Your browser doesn't support javascript.
loading
Synthesis, anti-proliferative and genotoxicity studies of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones and 6-chloro-5-(2-chloroethyl)-3-(alkyl/ary-2-ylidene)indolin-2-ones.
Meti, Gangadhar Y; Kamble, Atulkumar A; Kamble, Ravindra R; Somagond, Shilpa M; Devarajegowda, H C; Kumari, Sandhya; Kalthur, Guruprasad; Adiga, Satish K.
Afiliación
  • Meti GY; R. L. Fine Chemicals Ltd. Yelahanka, Bangalore 560064, India.
  • Kamble AA; Department of Studies in Chemistry, Karnatak University, Pavate Nagar, Dharwad 580003, India.
  • Kamble RR; Department of Studies in Chemistry, Karnatak University, Pavate Nagar, Dharwad 580003, India. Electronic address: kamchem9@gmail.com.
  • Somagond SM; Department of Studies in Chemistry, Karnatak University, Pavate Nagar, Dharwad 580003, India.
  • Devarajegowda HC; Department of Physics, Yuvaraja's College, Mysore 570005, India.
  • Kumari S; Division of Clinical Embryology, Kasturba Medical College, Manipal University, Manipal 576104, Karnataka, India.
  • Kalthur G; Division of Clinical Embryology, Kasturba Medical College, Manipal University, Manipal 576104, Karnataka, India.
  • Adiga SK; Division of Clinical Embryology, Kasturba Medical College, Manipal University, Manipal 576104, Karnataka, India.
Eur J Med Chem ; 121: 221-231, 2016 Oct 04.
Article en En | MEDLINE | ID: mdl-27240276
ABSTRACT
A series of 6-chloro-5-(2-substituted-ethyl)-1,3-dihydro-2H-indol-2-ones (3a-h) and 6-chloro-5-(2-chloroethyl)-3-(alkyl/aryl-2-ylidene)indolin-2-ones (5i-x) were synthesized. Compounds 3a-e, 5i-l and 5q-r were selected by NIH, USA for in vitro anti-proliferative screening. Based on the impressive growth inhibitory (GI %) effect by the compounds 3a-b and 3e which showed growth inhibition in the range 1.22-76.30%, 2.85-76.03% and 10.98-82.05% respectively at 10(-5) concentration, these compounds were further analyzed for anti-proliferative activity at 5 dose concentration and genotoxicity.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Indoles / Antineoplásicos Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2016 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Indoles / Antineoplásicos Límite: Humans Idioma: En Revista: Eur J Med Chem Año: 2016 Tipo del documento: Article País de afiliación: India