase I and II and ceramide-specific glycosyltransferase inhibitor.

    1 mg
    $25.00
    2 mg
    $40.00
    All 8 sizes
  • Rebaudioside A
    Cat. No.
    A12108

    Rebaudioside A

    Rebaudioside A is an α-glucosidase inhibitor that demonstrates an IC50 value of 35.01 μg/mL. This steviol glycoside enhances insulin secretion in pancreatic β cells through a glucose-dependent mechanism, which involves the inhibition of KATP channels and subsequent depolarization and calcium influx. Additionally, Rebaudioside A regulates cholesterol metabolism by activating the SREBP signaling pathway and inhibiting HMGCR, leading to increased LDL receptor expression. It is suitable for research in the areas of blood glucose and lipid regulation, as well as obesity management.

    1 g
    $20.00
    5 g
    $40.00
    All 6 sizes
  • Celgosivir
    Cat. No.
    A13118

    Celgosivir

    Synonyms: MDL 28574

    Celgosivir is an alpha-glucosidase I inhibitor for the potential treatment of HCV infection.

    1 mg
    $70.00
    2 mg
    $110.00
    All 8 sizes
  • Deoxynojirimycin
    Cat. No.
    A14383

    Deoxynojirimycin

    Synonyms: Duvoglustat; Moranolin; Moranoline; 1-Deoxynojirimycin

    Deoxynojirimycin is a Maltase-glucoamylase (a-glucosidase I and II) inhibitor. It interferes with N-linked glycosylation.

    2 mg
    $30.00
    5 mg
    $50.00
    All 8 sizes
  • Afegostat D-tartrate
    Cat. No.
    A14385

    Afegostat D-tartrate

    Synonyms: Isofagomine D-Tartrate; D-Isofagomine; iso-Fagomine

    Afegostat D-tartrate was an experimental drug for the treatment of certain forms of Gaucher's disease. The substance was used in form of the tartrate. Isofagomine (IFG) is an acid β-glucosidase (GCase) active site inhibitor that acts as a pharmacological chaperone.

    Out of stock

    All 4 sizes
  • Voglibose
    Cat. No.
    A14945

    Voglibose

    Voglibose is an N-substituted derivative of valiolamine, excellent inhibitory activity against alpha-glucosidases and its action against hyperglycemia and various disorders caused by hyperglycemia.

    10 mg
    $25.00
    25 mg
    $40.00
    All 7 sizes
  • Hexylresorcinol
    Cat. No.
    A16573

    Hexylresorcinol

    Synonyms: 4-Hexylresorcinol

    Hexylresorcinol (4-Hexylresorcinol) is a natural compound found in plants with antimicrobial, anthelmintic, antiseptic and antitumor activities. Hexylresorcinol can induce apoptosis in squamous carcinoma cells. Hexylresorcinol is a reversible and noncompetitive inhibitor of α-glucosidase. Hexylresorcinol has protective effects against oxidative DNA damage.

    500 mg
    $35.00
    1 g
    $45.00
    All 3 sizes
  • Ceftezole
    Cat. No.
    A17580

    Ceftezole

    Synonyms: CTZ

    Ceftezole is a broad-spectrum cephem antibiotic that effectively targets both gram-positive and gram-negative bacteria. Its primary mechanism involves inhibiting bacterial cell wall synthesis, making it valuable in combating various bacterial infections. Additionally, Ceftezole acts as an alpha-glucosidase inhibitor, demonstrating potential in in vivo anti-diabetic applications. It is suitable for use in microbiological research and studies related to diabetes management.

    25 mg
    $1,275.00
    50 mg
    $1,625.00
    All 3 sizes
  • Ceftezole sodium
    Cat. No.
    A17597

    Ceftezole sodium

    Synonyms: CTZ sodium

    Ceftezole sodium is a broad-spectrum cephem antibiotic primarily targeting various gram-positive and gram-negative bacteria. Its mechanism of action involves inhibiting bacterial cell wall synthesis, leading to cell lysis and death. Additionally, ceftezole sodium demonstrates alpha-glucosidase inhibition, contributing to its in vivo anti-diabetic effects. This compound is relevant for research in microbial resistance and diabetes therapeutic development.

    5 mg
    $20.00
    10 mg
    $30.00
    All 6 sizes
  • N-Nonyldeoxynojirimycin
    Cat. No.
    A19963

    N-Nonyldeoxynojirimycin

    Synonyms: NN-DNJ; Nonyl-DNJ

    N-Nonyldeoxynojirimycin (NN-DNJ) is a potent inhibitor of alpha-glucosidase and alpha-1,6-glucosidase (IC50s, 0.42, 8.4 μM, respectively), inhibits glycogen breakdown.

    1 mg
    $80.00
    5 mg
    $155.00
    All 6 sizes
  • ML198
    Cat. No.
    A22122

    ML198

    ML198 is a novel activator and non-inhibitory chaperone of glucocerebrosidase.

    2 mg
    $35.00
    5 mg
    $80.00
    All 7 sizes
  • Butyl isobutyl phthalate
    Cat. No.
    A22689

    Butyl isobutyl phthalate

    Butyl isobutyl phthalate is isolated from the rhizoid of Laminaria japonica. Butyl isobutyl phthalate is a non-competitive α-glucosidase inhibitor with an IC50 value of 38 μM.

    10 mg
    $25.00
    25 mg
    $40.00
    All 6 sizes
  • Tangshenoside I
    Cat. No.
    A22712

    Tangshenoside I

    Tangshenoside I, isolated from the roots of Codonopsis lanceolata, exhibits weak α-glucosidase inhibitory activities in vitro with an IC50 of 1.4 mM.

    1 mg
    $175.00
    5 mg
    $575.00
    All 3 sizes
  • Gnetol
    Cat. No.
    A24067

    Gnetol

    Gnetol is a bioactive phenolic compound isolated from the root of *Gnetum montanum* with diverse pharmacological properties. It potently inhibits cyclooxygenase-1 (COX-1) with an IC₅₀ of 0.78 μM and exhibits histone deacetylase (HDAC) inhibitory activity. Gnetol is also a strong tyrosinase inhibitor, with an IC₅₀ of 4.5 μM against murine tyrosinase, leading to suppression of melanin biosynthesis. In addition to its antioxidant, antiproliferative, anticancer, and hepatoprotective effects, Gnetol modulates metabolic enzymes in a concentration-dependent manner, including α-amylase, α-glucosidase, and adipogenesis pathways, making it a promising candidate for research in oncology, dermatology, and metabolic disorders.

    5 mg
    $54.00
    10 mg
    $93.00
    All 4 sizes
  • β-Amyrone
    Cat. No.
    A28354

    β-Amyrone

    Synonyms: β-Amyron

    β-Amyrone is a triterpene compound recognized for its anti-inflammatory properties, primarily through the inhibition of cyclooxygenase-2 (COX-2) expression. It demonstrates significant antifungal activity and exhibits antiviral effects against the Chikungunya virus. Additionally, β-Amyrone inhibits α-glucosidase and acetylcholinesterase (AChE) activities, making it a valuable compound for research in inflammation, infectious diseases, and obesity-related studies.

    Out of stock

    All 7 sizes
  • (-)-Pinoresinol
    Cat. No.
    A31189

    (-)-Pinoresinol

    (-)-Pinoresinol is a plant-derived tetrahydrofuran lignan that serves as an anti-inflammatory agent through the inhibition of α-glucosidase. This compound exhibits hypoglycemic properties and demonstrates chemopreventive potential by inducing apoptosis and causing G2/M phase cell cycle arrest. Its biological activities make it a valuable tool for research in inflammation and metabolic disorders.

    1 mg
    $90.00
    5 mg
    $290.00
    All 6 sizes
  • Malabaricone B
    Cat. No.
    A31404

    Malabaricone B

    Malabaricone B is a naturally occurring phenolic compound that functions as an α-glucosidase inhibitor, exhibiting an IC50 of 63.7 µM. This compound demonstrates significant biological activities, including anticancer, antimicrobial, antioxidant, and antidiabetic effects. It is suitable for research applications focused on metabolic regulation and the investigation of glycemic control.

    1 mg
    $55.00
    2 mg
    $80.00
    All 6 sizes
  • 3-Hydroxybakuchiol
    Cat. No.
    A31629

    3-Hydroxybakuchiol

    3-Hydroxybakuchiol is an electron transport chain (ETC) inhibitor known for its antitumor properties. It effectively induces apoptosis in tumor cells, contributing to its potential as a therapeutic agent in cancer research. Additionally, 3-Hydroxybakuchiol exhibits moderate inhibitory activity against α-glucosidase, with an IC50 value of 345 μM, further expanding its applications in biological studies.

    5 mg
    $425.00
    All 1 sizes
  • Caffeoyltryptophan
    Cat. No.
    A36227

    Caffeoyltryptophan

    Caffeoyltryptophan is a competitive inhibitor of protein tyrosine phosphatase 1B (PTP1B), exhibiting an IC50 of 16.99 μM. Additionally, it demonstrates inhibitory effects on α-glucosidase, linoleic acid peroxidation, and hemolysis. This compound is primarily utilized in research related to type 2 diabetes, offering insights into metabolic regulation and potential therapeutic avenues.

    1 mg
    $85.00
    2 mg
    $120.00
    All 6 sizes
  • Antidiabetic agent 2
    Cat. No.
    A36337

    Antidiabetic agent 2

    Antidiabetic agent 2 is a potent DPP-4 inhibitor that effectively promotes glucose uptake. This compound also inhibits PTP-1B, α-amylase, and α-glucosidase, exhibiting IC50 values of 0.036, 0.042, 0.241, and 0.185 μM, respectively. By decreasing blood glucose levels, Antidiabetic agent 2 serves as a valuable tool for research focused on diabetes management and the modulation of glucose homeostasis.

    Out of stock

    All 3 sizes
  • Ethyl-3,5-di-O-caffeoylquinate
    Cat. No.
    A36349

    Ethyl-3,5-di-O-caffeoylquinate

    Ethyl-3,5-di-O-caffeoylquinate is a derivative of ethyl caffeoylquinate, primarily targeting α-glucosidase and PTP1B enzymes. This compound demonstrates potential as an inhibitor of these critical enzymes, making it valuable for research in metabolic disorders and diabetes management. Isolated from the flower buds of Lonicera macranthoides, it also serves as an isomer of chlorogenic acid (ethyl dicaffeoylquinate), expanding its relevance in phytochemical studies and pharmacological applications.

    5 mg
    $375.00
    All 1 sizes
  • Chrysophanol triglucoside
    Cat. No.
    A36377

    Chrysophanol triglucoside

    Chrysophanol triglucoside is an anthraquinone with a specific inhibitory action on protein tyrosine phosphatase 1B (PTP1B) and α-glucosidase, demonstrating IC50 values of 80.17 µM and 197.06 µM, respectively. This compound is derived from Cassia obtusifolia and has potential applications in diabetes research, particularly in the study of glucose metabolism and insulin signaling pathways.

    1 mg
    $195.00
    All 1 sizes

Items 1-25 of 194

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