"Azides" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Organic or inorganic compounds that contain the -N3 group.
| Descriptor ID |
D001386
|
| MeSH Number(s) |
D01.625.100 D02.159
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Azides".
Below are MeSH descriptors whose meaning is more specific than "Azides".
This graph shows the total number of publications written about "Azides" by people in this website by year, and whether "Azides" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 0 | 1 | 1 |
| 2002 | 1 | 0 | 1 |
| 2005 | 0 | 2 | 2 |
| 2009 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Azides" by people in Profiles.
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Abebe F, Sutton T, Perkins P, Shaw R. Two colorimetric fluorescent turn-on chemosensors for detection of Al3+ and N3- : Synthesis, photophysical and computational studies. Luminescence. 2018 Nov; 33(7):1194-1201.
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Singh G, Kumar R, Swett J, Zajc B. Modular synthesis of N-vinyl benzotriazoles. Org Lett. 2013 Aug 16; 15(16):4086-9.
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Akula HK, Lakshman MK. Synthesis of deuterated 1,2,3-triazoles. J Org Chem. 2012 Oct 19; 77(20):8896-904.
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Kuang YH, Patel JP, Sodani K, Wu CP, Liao LQ, Patel A, Tiwari AK, Dai CL, Chen X, Fu LW, Ambudkar SV, Korlipara VL, Chen ZS. OSI-930 analogues as novel reversal agents for ABCG2-mediated multidrug resistance. Biochem Pharmacol. 2012 Sep 15; 84(6):766-74.
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Kumar R, Pradhan P, Zajc B. Facile synthesis of 4-vinyl- and 4-fluorovinyl-1,2,3-triazoles via bifunctional "click-olefination" reagents. Chem Commun (Camb). 2011 Apr 07; 47(13):3891-3.
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Lakshman MK, Singh MK, Parrish D, Balachandran R, Day BW. Azide-tetrazole equilibrium of C-6 azidopurine nucleosides and their ligation reactions with alkynes. J Org Chem. 2010 Apr 16; 75(8):2461-73.
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Balas L, Durand T, Saha S, Johnson I, Mukhopadhyay S. Total synthesis of photoactivatable or fluorescent anandamide probes: novel bioactive compounds with angiogenic activity. J Med Chem. 2009 Feb 26; 52(4):1005-17.
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Wu P, Ma D, Pierzchala M, Wu J, Yang LC, Mai X, Chang X, Schmidt-Glenewinkel T. The Drosophila acetylcholine receptor subunit D alpha5 is part of an alpha-bungarotoxin binding acetylcholine receptor. J Biol Chem. 2005 Jun 03; 280(22):20987-94.
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Jiang Y, Bhattacharjee H, Zhou T, Rosen BP, Ambudkar SV, Sauna ZE. Nonequivalence of the nucleotide binding domains of the ArsA ATPase. J Biol Chem. 2005 Mar 18; 280(11):9921-6.
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Jin S, Kurtz DM, Liu ZJ, Rose J, Wang BC. X-ray crystal structures of reduced rubrerythrin and its azide adduct: a structure-based mechanism for a non-heme diiron peroxidase. J Am Chem Soc. 2002 Aug 21; 124(33):9845-55.