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Displaying Products Alphabetically by Name (W)

Cat. No. Product Name / Activity
5455 W 54011
High affinity C5a receptor antagonist
1415 1400W dihydrochloride
Potent, highly selective iNOS inhibitor
0361 W-13 hydrochloride
Calmodulin antagonist
3602 W146
Potent and selective S1P1 receptor antagonist
0368 W-5 hydrochloride
Calmodulin antagonist
0369 W-7 hydrochloride
Calmodulin antagonist. Inhibits myosin light chain kinase
1253 (S)-WAY 100135 dihydrochloride
Potent and selective 5-HT1A antagonist
4380 WAY 100635 maleate
Potent 5-HT1A antagonist; also D4 agonist
1801 WAY 161503 hydrochloride
Potent and selective 5-HT2C agonist
2633 WAY 170523
Potent and selective inhibitor of MMP-13
5589 WAY 181187 oxalate
High affinity and selective 5-HT6 agonist
3904 WAY 208466 dihydrochloride
Selective 5-HT6 agonist
2652 WAY 213613
Potent, non-substrate EAAT2 inhibitor
5951 WAY 252623
Potent LXR agonist
3933 WAY 267464 dihydrochloride
Potent non-peptide oxytocin receptor agonist
4767 WAY 316606 hydrochloride
Secreted Frizzled-related protein-1 (sFRP-1) inhibitor; increases Wnt signaling
5323 WDR5 0103
WDR5 antagonist
2339 WEB 2086
Potent PAF receptor antagonist
5413 WH-4-023
Potent and selective Lck and Src inhibitor; also inhibits SIK
3115 WHI-P 154
JAK3 kinase inhibitor. Also inhibits EGFR
7580 WIC1
Inhibitor of Wnt/β-catenin signaling
4855 WIKI4
Potent tankyrase inhibitor
4736 WIN 18446
ALDH1A2 inhibitor
1038 WIN 55,212-2 mesylate
Selective high affinity CB2 agonist
1057 WIN 64338 hydrochloride
Bradykinin B2 antagonist
1800 WKYMVm
FPR1, FPR2 and FPR3 receptor agonist
6692 WM 1119
High affinity KAT6A (MOZ) competitive inhibitor
7366 WM 3835
Lysine acetyltransferase HBO1 (KAT7) inhibitor
6693 WM 8014
Potent and selective KAT6A and KAT6B inhibitor
8106 WNTinib
Inhibitor of mutant β-catenin signaling in hepatocellular carcinoma
7156 WQ 1
Potent and selective σ1 receptor antagonist; active in vivo
3356 WR 1065 dihydrochloride
p53 activator. Also ROS scavenger
2262 WRW4
Selective FPR2 antagonist
3040 WS 12
TRPM8 agonist; cooling agent
7055 WS 383
Potent, selective and reversible DCN1-UBC12 interaction inhibitor
7791 WS 6
Induces growth and proliferation of pancreatic islet cells, murine totipotent stem cells, GABAergic neurons and hippocampal neurons
5317 WWL 123
α/β-hydrolase domain 6 (ABHD6) inhibitor; antiepileptic
1312 WY 14643
Selective PPARα agonist
4282 WYE 687 dihydrochloride
Potent and selective mTOR inhibitor
6290 WZ 4002
Potent mutant-selective EGFR inhibitor
5177 WZ 4003
Potent and selective NUAK1/2 inhibitor
6143 WZB 117
GLUT inhibitor
4434 Wiskostatin
N-WASP inhibitor; inhibits Arp2/3 activation
2816 Withaferin A
Inhibits NF-κB activation
5148 Wnt-C59
Highly potent PORCN inhibitor
1232 Wortmannin
Potent, irreversible inhibitor of PI 3-kinase. Also inhibitor of PLK1

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