Rujukan S-Nitrosotiol

  1. ↑ "Nitroso" IUPAC nomenclature
  2. ↑ Zhang Y.; Hogg, N. (2005). "S-Nitrosothiols: cellular formation and transport". Free Radical Biology and Medicine. 38 (7): 831–838. doi:10.1016/j.freeradbiomed.2004.12.016. PMID 15749378.
  3. ↑ Diesen, Diana L.; Douglas T. Hess; Jonathan S. Stamler (2008). "Hypoxic vasodilation by red blood cells: evidence for an s-nitrosothiol-based signal". Circulation Research. 103 (5): 545–53. doi:10.1161/CIRCRESAHA.108.176867. PMC 2763414. PMID 18658051.
  4. ↑ Ernst van Faassen; Anatoly Fyodorovich Vanin (7 May 2007). Radicals for life: the various forms of nitric oxide. Elsevier. m/s. 204–. ISBN 978-0-444-52236-8. Dicapai pada 5 September 2011.
  5. ↑ Gaston, B.; Carver, J; Doctor, A; Palmer, LA (2003). "S-Nitrosylation Signaling in Cell Biology". Molecular Interventions. 3 (5): 253–63. doi:10.1124/mi.3.5.253. PMID 14993439. Unknown parameter |displayauthors= ignored (bantuan)
  6. ↑ Gaston, B.; Singel, D; Doctor, A; Stamler, JS (2006). "S-Nitrosothiol Signaling in Respiratory Biology". American Journal of Respiratory and Critical Care Medicine. 173 (11): 1186–1193. doi:10.1164/rccm.200510-1584PP. PMC 2662966. PMID 16528016. Unknown parameter |displayauthors= ignored (bantuan)
  7. ↑ Arulsamy, N.; Bohle, D. S.; Butt, J. A.; Irvine, G. J.; Jordan, P. A.; Sagan, E. (1999). "Interrelationships between Conformational Dynamics and the Redox Chemistry of S-Nitrosothiols". Journal of the American Chemical Society. 121 (30): 7115–7123. doi:10.1021/ja9901314.
  8. ↑ Wang, P. G.; Xian, M.; Tang, X.; Wu, X.; Wen, Z.; Cai, T.; Janczuk, A. J. (2002). "Nitric Oxide Donors: Chemical Activities and Biological Applications". Chemical Reviews. 102 (4): 1091–1134. doi:10.1021/cr000040l. PMID 11942788.
  9. ↑ Byler, D. M.; Susi, H (1981). "Vibrational spectra and normal coordinate analysis of methyl thionitrite and isotopic analogs". J. Mol. Struct. 77 (1–2): 25–36. Bibcode:1981JMoSt..77...25B. doi:10.1016/0022-2860(81)85264-7.
  10. ↑ Goto, K.; Hino, Y.; Kawashima, T.; Kaminaga, M.; Yano, E.; Yamamoto, G.; Takagi, N.; Nagase, S. (2000). "Synthesis and crystal structure of a stable S-nitrosothiol bearing a novel steric protection group and of the corresponding S-nitrothiol". Tetrahedron Letters. 41 (44): 8479–8483. doi:10.1016/S0040-4039(00)01487-8.
  11. ↑ Bartberger, M.D.; Houk, K.N.; Powell, S.C.; Mannion, J.D.; Lo, K.Y.; Stamler, J.S.; Toone, E.J. (2000). "Theory, Spectroscopy, and Crystallographic Analysis ofS-Nitrosothiols: Conformational Distribution Dictates Spectroscopic Behavior". J. Am. Chem. Soc. 122 (24): 5889–5890. doi:10.1021/ja994476y.
  12. ↑ Field, L.; Dilts, R.V.; Ravichandran, R.; Lenhert, P.G.; Carnahan, G.E. (1978). "An unusually stable thionitrite from N-acetyl-D,L-penicillamine; X-ray crystal and molecular structure of 2-(acetylamino)-2-carboxy-1,1-dimethylethyl thionitrite". J. Chem. Soc. Chem. Commun. (6): 249–250. doi:10.1039/c39780000249.

Templat:Nitric oxide signaling

Rujukan

WikiPedia: S-Nitrosotiol http://www.acdlabs.com/iupac/nomenclature/79/r79_5... https://doi.org/10.1016%2Fj.freeradbiomed.2004.12.... https://pubmed.ncbi.nlm.nih.gov/15749378 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC27634... https://doi.org/10.1161%2FCIRCRESAHA.108.176867 https://pubmed.ncbi.nlm.nih.gov/18658051 https://books.google.com/books?id=UJ4glFNEcn0C&pg=... https://doi.org/10.1124%2Fmi.3.5.253 https://pubmed.ncbi.nlm.nih.gov/14993439 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC26629...