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Displaying products by catalog number (1400 - 1499)

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Cat.No.
Product Name / Activity
1400SCH 202676 hydrobromide

Inhibitor of ligand binding to G-protein-coupled receptors

1401NU 1025

Potent PARP inhibitor

1402SB 203580 hydrochloride

Selective inhibitor of p38 MAPK; water-soluble

1403FPL 64176

Potent activator of Ca2+ channels (L-type)

1405(-)-Terreic acid

Selective inhibitor of BTK

1406Trichostatin A

Potent histone deacetylase inhibitor

1407PP 2

Potent, selective Src family kinase inhibitor

1408YM 022

Highly potent, selective non-peptide CCK2 antagonist

1409CGP 39551

Potent, selective and competitive NMDA antagonist

1410SDM25N hydrochloride

Potent, selective non-peptide δ antagonist

1411Noladin ether

Endogenous agonist for CB1 and GPR55

1412Chromanol 293B

IKs blocker. Also blocks ICFTR

1413NAS-181

Selective r5-HT1B antagonist. Active in vivo

1414Scopolamine hydrobromide

Non-selective muscarinic antagonist

14151400W dihydrochloride

Potent, highly selective iNOS inhibitor

1416Homoharringtonine

Inhibitor of protein synthesis. Antileukemic agent

1417Daidzein

Arrests cell cycle in G1 phase

1418Resveratrol

Cyclooxygenase inhibitor

1419Naloxone benzoylhydrazone

Full κ agonist, partial μ and δ agonist and antagonizes agonist-induced activation of NOP

1420D-myo-Inositol-1,3,4,5-tetrakisphosphate, octapotassium salt

Potent inhibitor of Ins(1,4,5)P3 5-phosphatase. Metabolite of Cat. No. 1482

1422DCEBIO

Activates Cl- conductance and hKCa3.1 channels

1425(S)-(+)-Dimethindene maleate

M2-selective antagonist

1426PPT

Subtype-selective ERα agonist

1427Citalopram hydrobromide

Highly potent and selective 5-HT uptake inhibitor

1428Amyloid β-Peptide (1-42) (human)

Predominant amyloid β-protein fragment

1429Amyloid β-peptide (25-35) (human)

Human amyloid β-protein fragment functionally required for neurotoxicity

1430DuP 697

Cyclooxygenase-2 (COX-2) inhibitor

1431DPDPE

Selective δ agonist

1435SQ 22536

Adenylyl cyclase inhibitor

1436MDL 12330A hydrochloride

Adenylyl cyclase inhibitor; also cyclic nucleotide PDE inhibitor

1437D609

Selective PC-PLC inhibitor

1439Ruthenium Red

Non-selective Ca2+ channel blocker (N- and P-type)

1440BMY 14802 hydrochloride

Sigma antagonist. Antipsychotic agent

1441BMS 182874 hydrochloride

Highly selective, orally active non-peptide ETA antagonist

1442BMY 45778

Non-prostanoid prostacyclin IP receptor partial agonist

1443Metastin (human)

Potent, endogenous ligand for kisspeptin receptor

1445N-Arachidonylglycine

Endocannabinoid. Suppresses pain in vivo

1446O-2093

Inhibitor of anandamide uptake

1447SKF 81297 hydrobromide

D1 agonist

1448Formoterol hemifumarate

Potent and selective β2 agonist

1450Galanin (1-15) (porcine, rat)

Galanin receptor agonist peptide

1451Galanin (2-29) (rat)

Selective GAL2 peptide agonist

1453Clemastine fumarate

H1 antagonist

1454GYKI 52466 dihydrochloride

Selective non-competitive AMPA antagonist

1455Orexin A (human, rat, mouse)

Endogenous agonist at OX1 and OX2

1456Orexin B (human)

Endogenous agonist at OX1 and OX2

1457Orexin B (mouse)

Endogenous agonist at OX1 and OX2

1458DAPK Substrate Peptide

Death associated protein kinase substrate (synthetic)

1459SU 4312

Potent inhibitor of VEGFR tyrosine kinase

1460PACOCF3

Phospholipase A2 inhibitor

1461Linomide

Immunomodulator with antiangiogenic properties

1462AACOCF3

Phospholipase A2 inhibitor

1463Ghrelin (human)

Endogenous ghrelin receptor agonist

1464TFLLR-NH2

PAR1-activating peptide

1465Ghrelin (rat)

Endogenous ghrelin receptor agonist

1466PPAHV

Non-pungent vanilloid receptor agonist

1467Daunorubicin hydrochloride

RNA synthesis inhibitor

1468SLIGRL-NH2

PAR2-activating peptide

1469CGP 37849

Potent and selective NMDA antagonist

1470Flecainide acetate

Cardiac Na+ channel blocker. Antiarrhythmic

1471Etomidate

GABA mimetic and GABA modulatory agent

1472Suramin hexasodium salt

Non-selective P2 antagonist

1475(-)-[3R,4S]-Chromanol 293B

IKs blocker. Enantiomer of Chromanol 293B (Cat. No. 1412)

1476Gap 27

Selective gap junction blocker

1477GR 127935 hydrochloride

Potent, selective 5-HT1B/1D antagonist

1478Proglumide sodium salt

Non-selective CCK antagonist; orally active

1479Mifepristone

Progesterone and glucocorticoid receptor antagonist

1480FIT

Irreversible δ agonist

1481(-)-5'-DMH-CBD

Metabolically stable anandamide transport inhibitor

1482D-myo-Inositol 1,4,5-trisphosphate, hexapotassium salt

Ca2+ mobilizing second messenger

1483GR 89696 fumarate

Subtype-selective κ agonist

1484Oleylethanolamide

Lipid mediator, anorexic actions; also GPR55 and PPARα agonist

1485DEA

Endogenous CB1 agonist

1486GR 231118

Potent NPY Y1 antagonist/NPY Y4 agonist. Binds to NPFF receptors

1487AY-NH2

Selective PAR4 agonist

1488tcY-NH2

Selective PAR4 antagonist

1489Mithramycin A

Inhibitor of DNA and RNA polymerase

1490MNI-caged-L-glutamate

Stable photoreleaser of L-glutamate

1493CGP 78608 hydrochloride

Potent, selective glycine-site NMDA antagonist

1494DPN

Highly potent ERβ agonist

1495Combretastatin A4

Antiangiogenic

1496SP 600125

Selective JNK inhibitor

1497Rimcazole dihydrochloride

σ2 antagonist. Also DAT inhibitor

1499CL 316243 disodium salt

Highly selective β3 agonist

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IVBM 2016

October 30 - November 3, 2016

Boston, MA, USA

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