Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Young S. Rho"'
Publikováno v:
Ethnicityhealth.
Racial disparities in care and outcome have been demonstrated for several cancers, but it is not clear that a similar discrepancy exists for pancreatic cancer. Furthermore, there are limited data describing the pancreatic cancer experience of Pacific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42c086c07484eb1d6824555d8162f391
https://pubmed.ncbi.nlm.nih.gov/36036201
https://pubmed.ncbi.nlm.nih.gov/36036201
Publikováno v:
HPB : the official journal of the International Hepato Pancreato Biliary Association. 23(7)
Background Hepatocellular carcinoma (HCC) is one of the few cancers that can be diagnosed based on imaging findings alone. The factors associated with the decision to perform a biopsy and the clinical impact have not been previously studied. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1065e8b691f219e72a1dbe17220f77f7
https://pubmed.ncbi.nlm.nih.gov/33229278
https://pubmed.ncbi.nlm.nih.gov/33229278
Publikováno v:
Bulletin of the Korean Chemical Society. 32:4171-4175
Bio-functionalized gold nanoparticles (AuNPs), which bio-specifically interact with biotin-(strept)avidin, were investigated in this study. AuNPs were functionalized with a synthetically-provided biotin-linked thiol (BLT), which was synthesized by am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0869b518682775c82ad812d9222429d
https://doi.org/10.5012/bkcs.2011.32.12.4171
https://doi.org/10.5012/bkcs.2011.32.12.4171
Publikováno v:
Bulletin of the Korean Chemical Society. 31:69-74
The new idarubicin analogues (12 and 13) with a glucose or galactoseas as a glycone were synthesized from daunomycin (2). (+)-4-Demethoxydaunomycinone (6) obtained from reaction of 2 with AlCl 3 was converted to 4-trifluoromethanesulfonyl daunomycino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a13d3d00ffe22db2d56fc11e70c44752
https://doi.org/10.5012/bkcs.2010.31.01.069
https://doi.org/10.5012/bkcs.2010.31.01.069
Publikováno v:
Bulletin of the Korean Chemical Society. 27:1359-1363
Novel anthracycline analogues 2-9 as potential anticancer agents were synthesized from daunomycin (1a) and doxorubicin (1b). Compounds 2, 6, and 7 were prepared by the nucleophilic displacement type esterification of a 14-bromodaunomycin (1c) with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ea89d990dde27c7ddfee2d0831c7022
https://doi.org/10.5012/bkcs.2006.27.9.1359
https://doi.org/10.5012/bkcs.2006.27.9.1359
Autor:
Pyoung Won Suh, Hyesun Kim, Dong Jin Yoo, Young S. Rho, Jihyung Park, Hong-Sig Sin, Gyuil Kim
Publikováno v:
Synthetic Communications. 34:1703-1722
Regiospecific syntheses of idarubicinone coupled with D‐glucuronic acid are described. Cyclization of dimethoxybenzene with carboxylic acid derivatives in polyphosphoric acid (PPA) in one step afforded the naphthalenones 7, which were transformed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a066705eb5ee85c9338258da5fc72f59
https://doi.org/10.1081/scc-120030758
https://doi.org/10.1081/scc-120030758
Publikováno v:
Synthetic Communications. 34:3497-3511
The first synthesis of new doxorubicin and daunomycin analogs containing glucuronic acid moieties instead of daunosamine are described. The desired products, daunomycinone‐7‐D‐glucuronide (DM7G, 10) and doxorubicinone‐7‐D‐glucuronide (DX7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78c918ed6d9beff17371bf36fe5bbdb1
https://doi.org/10.1081/scc-200030978
https://doi.org/10.1081/scc-200030978
Publikováno v:
Bulletin of the Korean Chemical Society. 23:1315-1327
The model compounds, 8-methoxypsoralen-CH 2 O(CH 2 ) n -adenine (MOPCH 2 OCnAd, n=2, 3, 5, 6, 8, and 10) in which 5 position of 8-methoxypsoralen (8-MOP) is linked by various lengths of polymethylene bridge to N 9 of adenine.UV absorption spectra are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cb4caae31bfc2769852a141e4308947
https://doi.org/10.5012/bkcs.2002.23.9.1315
https://doi.org/10.5012/bkcs.2002.23.9.1315
Autor:
Wan-Joong Kim, Young S. Rho, Dong Jin Yoo, Soon‐Ryang Chung, Gyuil Kim, Siho Park, Heun-Soo Kang
Publikováno v:
Synthetic Communications. 32:1961-1975
The new anthracycline analogues (2–10) as potential anticancer agents were synthesized from daunomycin (1a) and doxorubicin (1b). Compounds 2, 6, and 7 were prepared by the nucleophilic displacement type esterification of a 14-bromodaunomycin (1c)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17f1b83c6c469b6ff90a46e00a6f97f0
https://doi.org/10.1081/scc-120004846
https://doi.org/10.1081/scc-120004846
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aee9259f9572b6d9a827ee4b95531fef
https://doi.org/10.1002/chin.199718131
https://doi.org/10.1002/chin.199718131