TPT-004

SKU:BHB21902253
Overview
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TPT-004 (CAS 3032648-15-7) is an inhibitor supplied as a solid. Relevant to Metabolic Enzyme/Protease research. Molecular formula C18H20N6O3S, molecular weight 400.45 g/mol.
Purity 99.90%
CAS Number 3032648-15-7
Molecular Weight 400.45 g/mol
Form Solid
Storage Powder -20°C; in solvent -80°C
Options selector
Catalog no. Size
HY-157014-5MG 5 mg
HY-157014-10MG 10 mg
HY-157014-25MG 25 mg
HY-157014-50MG 50 mg
HY-157014-100MG 100 mg
HY-157014-200MG 200 mg
HY-157014-1MLX10MM 1 mL x 10 mM (in DMSO)
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 1 mL x 10 mM (in DMSO)
  • Lead time: varies by selected option.
  • Storage: Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: transfer to -20°C as soon as possible.
Field Specification
CAS no. 3032648-15-7
Applications
  • Functional Assay (In Vitro)
Molecular weight 400.45
Molecular formula C18H20N6O3S
Purity 99.90%
SMILES CCN1C2=C(C(NC1=O)=O)N(C(CC3=CN4C=C(SC4=N3)C)=N2)CC5COC5
Form Solid
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-157014
Main SKU BHB21902253
Inhibitors

Compound Overview

TPT-004 is a selective, orally active inhibitor of tryptophan hydroxylases (TPH), with IC50 values of 77 nM at TPH1 and 16 nM at TPH2. It shows selectivity for TPH1 relative to other members of the AAAH family and demonstrates efficacy in attenuating peripheral serotonin and reducing colorectal tumor growth in mice[1][2]. It is supplied as a white to off-white solid (C18H20N6O3S, MW 400.45) at 99.90% purity.

Physical & Chemical Properties

CAS Number 3032648-15-7
Molecular Formula C18H20N6O3S
Molecular Weight 400.45 g/mol
Purity 99.90%
Appearance Solid
Color White to off-white
SMILES CCN1C2=C(C(NC1=O)=O)N(C(CC3=CN4C=C(SC4=N3)C)=N2)CC5COC5
Signaling Pathway Metabolic Enzyme/Protease
Solubility In Vitro: DMSO: 125 mg/mL (312.15 mM; Requires sonication; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Storage Powder: -20°C, 3 years. In solvent: -80°C, 6 months; -20°C, 1 month.
Shipping Room temperature in continental US; may vary elsewhere.

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Specker E, et al. Structure-Based Design of Xanthine-Imidazopyridines and -Imidazothiazoles as Highly Potent and In Vivo Efficacious Tryptophan Hydroxylase Inhibitors. J Med Chem. 2023 Oct 31.

[2]. Wesolowski R,et al. Selectivity and Safety Characterization of a Xanthine-Imidazothiazole Lead Structure: a Novel Tryptophan Hydroxylase Inhibitor of Peripheral Serotonin Synthesis. ACS Pharmacol Transl Sci. 2025 May 19;8(6):1678-1693.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with the Safety Data Sheet and your institution's chemical hygiene plan.

In Vitro

SolventSolubilityNotes
DMSO125 mg/mL (312.15 mM)requires sonication; use freshly opened DMSO (absorbed moisture lowers solubility)

Aliquot the stock solution and store it at -80°C (up to 6 months) or -20°C (up to 1 month); avoid repeated freeze-thaw cycles.

Data provided by the manufacturer.

In Vitro

In serotonergic BON cells, TPT-004 (72 h) lowers intracellular serotonin levels along a dose-response curve with an IC50 of 0.952 μM[1].

TPT-004 inhibits phenylalanine hydroxylase (PAH) and tyrosine hydroxylase (TH), with IC50 values of 403.5 nM and 1.359 μM, respectively[2].

In Vivo

In the mouse colon carcinoma model MC38, TPT-004 (50 mg/kg; oral gavage; twice daily; for 20 days) reduces tumor growth[1].

Animal ModelFemale C57BL/6N mice (aged 8 weeks) were subcutaneously transplanted with MC38 tumor fragments[1].
Dosage50 mg/kg
AdministrationOral gavage; twice daily; for 20 days
ResultAttenuated the tumor-growth, especially in the initial growth phase.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price on some sizes?
A.Availability and lead time for those sizes are confirmed on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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