mesylate
Sign in to saveAlso known as methanesulfonate
thumb|230px|Mesylate anion ([[structural formula)]] thumb|230px|Mesylate anion (ball-and-stick model)
Research
38,245 papers- Synthesis and evaluation of bisulfate/mesylate-conjugated chlortetracycline with high solubility and bioavailability.Acta pharmaceutica (Zagreb, Croatia) · 2020
- Charge-assisted bond and molecular self-assembly drive the gelation of lenvatinib mesylate.International journal of pharmaceutics · 2021
- Amino acid analysis.Current protocols in protein science · 2001
- Camostat mesilate therapy for COVID-19.Internal and emergency medicine · 2020
- Validated GC-MS and LC-MS/MS Methods for ICH M7-Based Quantification of Alkyl Mesylate and Azido Genotoxic Impurities in Pharmaceutical Products.Biomedical chromatography : BMC · 2026
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Wikidata facts
- Subclass of
- chemical compound
Show 1 more fact
- Commons category
- Mesylates
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
6 sectionsContents
- Preparation
- Mesyl
- Pharmaceutical preparations
- Natural occurrence
- See also
- References
thumb|230px|Mesylate anion ([[structural formula)]] thumb|230px|Mesylate anion (ball-and-stick model)
In organosulfur chemistry, a mesylate is any salt or ester of methanesulfonic acid (). In salts, the mesylate is present as the anion. When modifying the international nonproprietary name of a pharmaceutical substance containing the group or anion, the spelling used is sometimes mesilate (as in imatinib mesilate, the mesylate salt of imatinib).
Excerpted from Wikipedia’s “mesylate” article, available under the CC BY-SA 4.0 licence.