TY - JOUR
T1 - Synthesis and evaluation of novel benzothiazole derivatives against human cervical cancer cell lines
AU - Kini, S.
AU - Swain, S.P.
AU - Gandhi, A.M.
N1 - Cited By :46
Export Date: 10 November 2017
CODEN: IJSID
Correspondence Address: Kini, S.; Dept. of Pharmaceutical Chemistry, Manipal College of Pharmaceutical Sciences, MAHE, Manipal-576 104, India; email: [email protected]
Chemicals/CAS: cisplatin, 15663-27-1, 26035-31-4, 96081-74-2
References: Dong- Fang, S., Bradshaw, T.D., Wrigley, S., McCall, C.J., Lelieveld, P., Fitchner, I., Stevens, M.F.G., (1996) J. Med. Chem, 39, p. 3375; Kochichiro, Y., Katsumi, G., Kazuya, Y., Tominori, M., Goro, T., (1990) J. Med. Chem, 33, p. 2192; Bhusari, K.P., Khadekar, P.B., Umathe, S.N., Bahekar, R.H., Rao, A.R., (2000) Indian. J. Heterocycl. Chem, 9, p. 213; Klein, L.L., Yeuns, C.M., Weissing, D.E., Lartey, P.A., Tonaka, S.K., Plattner, J.J., Mulford, D.J., (1994) J. Med. Chem, 37, p. 572; Verma, R.S., Singh, A.P., (1998) Indian. J. Chem, 27 B, p. 438; Mei-Sze, C., Dong- Fang, S., Wrigley, S., Bradshaw, T.D., Hutchinson, I., Shaw, P.N., Barrett, D.A., Stevens, M.F.G., (1999) J. Med. Chem, 42, p. 381; Goldin, A., Schepartz, S.A., Venditti, J.M., Devita, V.T., (1979) Methods in Cancer Research, 16, p. 165. , Academic Press
PY - 2007
Y1 - 2007
N2 - The 2-arylsubstituted benzothiazole derivatives were synthesized by refluxing o-aminothiophenol with substituted benzoic acids in the presence of polyphosphoric acid at 220°. 2-Mercaptothiazole was used along with thionyl chloride to get the carbothioates. The physical and spectral data such as mp, Rf, IR, NMR was obtained for the synthesized compounds and the structures were confirmed. The screening for antitumour activity was done as per the National Cancer Institute drug screening strategy 3 compounds were found to be significantly cytotoxic as compared to [2-(3-bromo-4-aminophenyl) benzothiazole] against the human cervical cancer cell lines.
AB - The 2-arylsubstituted benzothiazole derivatives were synthesized by refluxing o-aminothiophenol with substituted benzoic acids in the presence of polyphosphoric acid at 220°. 2-Mercaptothiazole was used along with thionyl chloride to get the carbothioates. The physical and spectral data such as mp, Rf, IR, NMR was obtained for the synthesized compounds and the structures were confirmed. The screening for antitumour activity was done as per the National Cancer Institute drug screening strategy 3 compounds were found to be significantly cytotoxic as compared to [2-(3-bromo-4-aminophenyl) benzothiazole] against the human cervical cancer cell lines.
M3 - Article
SN - 0250-474X
VL - 69
SP - 46
EP - 50
JO - Indian Journal of Pharmaceutical Sciences
JF - Indian Journal of Pharmaceutical Sciences
IS - 1
ER -
