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erythromycin oxime
Known as:
Erythromycin, 9-oxime
, Erythromycin-9-oxime
, Erythromycin A Oxime
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Erythromycin
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
The Oxime Portmanteau Motif: Released Heteroradicals Undergo Incisive EPR Interrogation and Deliver Diverse Heterocycles
J. Walton
Accounts of Chemical Research
2014
Corpus ID: 15835194
Conspectus Selective syntheses are now available for compounds of many classes, based on C-centered radicals, exploiting a…
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Highly Cited
2012
Highly Cited
2012
Nonquaternary reactivators for organophosphate-inhibited cholinesterases.
J. Kalisiak
,
E. C. Ralph
,
J. Cashman
Journal of Medicinal Chemistry
2012
Corpus ID: 207228299
A new class of amidine-oxime reactivators of organophosphate (OP)-inhibited cholinesterases (ChE) was synthesized and tested in…
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Highly Cited
2009
Highly Cited
2009
Cutting Edge: Necrosis Activates the NLRP3 Inflammasome1
Hanfen Li
,
Aditya Ambade
,
F. Re
Journal of Immunology
2009
Corpus ID: 5125197
Cells undergoing necrosis release endogenous danger signals that possess proinflammatory potential. In this study we show that…
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Highly Cited
2006
Highly Cited
2006
The identification of potent and selective imidazole-based inhibitors of B-Raf kinase.
A. Takle
,
Murray J. B. Brown
,
+10 authors
David M. Wilson
Bioorganic & Medicinal Chemistry Letters
2006
Corpus ID: 42775589
Review
2003
Review
2003
Development of radicicol analogues.
S. Soga
,
Y. Shiotsu
,
S. Akinaga
,
Sreenath V. Sharma
Current Cancer Drug Targets
2003
Corpus ID: 22735368
Radicicol, a macrocyclic antibiotic produced by fungi, was originally isolated many years ago, and was described as tyrosine…
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Highly Cited
2003
Highly Cited
2003
A Comparison of the Ability of a New Bispyridinium Oxime—1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium)butane Dibromide and Currently used Oximes to Reactivate Nerve Agent-inhibited Rat…
Kamil Kuca
,
Jiří Kassa
Journal of Enzyme Inhibition and Medicinal…
2003
Corpus ID: 10854766
The efficacy of a new bispyridinium oxime 1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium)butane dibromide, called…
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Review
2002
Review
2002
Review of Oximes in the Antidotal Treatment of Poisoning by Organophosphorus Nerve Agents
Jiří Kassa
Journal of Toxicology Clinical Toxicology
2002
Corpus ID: 20536869
The cholinesterase-inhibiting organophosphorus compounds referred to as nerve agents (soman, sarin, tabun, GF agent, and VX) are…
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Highly Cited
2001
Highly Cited
2001
SCH-C (SCH 351125), an orally bioavailable, small molecule antagonist of the chemokine receptor CCR5, is a potent inhibitor of HIV-1 infection in vitro and in vivo
J. Strizki
,
Serena Xu
,
+22 authors
B. Baroudy
Proceedings of the National Academy of Sciences…
2001
Corpus ID: 256474
We describe here the identification and properties of SCH-C (SCH 351125), a small molecule inhibitor of HIV-1 entry via the CCR5…
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Highly Cited
1993
Highly Cited
1993
Pharmacological modulation of soman-induced seizures
J. McDonough
,
T. Shih
Neuroscience and Biobehavioral Reviews
1993
Corpus ID: 24521785
Highly Cited
1974
Highly Cited
1974
The reactivatibility of cholinesterase inhibited by VX and sarin in man.
F. Sidell
,
W. Groff
Toxicology and Applied Pharmacology
1974
Corpus ID: 45065701
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