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Displaying Products by Catalog Number (2300 - 2399)

Cat No Product Name / Activity
2301 T 0070907
Highly potent and selective covalent PPARγ antagonist
2302 Sanguinarine chloride
Inhibitor of protein phosphatase 2C (PP2C)
2303 PNU 282987
Selective α7 nAChR agonist
2304 Devazepide
Selective, orally active CCK1 receptor antagonist
2305 Tautomycetin
Selective PP1 inhibitor
2306 15-deoxy-Δ-12,14-Prostaglandin J2
Endogenous PPARγ agonist
2307 Leukotriene B4
BLT1/BLT2 receptor agonist and potent chemotactic factor
2308 Tabimorelin hemifumarate
Potent, orally active ghrelin receptor agonist
2309 SR 142948
Highly potent NT receptor antagonist
2310 SR 49059
Selective, orally active vasopressin V1A receptor antagonist
2311 L-168,049
Potent, orally active human glucagon receptor antagonist
2312 DNQX disodium salt
Selective non-NMDA iGluR antagonist; water-soluble salt of DNQX (Cat. No. 0189)
2313 QX 314 chloride
Na+ channel blocker
2314 LOE 908 hydrochloride
Broad spectrum cation channel blocker; neuroprotective
2315 Immethridine dihydrobromide
Potent H3 agonist, highly selective over H4
2316 AMG 9810
Potent and selective, competitive antagonist of TRPV1
2318 Pravastatin sodium salt
HMG-CoA reductase inhibitor
2319 CALP2
Cell-permeable calmodulin antagonist
2320 TCS 184
Scrambled control peptide for use with TCS 183 (Cat. No. 2236)
2321 CALP3
Cell-permeable calmodulin agonist
2322 BTS 54-505 hydrochloride
Potent SNRI; active metabolite of sibutramine (Cat. No. 2290)
2324 Necrostatin-1
RIPK1 inhibitor; inhibits necroptosis
2329 Ro 10-5824 dihydrochloride
Selective D4 receptor partial agonist
2330 DMP 543
Potent, orally active ACh release enhancer
2332 (+)-Igmesine hydrochloride
Selective σ1 ligand; antidepressant
2333 JNJ 16259685
Highly potent, mGlu1-selective non-competitive antagonist
2337 Trequinsin hydrochloride
Extremely potent inhibitor of PDE3
2338 MK 571
Potent CysLT1 (LTD4) inverse agonist. Also MRP1 inhibitor
2339 WEB 2086
Potent PAF receptor antagonist
2341 A 80426 mesylate
High affinity α2 antagonist. Also 5-HT uptake inhibitor
2342 4-Methylhistamine dihydrochloride
Selective, high affinity H4 agonist
2344 CGH 2466 dihydrochloride
A1, A2B and A3 antagonist and inhibitor of p38 MAPK and PDE4
2345 ZK 200775
Competitive non-NMDA iGluR antagonist
2347 Salubrinal
Selective inhibitor of eIF2α dephosphorylation
2348 Gavestinel
Potent and selective NMDA antagonist; acts at the glycine site
2349 Dihydro-β-erythroidine hydrobromide
α4β2, muscle type and Torpedo nAChR antagonist
2370 Bombinakinin-GAP
Bioactive, bradykinin-related peptide
2371 Bombinakinin M
Potent bradykinin receptor agonist
2372 ABT 702 dihydrochloride
Adenosine kinase inhibitor; orally active
2373 T 0901317
Potent liver X receptor (LXR) agonist; also CAR inverse agonist
2374 GW 405833
Selective, high affinity CB2 receptor partial agonist
2382 EMD 386088 hydrochloride
Potent 5-HT6 agonist
2383 Bryostatin 1
Protein kinase C activator
2385 AMN 082 dihydrochloride
Selective mGlu7 agonist
2386 Fenobam
Potent and selective mGlu5 antagonist
2387 LY 320135
Selective CB1 inverse agonist
2390 LY 456236 hydrochloride
Selective mGlu1 antagonist
2391 Astressin 2B
Selective CRF2 antagonist
2392 JTE 013
S1P2 receptor antagonist
2394 SDZ NKT 343
Highly selective human NK1 antagonist
2395 Sertraline hydrochloride
5-HT re-uptake inhibitor
2396 Glimepiride
Kir6 (KATP) channel blocker
2397 Eplerenone
Selective mineralocorticoid receptor antagonist
2398 SNAP 5089
Subtype-selective α1A antagonist

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