Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rajesh Rengasamy"'
Autor:
Jin Kyung Rho, Jae Cheol Lee, Chang-Min Choi, Wonjun Ji, Rajesh Rengasamy, Jae-Sun Kim, Hyung Chul Ryu, Yun Jeong Kong, Sunho Lee, Sung-Eun Kim, Dong-Cheol Woo, Joongkee Min, Jeongin Cho, Chae Won Lee, Hyeonjeong Lee, Kyungtaek Im, Dong Ha Kim, Young Hoon Sung, Da-Som Kim, Yun Jung Choi
Supplementary Data from The Reversible Fourth-Generation EGFR Tyrosine Kinase Inhibitor OBX02–011 Overcomes C797S-Mediated Resistance in Lung Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c72e40a980b20a6f9965cf58c368e86
https://doi.org/10.1158/0008-5472.22431839
https://doi.org/10.1158/0008-5472.22431839
Autor:
Jin Kyung Rho, Jae Cheol Lee, Chang-Min Choi, Wonjun Ji, Rajesh Rengasamy, Jae-Sun Kim, Hyung Chul Ryu, Yun Jeong Kong, Sunho Lee, Sung-Eun Kim, Dong-Cheol Woo, Joongkee Min, Jeongin Cho, Chae Won Lee, Hyeonjeong Lee, Kyungtaek Im, Dong Ha Kim, Young Hoon Sung, Da-Som Kim, Yun Jung Choi
Osimertinib is an irreversible third-generation EGFR tyrosine kinase inhibitor (TKI) that was initially developed to overcome the EGFR T790M mutation and is used as a standard therapy in patients with advanced non–small cell lung cancer (NSCLC) wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adf0914a53516f4d5a152b844ddcf7e2
https://doi.org/10.1158/0008-5472.c.6514004.v1
https://doi.org/10.1158/0008-5472.c.6514004.v1
Autor:
Jin Kyung Rho, Jae Cheol Lee, Chang-Min Choi, Wonjun Ji, Rajesh Rengasamy, Jae-Sun Kim, Hyung Chul Ryu, Yun Jeong Kong, Sunho Lee, Sung-Eun Kim, Dong-Cheol Woo, Joongkee Min, Jeongin Cho, Chae Won Lee, Hyeonjeong Lee, Kyungtaek Im, Dong Ha Kim, Young Hoon Sung, Da-Som Kim, Yun Jung Choi
Supplementary Table from The Reversible Fourth-Generation EGFR Tyrosine Kinase Inhibitor OBX02–011 Overcomes C797S-Mediated Resistance in Lung Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::440dc418e274060ef1f59258e3aa59d8
https://doi.org/10.1158/0008-5472.22431836
https://doi.org/10.1158/0008-5472.22431836
Autor:
Yun Jung Choi, Da-Som Kim, Young Hoon Sung, Dong Ha Kim, Kyungtaek Im, Hyeonjeong Lee, Chae Won Lee, Jeongin Cho, Joongkee Min, Dong-Cheol Woo, Sung-Eun Kim, Sunho Lee, Yun Jeong Kong, Hyung Chul Ryu, Jae-Sun Kim, Rajesh Rengasamy, Wonjun Ji, Chang-Min Choi, Jae Cheol Lee, Jin Kyung Rho
Publikováno v:
Cancer research.
Osimertinib is an irreversible third-generation EGFR tyrosine kinase inhibitor (TKI) that was initially developed to overcome the EGFR T790M mutation and is used as a standard therapy in patients with advanced non–small cell lung cancer (NSCLC) wit
Autor:
Yun Jung Choi, Da-Som Kim, Young Hoon Sung, Dong Ha Kim, Kyungtaek Im, Hyeonjeong Lee, Chae Won Lee, Jeongin Cho, Joongkee Min, Dong-Cheol Woo, Sung-Eun Kim, Sunho Lee, Yun Jeong Kong, Hyung Chul Ryu, Jae-Sun Kim, Rajesh Rengasamy, Wonjun Ji, Chang-Min Choi, Jae Cheol Lee, Jin Kyung Rho
Publikováno v:
Cancer Research. :OF1-OF1
Publikováno v:
Journal of the Korean Society for Applied Biological Chemistry. 54:881-888
Azasugars derived from L-alanine and L-serine were screened for inhibitory activity against α-rhamnosidase. The enantiomers of 1,6-dideoxynojirimycin (ent-1,6-dDNJ) (1) and (2S,3R)-2-(hydroxymethyl)piperidin-3-ol (5) showed highly specific and poten
Publikováno v:
Bulletin of the Korean Chemical Society. 30:1531-1534
(2S,3R)-3-Hydroxy-2-(hydroxymethyl)-3,6-dihydro-2H-pyridine 8, an important precursor for the synthesis of polyhydroxylated piperidine azasugars, has been prepared from L -serine. Highly stereoselective nucleophilic addition to amino aldehyde 5 gave
Autor:
Ill-Yun Jeong, Woo Duck Seo, Rajesh Rengasamy, Ki Hun Park, Marcus J. Curtis-Long, Seong Hun Jeong
Publikováno v:
The Journal of Organic Chemistry. 73:2898-2901
(3R,4S)-3-Hydroxy-4-N-allyl-N-Boc-amino-1-pentene 10, an important precursor for the synthesis of polyhydroxylated piperidines, has been achieved as a single diastereomer without racemization via vinyl Grignard addition to N-Boc-N-allyl aminoaldehyde
A study involving scope in the condensation reaction of phenylsulfonylacetic acid with a series of carbonyl derivatives has been conducted. Reactivity trends favor formation of the corresponding vinyl sulfones when working with aryl aldehydes. Electr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b861af03abf57633a7582b92dd1a468
Publikováno v:
ChemInform. 40