All ProductsDisplaying Products Alphabetically by Name (K)
| Cat. No. | Product Name / Activity |
|---|---|
| 4986 | K 02288 |
| Type 1 BMP receptor inhibitor | |
| 6789 | K 03861 |
| Potent CDK2 inhibitor | |
| 7338 | K 22 |
| Inhibits coronavirus RNA replication; impairs double membrane vesicle (DMV) formation | |
| 1683 | K 252a |
| Protein kinase inhibitor | |
| 2070 | K 41498 |
| Highly selective and potent CRF2 antagonist | |
| 3144 | K 114 |
| Amyloid fibril-specific fluorescent probe. Used for: amyloid fibril detection. Application: fluorescence microscopy, confocal microscopy | |
| 5114 | K34c |
| Potent and selective α5β1 integrin inhibitor | |
| 4660 | KB SRC 4 |
| Potent and selective c-Src inhibitor | |
| 1244 | KB-R7943 mesylate |
| Na+/Ca2+ exchange inhibitor (reverse mode) | |
| 4324 | KC7F2 |
| HIF-1α inhibitor; down-regulates HIF-1α protein synthesis | |
| 2748 | KF 38789 |
| Selective inhibitor of P-selectin-mediated cell adhesion | |
| 5260 | KG 5 |
| PDGFRβ, B-Raf, c-Raf, FLT3 and KIT inhibitor | |
| 3834 | KH 7 |
| Selective soluble adenylyl cyclase inhibitor | |
| 4888 | KHS 101 hydrochloride |
| Selective inducer of neuronal differentiation in hippocampal neural progenitors | |
| 6787 | KI-7 |
| Positive allosteric modulator of A2B receptors | |
| 6984 | KIN001-266 |
| Potent and selective Tpl2 (MAP3K8) inhibitor | |
| 5306 | KJ Pyr 9 |
| High affinity Myc inhibitor | |
| 4685 | KL 001 |
| Cryptochrome protein stabilizer; lengthens circadian period | |
| 4872 | KML 29 |
| Highly potent and selective MAGL inhibitor | |
| 4130 | KN 92 |
| Inactive analog of KN 93. K+ channel (Kv) blocker | |
| 5215 | KN 93 phosphate |
| CaM kinase II inhibitor; water soluble version of KN 93 (Cat. No. 1278) | |
| 1277 | KN-62 |
| Non-competitive P2X7 antagonist | |
| 1278 | KN 93 |
| CaM kinase II inhibitor; also K+ channel blocker (KV) | |
| 5480 | KRIBB11 |
| HSF1 inhibitor | |
| 4169 | KS 176 |
| Selective BCRP inhibitor | |
| 6738 | KT 182 |
| Potent, selective and irreversible α/β-hydrolase domain 6 (ABHD6) inhibitor | |
| 1288 | KT 5720 |
| Selective protein kinase A inhibitor | |
| 1289 | KT 5823 |
| Selective protein kinase G inhibitor | |
| 4840 | KU 0060648 |
| Dual DNA-PK and PI 3-K inhibitor | |
| 3725 | KU 0063794 |
| Selective mTOR inhibitor | |
| 3544 | KU 55933 |
| Potent and selective ATM kinase inhibitor | |
| 4167 | KW 3902 |
| Selective A1 antagonist | |
| 4731 | KY 02111 |
| Inhibits canonical Wnt signaling. Promotes differentiation of human ESCs and iPSCs into cardiomyocytes | |
| 7002 | KYA 1797K |
| Wnt/β-catenin signaling inhibitor | |
| 5290 | KYL |
| EphA4 kinase inhibitor; neuroprotective | |
| 6272 | KYP 2047 |
| High affinity prolyl oligopeptidase inhibitor; anti-angiogenic, neuroprotective and brain penetrant | |
| 5026 | KYT 0353 |
| Potent and selective inhibitor of L-type amino acid transporter 1 (LAT1); active in vivo | |
| 3603 | Kaempferol |
| Proapoptotic; downregulates PLK1 expression and activates mitochondrial Ca2+ uniporter | |
| 7065 | Kainic acid (synthetic) |
| Kainate agonist; excitant and neurotoxin | |
| 4513 | Kartogenin |
| Potently induces chondrogenesis in MSCs | |
| 1398 | Kenpaullone |
| GSK-3β inhibitor; also inhibits cdks | |
| 3131 | Ketamine hydrochloride |
| Non-competitive NMDA receptor antagonist | |
| 6751 | (R)-(-)-Ketamine hydrochloride |
| NMDA antagonist; antidepressant; may not display psychotomimetic or addictive side effects of (S)-ketamine | |
| 4379 | (S)-(+)-Ketamine hydrochloride |
| NMDA receptor antagonist; enantiomer of ketamine hydrochloride (Cat. No. 3131); neuroprotective | |
| 0908 | Ketanserin tartrate |
| Selective 5-HT2A antagonist. Also antagonist at 5-HT1D | |
| 1103 | Ketoconazole |
| Cytochrome P450c17 inhibitor | |
| 5056 | Ki 16425 |
| LPA1 and LPA3 receptor antagonist | |
| 4481 | Ki 20227 |
| c-Fms inhibitor; suppresses osteolysis and osteoclast accumulation | |
| 2542 | Ki 8751 |
| Potent, selective VEGFR-2 inhibitor | |
| 3207 | Kifunensine |
| Inhibitor of class I α-mannosidases | |
| 6664 | Kinesore |
| Kinesin-1 modulator; cell permeable | |
| 2570 | Kisspeptin 10 (human) |
| Endogenous ligand for kisspeptin receptor | |
| 4243 | Kisspeptin 10 (rat) |
| Endogenous ligand for kisspeptin receptor | |
| 3881 | Kisspeptin 234 |
| Kisspeptin receptor antagonist; kisspeptin 10 (Cat. No. 2570) analog | |
| 7830 | Klotho-derived peptide 1 |
| TGF-β receptor 2 (TβR2) binding peptide; disrupts the TGF-β/TβR2 interaction | |
| 7847 | Klotho-derived peptide 6 |
| Wnt/β-catenin signaling inhibitor | |
| 3241 | Ko 143 |
| Potent and selective BCRP inhibitor | |
| 0223 | Kynurenic acid |
| Broad spectrum glutamatergic antagonist | |
| 3694 | Kynurenic acid sodium salt |
| Sodium salt of kynurenic acid (Cat. No. 0223) | |
| 7419 | Kyoto Probe-1 |
| Fluorescent probe that selectively identifies undifferentiated iPS/ES cells |
Tocris Products by Catalog Number
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