Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Vinod K. Sanna"'
Autor:
Vinod K. Sanna, Alka Madaan, Anand C. Burman, Vivek Kumar, Anu T. Singh, Raghuveer Irchhaiya, Pankaj Sharma, Pratibha Singh, Manu Jaggi
Publikováno v:
European Journal of Medicinal Chemistry. 44:3356-3362
A number of 1-propargyl-1,8-naphthyridine-3-carboxamide derivatives (15-35) have been synthesized and screened for their in vitro cytotoxicity and anti-inflammatory activity. Compounds 22, 31 and 34 have shown high cytotoxicity against a number of ca
Autor:
Manu Jaggi, Vinod K. Sanna, Pratibha Singh, Anand C. Burman, Nidhi Rani, Mukesh M. Mudgal, Anu T. Singh, Vivek Kumar, Raghuveer Irchhaiya, Pankaj Sharma, Amrita Jha
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 24:763-770
A new series of functionalized amino acid derivatives N-substituted 1-N-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-5-oxazolidine carboxamide (1-17) and 1-N-substituted-3-amino-2-hydroxy-3-phenylpropane-1-carboxamide (18-34) were synthesized and eval
Autor:
Raghuveer Irchhaiya, Nidhi Rani, Narendra Shriram Joshi, Pankaj Sharma, Pawan Aggarwal, Vivek Kumar, Anand C. Burman, Anu T. Singh, Vinod K. Sanna, Manu Jaggi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:5058-5062
A new series of betulinic acid derivatives have been synthesized by introducing heterocyclic ring between C-2 and C-3 positions of betulinic acid. Further modifications were also carried out by reduction of C-20(29) unsaturated bond and substitution
Autor:
Anu T. Singh, Anand C. Burman, Sarjana Dutt, Rama Mukherjee, Gurvinder Singh, Praveen Rajendran, Kakali Datta, Vinod K. Sanna, Manu Jaggi, Sudhanand Prasad
Publikováno v:
Investigational New Drugs. 26:505-516
We have reported earlier a novel combination of four structurally designed synthetic neuropeptide analogs of vasoactive intestinal peptide (VIP), bombesin, substance P and somatostatin, code-named DRF 7295 which have anti-tumor efficacy for adenocarc
Autor:
Anand C. Burman, Anu T. Singh, Manu Jaggi, Alka Madaan, Raghuveer Irchhaiya, Manupriya Vishnoi, Vinod K. Sanna, Pankaj Sharma, Vivek Kumar, Narendra Shriram Joshi
Publikováno v:
Journal of enzyme inhibition and medicinal chemistry. 24(5)
A number of 1,8-naphthyridine derivatives (22-62) have been synthesized and screened for their in vitro cytotoxicity against eight tumors and two non-tumor cell lines. Halogen substituted 1,8-naphthyridine-3-caboxamide derivatives showed potent activ
Autor:
Rama Mukherjee, Vinod K. Sanna, Anu T. Singh, Aji Abraham, Gurvinder Singh, Anand C. Burman, Sanjay K. Srivastava, Manu Jaggi, Beena Bhat, Shiv K. Agarwal
Publikováno v:
ChemInform. 37
A number of costunolide derivatives (4a-p) have been synthesized and evaluated for their in vitro cytotoxicity against eight tumor and a non-tumor cell lines. Compound 4d showed around 2-fold better cytotoxicity against SW-620 (colon) cell line with
Autor:
Vinod K. Sanna, Neena Gupta, Anu T. Singh, Archna Mathur, Manu Jaggi, Rama Mukherjee, Sudhanand Prasad, Kakali Datta, Praveen Rajendran
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 13(1)
Six octapeptide bombesin (BN) analogs were synthesized by substituting alpha-aminoisobutyric acid (Aib), in place of Ala9 or Gly11, or both, in the [D-Phe6, desMet14]-BN (6-14) sequence: D-Phe6-Gln7-Trp8-Ala9-Val10-Gly11-His12-Leu13-NH2 (P0). Additio
Autor:
Mukund K. Gurjar, Radhika D. Wakharkar, Anu T. Singh, Manu Jaggi, Hanumant B. Borate, Popat D. Shinde, Ritu Verma, Praveen Rajendran, Sarjana Dutt, Gurvinder Singh, Vinod K. Sanna, Manoj K. Singh, Sanjay K. Srivastava, Vishal A. Mahajan, Vinod H. Jadhav, Kakali Dutta, Karthik Krishnan, Anika Chaudhary, Shiv K. Agarwal, Rama Mukherjee
Publikováno v:
Journal of Medicinal Chemistry; Apr2007, Vol. 50 Issue 8, p1744-1753, 10p