You Searched For: Thiophene-3-carboxylic+acid+amide


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Supplier: ENZO LIFE SCIENCES
Description: AACOCF3 is a trifluoromethylketone derivative of arachidonic acid. It is a selective inhibitor of human cytosolic PLA2 and Ca2+-independent PLA2 (iPLA2, IC50=15 µM). It is active in intact platelets and U937 cells (IC50=8 µM). It also inhibits fatty acid amide hydrolase (100% at 7.5 µM).

Catalog Number: (APOSOR361268-250MG)
Supplier: Apollo Scientific
Description: 2-Hydroxymethylthiophen-4-boronic acid, pinacol ester 97%
UOM: 1 * 250 mg


Catalog Number: (71478-50MG)
Supplier: Merck
Description: Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent (CDA), has high enantioselectivity but low sensitivity as compared to other CDAs. It is generally used to assign the stereochemistry of amino acids in trace amounts.
UOM: 1 * 50 mg


Supplier: MP Biomedicals
Description: p-Nitrophenol is used as an indicator in 0.1% alcohol solutions. 4-Nitrophenol is used as a precursor to prepare phenetidine, acetophenetidine and pH indicator. Its carboxylate ester derivatives are involved as an active component for the construction of amide moieties in peptide synthesis.

Catalog Number: (APOSOR12587-250MG)
Supplier: Apollo Scientific
Description: 2-Methyl-6-oxo-1,6-dihydro-3,4'-bipyridine-5-carboxamide 98+%
UOM: 1 * 250 mg


Catalog Number: (APOSOR14727-1G)
Supplier: Apollo Scientific
Description: H-β-(3-Benzothienyl)-Ala-OH 95+%
UOM: 1 * 1 g


Catalog Number: (APOSOR51014-5G)
Supplier: Apollo Scientific
Description: (3-Dibenzothiophen-4-ylphenyl)boronic acid 99%
UOM: 1 * 5 g


Supplier: Thermo Fisher Scientific
Description: Carboxyl groups, in the form of carboxy termini, aspartate residues or glutamate residues, can be targeted for biotin labeling using amine-derivatised biotin molecules. This reaction is mediated by a class of crosslinkers known as carbodiimides and results in the formation of an amide bond. The reaction with EDC, the most common carbodiimide crosslinker, is generally performed in an MES buffer at pH 4,5 to 5 and requires just minutes to complete.
Catalog Number: (ACRO445580010)
Supplier: Thermo Fisher Scientific
Description: 1-[(2-Thienyl)methyl]-1H-pyrazole-4-boronic acid pinacol ester 97%
UOM: 1 * 1 g

MSDS


Catalog Number: (APOSOR912862-1G)
Supplier: Apollo Scientific
Description: Methyl-3-oxo-3-(2-thienyl)propanoate 95%
UOM: 1 * 1 g


Supplier: Thermo Fisher Scientific
Description: 3-(2-Thienyl)-L-alanine 95%
Supplier: Apollo Scientific
Description: Derivatised D- and L- amino acids can be resolved and quantified by HPLC. For reference see:Marfey, P. (1984) Carlsberg Res. Commun. 49, 591

Catalog Number: (APOSOR14732-5G)
Supplier: Apollo Scientific
Description: 3-(2-Thienyl)-L-alanine 95%
UOM: 1 * 5 g


Supplier: Apollo Scientific
Description: 3-Amino-3-(2-thienyl)propanoic acid

Supplier: G-Biosciences
Description: HOOK™ Biotin-PEG₂-Amine, and its long chain form, HOOK™ Biotin-PEG₃-Amine, are carboxyl reactive biotinylation reagents. These agents contain terminal amines and react with carboxyl groups found at the carboxyl termini, aspartate, and glutamate side chains. The reaction is mediated by a water-soluble carbodiimide (EDC). The carbodiimide activates the carboxyl group and reacts with the amines (-NH₂) on the biotinylation agent to form an amide bond. This reaction is rapid and takes just a few minutes to complete. Under these conditions, hydrazide-derivatives of biotin reagents may also react with the carboxyls.

Catalog Number: (324715-5)
Supplier: Merck Millipore (Calbiochem‎)
Description: Native endoproteinase Lys-C from <i>Lysobacter enzymogenes</i>. Serine protease that specifically hydrolyses amide and peptide ester bonds at the carboxylic side of lysine in peptides and proteins. Designed for protein sequencing or sequence verification, analysis of protein structural domains, and cleavage of fusion proteins. Inhibited by aprotinin, DFP, leupeptin, and TLCK. Suggested working concentration: 1:20 to 1:100 (protease: protein by weight) for sequence analysis.
UOM: 1 * 5 µG


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