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Indian Journal of Chemistry -Section B (IJC-B) >
IJC-B Vol.44B [2005] >
IJC-B Vol.44B(02) [February 2005] >
| Title: | Synthesis, hydrolysis over silica column, anticancer, anti-inflammatory and analgesic activity evaluation of some pyridine and pyrazine derivatives |
| Authors: | Sondhi, Sham M
Singh, Nirupma
Rajvanshi, Shefali
Johar, Monika
Shukla, Rakesh
Raghubir, Ram
Dastidar, Sunanda G |
| Issue Date: | Feb-2005 |
| Publisher: | CSIR |
| IPC Code: | Int.Cl.7 C 07 D 211/00, 231/00 // A 61 P 35/02, 29/00, 25/04 |
| Abstract: | Various 3,4-diaryl-2-iminothiazolines 1a-s
have been condensed with 4-cyanopyridine and 2-cyanopyrazine by refluxing in
methanol for about 16 hr to give corresponding 3,4-diaryl-2-imino-N-(4'-pyridyliminomethyl)-4-thiazoline (2a-k, n-p) and 3,
4-diaryl-2-imino-N-(2'-pyrazinyliminomethyl)-4-thiazoline
(3a-m, q-s) derivatives. In some cases when these pyridyl and pyrazinyl
derivatives are purified by column chromatography over silica gel these compounds
get hydrolysed to give corresponding 3,4-diaryl-2-imino-N-(4'-carbonylpyridyl)-4-thiazoline (2o,p) and
3,4-diaryl-2-imino-N-(2'-carbonylpyrazinyl)-4-thiazoline
(3q-s) derivatives. The structures of all synthesized compounds have
been confirmed by spectroscopic methods. Compounds 2a-c,e-h,k,n,p, 3a-i
and 3l,m,q are screened for anticancer activity against a small panel of
six human cancer cell lines consisting of prostate (DU 145) colon (HT 29)
breast (MCF 7) breast (MCF 7/ADR), CNS (U 251) and lung large (NCIH 460)
tumors. Best GI50 values are shown by 3f, 11.5  M (prostate tumor, cell line DU 145), 3f, 1.0 M (colon tumor, cell line HT 29), 2n, 6.2M (breast tumor, cell line MCF 7), 2p, 4.8M (breast tumor, cell line MCF 7/ADR), 2p, 6.3M (CNS tumor, cell line U 251) and 3f, 0.9 M (lung large carcinoma, cell line NCIH 460) respectively. Compound 3f
has shown good anticancer activity against three cancer cell lines, whereas
compounds 2n and 2p against one and two cancer cell lines
respectively. Antiinflammatory
activity evaluation of 2a-k,n,o,p, 3a-m and 3q,r,s has
been carried out and compounds 2a-h, 2j, 2o,p, 3a,b,c,g,m and 3r showed
13, 32.5, 48.8, 6.5, 13.9, 7.0, 4.3, 16.6, 20.0, 17.3, 27.7, 16.2, 18.4, 34.7,
15.6, 24.0 and 4.7% activity, respectively, at 100mg/kg p.o. Analgesic
activity, evaluation of
2a-k,n,o,p, 3a-m and 3q,r,s indicates that these compounds
possess 50, 25,75, 25, 50, 75, 50, 50, 25, 0.0, 50, 50, 0.0, 75, 50, 25, 25,
25, 75, 0.0, 25, 25, 25, 50, 50, 75, 25, 50, 75 and 50% analgesic activity at
100mg/kg p.o. |
| Page(s): | 387-399 |
| ISSN: | 0975-0983(Online); 0376-4699(Print) |
| Source: | IJC-B Vol.44B(02) [February 2005]
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