Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Krishnamurthi Vyas"'
Autor:
Shakil S. Sait, Krishnamurthi Vyas, A. Malleswara Reddy, S. Jayapal Reddy, Palavai Sripal Reddy
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 37:2490-2505
A novel gradient reversed-phase high-performance liquid chromatographic method has been developed for quantitative determination of Ropinirole hydrochloride and its six impurities in pharmaceutical dosage forms. Chromatographic separation has been ac
Autor:
Krishnamurthi Vyas, R. Pichai, L. Kalyanaraman, S.R. Narasimhan, R. Mohan Kumar, K. K. Sree Ganesh
Publikováno v:
Journal of Liquid Chromatography & Related Technologies. 35:1649-1661
This account details the structural modification of Calophyllolide 1, using Ritter reaction with various nitriles to study the antimicrobial properties. Ritter reaction of calophyllolide results in a 1:1 mixture of two structurally related compounds
Publikováno v:
Crystal Growth & Design. 9:4822-4829
Imiquimod free base 1, an immune response modifier, its hydrochloride salt 2, hydrochloride salt monohydrate 3, salts with maleic acid 4, fumaric acid 5, succinic acid 6, adipic acid 7, and 4-hydroxybenzoic acid 8 have been prepared and characterized
Autor:
Pooja Guleria, Krishnamurthi Vyas, B. Selva Kumar, N. M. Sekhar, Palle V. R. Acharyulu, J. Moses Babu, T. Lakshmi Kumar, Peddy Vishweshwar, A. Sivalakshmidevi
Publikováno v:
Journal of Inclusion Phenomena and Macrocyclic Chemistry. 66:261-269
Host–guest complexes of Docetaxel 1, an anti-cancer drug have been isolated and crystal structures are described. Docetaxel crystallized in the 1:1 molar ratio with n-butanol, dimethylformamide (DMF) and acetonitrile (ACN) during crystallization fr
Autor:
Krishnamurthi Vyas, B. Suresh Babu, B. Venkata Subbaiah, G. Sai Uday Kiran, J. Moses Babu, R. Vasu Dev, P. K. Dubey
Publikováno v:
Magnetic Resonance in Chemistry. 47:443-448
Three unknown impurities of Rabeprazole, a proton pump inhibitor, were formed in the formulated drug under the stress conditions, [40 degrees C/75% relative humidity (RH) for 6 months] with relative retention times (RRTs) 0.17, 0.22 and 0.28. The Imp
Autor:
Javed Iqbal, P. C. Sudhakar, Peddy Vishweshwar, Bukkapattanam R. Sreekanth, R. Srivijaya, Krishnamurthi Vyas, Moses Babu, P.K. Jayanthi
Publikováno v:
Journal of Molecular Structure. 885:45-49
Robustness of carboxylic acid–pyridine supramolecular heterosynthon was examined in three 1:2 binary co-crystals of 4,4′-bipyridine with monocarboxylic acids, (4,4′-bipyridine)·( dl -hydroxyphenylacetic acid)2, 1; (4,4′-bipyridine)0.5·(4-br
Publikováno v:
CrystEngComm. 10:283-287
Tegaserod is shown to exist in the tautomeric form II in the free base and also in a monohydrate. The Tegaserod nicotinate salt has a 6-fold better aqueous solubility than the marketed Tegaserod maleate (form A, Zelnorm™).
Autor:
Krishnamurthi Vyas, S. Ashok, Ganta Madhusudhan Reddy, B. Vijaya Bhaskar, K. Mukkanti, P. Pratap Reddy, J. Moses Babu, P. C. Sudhakar
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 45:201-210
Six impurities in pantoprazole sodium bulk drug substance were detected by a simple high performance liquid chromatographic method (HPLC) whose area percentage ranged from ∼0.05 to 0.34%. Liquid chromatography–mass spectrometry (LC–MS) was perf
Autor:
Krishnamurthi Vyas, Sunil Kumar Singh, K. Ravi Ganesh, R. Vasudev, Y. Koteswar Rao, K. Srinivas Rao, Javid Iqbal, J. Moses Babu, P. Praveen Kumar, V. Saibaba, S. Shivaramakrishna
Publikováno v:
European Journal of Medicinal Chemistry. 42:456-462
ortho-Acylation attempt of benzenesulfonamide afforded the corresponding hemiaminal as major product. The in situ reduction of the reaction mixture, reported herein, directly provided 2-hydroxyalkyl benzenesulfonamide, an important pharmacophoric ele
Autor:
Manojit Pal, R. Vasu Dev, Bukkapattanam R. Sreekanth, J. Moses Babu, Pazhanimuthu Annamalai, Venkateswara Rao Batchu, Sirisilla Raju, Nalivela Kumara Swamy, Khagga Mukkanti, Krishnamurthi Vyas, P. Rajender Kumar
Publikováno v:
Tetrahedron. 62:9554-9570
We herein report a highly convenient protocol for rapid construction of α-pyrone fused with thiophene. This includes one-pot and regioselective synthesis of 4,5-disubstituted and 5-substituted thieno[2,3- c ]pyran-7-ones, 6,7-disubstituted and 6-sub