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Displaying products by catalog number (2200 - 2299)

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Product Name / Activity
2200PD 160170

Selective non-peptide NPY Y1 receptor antagonist

2201PNU 22394 hydrochloride

5-HT2C agonist and 5-HT2A/2B partial agonist

2202Zatebradine hydrochloride

Blocks hyperpolarization-activated current (If)


Endogenous lipid; potentiates effects of endovanilloids at TRPV1 receptors


Endogenous lipid, active in vivo. Enhances effects of endovanilloids at TRPV1 receptors


Endogenous lipid; enhances activity of 2-arachidonylglycerol (Cat. No. 1298)

2207PDZ1 Domain inhibitor peptide

Disrupts interaction between GluR6 and PSD-95 PDZ1 domain

2208LY 255283

Selective, competitive BLT2 receptor antagonist

2211Carcinine ditrifluoroacetate

Highly selective H3 antagonist

2213N20C hydrochloride

Non-competitive NMDA receptor open-channel blocker

2214ABT 724 trihydrochloride

Potent, selective D4 partial agonist; proerectile

2216des-His1-[Glu9]-Glucagon (1-29) amide

Glucagon receptor antagonist


Potent, non-competitive EAAT inhibitor


Potent, non-competitive EAAT inhibitor


Fluorescent Ca2+ indicator

2221Rac1 Inhibitor W56

Selective inhibitor of Rac1-GEF interaction

2222Rac1 Inhibitor F56, control peptide

Control peptide version of Rac1 Inhibitor W56 (Cat. No. 2221)


Caged NMDA

2225MNI caged kainic acid

Caged kainic acid

2226Flutax 1

Fluorescent taxol derivative

2227CI 976

Selective ACAT inhibitor


Dihydroorotate dehydrogenase inhibitor

2229GW 0742

Highly selective, potent PPARδ agonist


Substrate-competitive inhibitor of GSK-3

2236TCS 183

Fragment 1-13 of GSK-3β sequence

2237BRL 50481

Selective PDE7 inhibitor

2238GW 441756

Potent, selective TrkA inhibitor

2239GW 583340 dihydrochloride

Potent dual EGFR/ErbB2 inhibitor; orally active

2241DMAB-anabaseine dihydrochloride

Partial agonist at α7 nAChR; also α4β2 antagonist

2242Octopamine hydrochloride

Invertebrate biogenic amine: activates β3 adrenoceptors

2243MEK Inhibitor Tocriset™

Selection of 3 MEK inhibitors (Cat. Nos. 1213, 1969 and 1144)

2244p38 MAPK Inhibitor Tocriset™

Selection of 3 p38 MAPK inhibitors (Cat. Nos. 1264, 1202 and 1962)

2250SL 0101-1

Selective ribosomal S6 kinase (RSK) inhibitor


Potent pro-apoptotic anticancer agent; activates caspase-3

2252Doxorubicin hydrochloride

Antitumor antibiotic agent. Inhibits DNA topoisomerase II

2253Go 6976

Potent protein kinase C inhibitor; selective for α and β isozymes

2254ACDPP hydrochloride

Selective mGlu5 receptor antagonist

2255CGS 9343B

Calmodulin antagonist

2257GIP (1-39)

Highly potent insulinotropic peptide

2258GLP-2 (human)

Endogenous hormone; displays intestinotrophic activity

2259GLP-2 (rat)

Endogenous hormone; displays intestinotrophic activity

2260[Des-octanoyl]-Ghrelin (human)

Major circulating form of ghrelin; devoid of activity at ghrelin receptor but is active in vivo


Potent, non-peptide ghrelin receptor agonist


Selective FPR2 antagonist

2264Motilin (human, porcine)

Endogenous peptide regulator of gastrointestinal motility

2265Lyn peptide inhibitor

Inhibits Lyn-dependent activities of IL-5 receptor; cell-permeable


Agonist selective for estrogen-related receptors ERRβ and ERRγ


Cell-permeable, potent and selective proteasome inhibitor

2268NNC 55-0396 dihydrochloride

Highly selective Ca2+ channel blocker (T-type)

2270SCH 58261

Potent, highly selective A2A antagonist

2272Ro 08-2750

Inhibits NGF binding to p75NTR and TrkA

2273PMPA (NMDA antagonist)

Competitive NMDA antagonist


Competitive NR2A antagonist


Selective cell-permeable CK2 inhibitor

2276FPL 55712

Leukotriene receptor antagonist


Caged D-aspartate; NMDA agonist

2280Raloxifene hydrochloride

Selective estrogen receptor modulator (SERM)


Very selective and potent A1 receptor agonist

2282Moxonidine hydrochloride

I1 receptor and α2-adrenoceptor agonist (I1 > α2)

2284SEW 2871

Cell-permeable, selective S1P1 receptor agonist

2285Go 6983

Broad spectrum PKC inhibitor


Protein kinase C inhibitor


Silent antagonist for putative abnormal-CBD (Cat. No. 1297) receptor

2289Lamotrigine isethionate

Inhibits glutamate release. Water-soluble salt of lamotrigine (Cat. No. 1611)

2290Sibutramine hydrochloride

5-HT and noradrenalin re-uptake inhibitor (SNRI)


Inhibits JAK2 autophosphorylation

2292AQ-RA 741

Selective, high affinity M2 antagonist


DNA methyltransferase and cytidine deaminase inhibitor


RNA synthesis inhibitor

2295(±)-Cloprostenol sodium salt

Water-soluble PGF2α analog and potent FP receptor agonist

2296Prostaglandin E2

Major endogenous prostanoid


Cytoprotective PGE1 analog

2299SCH 39166 hydrobromide

High affinity D1/D5 receptor antagonist

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