Page last updated: 2024-08-23

acarbose and ao 128

acarbose has been researched along with ao 128 in 13 studies

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (7.69)29.6817
2010's11 (84.62)24.3611
2020's1 (7.69)2.80

Authors

AuthorsStudies
Afshari, CA; Chen, Y; Dunn, RT; Hamadeh, HK; Kalanzi, J; Kalyanaraman, N; Morgan, RE; van Staden, CJ1
Anantaraju, HS; Anireddy, JS; Babu, BN; Dwivedi, S; Ethiraj, KS; Kasturi, S; Perumal, Y; Sigalapalli, DK; Surarapu, S; Uppalanchi, S1
Anireddy, JS; Bathini, NB; Dwivedi, S; Ethiraj, KS; Kasturi, SP; Sigalapalli, DK; Surarapu, S; Uppalanchi, S; Yogeeswari, P1
Anireddy, JS; Babu, BN; Bathoju, CC; Dwivedi, S; Ethiraj, KS; Kasturi, S; Perumal, Y; Sigalapalli, DK; Surarapu, S; Uppalanchi, S1
Ishikawa, F; Kinouchi, E; Marumoto, S; Morikawa, T; Nakamura, S; Nakanishi, I; Ninomiya, K; Sakano, M; Takashima, K; Tanabe, G1
Adachi, I; Asano, N; Ikeda, K; Imahori, T; Kamiyama, O; Kato, A; Kuriyama, C; Okamoto, T; Sanae, F; Takahata, H1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Adachi, I; Imahori, T; Kato, A; Murakami, K; Nakagawa, S; Natori, Y; Takahata, H; Yoshimura, Y1
Akaki, J; Minematsu, T; Morikawa, T; Muraoka, O; Ninomiya, K; Tanabe, G; Wu, X; Xie, W; Yoshikawa, M1
Amer, MF; Matsuoka, K; Minematsu, T; Muraoka, O; Tanabe, G; Wu, X; Xie, W; Yoshikawa, M1
Cong, W; Minematsu, T; Muraoka, O; Ninomiya, K; Otani, T; Tanabe, G; Yoshikawa, M1
Adachi, I; Hayashi, E; Hirono, S; Imahori, T; Kato, A; Koseki, J; Miyauchi, S; Nakagome, I; Nash, RJ; Natori, Y; Shimaoka, H; Takahata, H; Yoshimura, Y1
Adachi, I; Hirokami, Y; Kato, A; Kinami, K; Natori, Y; Sakuma, T; Sato, K; Takahata, H; Yoshimura, Y1

Other Studies

13 other study(ies) available for acarbose and ao 128

ArticleYear
A multifactorial approach to hepatobiliary transporter assessment enables improved therapeutic compound development.
    Toxicological sciences : an official journal of the Society of Toxicology, 2013, Volume: 136, Issue:1

    Topics: Animals; ATP Binding Cassette Transporter, Subfamily B; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Biological Transport; Chemical and Drug Induced Liver Injury; Cluster Analysis; Drug-Related Side Effects and Adverse Reactions; Humans; Liver; Male; Multidrug Resistance-Associated Proteins; Pharmacokinetics; Rats; Rats, Sprague-Dawley; Recombinant Proteins; Risk Assessment; Risk Factors; Toxicity Tests

2013
Synthesis and α-glucosidase inhibition activity of dihydroxy pyrrolidines.
    Bioorganic & medicinal chemistry letters, 2017, 06-15, Volume: 27, Issue:12

    Topics: alpha-Glucosidases; Dose-Response Relationship, Drug; Glycoside Hydrolase Inhibitors; Molecular Docking Simulation; Molecular Structure; Pyrrolidines; Saccharomyces cerevisiae; Structure-Activity Relationship

2017
Synthesis, molecular modeling and evaluation of α-glucosidase inhibition activity of 3,4-dihydroxy piperidines.
    European journal of medicinal chemistry, 2018, Apr-25, Volume: 150

    Topics: alpha-Glucosidases; Dose-Response Relationship, Drug; Glycoside Hydrolase Inhibitors; Humans; Models, Molecular; Molecular Structure; Piperidines; Structure-Activity Relationship

2018
Synthesis, molecular modeling and biological evaluation of aza-flavanones as α-glucosidase inhibitors.
    MedChemComm, 2017, Aug-01, Volume: 8, Issue:8

    Topics:

2017
Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase.
    Bioorganic & medicinal chemistry letters, 2021, 02-01, Volume: 33

    Topics: alpha-Glucosidases; Animals; Dose-Response Relationship, Drug; Glycoside Hydrolase Inhibitors; Humans; Intestines; Medicine, Ayurvedic; Molecular Conformation; Rats; Salacia; Structure-Activity Relationship; Sugar Alcohols; Sulfates

2021
In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures.
    Bioorganic & medicinal chemistry, 2008, Aug-01, Volume: 16, Issue:15

    Topics: Animals; Caco-2 Cells; Carbohydrate Conformation; Cells, Cultured; Dose-Response Relationship, Drug; Fibroblasts; Gaucher Disease; Glycogen; Glycoside Hydrolases; Hepatocytes; Humans; Imino Sugars; Lysosomes; Rats; Structure-Activity Relationship

2008
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
The synthesis and biological evaluation of 1-C-alkyl-L-arabinoiminofuranoses, a novel class of α-glucosidase inhibitors.
    Bioorganic & medicinal chemistry letters, 2011, Jan-15, Volume: 21, Issue:2

    Topics: alpha-Glucosidases; Animals; Diabetes Mellitus, Type 2; Enzyme Inhibitors; Glycoside Hydrolase Inhibitors; Humans; Hypoglycemic Agents; Imino Furanoses; Rats

2011
Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors.
    Bioorganic & medicinal chemistry, 2011, Mar-15, Volume: 19, Issue:6

    Topics: alpha-Glucosidases; Animals; Enzyme Inhibitors; Glycoside Hydrolase Inhibitors; Hypoglycemic Agents; Rats; Salacia; Structure-Activity Relationship; Sugar Alcohols; Thiophenes; Thiosugars

2011
Role of the side chain stereochemistry in the α-glucosidase inhibitory activity of kotalanol, a potent natural α-glucosidase inhibitor.
    Bioorganic & medicinal chemistry, 2011, Apr-01, Volume: 19, Issue:7

    Topics: alpha-Glucosidases; Enzyme Inhibitors; Glycoside Hydrolase Inhibitors; Molecular Structure; Monosaccharides; Plant Extracts; Stereoisomerism; Structure-Activity Relationship; Sulfates

2011
Biological evaluation of 3'-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3' position in the side chain on the α-glucosidase inhibitory activity.
    Bioorganic & medicinal chemistry letters, 2011, May-15, Volume: 21, Issue:10

    Topics: Enzyme Activation; Enzyme Inhibitors; Glycoside Hydrolase Inhibitors; Hydrophobic and Hydrophilic Interactions; Magnetic Resonance Spectroscopy; Molecular Structure; Sugar Alcohols; Sulfates

2011
α-1-C-butyl-1,4-dideoxy-1,4-imino-l-arabinitol as a second-generation iminosugar-based oral α-glucosidase inhibitor for improving postprandial hyperglycemia.
    Journal of medicinal chemistry, 2012, Dec-13, Volume: 55, Issue:23

    Topics: Administration, Oral; Animals; Enzyme Inhibitors; Glycoside Hydrolase Inhibitors; Humans; Hyperglycemia; Hypoglycemic Agents; Imino Sugars; Inhibitory Concentration 50; Male; Mice; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

2012
Synthesis and biological evaluation of α-1-C-4'-arylbutyl-L-arabinoiminofuranoses, a new class of α-glucosidase inhibitors.
    Bioorganic & medicinal chemistry letters, 2014, Aug-01, Volume: 24, Issue:15

    Topics: alpha-Glucosidases; Dose-Response Relationship, Drug; Glycoside Hydrolase Inhibitors; Humans; Imino Sugars; Intestines; Molecular Structure; Structure-Activity Relationship

2014