5-Tosyl-1-oxa-5-aza-7-cyclononyne | Chemical Substance Information | J-GLOBAL
N-[(2R,5R)-2α,4β-Diphenyl-6-oxo-7-oxa-1-azaspiro[4.4]nonane-3α-yl]-p-toluenesulfonamide | Chemical Substance Information | J-GLOBAL
Oxa-376 and Oxa-530 variants of β-lactamase: computational study uncovers potential therapeutic targets of Acinetobacter baumannii - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02939A
3-Benzyl-2-oxa-3,4-diaza-2H-benzo[f]indene-1(3H)-one | Chemical Substance Information | J-GLOBAL
3aS,7aα)-8,8-Dimethyl-3aβ,6β-methanospiro[1-oxa -2-thia(IV)-hydrindane-2,2′-[1-oxa-2-thia(IV)-3]cyclopentene]-5′-one | Chemical Substance Information | J-GLOBAL
Oxa-376 and Oxa-530 variants of β-lactamase: computational study uncovers potential therapeutic targets of Acinetobacter baumannii - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02939A
File:Oxaloacetate and pyruvate aminoacid synthesis.png - Wikipedia
1S,4S,5S,6S)-N,3-Diphenyl-8-methyl-2-oxa-3-phospha(V)-bicyclo[2.2.2]octa-7-ene-5,6-dicarbimide 3-oxide | Chemical Substance Information | J-GLOBAL
Multiscale Simulations Identify Origins of Differential Carbapenem Hydrolysis by the OXA-48 β-Lactamase | ACS Catalysis
Datasheet 212 Addressable Relay Module
Mechanistic Basis of OXA-48-like β-Lactamases' Hydrolysis of Carbapenems | ACS Infectious Diseases
1S,2R,7S)-8,9-(Methyliminobiscarbonyl)-12-oxa-3,4,8,9-tetraazapentacyclo[4.4.3.2<sup>2,5</sup>.2<sup>7,10</sup>.0<sup>1,6</sup>]heptadecane-3,14-diene 3,4-dioxide | Chemical Substance Information | J-GLOBAL
Programmable Ether Synthesis Enabled by Oxa-Matteson Reaction | Journal of the American Chemical Society
OXA APK for Android Download
Incomplete course import in Edx Studio · Issue #376 · microsoft/oxa-tools · GitHub
Recombinant Acinetobacter Beta-lactamase OXA-23 Protein [230-00712]
Oxa[7]helicenen | Chemical Substance Information | J-GLOBAL
Oxa-376 and Oxa-530 variants of β-lactamase: computational study uncovers potential therapeutic targets of Acinetobacter baumannii - RSC Advances (RSC Publishing) DOI:10.1039/D2RA02939A
1,3-Dihydroxy-2-[(1-oxa-4-azoniacyclohexane-4-yl)methyl]-4-oxo-1,2,3,4-tetrahydronaphthalene-2-ide | Chemical Substance Information | J-GLOBAL
OXA Blox by Functional Genomic Nutrition - Charny Healing
IJMS | Free Full-Text | Specific Amino Acid Substitutions in OXA-51-Type β-Lactamase Enhance Catalytic Activity to a Level Comparable to Carbapenemase OXA-23 and OXA-24/40
2-Phenyl-1-oxa-2-bora-2a-azoniaacenaphthylene | Chemical Substance Information | J-GLOBAL
2-(2-Methyl-1-oxa-2-azonia-2-cyclopentene-3-ylacetyl)naphthalene | Chemical Substance Information | J-GLOBAL