Eptazocine hydrobromide

BIOshell &#8482 160Ã… Peptide CN columns provide an alternative selectivity to the traditional C18 bonded phases. The introduction of the cyano group enables peptides and small proteins to be separated due to a combination of hydrophobicity and

Bis(hexamethylene)triamine (Bis-HEA, BHMT, BHMTA) is an aliphatic polyamine. It is a spermidine analog and has been reported to lack the enhancing effect on mitochondrial Ca(2+) accumulation but shows inhibitory effect on the Ca(2+) and Pi-induced

Bis(hexamethylene)triamine (Bis-HEA, BHMT, BHMTA) is an aliphatic polyamine. It is a spermidine analog and has been reported to lack the enhancing effect on mitochondrial Ca(2+) accumulation but shows inhibitory effect on the Ca(2+) and Pi-induced

Application Capsazepine has been used as a transient receptor potential vanilloid-1 (TRPV1) antagonist: to study its effect on capsaicin induced extracellular signal-regulated kinase (ERK) phosphorylation to study the role of TRPV1 in central

Application Capsazepine has been used as a transient receptor potential vanilloid-1 (TRPV1) antagonist: to study its effect on capsaicin induced extracellular signal-regulated kinase (ERK) phosphorylation to study the role of TRPV1 in central

Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide is a novel anticancer agent derived from a hydroxamic acid and has demonstrated to produce severe central nervous system (CNS) toxicity.In

Product description：Number of SamplesSufficient for 25 samplesAmount of SamplesUp to 1 nmol of glycolipidSuitable of Samples Isolated glycolipids containing a ceramide backbone.Suggested usage1. Pipette 5 μl of LZ-CER-BUFFX4 into an Eppendorf tube,

General description This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the

A cell-permeable trisubstituted thiazole compound that acts as a potent and selective inhibitor of COX-1 (IC 50 = 28 nM and 65 &#181M for human recombinant COX-1 and COX-2, respectively). Displays ~2,300 fold greater selectivity towards inhibition

CU NHETAMIDE ARYLATION MICRO V1

A potent multitargeted inhibitor of histone deacetylase (HDAC) and the receptor kinases epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 2 (HER2), with IC50 values of 4.4, 2.

ETHYL 3-ACETAMIDO-4-HYDROXYBENZOATE