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Displaying products by catalog number (5700 - 5799)

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Cat.No.
Product Name / Activity
5701AMG 853

Potent dual CRTH2 and prostaglandin D2 (PGD2) receptor antagonist

5702DiD perchlorate

Lipophilic fluorescent reagent; shown to stain HSCs

5707RA 839

Nrf2 activator; inhibits Nrf2/Keap1 interaction

5708BAY 41-8543

Guanylyl cyclase (sGC) stimulator

5710NFAT inhibitor, Cell Permeable

Cell permeable NFAT inhibitor

5711Nilvadipine

Syk kinase inhibitor; inhibits Aβ production

57124-ethynyl-N-ethyl-1,8-naphthalimide

Click-activated fluorescent probe

5713MS 023 dihydrochloride

Potent and selective type I PRMT inhibitor

5714S 2101

LSD1 inhibitor

5715(±)-ADX 71743

Negative allosteric modulator at mGlu7; brain penetrant

5716PF 06447475

Potent LRRK2 inhibitor; neuroprotective

5719SKF 82958 hydrobromide

D1 agonist

5722Ogerin

Selective positive allosteric modulator at GPR68

5724NQ 301

Selective CD45 inhibitor

5725ML 352 hydrochloride

High affinity and selective presynaptic choline transporter (CHT) inhibitor

5727MC 1742

Potent class I and IIb HDAC inhibitor

5728EXP 3174

Potent and selective AT1 receptor antagonist

5734L-Dehydroascorbic acid

GLUT1 substrate; oxidized form of L-Ascorbic acid

5735S3QEL 2

Suppressor of complex III superoxide production

5736Aphidicolin

DNA polymerase α, δ and ε inhibitor

5737BAM 15

Mitochondrial protonophore uncoupler

5738ML 382

MrgX1 (SNSR4) positive allosteric modulator

5739Prostratin

PKC activator; also NF-κB activator

57406-Hydroxy-DL-DOPA

Allosteric inhibitor of RAD52; also APE1 inhibitor

5742AZ PFKFB3 67

Potent and selective PFKFB3 inhibitor

5744NVS-CECR2-1

Potent and selective inhibitor of cat eye syndrome chromosome region, candidate 2 (CECR2)

5747Apcin

Cdc20 inhibitor; inhibits Cdc20-substrate interaction

5748DAPI

Fluorescent DNA stain

5751PF 3084014 hydrobromide

Potent γ-secretase inhibitor

5752PF 06260933 dihydrochloride

MAP4K4 (HGK) inhibitor; also inhibits MINK and TNIK

5754PF 543 hydrochloride

Potent and selective SphK1 inhibitor

5756MLi-2

Potent and selective LRRK2 inhibitor

5757Tariquidar dihydrochloride

Potent P-glycoprotein (P-gp) inhibitor

5759SW 033291

High affinity 15-PGDH inhibitor; promotes hematopoiesis and hepatocyte proliferation

5760P-3FAX-Neu5Ac

Sialic acid analog; sialyltransferase inhibitor

5761RG 102240

Gene switch ligand for use in induceable gene expression systems

5762BMS 795311

Potent cholesteryl ester transfer protein (CETP) inhibitor

5763(R)-Citalopram oxalate

Enantiomer of escitalopram oxalate (Cat. No. 1427)

5764Deferoxamine mesylate

Iron chelator; also hypoxia mimetic

57654-azido-N-ethyl-1,8-naphthalimide

Click-activated fluorescent probe

5766A 971432

Potent and selective S1P5 agonist

5769TM 5275 sodium salt

Plasminogen activator inhibitor-1 (PAI-1) inhibitor; orally bioavailable

5770MONNA

Potent TMEM16A (Anoctamin-1) blocker

5772Sacubitril calcium

Membrane metallo-endopeptidase (neprilysin) inhibitor prodrug; orally bioavailable

5773Akti-1/2

Potent and selective dual Akt1 and 2 inhibitor

5774DEL 22379

ERK dimerization inhibitor

5775AZ 6102

Potent TNKS1/2 inhibitor

57782-Phospho-L-ascorbic acid trisodium salt

Ascorbic acid derivative; maintains differentiation potential in bone marrow-derived MSCs

5779NSC 23005 sodium

Potently promotes HSC expansion ; p18INK inhibitor

5781A 425619

Potent TRPV1 antagonist

5786NI 42

High affinity BRPF inhibitor

5789AM 4668

Potent FFA1 (GPR40) agonist

5790PF 05175157

Acetyl-CoA carboxylase (ACC) 1 and 2 inhibitor

5791Bz 423

ATP synthase inhibitor; proapoptotic

5792ProTx III

Potent Nav1.7 blocker; analgesic

5794LM 10

Selective tryptophan 2,3-dioxygenase (TDO) inhibitor

5795ATI 2341

CXCR4 allosteric agonist

5796Azoramide

Unfolded protein response (UPR) modulator

5798Irbesartan

Potent AT1 antagonist

5799Mitoglitazone

Insulin sensitizer; exhibits low binding affinity at PPARγ

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