Carboxylic acid salts
TARGETMOL CHEMICALS INC TILUDRONATE DISODIUM 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Tiludronate disodium (Tiludronic acid disodium) is an osteoclast vacuolar H(+)-ATPase inhibitor with antiresorptive and anti-inflammatory properties. Tiludronate disodium can be used in studies about metabolic bone disorders. purity: 100%
eMolecules 3-N-DI-BOC-2-METHYL-PROPIONIC ACID | 357610-29-8 | MFCD24475052 | 5g
AstaTech | 3-N-DI-BOC-2-METHYL-PROPIONIC ACID | 5g | 338839279 | 70023 | 95.000 | 357610-29-8 | MFCD24475052 | 303.355 | C14H25NO6
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Chem-Impex International, Inc. a-Ketoglutaric acid disodium salt dihydrate | 305-72-6 | MFCD00150702 | 25G
a-Ketoglutaric acid disodium salt dihydrate, 305-72-6, MFCD00150702, 25G
eMolecules Ambeed / Copper(II) 2-ethylhexanoate / 1g / 588343068 / A652646 / / 149-11-1 / MFCD00015695 / 349.958 / C16H30CuO4
Ambeed / Copper(II) 2-ethylhexanoate / 1g / 588343068 / A652646 / / 149-11-1 / MFCD00015695 / 349.958 / C16H30CuO4
AdipoGen R-3-Hydroxyisobutyric acid Na
Chemical. CAS 1228078-57-6. Formula C4H7O3 . Na. MW 103.1 . 23.0. Synthetic. Intermediate formed in the valine catabolism. It is a reactant of the enzymes involved in branched chain amino acid metabolism 3-hydroxyisobutyrate dehydrogenase and 3-hydroxyisobutyryl-CoA hydrolase and it was found to have increased concentrations in MS patient metabolic profiles. This compound may be used to study the distribution, characterization and kinetics of these enzymes. Shown to inhibit key enzymes of the energy metabolism.
TARGETMOL CHEMICALS INC BUCINDOLOL FORMATE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Bucindolol Formatel is a blocker of (beta)1-adrenergic receptor. Bucindolol exhibits intrinsic sympathomimetic activity. Bucindolol can be used in the research of heart failure.
Apexbio Technology LLC AVE 0991 sodium salt 306288-04-0 5mg
AVE 0991 sodium salt (CAS 306288-04-0) is a synthetic non-peptide agonist of the angiotensin-(1-7) receptor Mas Acting as a functional mimic of angiotensin-(1-7) AVE 0991 competitively binds to endothelial cell membranes with an IC50 of 21 35 nM in bovine aortic endothelial cells In vitro treatment with AVE 0991 promotes nitric oxide release to levels significantly greater than angiotensin-(1-7) In vivo AVE 0991 reduces urine volume and increases urine osmolality in mice effects reversed by angiotensin II antagonists indicating receptor specificity It also inhibits atherogenesis in ApoE knockout mice supporting its application in cardiovascular and renal research