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thiazoles and thiazolo(3,2-a)perimidine

thiazoles has been researched along with thiazolo(3,2-a)perimidine in 15 studies

Research

Studies (15)

TimeframeStudies, this research(%)All Research%
pre-19901 (6.67)18.7374
1990's0 (0.00)18.2507
2000's1 (6.67)29.6817
2010's12 (80.00)24.3611
2020's1 (6.67)2.80

Authors

AuthorsStudies
Chen, HH; Lin, YO; Liu, KC1
Austin, C; Austin, R; Bonnert, R; Cage, P; Christie, J; Christie, M; Dixon, C; Hill, S; Hunt, F; Jewell, R; Martin, I; Robinson, D; Willis, P1
Cao, C; Li, X; Li, Y; Liu, Z; Wang, R; Xu, Y; Yu, B; Zhang, X; Zhang, Z; Zhou, B; Zhou, J; Zhou, M1
Aertgeerts, K; Arita, T; Hirose, M; Imada, T; Ishikawa, T; Kawamoto, T; Miyazaki, T; Ohashi, T; Okaniwa, M; Sang, BC; Sumita, A; Takagi, T; Tanaka, Y; Tsutsumi, S; Yabuki, M; Yano, J; Yoshida, S1
Li, C; Li, Y; Wang, R; Xu, Y; Yu, B; Zhang, Z; Zhou, M1
Bharate, SB; Bhushan, S; Guru, SK; Jain, SK; Kour, S; Sharma, PR; Sharma, R; Singh, B; Singh, SK; Vishwakarma, RA1
Chen, L; Mahulikar, P; Nandre, J; Patil, S; Patil, U; Patil, V; Prior, T; Redshaw, C; Sahoo, S; Yu, F1
Fahmy, H; Kuppast, B1
Fu, DJ; Geng, PF; Li, ZH; Liu, HM; Liu, XQ; Ma, JL; Wang, B; Wang, C; Wei, HM; Yu, B; Zhang, J; Zhao, B; Zhao, TQ1
Fahmy, H; Kuppast, B; Liapakis, G; Spyridaki, K; Teleb, M1
Geng, PF; Li, ZH; Liu, HM; Liu, XQ; Ma, JL; Wang, B; Yu, B; Zhang, J; Zhang, XH; Zhao, B; Zhao, TQ1
Bian, X; Huang, X; Huang, Z; Jiao, W; Li, Y; Luo, L; Meng, Y; Sun, L; Sun, Q; Tang, J; Wang, K; Wang, X; Yang, T; Zhang, F1
Deng, YH; Liu, JP; Liu, Y; Sun, LP; Xue, WJ; Yan, ZH1
Azouz, AA; Bakr, RB; Ghoneim, AA1
Cheng, M; Li, R; Wang, H; Wang, J1

Reviews

1 review(s) available for thiazoles and thiazolo(3,2-a)perimidine

ArticleYear
Thiazolo[4,5-d]pyrimidines as a privileged scaffold in drug discovery.
    European journal of medicinal chemistry, 2016, May-04, Volume: 113

    Topics: Anti-Infective Agents; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Antiviral Agents; Chemokines; Drug Discovery; Humans; Molecular Structure; Receptors, Corticotropin-Releasing Hormone; Thiazoles

2016

Other Studies

14 other study(ies) available for thiazoles and thiazolo(3,2-a)perimidine

ArticleYear
[Synthesis and testing of thiazolo[3,2-a]perimidine for anorectic activity].
    Archiv der Pharmazie, 1983, Volume: 316, Issue:8

    Topics: Animals; Appetite Depressants; Mice; Thiazoles

1983
SAR studies on thiazolo[4,5-d]pyrimidine based CXCR2 antagonists involving a novel tandem displacement reaction.
    Bioorganic & medicinal chemistry letters, 2007, May-15, Volume: 17, Issue:10

    Topics: Animals; Humans; Rats; Receptors, Cytokine; Receptors, Interleukin-8B; Structure-Activity Relationship; Thiazoles

2007
Discovery and development of thiazolo[3,2-a]pyrimidinone derivatives as general inhibitors of Bcl-2 family proteins.
    ChemMedChem, 2011, May-02, Volume: 6, Issue:5

    Topics: Binding Sites; Biphenyl Compounds; Drug Evaluation, Preclinical; Molecular Dynamics Simulation; Proto-Oncogene Proteins c-bcl-2; Pyrimidines; Stereoisomerism; Thiazoles

2011
Design and synthesis of novel DFG-out RAF/vascular endothelial growth factor receptor 2 (VEGFR2) inhibitors: 3. Evaluation of 5-amino-linked thiazolo[5,4-d]pyrimidine and thiazolo[5,4-b]pyridine derivatives.
    Bioorganic & medicinal chemistry, 2012, Sep-15, Volume: 20, Issue:18

    Topics: Animals; Antineoplastic Agents; Cell Proliferation; Crystallography, X-Ray; Dose-Response Relationship, Drug; Drug Design; HT29 Cells; Human Umbilical Vein Endothelial Cells; Humans; Mice; Microsomes; Models, Molecular; Molecular Structure; Neoplasms, Experimental; Protein Kinase Inhibitors; Rats; Rats, Inbred F344; Structure-Activity Relationship; Thiazoles; Vascular Endothelial Growth Factor Receptor-2; Xenograft Model Antitumor Assays

2012
Characterization of the stereochemical structures of 2H-thiazolo[3,2-a]pyrimidine compounds and their binding affinities for anti-apoptotic Bcl-2 family proteins.
    ChemMedChem, 2013, Volume: 8, Issue:8

    Topics: bcl-X Protein; Binding Sites; Circular Dichroism; Crystallography, X-Ray; Kinetics; Molecular Conformation; Myeloid Cell Leukemia Sequence 1 Protein; Protein Binding; Protein Structure, Tertiary; Proto-Oncogene Proteins c-bcl-2; Stereoisomerism; Thiazoles

2013
Synthesis, antiproliferative and apoptosis-inducing activity of thiazolo[5,4-d]pyrimidines.
    European journal of medicinal chemistry, 2013, Volume: 70

    Topics: Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; HL-60 Cells; Humans; Molecular Structure; Structure-Activity Relationship; Thiazoles

2013
A novel fluorescent "turn-on" chemosensor for nanomolar detection of Fe(III) from aqueous solution and its application in living cells imaging.
    Biosensors & bioelectronics, 2014, Nov-15, Volume: 61

    Topics: Cell Line; Cell Survival; Ferric Compounds; Fluorescent Dyes; Hep G2 Cells; Humans; Iron; Limit of Detection; Liver; Microscopy, Fluorescence; Optical Imaging; Spectrometry, Fluorescence; Thiazoles

2014
Identification of thiazolo[5,4-d]pyrimidine derivatives as potent antiproliferative agents through the drug repurposing strategy.
    European journal of medicinal chemistry, 2017, Jul-28, Volume: 135

    Topics: Antineoplastic Agents; Apoptosis; Cell Line; Cell Proliferation; Dose-Response Relationship, Drug; Humans; Molecular Structure; Structure-Activity Relationship; Thiazoles

2017
Synthesis of 2-imino and 2-hydrazono thiazolo[4,5-d]pyrimidines as corticotropin releasing factor (CRF) antagonists.
    European journal of medicinal chemistry, 2017, Sep-29, Volume: 138

    Topics: Corticotropin-Releasing Hormone; Dose-Response Relationship, Drug; HEK293 Cells; Humans; Molecular Structure; Structure-Activity Relationship; Thiazoles

2017
Design, synthesis and antiproliferative activity of thiazolo[5,4-d]pyrimidine derivatives through the atom replacement strategy.
    European journal of medicinal chemistry, 2017, Sep-29, Volume: 138

    Topics: Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; Drug Screening Assays, Antitumor; Humans; Molecular Structure; Structure-Activity Relationship; Thiazoles

2017
Design and Synthesis of Novel Positive Allosteric Modulators of α7 Nicotinic Acetylcholine Receptors with the Ability To Rescue Auditory Gating Deficit in Mice.
    Journal of medicinal chemistry, 2019, 01-10, Volume: 62, Issue:1

    Topics: Acetylcholine; Administration, Oral; Allosteric Regulation; alpha7 Nicotinic Acetylcholine Receptor; Animals; Blood-Brain Barrier; Disease Models, Animal; Drug Design; Evoked Potentials; Half-Life; Humans; Mice; Oocysts; Rats; Schizophrenia; Structure-Activity Relationship; Thiazoles; Xenopus laevis

2019
Phenyl and Diaryl Ureas with Thiazolo[5,4-d]pyrimidine Scaffold as Angiogenesis Inhibitors: Design, Synthesis and Biological Evaluation.
    Chemistry & biodiversity, 2019, Volume: 16, Issue:4

    Topics: Angiogenesis Inhibitors; Cell Movement; Cell Proliferation; Dose-Response Relationship, Drug; Drug Design; Human Umbilical Vein Endothelial Cells; Humans; Molecular Structure; Neovascularization, Pathologic; Structure-Activity Relationship; Thiazoles; Urea; Wound Healing

2019
Selective cyclooxygenase inhibition and ulcerogenic liability of some newly prepared anti-inflammatory agents having thiazolo[4,5-d]pyrimidine scaffold.
    Bioorganic chemistry, 2019, Volume: 88

    Topics: Animals; Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Dose-Response Relationship, Drug; Edema; Formaldehyde; Indomethacin; Male; Molecular Docking Simulation; Molecular Structure; Rats; Rats, Wistar; Sheep; Structure-Activity Relationship; Thiazoles; Ulcer

2019
PB-10, a thiazolo[4,5-d] pyrimidine derivative, targets p21-activated kinase 4 in human colorectal cancer cells.
    Bioorganic & medicinal chemistry letters, 2020, 01-15, Volume: 30, Issue:2

    Topics: Binding Sites; Cell Adhesion; Cell Movement; Cell Proliferation; Colorectal Neoplasms; Drug Design; G1 Phase Cell Cycle Checkpoints; HCT116 Cells; Humans; Molecular Docking Simulation; p21-Activated Kinases; Protein Kinase Inhibitors; Pyrimidines; RNA Interference; RNA, Small Interfering; Thiazoles

2020