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BAM (8-22)

/products/reagent/bam-(8-22)-92-1215
MAS-related GPR, member X1 (MRGPRX1)
Orphan receptor. Probably involved in the function of nociceptive neurons. May regulate nociceptor function and/or development, including the sensation or modulation of pain. Potently activated by enkephalins including BAM22 (bovine adrenal medulla peptide 22) and BAM (8-22). ...
/target-data-sheets/gpcr/mrgprx1 2/12/2015 9:45:12 PM
PathHunter® CHO-K1 MRGPRX1 β-Arrestin Cell Line

/products/cell-line/cho-k1-mrgprx1-β-arrestin-cell-line-93-0919c2
RBL-2H3 MRGPRX1 Gq Cell Line

/products/cell-line/rbl-2h3-mrgprx1-gq-cell-line-95-1019c11
ChemiScreen™ MRGPRX1 Receptor Stable Cell Line

/products/cell-line/stable-cell-line/hts122c
Ready-to-Assay™ MRGPRX1 Receptor Frozen Cells

/products/frozen-cells/hts122rta
The discovery of 2-amino-3,5-diarylbenzamide inhibitors of IKK-alpha and IKK-beta kinases.
A potent and selective series of 2-amino-3,5-diarylbenzamide inhibitors of IKK-alpha and IKK-beta is described. The most potent compounds are 8h, 8r and 8v, with IKK-beta inhibitory potencies of pIC(50) 7.0, 6.8 and 6.8, respectively. The series has excellent selectivity, both...
/tools-resources/publications-references/publications/the-discovery-of-2-amino-3-5-diarylbenzamide-inhib 10/3/2012 5:51:37 PM
Biphenyl amide p38 kinase inhibitors 3: Improvement of cellular and in vivo activity.
The biphenyl amides (BPAs) are a novel series of p38alpha MAP kinase inhibitor. The optimisation of the series to give compounds that are potent in an in vivo disease model is discussed. SAR is presented and rationalised with reference to the crystallographic binding mode.
/tools-resources/publications-references/publications/biphenyl-amide-p38-kinase-inhibitors-3-improvement 10/3/2012 5:51:34 PM
The discovery and initial optimisation of pyrrole-2-carboxamides as inhibitors of p38alpha MAP kinase.
A novel pyrrole-2-carboxamide series of p38alpha inhibitors, discovered through the application of virtual screening, is presented. Following evaluation of activity, selectivity and developability properties of commercially available analogues, a synthesis program enabled rapi...
/tools-resources/publications-references/publications/the-discovery-and-initial-optimisation-of-pyrrole 10/3/2012 5:51:31 PM
An orally bioavailable positive allosteric modulator of the mGlu4 receptor with efficacy in an animal model of motor dysfunction.
A high-throughput screening campaign identified 4-((E)-styryl)-pyrimidin-2-ylamine (11) as a positive allosteric modulator of the metabotropic glutamate (mGlu) receptor subtype 4. An evaluation of the structure-activity relationships (SAR) of 11 is described and the efficacy o...
/tools-resources/publications-references/publications/an-orally-bioavailable-positive-allosteric-modulat 10/3/2012 5:51:25 PM
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