Weight | 95.099 g/mol |
---|---|
Formula | CH3O3S- |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Methanesulfonate (16053-58-0)
Score:
#1976 in Biology
,
#2404 in Chemistry
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- Sigma-Aldrich - Search for Methanesulfonate
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- Population Pharmacokinetics of Colistin Methanesulfonate and Formed Colistin in Critically Ill Patients from a Multicenter Study Provide Dosing Suggestions for Various Categories of Patients (Antimicrobial Agents and Chemotherapy, 2011)
- Facile synthesis of methanesulfonate esters (Journal of Organic Chemistry, 1970)
- The BRC repeats in BRCA2 are critical for RAD51 binding and resistance to methyl methanesulfonate treatment (Proceedings of the National Academy of Sciences of the United States of America, 1998)
- Population pharmacokinetic analysis of colistin methanesulfonate and colistin after intravenous administration in critically ill patients with infections caused by gram-negative bacteria. (Antimicrobial Agents and Chemotherapy, 2009)
- A genome-wide screen for methyl methanesulfonate-sensitive mutants reveals genes required for S phase progression in the presence of DNA damage (Proceedings of the National Academy of Sciences of the United States of America, 2002)
- Alteration of Seed Fatty Acid Composition by an Ethyl Methanesulfonate-Induced Mutation in Arabidopsis thaliana Affecting Diacylglycerol Acyltransferase Activity (Plant Physiology, 1995)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCS(=O)(=O)[O-]
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InChIKeyAFVFQIVMOAPDHO-UHFFFAOYSA-M
- Pubchem - Methanesulfonate
- Wikipedia - methanesulfonate
In chemistry, a mesylate is any salt or ester of methanesulfonic acid (CH3SO3H). In salts, the mesylate is present as the CH3SO3 anion. When modifying the International Nonproprietary Name of a pharmaceutical substance containing the group or anion, the correct spelling is mesilate (as in imatinib mesilate, the mesylate salt of imatinib).
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