G. Surineni

发表

Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions

Arunasree M. Kalle, S. Kantevari, S. Chakravarty, 2019, ACS omega.

Comparative Analysis of Whole-Genome and Methylome Profiles of a Smooth and a Rough Mycobacterium abscessus Clinical Strain

Md. Mahmudul Islam, Amjad Ali, Tianyu Zhang, 2019, G3: Genes, Genomes, Genetics.

Rational design, synthesis and evaluation of novel-substituted 1,2,3-triazolylmethyl carbazoles as potent inhibitors of Mycobacterium tuberculosis

P. Yogeeswari, D. Sriram, S. Kantevari, 2014, Medicinal Chemistry Research.

Discovery of novel verinurad analogs as dual inhibitors of URAT1 and GLUT9 with improved Druggability for the treatment of hyperuricemia.

Jianjun Chen, Jian Luo, Ting Wu, 2021, European journal of medicinal chemistry.

Design, synthesis, and in vitro biological evaluation of novel benzimidazole tethered allylidenehydrazinylmethylthiazole derivatives as potent inhibitors of Mycobacterium tuberculosis.

Tianyu Zhang, H. A. Hameed, Md Mahmudul Islam, 2019, MedChemComm.

Design and synthesis of novel carbazole tethered pyrrole derivatives as potent inhibitors of Mycobacterium tuberculosis.

P. Yogeeswari, D. Sriram, S. Kantevari, 2015, Bioorganic & medicinal chemistry letters.

Rational design, synthesis and evaluation of novel-substituted 1,2,3-triazolylmethyl carbazoles as potent inhibitors of Mycobacterium tuberculosis

P. Yogeeswari, D. Sriram, S. Kantevari, 2015, Medicinal Chemistry Research.

Dibenzofuran, dibenzothiophene and N-methyl carbazole tethered 2-aminothiazoles and their cinnamamides as potent inhibitors of Mycobacterium tuberculosis.

P. Yogeeswari, D. Sriram, S. Kantevari, 2018, Bioorganic & medicinal chemistry letters.

Synthesis, in vitro, and in vivo (Zebra fish) antitubercular activity of 7,8-dihydroquinolin-5(6H)-ylidenehydrazinecarbothioamides.

D. Sriram, B. Sridhar, S. Kantevari, 2020, Bioorganic chemistry.

Quinoline Derivatives Kill Mycobacterium tuberculosis by Activating Glutamate Kinase.

Tianyu Zhang, Yaoju Tan, Shouyong Tan, 2019, Cell chemical biology.

Detection of novel mutations associated with independent resistance and cross-resistance to isoniazid and prothionamide in Mycobacterium tuberculosis clinical isolates.

X. Li, W. Yew, H. A. Hameed, 2019, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

Click-based synthesis and antitubercular evaluation of dibenzofuran tethered thiazolyl-1,2,3-triazolyl acetamides.

P. Yogeeswari, D. Sriram, S. Kantevari, 2016, Bioorganic & medicinal chemistry letters.

Discovery of novel benzohydroxamate-based histone deacetylase 6 (HDAC6) inhibitors with the ability to potentiate anti-PD-L1 immunotherapy in melanoma

Ting Yu, Bulian Deng, Jianjun Chen, 2023, Journal of enzyme inhibition and medicinal chemistry.

Design, synthesis, and in vitro biological evaluation of novel benzimidazole tethered allylidenehydrazinylmethylthiazole derivatives as potent inhibitors of Mycobacterium tuberculosis.

Tianyu Zhang, H. A. Hameed, C. Chhotaray, 2019, MedChemComm.