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Displaying products by catalog number (2300 - 2399)

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Product Name / Activity
2301T 0070907

Highly potent and selective PPARγ antagonist

2302Sanguinarine chloride

Inhibitor of protein phosphatase 2C (PP2C)

2303PNU 282987

Selective α7 nAChR agonist


Selective, orally active CCK1 receptor antagonist


Selective PP1 inhibitor

230615-deoxy-Δ-12,14-Prostaglandin J2

Endogenous PPARγ agonist

2307Leukotriene B4

BLT1/BLT2 receptor agonist and potent chemotactic factor

2308Tabimorelin hemifumarate

Potent, orally active ghrelin receptor agonist

2309SR 142948

Highly potent NT receptor antagonist

2310SR 49059

Selective, orally active vasopressin V1A receptor antagonist


Potent, orally active human glucagon receptor antagonist

2312DNQX disodium salt

Selective non-NMDA antagonist. Water-soluble salt of DNQX (Cat. No. 0189)

2313QX 314 chloride

Na+ channel blocker

2314LOE 908 hydrochloride

Broad spectrum cation channel blocker; neuroprotective

2315Immethridine dihydrobromide

Potent H3 agonist, highly selective over H4

2316AMG 9810

Potent and selective, competitive antagonist of TRPV1

2318Pravastatin sodium salt

HMG-CoA reductase inhibitor


Cell-permeable calmodulin antagonist

2320TCS 184

Scrambled control peptide for use with TCS 183 (Cat. No. 2236)


Cell-permeable calmodulin agonist

2322BTS 54-505 hydrochloride

Potent SNRI; active metabolite of sibutramine (Cat. No. 2290)


RIPK1 inhibitor; inhibits necroptosis

2327WIN 55,212-3 mesylate

CB2 antagonist/CB1 partial inverse agonist; enantiomer of WIN 55,212-2 (Cat. No. 1038)

2329Ro 10-5824 dihydrochloride

Selective D4 receptor partial agonist

2330DMP 543

Potent and selective K2P3.1 (TASK-1) channel blocker

2332(+)-Igmesine hydrochloride

Selective σ1 ligand; antidepressant

2333JNJ 16259685

Extremely potent, mGlu1-selective non-competitive antagonist


Endocytosis blocker

2337Trequinsin hydrochloride

Extremely potent inhibitor of PDE3

2338MK 571

Potent CysLT1 (LTD4) inverse agonist. Also MRP1 inhibitor

2339WEB 2086

Potent PAF receptor antagonist

2341A 80426 mesylate

High affinity α2 antagonist. Also 5-HT uptake inhibitor

23424-Methylhistamine dihydrochloride

Selective, high affinity H4 agonist

2344CGH 2466 dihydrochloride

A1, A2B and A3 antagonist and inhibitor of p38 MAPK and PDE4

2345ZK 200775

Competitive AMPA/kainate antagonist


Selective inhibitor of eIF2α dephosphorylation


Potent and selective glycine site antagonist; orally available and active in vivo

2349Dihydro-β-erythroidine hydrobromide

Inhibitor of α4β2, muscle type and Torepedo nAChRs


Bioactive, bradykinin-related peptide

2371Bombinakinin M

Potent bradykinin receptor agonist

2372ABT 702 dihydrochloride

Adenosine kinase inhibitor; orally active

2373T 0901317

Potent liver X receptor (LXR) agonist; also CAR inverse agonist

2374GW 405833

Selective, high affinity CB2 receptor partial agonist

2382EMD 386088 hydrochloride

Potent 5-HT6 agonist

2383Bryostatin 1

Protein kinase C activator

2385AMN 082 dihydrochloride

The first selective mGlu7 agonist


Potent and selective mGlu5 antagonist

2387LY 320135

Selective CB1 receptor antagonist/inverse agonist

2390LY 456236 hydrochloride

Selective mGlu1 antagonist

2391Astressin 2B

Selective CRF2 antagonist

2392JTE 013

S1P2 receptor antagonist

2394SDZ NKT 343

Highly selective, human NK1 antagonist

2395Sertraline hydrochloride

5-HT re-uptake inhibitor


Kir6 (KATP) channel blocker


Selective mineralocorticoid receptor antagonist

2398SNAP 5089

Subtype-selective α1A antagonist

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