M. Arifuddin

发表

Development of quinoline‐based hybrid as inhibitor of methionine aminopeptidase 1 from Leishmania donovani

I. Qureshi, Sonali Bhandari, Saleem Yousuf Bhat, 2020, Chemical biology & drug design.

Synthesis and Biological Evaluation of 4‐Sulfamoylphenyl/Sulfocoumarin Carboxamides as Selective Inhibitors of Carbonic Anhydrase Isoforms hCA II, IX, and XII

C. Supuran, A. Angeli, M. Arifuddin, 2018, ChemMedChem.

Sulfocoumarin‐, Coumarin‐, 4‐Sulfamoylphenyl‐Bearing Indazole‐3‐carboxamide Hybrids: Synthesis and Selective Inhibition of Tumor‐Associated Carbonic Anhydrase Isozymes IX and XII

C. Supuran, A. Angeli, M. Arifuddin, 2017, ChemMedChem.

Anti-nociceptive mechanisms of flavonoids-rich methanolic extract from Terminalia coriacea (Roxb.) Wight & Arn. leaves.

M. M. Al-Sanea, Z. Zakaria, N. Ahmed, 2018, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

DABCO mediated one pot synthesis of 2‐(3‐benzyl‐2, 6‐dioxo‐3, 6‐dihydropyrimidin‐1[ 2 H ]‐yl)‐ N ‐(4‐(1, 3‐dioxo‐1 H ‐benzo [ de ]isoquinolin‐2[ 3 H ]‐yl) aryl) acetamides as antimicrobial agents

M. Arifuddin, Sakram Boda, Rambabu Sirgamalla, 2020 .

Mild and Efficient Nitration of Aromatic Compounds Mediated by Transition-Metal Complexes

S. Amina, K. Rajanna, Y. Kumar, 2011 .

Metal‐Free C−C Bond Cleavage: One‐Pot Access to 1,4‐Benzoquinone‐linked N‐Formyl Amides/Sulfonamides/Carbamates using Oxone

A. Kamal, Chander S Digwal, P. Ramya, 2017 .

Synthesis and biological evaluation of novel 4, 7-disubstituted coumarins as selective tumor-associated carbonic anhydrase IX and XII inhibitors.

C. Supuran, K. Chandra, A. Angeli, 2021, Bioorganic & medicinal chemistry letters.

Werner transition‐metal complex (WTMC)‐mediated mild and efficient chemo‐selective acylation of phenols and anilines under solvent‐free condition

S. Haque, M. Arifuddin, Abdulla Sarief, 2018 .

Discovery of 4-sulfamoyl-phenyl-β-lactams as a new class of potent carbonic anhydrase isoforms I, II, IV and VII inhibitors: The first example of subnanomolar CA IV inhibitors.

S. M. Monti, A. Angeli, Mallika Alvala, 2017, Bioorganic & medicinal chemistry.

An efficient reduction of azides to amines: synthesis of DNA interactive pyrrolo[2,1-c][1,4]benzodiazepines

A. Kamal, M. Arifuddin, E. Laxman, 2000 .

TRANSITION METAL COMPLEXES MEDIATED EFFICIENT AND FACILE CLEAVAGE OF OXIMES AND PHENYLHYDRAZONE TO CARBONYL COMPOUNDS

S. Wajid, Tasneem Mohammed, M. Arifuddin, 2015 .

Enantioselective ring opening of epoxides with trimethylsilyl azide (TMSN3) in the presence of β-cyclodextrin: an efficient route to 1,2-azido alcohols

A. Kamal, M. Arifuddin, M. V. Rao, 1999 .

Iodine-mediated one-pot intramolecular decarboxylation domino reaction for accessing functionalised 2-(1,3,4-oxadiazol-2-yl)anilines with carbonic anhydrase inhibitory action

C. Supuran, A. Angeli, N. Nagesh, 2018, Journal of enzyme inhibition and medicinal chemistry.

Ultrasound assisted, VOSO4 catalyzed synthesis of 4-thiazolidinones: Antimicrobial evaluation of indazole-4-thiazolidinone derivatives

C. Kumar, A. Kamal, P. Ramya, 2017 .

Design, synthesis, biological evaluation and QSAR studies of novel bisepipodophyllotoxins as cytotoxic agents.

A. Kamal, S. Dastidar, G. Khanna, 2004, Bioorganic & medicinal chemistry.

An Efficient and Rapid Regeneration of Carbonyl Compounds from Their N,N-Dimethylhydrazones in Presence of Chlorotrimethylsilane/Sodium Iodide

A. Kamal, M. Arifuddin, K. V. Ramana, 1999 .

Ultrasonic activated efficient method for the cleavage of epoxides with aromatic amines.

S. Adil, A. Kamal, M. Arifuddin, 2005, Ultrasonics sonochemistry.

Bi(OTf)(3)-catalyzed regioselective ring opening of epoxides with phenols: Facile synthesis of 1,3-diaryloxy-2-propanols

A. Kamal, Mahendra Sandbhor, M. Arifuddin, 2005 .

An Efficient Reduction of Azides to Amines: Synthesis of DNA Interactive Pyrrolo[2,1-c][1,4]benzodiazepines.

A. Kamal, M. Arifuddin, E. Laxman, 2000 .

Design, synthesis and biological evaluation of coumarin linked 1,2,4-oxadiazoles as selective carbonic anhydrase IX and XII inhibitors.

C. Supuran, A. Angeli, Pavitra S Thacker, 2020, Bioorganic chemistry.

Saccharomyces cerevisiae (Baker’s Yeast) catalyzed efficient and facile chemo-selective synthesis of aldimines

M. Arifuddin, Q. Ullah, Samreen Kauser, 2023, Results in Chemistry.

Coumarin‐Thiourea Hybrids Show Potent Carbonic Anhydrase IX and XIII Inhibitory Action

C. Supuran, A. Angeli, Priti Singh, 2020, ChemMedChem.

Synthesis and Biological Evaluation of Imidazo[2,1-b]Thiazole based Sulfonyl Piperazines as Novel Carbonic Anhydrase II Inhibitors

C. Supuran, A. Angeli, Mallika Alvala, 2020, Metabolites.

Facile and Rapid Regeneration of Carbonyl Compounds from Their N,N-Dimethylhydrazones by Employing Transition Metal Complexes.

A. Kamal, M. Arifuddin, M. V. Rao, 2001 .

New coumarin/sulfocoumarin linked phenylacrylamides as selective transmembrane carbonic anhydrase inhibitors: Synthesis and in-vitro biological evaluation.

C. Supuran, A. Angeli, Priti Singh, 2020, Bioorganic & medicinal chemistry.

Design, Synthesis, and Biological Evaluation of 1,2,3-Triazole-linked triazino[5,6-b]indole-benzene sulfonamide Conjugates as Potent Carbonic Anhydrase I, II, IX, and XIII Inhibitors

C. Supuran, A. Angeli, Pavitra S Thacker, 2020, Metabolites.

Design, synthesis and biological evaluation of coumarin-3-carboxamides as selective carbonic anhydrase IX and XII inhibitors.

C. Supuran, A. Angeli, Mallika Alvala, 2019, Bioorganic chemistry.

Synthesis of 4β-amido and 4β-sulphonamido analogues of podophyllotoxin as potential antitumour agents

A. Kamal, S. Dastidar, M. Arifuddin, 2003 .

An efficient and facile nitration of phenols with nitric acid/zinc chloride under ultrasonic conditions.

A. Kamal, M. Arifuddin, B. A. Kumar, 2004, Ultrasonics sonochemistry.

Improved Efficient Conversion of Aldehydes to Nitriles via Their N, N-Dimethyl Hydrazones

A. Kamal, M. Arifuddin, Mohammed Arifuddin, 1998 .

Facile Transformation of N,N-Dimethylhydrazones and Tosylhydrazones to Ketones with Dimethyl Sulfate and Potassium Carbonate

A. Kamal, M. Arifuddin, N. Venugopalrao, 1998 .

EFFECT OF VISIBLE LIGHT ON AMINO ACIDS—I. TRYPTOPHAN

K. T. Augusti, M. Arifuddin, S. Gurnani, 1966, Photochemistry and photobiology.

EFFECT OF VISIBLE LIGHT ON AMINO ACIDS—II. HISTIDINE

M. Arifuddin, S. Gurnani, 1966, Photochemistry and photobiology.

Indole alkaloids and anti-nociceptive mechanisms of Tabernaemontana divaricata (L.) R. Br. flower methanolic extract.

N. Ahmed, Misbah, M. Arifuddin, 2018, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Synthesis and Biological Evaluation of Coumarin-Linked 4-Anilinomethyl-1,2,3-Triazoles as Potent Inhibitors of Carbonic Anhydrases IX and XIII Involved in Tumorigenesis

C. Supuran, A. Angeli, B. Swain, 2021, Metabolites.

PET radiotracers and fluorescent probes for imaging human carbonic anhydrase IX and XII in hypoxic tumors.

C. Supuran, Pavitra S Thacker, M. Arifuddin, 2023, Bioorganic chemistry.

Synthesis and biological evaluation of new 4β-anilino- and 4β-imido-substituted podophyllotoxin congeners

A. Kamal, S. Dastidar, A. K. Kondapi, 2005 .

Anticancer carbonic anhydrase inhibitors: a patent and literature update 2018-2022

C. Supuran, M. Arifuddin, S. G. Nerella, 2022, Expert opinion on therapeutic patents.

Design, Synthesis and Biological Assessment of Rhodanine-Linked Benzenesulfonamide Derivatives as Selective and Potent Human Carbonic Anhydrase Inhibitors

S. Carradori, C. Supuran, A. Angeli, 2022, Molecules.

Synthesis and biological evaluation of novel 8-substituted quinoline-2-carboxamides as carbonic anhydrase inhibitors

C. Supuran, A. Angeli, Pavitra S Thacker, 2019, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and carbonic anhydrase inhibition studies of sulfonamide based indole-1,2,3-triazole chalcone hybrids.

C. Supuran, A. Angeli, Priti Singh, 2020, Bioorganic chemistry.

Synthesis of a new series of 3-functionalised-1-phenyl-1,2,3-triazole sulfamoylbenzamides as carbonic anhydrase I, II, IV and IX inhibitors

C. Supuran, A. Angeli, Priti Singh, 2019, Journal of enzyme inhibition and medicinal chemistry.

Development of sulfonamides incorporating phenylacrylamido functionalities as carbonic anhydrase isoforms I, II, IX and XII inhibitors.

C. Supuran, C. Capasso, A. Angeli, 2017, Bioorganic & medicinal chemistry.

Synthesis of a new series of quinoline/pyridine indole-3-sulfonamide hybrids as selective carbonic anhydrase IX inhibitors.

C. Supuran, A. Angeli, B. Swain, 2022, Bioorganic & medicinal chemistry letters.

Exploration of 2-phenylquinoline-4-carboxamide linked benzene sulfonamide derivatives as isoform selective inhibitors of transmembrane human carbonic anhydrases.

C. Supuran, A. Angeli, Priti Singh, 2022, European journal of medicinal chemistry.

Design and development of novel series of indole‐3‐sulfonamide ureido derivatives as selective carbonic anhydrase II inhibitors

C. Supuran, A. Angeli, Priti Singh, 2021, Archiv der Pharmazie.

Discovery of a novel series of indolylchalcone-benzenesulfonamide hybrids acting as selective carbonic anhydrase II inhibitors.

C. Supuran, A. Angeli, Priti Singh, 2021, Bioorganic chemistry.

Synthesis and biological evaluation of some coumarin hybrids as selective carbonic anhydrase IX and XII inhibitors.

C. Supuran, A. Angeli, Mallika Alvala, 2020, Bioorganic chemistry.

Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors

C. Supuran, A. Angeli, A. Kamal, 2017, Journal of enzyme inhibition and medicinal chemistry.

Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors

C. Supuran, A. Angeli, Priti Singh, 2021 .

Design, synthesis, SAR, and biological evaluation of saccharin‐based hybrids as carbonic anhydrase inhibitors

C. Supuran, A. Angeli, S. Nanduri, 2022, Archiv der Pharmazie.

Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors.

C. Supuran, A. Angeli, Priti Singh, 2019, Bioorganic & medicinal chemistry.

3-Functionalised Benzenesulphonamide based 1,3,4-oxadiazoles as Selective Carbonic Anhydrase XIII Inhibitors: Design, Synthesis and Biological Evaluation.

Abhay, C. Supuran, A. Angeli, 2021, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of coumarin‐thiazole hybrids as selective carbonic anhydrase IX and XII inhibitors

C. Supuran, A. Angeli, N. S. Goud, 2022, Archiv der Pharmazie.

Synthesis and characterization of quinoline-carbaldehyde derivatives as novel inhibitors for leishmanial methionine aminopeptidase 1.

I. Qureshi, P. Jagruthi, M. Arifuddin, 2019, European journal of medicinal chemistry.

Transition Metal Ions as Efficient Catalysts for Vilsmeier–Haack Formylation of Hydrocarbons with Reagents: Kinetics and Mechanism

K. Rajanna, M. Arifuddin, K. Rajendar Reddy, 2016, Journal of Solution Chemistry.

A one-pot, efficient and facile synthesis of 4β-arylaminopodophyllotoxins: Synthesis of NPF and GL-331 as DNA topoisomerase II inhibitors

A. Kamal, M. Arifuddin, B. A. Kumar, 2003 .

Novel ureidosulfocoumarin derivatives as selective and potent carbonic anhydrase IX and XII inhibitors: Design, synthesis and biological evaluation.

C. Supuran, A. Angeli, Priti Singh, 2021, ChemMedChem.

Exploration of seryl tRNA synthetase to identify potent inhibitors against leishmanial parasites.

I. Qureshi, Rahila Qureshi, M. Arifuddin, 2023, International journal of biological macromolecules.

Development of 2-chloroquinoline based heterocyclic frameworks as dual inhibitors of SARS-CoV-2 MPro and PLPro

A. Addlagatta, S. S. Jadav, S. Are, 2023, International Journal of Biological Macromolecules.