Search for new products by date added, alphabetically, or by pharmacological action.
New products are an essential component of our range. Introductions are made on an ongoing basis, with hundreds of new small molecules and peptides being added every year. Our aim is to find the latest, otherwise unobtainable research tools, and bring them to the market as quickly as we can. New products can be identified throughout the Tocris website by the New symbol.
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| Cat No | Product Name / Activity | Date Added |
|---|---|---|
| 6817 | BAY 8002 | May 2019 |
| Potent dual MCT1/2 inhibitor; orally available | ||
| 6782 | Indisulam | May 2019 |
| Molecular glue; pre-mRNA splicing modulator | ||
| 6898 | Mitochondrial fusion promoter M1 | May 2019 |
| Mitochondrial fusion promoter | ||
| 6835 | ABT 737 | May 2019 |
| Bcl-2 family inhibitor; mimics BH3 and induces apoptosis in cancer cell lines | ||
| 6861 | Anle138b | May 2019 |
| Oligomeric aggregation inhibitor; inhibits prion protein and α-synuclein aggregate formation | ||
| 6313 | A 33 | May 2019 |
| Potent and selective PDE4B inhibitor | ||
| 6949 | Thalidomide - linker 10 | May 2019 |
| Thalidomide-alkylC2-amine | ||
| 6951 | Thalidomide - linker 12 | May 2019 |
| Thalidomide-PEG5-ethylamine | ||
| 6792 | Omipalisib | May 2019 |
| Highly potent PI 3-kinase inhibitor; also potent inhibitor of mTOR and DNA-PK | ||
| 6717 | FFN 270 | May 2019 |
| Fluorescent substrate for NET and VMAT2 | ||
| 5026 | KYT 0353 | May 2019 |
| Potent and selective inhibitor of L-type amino acid transporter 1 (LAT1); active in vivo | ||
| 6935 | GSK J5 HCl | May 2019 |
| Inactive isomer of GSK J4 (Cat. No. 4594); cell permeable | ||
| 6881 | SB 4 | May 2019 |
| Potent BMP4 agonist | ||
| 6882 | DiFMUP | May 2019 |
| Fluorescent phophatase substrate | ||
| 6815 | Selumetinib | May 2019 |
| Potent and selective MEK inhibitor; orally bioavailable | ||
| 6690 | Ceralifimod | May 2019 |
| Highly potent and selective S1P1 and S1P5 agonist | ||
| 6868 | 8-Azaadenosine | May 2019 |
| ADAR1 (adenosine deaminases acting on double-stranded RNA) inhibitor; inhibits leukemia stem cell self-renewal | ||
| 6840 | AD 01 | May 2019 |
| FKBPL (FK506-binding protein like)-based peptide; inhibits breast cancer stem cell self-renewal; also antiangiogenic | ||
| 6832 | Ec2la | May 2019 |
| CB2 receptor positive allosteric modulator; active in vivo | ||
| 6845 | RCM 1 | May 2019 |
| FOXM1 inhibitor | ||
| 6708 | SAH-EZH2 | May 2019 |
| EZH2/EDD interaction inhibitor; suppresses PCR2 complex function | ||
| 6362 | GSK 143 | May 2019 |
| Syk inhibitor | ||
| 6829 | (R)-Shikonin | May 2019 |
| PTEN inhibitor; induces necroptosis; anti-inflammatory | ||
| 6771 | PHPS1 sodium salt | May 2019 |
| Shp2 (PTPN11) inhibitor | ||
| 6907 | VH 032 - linker 12 | Apr 2019 |
| VH 032-PEG2-amine | ||
| 6867 | Rhein | Apr 2019 |
| FTO (mRNA N6-methyladenine demethylase) inhibitor; also inhibits ALKBH2 and ALKBH3 | ||
| 6434 | DFHO | Apr 2019 |
| Mimic of RFP fluorophore for imaging RNA in living cells | ||
| 6763 | AVE 1625 | Apr 2019 |
| Potent and selective CB1 receptor antagonist | ||
| 6749 | TH 5487 | Apr 2019 |
| Selective 8-oxoguanine DNA glycosylase 1 (OGG1) inhibitor | ||
| 6679 | VH 032 - linker 4 | Apr 2019 |
| VH 032-PEG3-CH2CH2COOH | ||
| 6378 | JMS 17-2 hydrochloride | Apr 2019 |
| CX3CR1 antagonist | ||
| 6355 | VU 0650991 | Apr 2019 |
| Non-competitive GLP-1 antagonist; orally bioavailable and brain penetrant | ||
| 6852 | VH 032 - linker 7 | Apr 2019 |
| VH 032-AlkylC2-Amine | ||
| 6864 | Ticagrelor | Apr 2019 |
| High affinity and reversible P2Y12 antagonist; displays inverse agonism in vitro; also inhibits ENT1 | ||
| 6814 | Sorafenib | Apr 2019 |
| Potent Raf-1 inhibitor; also inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and cKIT | ||
| 6762 | Urolithin A | Apr 2019 |
| PI 3-K/Akt/mTOR signaling inhibitor; blocks phosphorylation of Akt and p70S6K in vitro | ||
| 6575 | StRIP16 | Apr 2019 |
| Rab8a GTPase-binding stapled peptide | ||
| 6740 | Siramesine hydrochloride | Apr 2019 |
| High affinity σ agonist (σ2 > σ1) | ||
| 6634 | Surfen | Apr 2019 |
| Heparin sulfate antagonist | ||
| 6510 | LNT 1 | Apr 2019 |
| Potent flap endonuclease 1 (FEN1) inhibitor; induces DNA damage response | ||
| 6451 | Pexacerfont | Apr 2019 |
| Potent and selective CRF1 antagonist; anxiolytic | ||
| 6856 | α-Mangostin | Apr 2019 |
| Inhibits proliferation and induces apoptosis selectively in pancreatic CSCs and cancer cell lines | ||
| 6813 | Ibrutinib | Apr 2019 |
| Potent and selective BTK inhibitor | ||
| 6811 | Lapatinib | Apr 2019 |
| Potent and selective dual ErbB2 (HER-2) and EGFR inhibitor | ||
| 6785 | E 7820 | Apr 2019 |
| α2 integrin inhibitor; anti-angiogenic | ||
| 6747 | TL 13-22 | Apr 2019 |
| Negative control for TL 13-12 | ||
| 6744 | TL 13-12 | Apr 2019 |
| Selective ALK degrader | ||
| 6748 | PRX 07034 | Apr 2019 |
| Potent and selective 5-HT6 antagonist | ||
| 5862 | ARN 14686 | Apr 2019 |
| Potent N-acylethanolamine acid amidase inhibitor; NAAA activity-based protein profiling (ABPP) probe | ||
| 6806 | AZ 3451 | Apr 2019 |
| Potent negative allosteric modulator of PAR2 | ||
| 6853 | VH 032 - linker 8 | Apr 2019 |
| VH 032-AlkylC6-Amine | ||
| 6746 | TL 13-110 | Apr 2019 |
| Negative control for TL 13-112 | ||
| 6745 | TL 13-112 | Apr 2019 |
| Selective ALK Degrader | ||
| 6502 | Janelia Fluor® 549, Tetrazine | Apr 2019 |
| Cell permeable yellow fluorescent dye; supplied as a tetrazine for 'click' chemistry | ||
| 6246 | BF 738735 | Apr 2019 |
| Potent and selective PI 4-kinase IIIβ inhibitor; broad spectrum enterovirus replication inhibitor | ||
| 6880 | VH 032 - linker 10 | Apr 2019 |
| VH 032-alkylC10-amine | ||
| 6879 | VH 032 - linker 9 | Apr 2019 |
| VH 032-PEG1-amine | ||
| 6890 | VH 032 - linker 11 | Apr 2019 |
| VH 032-AlkylC8-Amine | ||
| 6865 | uPSEM 792 hydrochloride | Apr 2019 |
| Highly potent PSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | ||
| 6818 | Artemether | Mar 2019 |
| Antimalarial; also inhibits neuroinflammation | ||
| 6866 | uPSEM 817 tartrate | Mar 2019 |
| Highly potent and selective uPSAM4-GlyR and PSAM4-5-HT3 chimeric ion channel agonist; brain-penetrant | ||
| 6784 | FTBMT | Mar 2019 |
| Potent and selective GPR52 agonist; orally bioavailable and BBB permeable | ||
| 6770 | ABT 639 | Mar 2019 |
| CaV3.2 and CaV3.1 channel blocker; orally bioavailable | ||
| 6752 | LDC 000067 | Mar 2019 |
| Potent and selective CDK9 inhibitor | ||
| 6766 | AC 1903 | Mar 2019 |
| Selective TRPC5 blocker | ||
| 6787 | KI-7 | Mar 2019 |
| A2B receptor positive allosteric modulator | ||
| 6753 | CHS 828 | Mar 2019 |
| NAMPT inhibitor; active in vivo and cytotoxic | ||
| 6728 | RGFP 966 | Mar 2019 |
| Potent and selective HDAC3 inhibitor | ||
| 6830 | Conivaptan hydrochloride | Mar 2019 |
| Very high affinity vasopressin V1A and V2 antagonist; orally bioavailable | ||
| 6819 | Mefloquine hydrochloride | Mar 2019 |
| Cx36 and Cx50 gap channel blocker; also antimalarial and antischistosomal | ||
| 6706 | DPNB-ABT 594 | Mar 2019 |
| Caged ABT 594; suitable for one- or two-photon photolysis | ||
| 6429 | ML 210 | Mar 2019 |
| Selectively kills mutant HRAS-expressing cells; glutathione peroxidase inhibitor; induces ferroptosis | ||
| 6827 | Artesunate | Mar 2019 |
| Suppresses ROS-induced activation of the NLRP3 inflammasome; antimalarial | ||
| 6490 | GNE 2861 | Mar 2019 |
| Group II PAK inhibitor; potently inhibits PAK4 and PAK 6 | ||
| 1304 | BW-B 70C | Mar 2019 |
| 5-Lipoxygenase inhibitor | ||
| 6850 | Thalidomide - linker 6 | Mar 2019 |
| Thalidomide-AlkylC2-Amine | ||
| 6834 | Auxin | Mar 2019 |
| Chemical dimerizer used in auxin-inducible degron (AID) system; phytohormone | ||
| 6755 | Darapladib | Mar 2019 |
| Potent lp-PLA2 inhibitor | ||
| 6692 | WM 1119 | Mar 2019 |
| High affinity KAT6A (MOZ) competitive inhibitor | ||
| 6605 | dTAG-13 | Mar 2019 |
| Degrades mutant FKBPF36V fusion proteins; useful alternative to genetic methods for target validation | ||
| 6439 | JNJ 0966 | Mar 2019 |
| Pro-MMP9 activation inhibitor | ||
| 6812 | Afatinib dimaleate | Mar 2019 |
| Potent dual specificity EGFR/HER2 inhibitor; active in vivo | ||
| 6760 | Raphin 1 | Mar 2019 |
| Inhibitor of the regulatory subunit PPP1R15B of protein phosphatase 1; orally bioavailable and brain penetrant | ||
| 6754 | LJI308 | Mar 2019 |
| Potent pan-RSK inhibitor | ||
| 6851 | Pomalidomide - linker 7 | Mar 2019 |
| Pomalidomide-alkylC2-amine | ||
| 6664 | Kinesore | Mar 2019 |
| Kinesin-1 modulator; cell permeable | ||
| 6272 | KYP 2047 | Mar 2019 |
| High affinity prolyl oligopeptidase inhibitor; anti-angiogenic, neuroprotective and brain penetrant | ||
| 6816 | Sitagliptin phosphate | Feb 2019 |
| Potent and selective DPP IV inhibitor | ||
| 6809 | L-DON | Feb 2019 |
| Glutaminase inhibitor; also inhibits other glutamine-using enzymes and transporters | ||
| 6802 | 6 TMR Tre | Feb 2019 |
| Fluorescent trehalose; selectively labels mycobacterial cell envelope | ||
| 6724 | CBA | Feb 2019 |
| Selective TRPM4 blocker | ||
| 6702 | Cerulenin | Feb 2019 |
| Irreversible fatty acid synthase inhibitor | ||
| 6518 | BI 01383298 | Feb 2019 |
| Potent and selective SLC13A5 (Na+/citrate cotransporter) inhibitor | ||
| 6798 | Click N-Acetylmuramic acid - alkyne | Feb 2019 |
| Bacterial peptidoglycan derivative; suitable for 'click'-conjugation to fluorescent dyes | ||
| 6786 | BzF | Feb 2019 |
| Photoreactive unnatural amino acid | ||
| 6653 | FM19G11 | Feb 2019 |
| HIF α-subunit inhibitor | ||
| 6266 | Taxol Janelia Fluor® 646 | Feb 2019 |
| Red fluorescent taxol derivative | ||
| 3719 | Talabostat mesylate | Feb 2019 |
| Potent DPP IV inhibitor; activates NLRP1b inflammasome | ||
| 6759 | AA 147 | Feb 2019 |
| ER proteostasis regulator | ||
| 6597 | SPRi 3 | Feb 2019 |
| Potent sepiapterin reductase (SPR) inhibitor; attenuates proliferation of CD4+ T cells | ||
| 6719 | YH 239-EE | Feb 2019 |
| Promotes survival of muscle stem cells (MuSCs); MDM2 inhibitor; activates p53 activity | ||
| 6793 | Dasatinib | Feb 2019 |
| Highly potent pan-Src/Bcr-Abl inhibitor | ||
| 6659 | sBADA | Feb 2019 |
| Green fluorescent D-amino acid for labeling peptidoglycans in bacteria | ||
| 6705 | Diminazene aceturate | Feb 2019 |
| ASIC blocker; antihyperalgesic | ||
| 6577 | Pyridone 6 | Feb 2019 |
| Potent pan-JAK inhibitor; induces intermediate mesoderm; cell-permeable | ||
| 6566 | STAD 2 | Feb 2019 |
| AKAP disruptor; selectively binds PKA-RII and blocks its interaction with AKAP; cell permeable | ||
| 6567 | RI-STAD 2 | Feb 2019 |
| AKAP disruptor; selectively binds PKA-RI with high affinity and blocks its interaction with AKAP; cell permeable | ||
| 6695 | CHIR 98014 | Feb 2019 |
| Highly potent and selective GSK-3 inhibitor | ||
| 6535 | NVP 2 | Feb 2019 |
| Potent and selective ATP-competitive CDK9 inhibitor | ||
| 6470 | A 410099.1 | Feb 2019 |
| High affinity XIAP antagonist; active in vivo | ||
| 6621 | TFAX 488, TFP | Jan 2019 |
| Green fluorescent dye; amine reactive | ||
| 6715 | A 71915 | Jan 2019 |
| Highly potent and competitive NPRA antagonist | ||
| 6644 | KuWal151 | Jan 2019 |
| Potent and selective CLK inhibitor | ||
| 6668 | ML 184 | Jan 2019 |
| Selective GPR55 agonist; also promotes NSC proliferation and differentiation | ||
| 6245 | SM 16 | Jan 2019 |
| Potent TGF-βRI inhibitor; orally bioavailable | ||
| 6777 | TAK 375 | Jan 2019 |
| Very high affinity and selective melatonin receptor agonist | ||
| 6698 | ELA-11 (human) | Jan 2019 |
| High affinity apelin agonist | ||
| 6697 | ELA-21 (human) | Jan 2019 |
| High affinity apelin agonist | ||
| 6788 | Quizartinib | Jan 2019 |
| Highly potent FLT3 inhibitor | ||
| 6774 | 16673-34-0 NLRP3i | Jan 2019 |
| NLRP3 inflammasome inhibitor | ||
| 6726 | T-peptide | Jan 2019 |
| Cytotoxic Tau peptide; cell permeable | ||
| 6709 | GSK 2018682 | Jan 2019 |
| S1P1 and S1P5 agonist | ||
| 6607 | dTRIM 24 | Jan 2019 |
| TRIM24 degrading PROTAC | ||
| 6553 | JF-NP-26 | Jan 2019 |
| Caged Raseglurant (Cat. No. 4416) | ||
| 6334 | THDOC | Jan 2019 |
| Positive modulator of GABAA receptors; endogenous neurosteroid | ||
| 5984 | LY 2955303 | Jan 2019 |
| High affinity and selective RARγ antagonist | ||
| 6606 | dBRD9 | Jan 2019 |
| Potent and selective BRD9 degrading PROTAC | ||
| 6598 | OD 36 hydrochloride | Jan 2019 |
| Potent RIP2 kinase inhibitor | ||
| 6243 | ML 385 | Jan 2019 |
| Nrf2 inhibitor; phenotypically lethal | ||
| 6686 | Thalidomide - linker 5 | Jan 2019 |
| Thalidomide-PEG2-alkyne | ||
| 6683 | VH 032, propargyl | Jan 2019 |
| Alkyne-functionalized VH 032; 'click' VHL ligand for PROTACs | ||
| 6689 | GI 530159 | Jan 2019 |
| TREK1 and TREK2 channel activator | ||
| 6352 | (S)-ZINC 3573 | Jan 2019 |
| Negative control for (R)-ZINC 3573 | ||
| 6681 | Pomalidomide - linker 2 | Jan 2019 |
| Pomalidomide-PEG3-carboxylic acid | ||
| 6685 | Thalidomide, propargyl | Jan 2019 |
| Alkyne-functionalized Thalidomide; 'click' cereblon ligand for PROTACs | ||
| 6682 | Pomalidomide - linker 3 | Jan 2019 |
| Pomalidomide-alkylC5-carboxylic acid | ||
| 6680 | VH 032 - linker 5 | Jan 2019 |
| VH 032-alkylC4-terminal carboxylic acid | ||
| 6699 | [D-Ala2]-GIP (human) | Jan 2019 |
| Highly potent GIP agonist | ||
| 6684 | VH 032 - linker 6 | Jan 2019 |
| VH 032-PEG2-alkyne | ||
| 6541 | AZD 2098 | Jan 2019 |
| Potent and selective CCR4 antagonist | ||
| 6369 | GNE 9278 | Jan 2019 |
| Positive allosteric modulator of NMDA receptors; acts in transmembrane domain | ||
| 6351 | (R)-ZINC 3573 | Jan 2019 |
| MRGPRX2 agonist | ||
| 6340 | Epiblastin A | Jan 2019 |
| CK1 inhibitor; converts epiblast stem cells to ESCs and promotes ESC self-renewal | ||
| 6742 | Acetazolamide | Dec 2018 |
| Carbonic anhydrase inhibitor | ||
| 6582 | D-3 | Dec 2018 |
| Selective PSC eliminating agent | ||
| 6488 | 5(6)-SFX (Fluorescein), SE | Dec 2018 |
| Green fluorescent dye for the labeling of primary amines | ||
| 6712 | A 77-01 | Dec 2018 |
| Potent inhibitor of TGF-βRI | ||
| 6618 | MB 05032 | Dec 2018 |
| Potent FBPase inhibitor; promotes HSC expansion | ||
| 6590 | Janelia Fluor® 646, Maleimide | Dec 2018 |
| Red fluorescent dye, supplied with a maleimide reactive group | ||
| 6530 | R 121919 hydrochloride | Dec 2018 |
| High affinity CRF1 antagonist; orally bioavailable | ||
| 6587 | TAK 242 | Dec 2018 |
| TLR4 signaling inhibitor | ||
| 6579 | BAY 826 | Dec 2018 |
| Potent Tie2 inhibitor | ||
| 6710 | Darunavir | Dec 2018 |
| Highly potent HIV protease inhibitor | ||
| 6625 | TFAX 594, SE | Dec 2018 |
| Red fluorescent dye; amine reactive | ||
| 6622 | Phalloidin-TFAX 488 | Dec 2018 |
| Green fluorescent cytoskeletal stain; binds F-actin | ||
| 6624 | TFAX 568, SE | Dec 2018 |
| Orange fluorescent dye; amine reactive | ||
| TB4423-GMP | CHIR 99021 | Dec 2018 |
| CHIR 99021 synthesized to cGMP guidelines | ||
| 5497 | ent-LP 99 | Dec 2018 |
| Negative Control for LP 99 | ||
| 5782 | Phalloidin-FITC | Dec 2018 |
| Green fluorescent cytoskeleton stain | ||
| 5783 | Phalloidin-TRITC | Dec 2018 |
| Red-orange fluorescent cytoskeleton stain | ||
| 6279 | JNJ 39758979 dihydrochloride | Dec 2018 |
| High affinity and selective histamine H4 receptor antagonist; orally bioavailable | ||
| 6652 | NGI 1 | Dec 2018 |
| Oligosaccharyltransferase (OST) inhibitor; anti-flaviviral | ||
| 6676 | IC 261 | Dec 2018 |
| CK1 inhibitor; displays selectivity for CK1δ and CK1ε | ||
| 6654 | VAS 2870 | Dec 2018 |
| NADPH oxidase (Nox) inhibitor | ||
| 5496 | LP 99 | Dec 2018 |
| Selective BRD7 and BRD9 inhibitor | ||
| 6177 | AZ 13705339 | Dec 2018 |
| Highly potent PAK1 and PAK2 inhibitor | ||
| 6704 | Indo 1AM | Nov 2018 |
| Fluorescent Ca2+ indicator |