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MAPK/ERK Pathway ERK JNK KLF MEK MLK MNK p38 MAPK Raf RSK MAP4K4
Membrane Transporter/Ion Channel AMPAR BCRP CFTR Chloride Channel CRAC Channel CRM1 EAAT2 HCN Channel MAT MCT Na+/Ca2+ Exchanger NKCC P2X Receptor P-gp Potassium Channel Proton Pump Sodium Channel TRPV URAT1 VDAC GABA Receptor IBAT Oct SGLT AChR ATPase Calcium Channel EAAT1 GlyT1 Na+/K+ ATPase NBC NMDAR TRP Channel SLC PIEZO1
Metabolic Enzyme 15-PGDH ACC ACE Adenosine Deaminase Adenosine Kinase AhR ALDH Aldose Reductase Aminopeptidase ATP Citrate Lyase Carbonic Anhydrase Cathepsin CETP COMT CPA Decarboxylase Dehydrogenase DGAT DHFR Elastase Enolase FAAH FABP Factor Xa FAS Ferroptosis FXR Glucokinase GLUT1 GSNOR GST Hexokinase HIF HIV Integrase HMGCR HSP Hydroxylase IDH IDO Lipase Lipoxygenase LXR MAO Mineralocorticoid Receptor NAE NAMPT Neprilysin P450 PAI-1 More >>
Neuronal Signaling AChE Adenosine Kinase Adrenergic Receptor AMPAR Amyloid-β CaMK CGRP Receptor COMT COX DAT Dopamine Receptor FAAH GABA Receptor GlyT1 Histamine Receptor Imidazoline Receptor MAO mGluR MT Receptor NK Receptor NMDAR Opioid Receptor OX Receptor P2X Receptor P-gp Secretase SSRIs Substance P Choline Cholinesterase Enkephalinase Glucosylceramide Synthase RAGE 5-HT Receptor AChR PIEZO1
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TGF-beta/Smad TGF-beta Receptor Smad TGF-beta
Stem Cells/Wnt Casein Kinase ERK Gli GSK-3 Hedgehog JAK MST Notch PKA PORCN ROCK Secretase sFRP-1 Smo STAT Wnt YAP β-catenin BMI-1
Phosphatase
Ubiquitin APC DUB NAE p97 Proteasome E1/E2/E3 Enzyme
NF-kB HDAC IKK MALT1 NF-kB NOD1 Nrf2 PPAR RIP Kinase TAK1
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Bombesin Receptor

Bombesin Receptor

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Cat. No.	Product Name	CAS No.	Information
CSN21385	PD176252	204067-01-6	PD176252 is a potent antagonist of neuromedin-B preferring BB1 and gastrin-releasing peptide-preferring BB2 receptor with Kis of 017 nM and 1 nM for human BB1 and BB2 receptors and 066 nM 16 nM for Rat BB1 and BB2 receptors respectively also an agonist of N-Formyl peptide receptor12 FPR1FPR2 with EC50s of 031 and 066 M in HL-60 cells
CSN24208	ML-18	1422269-30-4	ML-18 is a Bombesin receptor subtype 3 (BRS-3) antagonist with IC50 = 4.8 μM. It also binds GRPR with IC50 = 16 μM.

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Bombesin Receptor

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