[HTML][HTML] RXDX-101 inhibitor

C Atsriku, M Hoffmann, Y Ye, G Kumar, S Surapaneni - rxdx-101inhibitor.com
The disposition of tanzisertib [(1S, 4R)-4-(9-((S) tetrahydrofuran-3-yl)-8-(2, 4, 6-
trifluorophenyla-mino)-9H-purin-2-ylamino) cyclohexanol], a potent, orally active c-Jun …

Metabolism and disposition of a potent and selective JNK inhibitor [14C]tanzisertib following oral administration to rats, dogs and humans

C Atsriku, M Hoffmann, Y Ye, G Kumar… - Xenobiotica, 2015 - Taylor & Francis
The disposition of tanzisertib [(1S, 4R)-4-(9-((S) tetrahydrofuran-3-yl)-8-(2, 4, 6-
trifluorophenylamino)-9H-purin-2-ylamino) cyclohexanol], a potent, orally active c-Jun amino …

[HTML][HTML] ZM-306416 is a VEGFR antagonist and a potent inhibitor of EGFR function Menu

C Atsriku, M Hoffmann, M Moghaddam, G Kumar… - zm306416inhibitor.com
In vitro metabolism of Tanzisertib [(1S, 4R)-4-(9-((S) tetrahydrofuran-3-yl)-8-(2, 4, 6-
trifluorophe-nylamino)-9H-purin-2-ylamino) cyclohexanol], a potent, selective c-Jun amino …

Discovery of the c-Jun N-terminal kinase inhibitor CC-90001

MA Nagy, R Hilgraf, DS Mortensen… - Journal of Medicinal …, 2021 - ACS Publications
As a result of emerging biological data suggesting that within the c-Jun N-terminal kinase
(JNK) family, JNK1 and not JNK2 or JNK3 may be primarily responsible for fibrosis …

Quinazoline derivatives as medicaments

S Chakravarty, S Dugar, JJ Perumattam… - US Patent …, 2001 - Google Patents
US6277989B1 - Quinazoline derivatives as medicaments - Google Patents US6277989B1 -
Quinazoline derivatives as medicaments - Google Patents Quinazoline derivatives as …

Quinazoline derivatives as medicaments

S Chakravarty, S Dugar, JJ Perumattam… - US Patent …, 2005 - Google Patents
US6903096B2 - Quinazoline derivatives as medicaments - Google Patents US6903096B2 -
Quinazoline derivatives as medicaments - Google Patents Quinazoline derivatives as …

Antiproliferative activity and mechanism of action of DZ-3358, a novel pyrimidinyl pyrazole derivative.

M Iwahana, Y Ochi, A Ejima - Anticancer research, 2000 - europepmc.org
The novel pyrimidinyl pyrazole derivative, 1-[5-methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-3-[4-(3-
chlorophenyl)-1-piperazinyl]-1-trans-propene hydrochloride (DZ-3358), was found through …

[HTML][HTML] A selective small-molecule inhibitor of c-Jun N-terminal kinase 1

K Yao, YY Cho, AM Bode, A Vummenthala, JG Park… - FEBS letters, 2009 - Elsevier
Indiscriminately suppressing total c-Jun N-terminal kinase (JNK) activity is not an
appropriate strategy because each JNK appears to have a distinct function in cancer …

Pyrrolo [1, 2-d][1, 2-4] triazine as inhibitors of c-Jun N terminal kinases (JNK) and p-38 kinases

Q Dong - US Patent 7,855,288, 2010 - Google Patents
BACKGROUND A large number of cytokines participate in the inflamma tory response,
including IL-1, IL6, IL-8 and TNF-C. Over production of cytokines such as IL-1 and TNF-C …

Tumor Selective Effect of RS-1541 (Palmitoyl-Rhizoxin) in M5076 Sarcoma and Host Tissues in Vivo

T Tokui, N Maeda, C Kuroiwa, K Sasagawa… - Pharmaceutical …, 1995 - Springer
Abstract RS-1541 is a 13-O-palmitoyl derivative of rhizoxin, an inhibitor of tubulin
polymerization. After intravenous administration of RS-1541 to mice bearing M5076 …