In silco studies on modified hydroxamic acid and valporic acid as potential inhibitors for HDAC2

Histone deacetylases2, Class 1 HDAC family are emerged as an important therapeutic target for the treatment of various cancers. HDAC2 inhibitors are potent anti-cancer agents. Two inhibitors of HDAC2 are Hydroxamic acid and Valporic acid which are potent inducers of growth arrest, differentiation, a...

Cur síos iomlán

Sábháilte in:
Sonraí bibleagrafaíochta
Príomhchruthaitheoirí: Naresh Kandakatla (Údar), Shikha Rathaur (Údar), Smruti Sandhya Sahoo (Údar), Geetha Ramakrishnan (Údar)
Formáid: LEABHAR
Foilsithe / Cruthaithe: Bangladesh Pharmacological Society, 2013-08-01T00:00:00Z.
Ábhair:
Rochtain ar líne:Connect to this object online.
Clibeanna: Cuir clib leis
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!

Ar líne

Connect to this object online.

3rd Floor Main Library

Sonraí sealbhúcháin ó 3rd Floor Main Library
Gairmuimhir: A1234.567
Cóip 1 Ar fáil