All ProductsDisplaying Products Alphabetically by Name (N)
| Cat. No. | Product Name / Activity |
|---|---|
| 7874 | N-Acetylcysteine |
| Glutathione (GSH) precursor; maintains stem cell function in culture. | |
| 7716 | N-methylated pomalidomide |
| Functionalized cereblon ligand for generating Degrader negative controls; also used as Pomalidomide negative control | |
| 3905 | NAADP tetrasodium salt |
| Ca2+ mobilizing agent | |
| 6648 | NADA-green |
| Fluorescent D-amino acid for labeling peptidoglycans in live bacteria | |
| 5515 | NADPH reduced form tetrasodium salt |
| Cofactor for many anabolic enzymes | |
| 7004 | NAI |
| Reagent for RNA SHAPE-MaP experiments in vivo; cell permeable | |
| 0665 | L-NAME hydrochloride |
| Non-selective NOS inhibitor | |
| 7842 | NAMPT PROTAC® A7 |
| Potent and selective nicotinamide phosphoribosyl transferase (NAMPT) Degrader (PROTAC®) | |
| 0553 | NAN-190 hydrobromide |
| 5-HT1A antagonist | |
| 5986 | NAV 2729 |
| Selective ARF6 inhibitor | |
| 7538 | NBD-PE |
| Green-fluorescent label for lysosomal lipid bodies. Used for: Application: confocal microscopy | |
| 6065 | 2-NBDG |
| Fluorescent glucose uptake indicator | |
| 1591 | NBI 27914 hydrochloride |
| Selective non-peptide CRF1 antagonist | |
| 5192 | NBI 31772 |
| High affinity insulin-like growth factor-I binding protein IGFBP inhibitor | |
| 3100 | NBI 35965 hydrochloride |
| Potent and selective CRF1 antagonist | |
| 4528 | (±)-NBI 74330 |
| Potent and selective CXCR3 antagonist | |
| 2924 | NBMPR |
| Equilibrative nucleoside transporter 1 (ENT1) inhibitor | |
| 5171 | NBOH-2C-CN hydrochloride |
| High affinity and selective 5-HT2A agonist | |
| 0373 | NBQX |
| Potent AMPA antagonist; more selective than CNQX (Cat. No. 0190) | |
| 1044 | NBQX disodium salt |
| Potent AMPA antagonist; more water soluble form of NBQX (Cat. No. 0373) | |
| 5150 | NCL 00017509 |
| Potent and reversible NIMA related kinase 2 (Nek2) inhibitor | |
| 7551 | NCT 02 |
| Molecular glue; induces degradation of CCNK and CDK12 | |
| 5934 | NCT 501 hydrochloride |
| Potent and selective ALDH1A1 inhibitor | |
| 7388 | ND1-YL2 |
| SRC-1 peptide-based Degrader (PROTAC®); active in vivo | |
| 7808 | NDT 30805 |
| Potent NLRP3 inflammasome inhibitor | |
| 3333 | NDT 9513727 |
| Potent, selective human C5a receptor negative allosteric modulator (NAM) | |
| 3133 | NE 100 hydrochloride |
| Selective σ1 antagonist | |
| 1691 | NECA |
| High affinity adenosine agonist | |
| 5746 | NESS 0327 |
| Ultra-high affinity and selective CB1 antagonist | |
| 1240 | NF 023 |
| Selective and competitive P2X1 antagonist | |
| 2548 | NF 110 |
| Potent P2X3 antagonist | |
| 2450 | NF 157 |
| Selective P2Y11 and P2X1 antagonist | |
| 1199 | NF 279 |
| Potent and selective P2X1 antagonist | |
| 1391 | NF 449 |
| Highly selective P2X1 antagonist | |
| 3892 | NF 546 |
| Selective P2Y11 agonist | |
| 3930 | NFAT Inhibitor |
| Inhibitor of calcineurin-mediated NFAT activation | |
| 5710 | NFAT inhibitor, Cell Permeable |
| Cell permeable NFAT inhibitor | |
| 5429 | NG 25 |
| TGF-β-activated kinase (TAK1) inhibitor | |
| 2635 | NGB 2904 |
| Potent and selective D3 antagonist | |
| 6652 | NGI 1 |
| Oligosaccharyltransferase (OST) inhibitor; anti-flaviviral | |
| 3439 | NH 125 |
| CaM kinase III (eEF-2 kinase) inhibitor | |
| 5363 | NHI 2 |
| LDHA inhibitor | |
| 5546 | NI 57 |
| Potent and selective BRPF bromodomain inhibitor | |
| 8175 | NIBR LTSi |
| Potent and selective LATS inhibitor; activates YAP signaling | |
| 8088 | NICE 01 |
| Heterobifunctional compound for nuclear import of FKBPF36V tagged proteins | |
| 7136 | NIKi |
| Potent NIK inhibitor | |
| 0546 | L-NIO dihydrochloride |
| NOS inhibitor | |
| 7626 | NIR Dye s775z, NHS |
| Bright and photostable non-aggregating near-IR cyanine dye (Reactive group: NHS ester). Suitable for in vivo imaging | |
| 6045 | NITD 008 |
| Antiflaviviral; active against Zika, Dengue and Hepatitis C viruses | |
| 5293 | NK 252 |
| Nrf2 activator | |
| 1603 | NKH 477 |
| Water-soluble adenylyl cyclase activator | |
| 5071 | NKY 80 |
| Adenylyl cyclase inhibitor | |
| 6531 | NLS-StAx-h |
| Wnt signaling inhibitor; inhibits β-catenin-transcription factor interactions | |
| 0114 | NMDA |
| Selective NMDA agonist | |
| 6180 | NMS 873 |
| Potent and selective p97 ATPase (VCP) allosteric inhibitor | |
| 6807 | NNC 0640 |
| Negative allosteric modulator of glucagon and GLP-1 receptors | |
| 2440 | NNC 26-9100 |
| Selective sst4 agonist | |
| 2268 | NNC 55-0396 dihydrochloride |
| Highly selective CaV3.x blocker | |
| 1779 | NNC 711 |
| Selective GAT-1 inhibitor | |
| 6900 | NNMTi |
| Nicotinamide N-methyltransferase (NNMT) inhibitor; promotes myoblast differentiation | |
| 3512 | NPE-caged-proton |
| Caged proton | |
| 0593 | NPPB |
| Inhibits calcium-sensitive chloride currents | |
| 3626 | NPS 2143 hydrochloride |
| Selective calcium-sensing receptor (CaSR) antagonist; orally active calcilytic agent | |
| 4134 | NPS 2390 |
| Group I mGlu antagonist | |
| 7572 | NR 162 |
| Potent and selective calcium/calmodulin-dependent serine protein kinase (CASK) inhibitor | |
| 7177 | NR 7h |
| Potent and selective p38α and p38β Degrader (PROTAC®); active in vivo | |
| 7509 | NR12S |
| Fluorogenic lipid membrane dye. Used for: staining lipid at the outer leaflet of vesicles and cell membranes, suitable for live cell imaging. Application: fluorescence microscopy | |
| 7990 | NRX 252114 |
| Molecular glue Degrader of mutant β-catenin | |
| 4788 | NS 11021 |
| KCa1.1 (BK) channel activator | |
| 3804 | NS 1619 |
| KCa1.1 (BK) channel activator | |
| 3062 | NS 1643 |
| KV11.1 (hERG) channel activator; antiarrhythmic | |
| 2995 | NS 1738 |
| Positive allosteric modulator of α7 nAChRs; active in vivo | |
| 5276 | NS 19504 |
| KCa1.1 (BK) channel activator | |
| 4517 | NS 2028 |
| Potent soluble guanylyl cyclase (sGC) inhibitor | |
| 3895 | NS 309 |
| Positive modulator of KCa2 (SK) and KCa3.1 (IK) channels | |
| 4462 | NS 3623 |
| KV11.1 (hERG) and KV4.3 channel activator; antiarrhythmic | |
| 6973 | NS 3728 |
| VRAC blocker | |
| 4831 | NS 3861 |
| α3β2 full agonist; also α3β4 partial agonist | |
| 0942 | NS 398 |
| Cyclooxygenase-2 (COX-2) inhibitor | |
| 4166 | NS 5806 |
| KV4.3 channel activator | |
| 4597 | NS 8593 hydrochloride |
| Selective negative modulator of KCa2 (SK) channels; inhibits SK currents | |
| 5112 | NS 9283 |
| Positive allosteric modulator of α4β2 nAChRs | |
| 2161 | NSC 23766 |
| Selective inhibitor of Rac1-GEF interaction; antioncogenic | |
| 4902 | NSC 405020 |
| Histone deacetylase inhibitor | |
| 5340 | NSC 617145 |
| Werner syndrome helicase (WRN) inhibitor | |
| 4993 | NSC 624206 |
| Ubiquitin-activating enzyme (E1) inhibitor | |
| 5287 | NSC 636819 |
| KDM4A/KDM4B inhibitor | |
| 5813 | NSC 668036 |
| Wnt signaling inhibitor; binds the PDZ domain of the Dishevelled (Dvl) protein | |
| 4655 | NSC 74859 |
| Selective STAT3 inhibitor | |
| 5438 | NTRC 824 |
| Potent and selective non-peptide NTS2 antagonist | |
| 3301 | NU 6140 |
| Cdk2 inhibitor; also potent inhibitor of aurora kinase A and B | |
| 3712 | NU 7441 |
| Potent and selective DNA-PK inhibitor | |
| 4903 | NU 9056 |
| Inhibitor of KAT5 (Tip60) | |
| 6535 | NVP 2 |
| Potent and selective ATP-competitive CDK9 inhibitor | |
| 3960 | NVP 231 |
| Potent, selective and reversible CerK inhibitor | |
| 5247 | NVP ADW 742 |
| ATP-competitive inhibitor of IGF1R | |
| 7482 | NVS MLLT-1 |
| Selective MLLT1/3 inhibitor | |
| 6132 | NVS PAK1 1 |
| Potent and selective PAK1 inhibitor | |
| 6133 | NVS PAK1 C |
| Negative control of NVS PAK1 1 (Cat. No. 6132) | |
| 5744 | NVS-CECR2-1 |
| Potent and selective CECR2 inhibitor | |
| 8120 | NVS-STG2 |
| STING agonist, molecular glue that causes oligomerization of STING | |
| 8950 | NX 1607 New |
| CBL-B intramolecular glue inhibitor | |
| 8951 | NX 2127 New |
| Potent BTK Degrader (PROTAC®) | |
| 8856 | NX 5948 |
| Potent and selective BTK Degrader (PROTAC®) | |
| 3081 | Nafamostat mesylate |
| Serine protease inhibitor; inhibits tryptase | |
| 4085 | Nalmefene hydrochloride |
| Opioid receptor antagonist | |
| 0599 | Naloxone hydrochloride |
| Non-selective opioid antagonist | |
| 0677 | Naltrexone hydrochloride |
| Non-selective opioid antagonist | |
| 5522 | Napabucasin |
| STAT3 inhibitor; also blocks cancer stem cell self-renewal | |
| 3063 | 1-Naphthyl PP1 |
| Src family kinase inhibitor; also inhibits c-Abl | |
| 3715 | Narciclasine |
| Stimulates RhoA activation; antiproliferative agent that slows cell cycle progression | |
| 2766 | Naspm trihydrochloride |
| Ca2+-permeable AMPA antagonist | |
| 4231 | Nateglinide |
| Kir6 (KATP) blocker; displays high affinity for SUR1/Kir6.2 channels | |
| 3517 | Nebivolol hydrochloride |
| Highly selective β1-adrenoceptor antagonist | |
| 2324 | Necrostatin-1 |
| RIP1 kinase inhibitor; inhibits necroptosis | |
| 5025 | Necrosulfonamide |
| Necroptosis inhibitor; also inhibits pyroptosis | |
| 3954 | trans-Ned 19 |
| NAADP antagonist; inhibits Ca2+ release | |
| 2851 | Nefiracetam |
| Cognitive enhancer | |
| 6359 | Nelarabine |
| Purine nuceloside analog; inhibits DNA synthesis | |
| 3766 | Nelfinavir mesylate |
| Potent HIV-1 protease inhibitor | |
| 1746 | Nemonapride |
| Highly potent D2-like antagonist; also 5-HT1A agonist | |
| 5037 | Nepicastat hydrochloride |
| Potent and selective dopamine β-hydroxylase (DBH) inhibitor; orally bioavailable | |
| 7371 | Neratinib |
| Potent HER2 receptor tyrosine kinase and EGFR kinase inhibitor | |
| 1582 | Neurokinin B (human, porcine) |
| Endogenous tachykinin peptide | |
| 3137 | Neuropeptide FF |
| Endogenous NPFF1 and NPFF2 agonist; also MRGPRA agonist | |
| 5857 | Neuropeptide S (Mouse) |
| Endogenous Neuropeptide S receptor agonist | |
| 1153 | Neuropeptide Y (human, rat) |
| Influences feeding and sexual behavior | |
| 1176 | [Leu31,Pro34]-Neuropeptide Y (human, rat) |
| NPY Y1 receptor agonist | |
| 1909 | Neurotensin |
| Endogenous neurotransmitter and endocrine modulator | |
| 6089 | Nexinhib20 |
| Rab27 inhibitor; inhibits neutrophil exocytosis; active in vivo | |
| 4079 | Niclosamide |
| STAT3 inhibitor; also inhibits mTORC1 signaling | |
| 4106 | Nicotinamide |
| PARP-1 inhibitor | |
| 6018 | Nicotinamide Riboside |
| NAD+ precursor; substrate for nicotinamide riboside kinases | |
| TB4106-RMU | Nicotinamide |
| Nicotinamide synthesized to Ancillary Material Grade | |
| 3546 | (-)-Nicotine ditartrate |
| Prototypical nAChR agonist | |
| 1075 | Nifedipine |
| CaV1.x blocker | |
| 4312 | Nigericin sodium salt |
| Selective K+ ionophore | |
| 7387 | Nile Red |
| Fluorogenic lipid membrane dye. Used for: intracellular lipid droplets and neutral lipids staining, suitable for live cell imaging. Application: fluorescence microscopy | |
| 7289 | Nimbolide |
| RNF114 inhibitor | |
| 0600 | Nimodipine |
| CaV1.x blocker | |
| 7049 | Nintedanib |
| Potent VEGFR, PDGFR and FGFR inhibitor | |
| 1025 | Nisoxetine hydrochloride |
| Noradrenalin re-uptake inhibitor | |
| 7234 | Nitazoxanide |
| Pyruvate flavodoxin/ferredoxin oxidoreductase inhibitor; also inhibits Wnt signaling; broad spectrum anti-infective | |
| 0910 | Nociceptin |
| Endogenous NOP agonist | |
| 1228 | Nocodazole |
| Microtubule inhibitor | |
| 1992 | Nomifensine |
| Potent noradrenalin and dopamine uptake inhibitor. Antidepressant | |
| 3691 | N-Nonyldeoxynojirimycin |
| Glucosidase inhibitor | |
| 6370 | Nor NOHA monoacetate |
| Arginase inhibitor | |
| 5169 | Noradrenaline bitartrate |
| Endogenous adrenergic hormone and neurotransmitter | |
| 1970 | Norketamine hydrochloride |
| Potent non-competitive NMDA antagonist; antinociceptive | |
| 5996 | (R)-Norketamine hydrochloride |
| NMDA receptor modulator; analgesic | |
| 6112 | (S)-Norketamine hydrochloride |
| NMDA receptor modulator; analgesic | |
| 8935 | NucleoLIVE™ Non-Toxic Dye New |
| Ready-to-use fluorescent nuclear stain for live cell imaging, cell toxicity, viability and morphology of 2D and 3D cell cultures | |
| 3984 | Nutlin-3 |
| MDM2 antagonist; inhibits MDM2-p53 interaction | |
| 6075 | Nutlin 3a |
| MDM2 antagonist; active enantiomer of Nutlin-3 (Cat. No. 3984) |
Tocris Products by Catalog Number
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