Radiochemical Catalog

Radiochemical Catalog

RC Tritec, an expert in tritium-labeling, provides high-quality tritium-labeled radiochemicals, suitable for your research, such as metabolic studies, mechanistic studies or high throughput screenings. The catalog is based on our knowledge and our constant efforts to ensure a high level of scientific research.

Our long-standing experience in tritium-labeling enables us to provide premium quality labeled radiochemicals. We guarantee a reliable biological activity as well as reproducible results. Always. RC Tritec is your partner of choice in tritium-labeling and our scientists have selected a variety of molecules, from tritiated water to complex natural products to help you with your research and addressing critical questions. Our catalog relies on actual hot topics in research and will be constantly updated. Upon your request, we are willing to include your tritium-labeled compound into our catalog to ensure a constant supply of your high quality radioligand.

Please have a look into our catalog whether your desired compound is available. Alternatively, tritium-custom synthesis is possible. We will be very pleased to help and convince you with our various labeling strategies.

All compounds are purified by HPLC and are provided together with a Certificate of Analysis and a stability declaration. We provide a fast and safe world-wide delivery of our compounds to your laboratory.

List of catalog radiochemicals available at RC TRITEC (OVERVIEW)

[H-3]Gamma-AMINOBUTYRIC ACID (GABA)

Ligand of GABA(A), GABA(B) Receptors and GABA Transporters.

[H-3](+)-MK-801

Potent noncompetitive antagonist of the NMDA receptor.

[H-3]1,3-DI-O-TOLYLGUANIDINE (DTG)

Sigma receptor agonist with neuroprotective and antidepressant effects.

[H-3]4-DAMP IODIDE

Selective M₃ muscarinic acetylcholine receptor (mAChR) antagonist.

[H-3]7-OH-DPAT

Selective agonist at the dopamine D₃ receptor.

[H-3]8-OH-DPAT

Serotonin receptor agonist specific for the 5-HT_1A and 5-HT₇ receptors, and serotonin reuptake inhibitor.

[H-3]ACETIC ACID SODIUM SALT

Acetylation reagent.

[H-3]AF-DX 384

Potent muscarinic M₂/M₄ selective antagonist (acetylcholine receptor).

[H-3]Alpha-Estradiol

Weak agonist of nuclear estrogen receptors

[H-3]ATAZANAVIR

Azapeptide and HIV-protease inhibitor. Antiviral.

[H-3]ATORVASTATIN, CALCIUM SALT

A selective, competitive HMG-CoA reductase inhibitor.

[H-3]ATOVAQUONE

Antiprotozoal, antimalarial agent, inhibitor of STAT3 (antipneumocystic).

[H-3]BATRACHOTOXININ A, 20-ALPHA-BENZOATE

Sodium channel agonist and extremely potent cardiotoxic and neurotoxic steroidal alkaloids.

[H-3]BBAC

Dual antagonist of OX1R, OX2R and TCS 1102.

[H-3]Beta-Estradiol

Agonist of the estrogen receptor (ER), a nuclear steroid hormone receptor.

[H-3]BICTEGRAVIR

Potent inhibitor of HIV-1 integrase and antiviral agent.

[H-3]BMS-955176

HIV maturation inhibitor and preventor of viral reproduction in host CD4+ T cells.

[H-3]BRADYKININ

Potent endothelium-dependent vasodilator and mild diuretic.

[H-3]BRADYKININ-(LYS-DES-ARG9)

Specific Bradykinin B₁ antagonist.

[H-3]Brodifacoum

4-hydroxycoumarin vitamin K antagonist anticoagulant poison.

[H-3]CIS-(+)-DILTIAZEM

Potent calcium channel blocker and antihypertensive.

[H-3]CELECOXIB

Selective cyclooxygenase-2 (COX-2) inhibitor and a nonsteroidal anti-inflammatory drug (NSAID).

[H-3]CITALOPRAM

Selective serotonin reuptake inhibitor (SSRI).

[H-3]CLOMIPRAMINE

Serotonin, norepinephrine and dopamine transporter blocker.

[H-3]COLCHICINE

Glycine receptor antagonists, antimitotic agent and stimulant of intrinsic GTPase activity of tubulin.

[H-3]Cyclic adenosine monophosphate

Second messenger for intracellular signal transduction

[H-3]Cyclic guanosine monophosphate

Regulator of and secondary messenger for various cellular processes.

[H-3]CYTISINE

Toxic priniciple in seed of Laburnum anagyroides and other Leguminosae. A neuronal nicotinic acetylcholine agonist.

[H-3]DAMGO

Synthetic opioid peptide, synthetic opioid analog with high specificity for the μ-opioid receptor.

[H-3]D/L-2,5-DIMETHOXY-4-IODOAMPHETAMINE HYDROCHLORIDE

5-HT_2A/2C agonist and hallucinogenic agent.

[H-3]D/L-ROSIGLITAZONE

Insulin sensitizer (antidiabetic drug).

[H-3]DARUNAVIR

HIV-1-protease inhibitor.

[H-3]Difenacoum

Anti-coagulant of the 4-hydroxycoumarin vitamin K antagonist type.

[H-3]DIGOXIN

Unselective Na⁺/K⁺-ATPase inhibitor.

[H-3]DEXAMETHASONE

Anti-inflammatory agent.

[H-3]DOFETILIDE

Potassium channel blocker and antidysrhythmic drug.

[H-3]DOLUTEGRAVIR

HIV integrase inhibitor.

[H-3]DOPAMINE

Binding affinity at dopamine receptors and at hTAAR₁, DAT and VMAT2.

[H-3]DPA-714

TSPO radioligand and selective ligand for the translocator protein.

[H-3]DPCPX

Potent and very selective A₁-adenosine receptor antagonist.

[H-3]EMPA

Highly potent, selective and brain penetrable OX₂ antagonist.

[H-3]Epibatidine

Selective α4β2 nicotinic agonist.

[H-3]FALLYPRIDE

Selective dopamine D₂/D₃ receptor antagonist.

[H-3]FLUMAZENIL

GABA_A receptor antagonist, inhibitor at the benzodiazepine recognition site on the GABA/benzodiazepine receptor complex.

[H-3]FLUDROCORTISONE ACETATE

Powerful mineralocorticoid.

[H-3]GLIBENCLAMIDE

Inhibitor of the ATP-sensitive potassium channels (KATP).

[H-3]GR 113808

Potent, selective 5-HT4 antagonist.

[H-3]GR125743

Selective antagonist at serotonin 5-HT1B and 5-HT1D receptors.

[H-3]GSK1059865

Selective orexin/hypocretin receptor type 1 antagonist.

[H-3]ICI 118,551 HYDROCHLORIDE

Highly selective, potent β₂-adrenoceptor antagonist.

[H-3]IMIPRAMINE HYDROCHLORIDE

Blocker of norepinephrine, serotonin and dopamine D₂ transporters.

[H-3]INDOLE-3-ACETIC ACID

Plant growth regulator; Inducer of cell division and cell elongation.

[H-3]KALLIDIN, (DES-ARG10, LEU9)

Bradykinin B₁ selective antagonist.

[H-3]KETANSERIN HYDROCHLORIDE

Selective 5-HT_2A receptor antagonist with affinity for multiple GPCR receptors.

[H-3]L-655,708

Subtype-selective inverse agonist of the benzodiazepine binding site of the GABA_A receptor.

[H-3]LAURIC ACID

Saturated medium-chain fatty acid.

[H-3]Latanoprost

Selective agonist at the prostaglandine F receptor.

[H-3]LOPINAVIR

Selective HIV protease inhibitor. Antiviral. It is a COVID19-related research product.

[H-3]LY2119620

High-affinity M₂/M₄ receptor-selective positive allosteric modulator (PAM).

[H-3]LY 341495

Potent and selective orthosteric antagonist for the group II metabotropic glutamate receptors.

[H-3]LYSOPHOSPHATIDIC ACID, L-ALPHA-1-OLEOYL

Potent mitogen and a ligand activator for EDG-2, EDG-4, and EDG-7.

[H-3]MESULERGINE

Agonist of dopamine D2-like receptors and serotonin 5-HT6 receptors and an antagonist of serotonin 5-HT2A, 5-HT2B, 5-HT2C, and 5-HT7 receptors.

[H-3]METHYLSPIPERONE

Selective dopamine D₂ receptor antagonist and serotonin 5-HT2A receptor antagonist.

[H-3]MLN-4760

Potent and selective inhibitor of human angiotensin-converting enzyme 2 (ACE2).

[H-3]M-MPEP

Potent, subtype selective mGluR5 antagonist and negative allosteric modulator (NAM) ligand for the mGlu5 receptor.

[H-3]MONTELUKAST

Leukotriene receptor antagonist, inhibitor of the drug metabolizing enzyme CYP2C8.

[H-3]MPP⁺ ACETATE

Neurotoxin and inhibitor of a complex I in mitochondria.

[H-3]MUSCIMOL

Potent GABAA receptor agonist and partial GABAA-ρ receptor agonist.

[H-3]N-acetylneuraminic acid

Predominant sialic acid found in human cells.

[H-3]NECA

Potent, non-selective adenosine receptor agonist.

[H-3]Naltrexone

Selective antagonist of the µ-opioid receptor.

[H-3]NALTRINDOLE HYDROCHLORIDE

Highly selective delta opioid (DOR) receptor antagonist.

[H-3]9-CIS RETINOIC ACID

Antagonist of the serotonin 5-HT_1A receptor.

[H-3]NICOTINAMIDE

Dietary supplement.

[H-3]NISOXETINE HYDROCHLORIDE

Selective and potent inhibitor of norepinephrine transporter.

[H-3]NITRENDIPINE

L-type calcium channel blocker.

[H-3]NNC-112

Selective and highly potent dopamine D₁ receptor antagonist.

[H-3]NOCICEPTIN

Neuropeptide and endogenous ligand of the N/OFQ peptide receptor (NOP, ORL-1).

[H-3]NOREPINEPHRINE

Neurotransmitter, binds and activates adrenergic receptors.

[H-3]N-SUCCINIMIDYL PROPIONATE

Labeling reagent for proteins and antibodies.

[H-3]OUABAIN

Unselective Na⁺/K⁺-ATPase inhibitor.

[H-3]PAROXETIN

Selective serotonin reuptake inhibitor (SSRI) antidepressant.

[H-3]PBR28

Translocator protein (TSPO) ligand.

[H-3]Pergafast 201

Endocrine disrupting chemical interfering and preventing the binding of natural hormones to their receptors.

[H-3]PIRENZEPINE

M₁ selective antagonist and selective muscarinic acetylcholine receptor.

[H-3]PK 11195

High affinity peripheral benzodiazepine receptor (PBR) ligand and membrane-ATPase blocker.

[H-3]PLATELET ACTIVATING FACTOR C18

Potent leukocyte functions modulator.

[H-3]R/S-Nicotine

Receptor agonist for most nicotinic acetylcholine receptors

[H-3]RACLOPRIDE

Selective antagonist of the dopamine D₂ receptor.

[H-3]RETINOIC ACID, ALL TRANS

Activator of retinoic acid receptors.

[H-3]RITONAVIR

Selective HIV protease inhibitor.

[H-3]RX 821002

Selective α2-adrenoceptor antagonist.

[H-3]SAREDUTANT

Neurokinin-2 antagonist.

[H-3]SB 269970

Potent and selective 5-HT₇ receptor antagonist.

[H-3]SB 674042

Potent and selective non-peptide orexin OX₁ receptor antagonist.

[H-3]SCH 23390

Dopamine D₁ and D₅ receptor antagonist.

[H-3]SCOPOLAMINE METHYL CHLORIDE

Antagonist of muscarinic acetylcholine receptors.

[H-3]SERTINDOLE

Activity at dopamine and serotonin receptors with high affinity to D2, 5-HT2 and α1 receptors.

[H-3]SIL26

α-Synuclein ligand.

[H-3]6-OH-BTA-1

Used clinically as treatment for spinocerebellar degradation

[H-3]SN-38

Antineoplastic agent, metabolite of Irinotecan, a DNA topoisomerase inhibitor.

[H-3]SODIUM TETRAHYDROBORATE

Reducing agent.

[H-3]SPIPERONE

Dopamine D_2/3 receptor, 5-HT_1A/2A and alpha-adrenergic receptor antagonist.

[H-3]SR 141716A

Potent and selective agonist of the cannabinoid receptor CB₁.

[H-3]SUBSTANCE P

Neuropeptide, neurotransmitter and neuromodulator, ligand for neurokinin 1 receptor.

[H-3]SynVesT-1

PET radiotracer for the imaging of Synaptic Vesicle Glycoprotein 2A (SV2A).

[H-3]T0901317

Potent and selective agonist for both liver X receptor (LXR) and farnesoid X receptor (FXR).

[H-3]T-807

Novel tau positron emission tomography (PET) tracer.

[H-3]TAMOXIFEN

Antineoplastic nonsteroidal selective estrogen receptor modulator (SERM).

[H-3]TEMSAVIR

Potent HIV-1 attachment inhibitor.

[H-3]TENOFOVIR ALAFENAMIDE

Reverse transcriptase inhibitor.

[H-3]Thyrotropin Releasing Hormone

Used clinically as treatment for spinocerebellar degradation

[H-3]TIAGABINE

GABA reuptake inhibitor (GRI).

[H-3]TOLCAPONE

Selective, potent and reversible nitrocatechol-type inhibitor of the enzyme catechol-O-methyltransferase (COMT).

[H-3]Troglitazone

Activator of peroxisome proliferator-activated receptors (PPARs).

[H-3]L-Tyrosine

Non-essential proteinogenic amino acid involved in signal transduction as receiver of phosphate groups.

[H-3]UCB-J

Synaptic density marker, binds to vesicle glycoprotein 2_A (SV2A).

[H-3]Vasopressin

Regulator of body fluid tonicity

[H-3]WAY100635

Antagonist of the serotonin 5-HT_1A receptor.

[H-3]WB-4101

Antagonist at the α_1B-adrenergic receptor.

Our website uses cookies so that we can continually improve the page and provide you with an optimized visitor experience. If you continue reading this website, you agree to the use of cookies.
Further information regarding cookies can be found in the disclaimer.

If you want to prevent the setting of cookies (for example, Google Analytics), you can set this up by using this browser add-on.