Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Annadka Shrinidhi"'
Autor:
Kyung Lock Kim, Gihyun Sung, Jaehwan Sim, James Murray, Meng Li, Ara Lee, Annadka Shrinidhi, Kyeng Min Park, Kimoon Kim
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Although protein-ligand pairs are useful tools for bioimaging, they are susceptible to enzymatic degradation and interference from endogenous species. Here, the authors show that a synthetic and bioorthogonal cucurbit[7]uril-guest binding pair can be
Externí odkaz:
https://doaj.org/article/6b1df780ac2341cc9ff12fa02ca90191
Autor:
Nader S. Abutaleb, Annadka Shrinidhi, Aloka B. Bandara, Mohamed N. Seleem, Daniel P. Flaherty
Publikováno v:
ACS Medicinal Chemistry Letters. 14:487-492
Autor:
Annadka Shrinidhi, Charles L. Perrin
Publikováno v:
ACS omega, vol 7, iss 26
Alkylation of aromatics and formation of a new C-C bond is usually achieved by the electrophilic attack of an activated carbon species on an electron-rich aromatic ring. Herein, we report an alternative method for alkylation of aromatics via nucleoph
Autor:
Annadka Shrinidhi, Charles L. Perrin
Publikováno v:
Organic letters, vol 23, iss 17
Enediynes are widely studied to understand their cycloaromatization and the trapping of the resulting p-dehydrobenzene diradical. However, few model substrates are known, and they are hard to synthesize and difficult to handle. Herein we report cyclo
Autor:
Hasanul Banna, Gihyun Sung, Jaeyeon An, Annadka Shrinidhi, Kyeng Min Park, Junghyun Kim, Kimoon Kim, Sungwan Kim
Publikováno v:
Nature Biomedical Engineering. 4:1044-1052
Efficient purification is crucial to providing large quantities of recombinant therapeutic proteins, such as monoclonal antibodies and cytokines. However, affinity techniques for manufacturing protein therapeutics that use biomolecule-conjugated agar
Autor:
Roberto Butera, Annadka Shrinidhi, Alexander Dömling, Justyna Kalinowska-Tłuścik, Katarzyna Kurpiewska
Publikováno v:
Chemical communications (Cambridge, England), 56(73), 10662-10665. ROYAL SOC CHEMISTRY
Oligoisocyanides are attractive synthetic targets, however, only a few are known. Here, we describe the smallest stable tetraisocyanide possible, the 1,3-diisocyano-2,2-bis(isocyano-methyl)propane (1) with S4 symmetry. Its four-step synthesis, struct
Publikováno v:
Organic & Biomolecular Chemistry. 17:6215-6220
Here we report the endocytosis and excretion pathways of two different dye-conjugated cucurbit[7]urils, (cyanine 3-conjugated CB[7] and rhodamine X-conjugated CB[7]), which have great potential as molecular probes for live cell imaging. The dye-CB[7]
Autor:
Roberto, Butera, Annadka, Shrinidhi, Katarzyna, Kurpiewska, Justyna, Kalinowska-Tłuścik, Alexander, Dömling
Publikováno v:
Chemical communications (Cambridge, England). 56(73)
Oligoisocyanides are attractive synthetic targets, however, only a few are known. Here, we describe the smallest stable tetraisocyanide possible, the 1,3-diisocyano-2,2-bis(isocyano-methyl)propane (1) with S4 symmetry. Its four-step synthesis, struct
Autor:
Annadka Shrinidhi, Charles L. Perrin
Publikováno v:
Chemical science, vol 11, iss 32
Chemical Science
Chemical Science
Large-ring cycloalkylamines are slightly less basic than other cycloalkylamines such as cyclohexylamine, even though all have tetrahedral carbons and are strain-free. To understand why, enthalpy and entropy for protonation of a series of cycloalkylam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59318c31c6dbba9da31ecf07ca47dd47
https://escholarship.org/uc/item/7hb5j64t
https://escholarship.org/uc/item/7hb5j64t
Autor:
James Brooke Murray, Kimoon Kim, Kangkyun Baek, Ki Hean Kim, Won Hyuk Jang, Young Ho Ko, Sungwan Kim, Jejoong Yoo, Annadka Shrinidhi, Kyeng Min Park, Jun-Seok Lee
Publikováno v:
Angewandte Chemie. 130:3186-3190
Serendipitously, mono-allyloxylated cucurbit[7]uril (AO1 CB[7]) was discovered to act as an unconventional amphiphile which self-assembles into light-responsive vesicles (AO1 CB[7]VC) in water. Although the mono-allyloxy group, directly tethered on t