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Novel triazolothiadiazines act as potent anticancer agents in liver cancer cells through Akt and ASK-1 proteins

Bioorganic & medicinal chemistry, 2016-02, Vol.24 (4), p.858-872

2016

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Design, Synthesis and Biological Evaluation of Novel Triazolothiadiazoles Derived from NSAIDs as Anticancer Agents

Anti-cancer agents in medicinal chemistry, 2022-01, Vol.22 (7), p.1340

2022

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Bioequivalence study of two favipiravir tablet formulations in healthy male subjects

International journal of clinical pharmacology and therapeutics, 2021-05, Vol.59 (5), p.409

2021

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Synthesis of 3,6-disubstituted 7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines as novel analgesic/anti-inflammatory compounds

European journal of medicinal chemistry, 2009-11, Vol.44 (11), p.4528-4538

2009

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The Relative Bioavailability Study of Two Cefdinir Formulations in Healthy Males Under Fasting Conditions

FABAD journal of pharmaceutical sciences, 2023-03, Vol.48 (1), p.25-36

2023

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Design and synthesis of some thiazolotriazolyl esters as anti-inflammatory and analgesic agents

Medicinal chemistry research, 2012-02, Vol.21 (2), p.192-201

2012

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Synthesis and structural characterization of 3-[1-[4-(2-methylpropyl)phenyl]ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4- b ]-1,3,4-thiadiazole

Powder diffraction, 2019-12, Vol.34 (4), p.325-330

2019

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A new triazolothiadiazine derivative inhibits stemness and induces cell death in HCC by oxidative stress dependent JNK pathway activation

Scientific reports, 2022-09, Vol.12 (1), p.15139-15139, Article 15139

2022

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The Bioequivalence Study of Two Dexketoprofen 25 mg Film-Coated Tablet Formulations in Healthy Males Under Fasting Conditions

Turkish journal of pharmaceutical sciences, 2023-04, Vol.20 (2), p.115-120

2023

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Structure determination of two structural analogs, named 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16F2N4S) and 3-[1-(2-fluoro-4-biphenyl)ethyl]-6-(4-chlorophenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole (C23H16ClFN4S) by synchrotron X-ray powder diffraction

Powder diffraction, 2017-12, Vol.32 (4), p.279-289

2017

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Structure elucidation of 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine, C23H18Cl2N4OS from synchrotron X-ray powder diffraction

Powder diffraction, 2017-12, Vol.32 (4), p.271-278

2017

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Structure elucidation of 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7 H -1,2,4-triazolo[3,4- b ]-1,3,4-thiadiazine, C 23 H 18 Cl 2 N 4 OS from synchrotron X-ray powder diffraction

Powder diffraction, 2017-12, Vol.32 (4), p.271-278

2017

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Novel 3,6-Disubstituted 7H-1,2,4-Triazolo[3,4-b][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic / Anti-inflammatory, Antioxidant Activities

Archiv der Pharmazie (Weinheim), 2009-05, Vol.342 (5), p.291-298

2009

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A joint theoretical and experimental structural study of two novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives

Structural chemistry, 2010-08, Vol.21 (4), p.795-802

2010

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COMPUTATIONAL IDENTIFICATION OF NOVEL TARGETS FOR DRUG CANDIDATE COMPOUNDS

Journal of Research in Pharmacy, 2023, Vol.27_special_issue_3 (27_special_issue_3), p.9-12

2023

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Novel 3,6‐Disubstituted 7 H ‐1,2,4‐Triazolo[3,4‐ b ][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic / Anti‐inflammatory, Antioxidant Activities

Archiv der Pharmazie (Weinheim), 2009-05, Vol.342 (5), p.291-298

2009

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Synthesis of 3,6-disubstituted 7 H-1,2,4-triazolo[3,4- b]-1,3,4-thiadiazines as novel analgesic/anti-inflammatory compounds

European journal of medicinal chemistry, 2009, Vol.44 (11), p.4528-4538

2009

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ChemInform Abstract: Novel 3,6-Disubstituted 7H-1,2,4-Triazolo[3,4-b][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic/Antiinflammatory, Antioxidant Activities

ChemInform, 2009-09, Vol.40 (38), p.no-no

2009

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Novel triazolothiadiazines act as potent anticancer agents in liver cancer cells through Akt and ASK-1 proteins

Design, Synthesis and Biological Evaluation of Novel Triazolothiadiazoles Derived from NSAIDs as Anticancer Agents

Bioequivalence study of two favipiravir tablet formulations in healthy male subjects

Synthesis of 3,6-disubstituted 7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines as novel analgesic/anti-inflammatory compounds

The Relative Bioavailability Study of Two Cefdinir Formulations in Healthy Males Under Fasting Conditions

Design and synthesis of some thiazolotriazolyl esters as anti-inflammatory and analgesic agents

Synthesis and structural characterization of 3-[1-[4-(2-methylpropyl)phenyl]ethyl]-6-(4-fluorophenyl)-1,2,4-triazolo[3,4- b ]-1,3,4-thiadiazole

A new triazolothiadiazine derivative inhibits stemness and induces cell death in HCC by oxidative stress dependent JNK pathway activation

The Bioequivalence Study of Two Dexketoprofen 25 mg Film-Coated Tablet Formulations in Healthy Males Under Fasting Conditions

Structure elucidation of 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine, C23H18Cl2N4OS from synchrotron X-ray powder diffraction

Structure elucidation of 3-[1-(6-methoxy-2-naphtyl)ethyl]-6-(2,4-dichlorophenyl)-7 H -1,2,4-triazolo[3,4- b ]-1,3,4-thiadiazine, C 23 H 18 Cl 2 N 4 OS from synchrotron X-ray powder diffraction

Novel 3,6-Disubstituted 7H-1,2,4-Triazolo[3,4-b][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic / Anti-inflammatory, Antioxidant Activities

A joint theoretical and experimental structural study of two novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine derivatives

COMPUTATIONAL IDENTIFICATION OF NOVEL TARGETS FOR DRUG CANDIDATE COMPOUNDS

Novel 3,6‐Disubstituted 7 H ‐1,2,4‐Triazolo[3,4‐ b ][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic / Anti‐inflammatory, Antioxidant Activities

Synthesis of 3,6-disubstituted 7 H-1,2,4-triazolo[3,4- b]-1,3,4-thiadiazines as novel analgesic/anti-inflammatory compounds

ChemInform Abstract: Novel 3,6-Disubstituted 7H-1,2,4-Triazolo[3,4-b][1,3,4]thiadiazines: Synthesis, Characterization, and Evaluation of Analgesic/Antiinflammatory, Antioxidant Activities

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