All ProductsDisplaying Products Alphabetically by Name (H)
| Cat. No. | Product Name / Activity |
|---|---|
| 2414 | H 1152 dihydrochloride |
| Selective Rho-kinase (ROCK) inhibitor | |
| 2485 | Glycyl-H 1152 dihydrochloride |
| Selective Rho-kinase (ROCK) inhibitor. More selective analog of H 1152 dihydrochloride (Cat. No. 2414) | |
| 6675 | H 151 |
| STING antagonist | |
| 2910 | H 89 dihydrochloride |
| Protein kinase A inhibitor | |
| 5935 | H2DCFDA |
| Fluorescent ROS indicator; cell permeable | |
| 0542 | H-7 dihydrochloride |
| Protein kinase inhibitor | |
| 4196 | HA 130 |
| Potent and selective autotaxin inhibitor | |
| 0281 | (R)-(+)-HA-966 |
| NMDA partial agonist/antagonist; acts at glycine site | |
| 6647 | HADA |
| Blue fluorescent D-amino acid for labeling peptidoglycans in live bacteria | |
| 8831 | HB-2-30 |
| Fluorescent TG2/LRP1 substrate for imaging endocytosis | |
| 7277 | HBC 530 |
| GFP fluorophore mimic for imaging RNA in live cells; activated by binding to Pepper aptamers; suitable for confocal and two-photon microscopy | |
| 4285 | HBX 41108 |
| Selective USP7 inhibitor | |
| 2896 | HC 030031 |
| Selective TRPA1 blocker | |
| 4100 | HC 067047 |
| Potent and selective TRPV4 antagonist | |
| 7882 | HDAC4 CHDI Degrader 11 |
| Potent and selective HDAC4 Degrader (PROTAC®) | |
| 0535 | HEAT hydrochloride |
| Highly selective α1 antagonist | |
| 1579 | HEMADO |
| High affinity selective A3 agonist | |
| 7940 | HEMTAC 26 |
| CDK6 and CDK4 HSP90-mediated targeting chimera (HEMTAC) Degrader | |
| 3173 | HEPES |
| Multipurpose HEPES buffer; used in cell culture | |
| 7886 | HER2 PROTAC® CH7C4 |
| Potent and selective HER2 targeting Degrader (PROTAC®) | |
| 7828 | HHP 9 |
| BET bromodomain Degrader (PROTAC®); also potent Hedgehog pathway inhibitor | |
| 5961 | HIOC |
| Selective TrkB receptor agonist; neuroprotectant | |
| 4844 | HJC 0350 |
| Selective Epac2 inhibitor | |
| 6110 | HJC 0416 hydrochloride |
| STAT3 inhibitor | |
| 3503 | HLI 373 |
| Hdm2 inhibitor; activates p53-dependent transcription | |
| 7312 | HM Janelia Fluor® 526, NHS ester |
| Fluorogenic spontaneously blinking yellow-emitting dye (Reactive group: NHS ester). Application: dSTORM, SMLSM, STED, SIM and confocal microscopy | |
| 5011 | HMR 1556 |
| Potent and selective Iks channel blocker | |
| 3014 | HOE 140 |
| Potent and selective B2 antagonist | |
| 3530 | HQL 79 |
| Human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor | |
| 1831 | HS 014 |
| Selective MC4 receptor antagonist | |
| 1832 | HS 024 |
| Highly potent MC4 receptor antagonist | |
| 5622 | HTH 01-015 |
| Potent and selective NUAK1 inhibitor | |
| 0646 | HTMT dimaleate |
| H1/ H2 agonist | |
| 3088 | HU 308 |
| Potent and selective CB2 agonist | |
| 3912 | HX 531 |
| Potent RXR antagonist | |
| 4991 | HaXS8 |
| Chemical dimerizer | |
| 1993 | Halofuginone hydrobromide |
| High affinity competitive prolyl-tRNA synthetase inhibitor | |
| 0931 | Haloperidol hydrochloride |
| Dopamine antagonist; displays some D2 selectivity | |
| 5075 | Harmine |
| Potent and selective DYRK1A inhibitor | |
| 5433 | Heclin |
| HECT E3 ubiquitin ligase inhibitor | |
| 3791 | Hemopressin (human, mouse) |
| Selective CB1 inverse agonist | |
| 2812 | Heparin sodium salt |
| Anticoagulant | |
| 3988 | Hesperadin hydrochloride |
| Potent Aurora kinase B inhibitor | |
| 7751 | 1-Hex-GlcNAlk |
| Metabolic chemical reporter for studying glycosylation and glycoproteins | |
| 7807 | Hh-Ag1.5 |
| Potent and high affinity Smo receptor agonist | |
| 3545 | Histamine dihydrochloride |
| Endogenous histamine receptor agonist | |
| 5117 | Hoechst 33342 |
| Blue-fluorescent dye for DNA staining. Cell permeable. Used for: nuclear counterstain, apoptosis analysis, fixed and live-cell staining. Application: flow cytometry, confocal microscopy | |
| 7313 | Hoechst Janelia Fluor® 526 |
| Fluorogenic, green-emitting DNA probe. Used for: fixed and live-cell imaging. Application: confocal microscopy, flow cytometry, super resolution microscopy (SRM) | |
| 6804 | Hoechst Janelia Fluor® 646 |
| Fluorogenic, red-emitting DNA probe. Used for: fixed and live-cell imaging. Application: confocal microscopy, super resolution microscopy (SRM) (PALM, PAINT), lattice light sheet microscopy | |
| 1416 | Homoharringtonine |
| Inhibitor of protein synthesis; antileukemic agent | |
| 4093 | Hydrocortisone |
| Adrenal glucocorticoid; immunosuppressant | |
| 5364 | Hydroxy Dynasore |
| Dynamin inhibitor; analog of dynasore (Cat. No. 2897) | |
| 0183 | L-(-)-threo-3-Hydroxyaspartic acid |
| Transportable EAAT1-4 inhibitor/non-transportable EAAT5 inhibitor | |
| 5648 | Hydroxychloroquine sulfate |
| Autophagy inhibitor; also TLR9 inhibitor | |
| 4474 | 20(S)-Hydroxycholesterol |
| Allosteric activator of Hedgehog (Hh) signaling; induces Smo accumulation | |
| 5741 | 25-Hydroxycholesterol |
| Inhibits hepatitis C viral life cycle; also α-crystallin (cryAB) chaperone | |
| 3907 | 27-Hydroxycholesterol |
| LXR agonist; also ER partial agonist | |
| 2547 | 6-Hydroxydopamine hydrobromide |
| Selective catecholaminergic neurotoxin | |
| 6124 | (R)-2-Hydroxyglutaric acid disodium salt |
| KDM4A inhibitor; also NF-κB activator | |
| 6122 | (RS)-2-Hydroxyglutaric acid disodium salt |
| Metabolite | |
| 6094 | 2R,6R-Hydroxynorketamine hydrochloride |
| Enhances AMPA currents; decreases D-serine (a NMDA co-agonist); lacks ketamine-related side effects | |
| 6095 | 2S,6S-Hydroxynorketamine hydrochloride |
| Decreases D-serine (a NMDA co-agonist); antidepressant | |
| 5982 | cis-6-Hydroxynorketamine hydrochloride |
| Enhances AMPA currents: antidepressant | |
| 0708 | 2-Hydroxypropyl-β-cyclodextrin |
| Solubilization agent | |
| 0245 | 2-Hydroxysaclofen |
| Selective GABAB antagonist; more potent than Saclofen (Cat. No. 0246) | |
| 3412 | (Z)-4-Hydroxytamoxifen |
| Metabolite of tamoxifen (Cat. No. 0999) | |
| 4137 | Hygromycin B |
| Aminoglycoside antibiotic; active against prokaryotic and eukaryotic cells | |
| 0208 | Hypotaurine |
| Non-selective endogenous glycine receptor agonist |
Tocris Products by Catalog Number
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