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Displaying products by catalog number (3300 - 3399)

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5100 5200 5300 5400 5500 5600 5700 5800 5900 6000
Cat.No.
Product Name / Activity
3300SU 5402

Potent FGFR and VEGFR inhibitor

3301NU 6140

Cyclin-dependent kinase 2 (cdk2) inhibitor

3302CD 3254

Potent and selective RXRα agonist.

3303UVI 3003

RXR antagonist

3304SU 16f

Potent and selective PDGFRβ inhibitor

3305Alfuzosin hydrochloride

Uroselective α1 antagonist

33068-(3-Chlorostyryl)caffeine

Selective A2A antagonist. Also MAO-B inhibitor

3307PF 750

Selective FAAH inhibitor

3308Zileuton

Orally active 5-LOX inhibitor

3309Fluvastatin sodium

Potent HMG-CoA reductase inhibitor

3311VU 0155041 sodium salt

Potent, positive allosteric mGlu4 agonist. Sodium salt of VU 0155041 (Cat. No. 3248)

3312BzATP triethylammonium salt

Photoaffinity label for ATPase; also P2X7 agonist and P2X1/P2Y1 partial agonist

3313rac BHFF

Potent, selective GABAB positive allosteric modulator

3314BI 78D3

Selective, competitive JNK inhibitor

3315RS 25344 hydrochloride

Potent PDE4 inhibitor

3316PF 670462

Potent and selective CK1ε and CK1δ inhibitor

3317AZ 11645373

Potent and selective human P2X7 antagonist

3318SC 514

IKKβ inhibitor; attenuates NF-κB-induced gene expression

3319ARL 17477 dihydrochloride

Selective nNOS inhibitor

3321AR-C 66096 tetrasodium salt

Potent and selective P2Y12 antagonist

3322ZD 9379

Brain penetrant NMDA antagonist; acts at glycine site

3323AZ 10606120 dihydrochloride

Potent P2X7 receptor antagonist

3324QS 11

ARFGAP1 inhibitor; modulates Wnt/β-catenin signaling

3325VU 1545

mGlu5 positive allosteric modulator

3326BGC 20-761

High affinity 5-HT6 antagonist

3327CID 755673

Selective protein kinase D inhibitor

3328Desformylflustrabromine hydrochloride

Positive allosteric modulator of α4β2; also muscle-type nAChR inhibitor

3330NPEC-caged-(S)-3,4-DCPG

Caged (S)-3,4-DCPG

3331NPEC-caged-(1S,3R)-ACPD

Caged (1S,3R)-ACPD

3332NPEC-caged-LY 379268

Caged group II mGlu receptor agonist

3333NDT 9513727

Potent, selective human C5a receptor antagonist

3335SU 6668

PDGFR, VEGFR and FGFR inhibitor

3336A 769662

Potent AMPK activator

3337CART (55-102) (rat)

Neuromodulatory neuropeptide fragment; satiety factor

3338CART (55-102) (human)

Neuromodulatory neuropeptide fragment; satiety factor

3339CART (62-76) (rat, human)

Neuromodulating neuropeptide fragment; inhibits food intake in vivo

3341JK 184

Alcohol dehydrogenase 7 inhibitor; inhibits downstream Hh signaling pathway

3342L-798,106

Potent and highly selective EP3 antagonist

3343Ro 8-4304 hydrochloride

NR2B-selective NMDA antagonist

3344SLV 320

Potent and selective A1 antagonist

3346ATC 0175 hydrochloride

MCH1 antagonist; also 5-HT2B antagonist and 5-HT1A partial agonist

3347SNAP 94847 hydrochloride

Potent and selective MCH1 antagonist

334810Panx

Panx-1 mimetic inhibitory peptide; blocks pannexin-1 gap junctions

3349Biocytin

Versatile marker for neuroanatomical investigations

3350LY 393558

Dual 5-HT1B/1D antagonist and 5-HT re-uptake inhibitor

3351Selexipag

Selective prostacyclin IP1 receptor agonist

3352JNJ 28871063 hydrochloride

Potent ErbB receptor family inhibitor

3353PSN 375963 hydrochloride

GPR119 receptor agonist

3354PF 429242

Competitive inhibitor of SREBP site 1 protease

3355PNU 177864 hydrochloride

Highly selective D3 antagonist

3356WR 1065

p53 activator. Also ROS scavenger

3357Ellipticine

Antitumor and intercalating agent; inhibits DNA topoisomerase II

3358MG 101

Calpain inhibitor; activates p53-dependent apoptosis

3359ATC 0065

Potent and selective MCH1 antagonist

3360CGP 52411

EGFR inhibitor. Also inhibits Aβ42 fibril formation

3361JNJ 17203212

Reversible, competitive and potent TRPV1 antagonist

3362MIRA-1

Restores mutant p53 activity; proapoptotic

3364BIX 01294

GLP and G9a inhibitor

3365Tenovin-1

Protects against MDM2-mediated p53 degradation

3366WAY 200070

Selective ERβ agonist

3367AT 101

Downregulates Bcl-2 and Mcl-1; pro-apoptotic

3368SB 271046 hydrochloride

Selective, orally active 5-HT6 antagonist

3369AC 55541

Potent and selective PAR2 agonist

3370AC 264613

PAR2 receptor agonist

3371TCS OX2 29

Potent and selective OX2 antagonist

3373Valinomycin

Selective K+ ionophore

3374Cortistatin 14

Endogenous neuropeptide; binds sst1 - sst5 and ghrelin receptor

3375Dolastatin 10 trifluoroacetate

Tubulin polymerization inhibitor

3377(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin

Selective vasopressin V1A antagonist

3378EIPA

Inhibits TRPP3-mediated currents; also inhibits the Na+/H+ exchanger (NHE)

3379Phenamil

Inhibits TRPP3-mediated currents; also inhibits epithelial Na+ channels

3380Benzamil

NCX inhibitor, Deg/ENaC channel blocker; amiloride (Cat. No. 0890) derivative

3381AM 1172

Anandamide uptake inhibitor; also FAAH inhibitor and CB receptor partial agonist

3383VU 152100

Positive allosteric modulator of M4 receptors

3384(Z)-Pugnac

O-GlcNAcase and β-hexosaminidase inhibitor

3385GW 791343 hydrochloride

P2X7 allosteric modulator

3387Gedunin

Hsp90 inhibitor; exhibits anticancer and antimalarial activity

3388Anastrozole

Potent aromatase (CYP19) inhibitor

3389Bicalutamide

Non-steroidal androgen receptor antagonist

3390Thymosin β4

Potent actin polymerization regulator

3391Amyloid β-peptide (42-1) (human)

Inactive control peptide for amyloid β-peptide (1-42) (Cat. No. 1428)

3392VKGILS-NH2

Control peptide for SLIGKV-NH2 (Cat. No. 3010)

3393RLLFT-NH2

Control peptide for TFLLR-NH2 (Cat. No. 1464)

3394LRGILS-NH2

Control peptide for SLIGRL-NH2 (Cat. No. 1468)

3395Lestaurtinib

JAK2, FLT3 and TrkA inhibitor; also inhibits AurA and AurB

3396Desmopressin

Synthetic vasopressin analog; V1B and V2 agonist

3397LY 2365109 hydrochloride

Potent and selective GlyT1 inhibitor

3399Myelin Basic Protein (87-99)

Major antigenic component implicated in the pathophysiology of multiple sclerosis

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