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TH588

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Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:TH588 HYDROCHLORIDE
CAS:1609960-31-7
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: career henan chemical co
Tel: +86-0371-86658258 +8613203830695
Email: sales@coreychem.com
Products Intro: Product Name:N4-Cyclopropyl-6-(2,3-dichlorophenyl)-2,4-pyrimidinediamine;TH588;N4-cyclopropyl-6-(2,3-dic
CAS:1609960-31-7
Purity:95%~99% Package:1KG;1USD
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:TH588
CAS:1609960-31-7
Purity:99.82% Package:5mg;34USD|10mg;50USD|25mg;77USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Products Intro: Product Name:TH-588
CAS:1609960-31-7
Purity:99% Package:10kg 25kg 200 kilograms per barrel Remarks:good
Company Name: Zhejiang J&C Biological Technology Co.,Limited
Tel: +1-2135480471 +1-2135480471;
Email: sales@sarms4muscle.com
Products Intro: Product Name:TH588
CAS:1609960-31-7
Purity:99% Package:5KG;1KG Remarks:TH588

TH588 manufacturers

  • TH588
  • TH588 pictures
  • $57.00 / 5mg
  • 2026-04-21
  • CAS:1609960-31-7
  • Min. Order:
  • Purity: 99.52%
  • Supply Ability: 10g
TH588 Basic information
Product Name:TH588
Synonyms:N4-Cyclopropyl-6-(2,3-dichlorophenyl)-2,4-pyrimidinediamine;TH588;N4-cyclopropyl-6-(2,3-dichlorophenyl)pyrimidine-2,4-diamine;TH588(TH-588);6-(2,3-dichlorophenyl)-N4-cyclopropylpyrimidine-2,4-diamine;TH 588;TH-588;TH588;CS-1701;TH588, >98%
CAS:1609960-31-7
MF:C13H12Cl2N4
MW:295.17
EINECS:
Product Categories:Inhibitors
Mol File:1609960-31-7.mol
TH588 Structure
TH588 Chemical Properties
Boiling point 545.7±60.0 °C(Predicted)
density 1.505±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Soluble in DMSO (up to 5 mg/ml).
form powder
pka5.90±0.10(Predicted)
color white to light brown
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChI1S/C13H12Cl2N4.ClH/c14-9-3-1-2-8(12(9)15)10-6-11(17-7-4-5-7)19-13(16)18-10;/h1-3,6-7H,4-5H2,(H3,16,17,18,19);1H
InChIKeyFBHMEHNWFXCSKE-UHFFFAOYSA-N
SMILESClC1=CC=CC(C2=NC(N)=NC(NC3CC3)=C2)=C1Cl.Cl
Safety Information
WGK Germany 3
Storage Class11 - Combustible Solids
MSDS Information
TH588 Usage And Synthesis
DescriptionTH588 (1609960-31-7) is a first-in-class nudix hydrolase family inhibitor.1MTH1/NUDT1 is a family member that “sanitizes” oxidized deoxynucleotide triphosphates (dNTP) preventing their incorporation into DNA and thus avoiding DNA damage and cell death. TH588 inhibits MTH1/NUDT1 (IC50= 5 nM) leading to cell death in several cancer cell lines while not affecting normal cells. Activein vitroandin vivo. Recent evidence has raised doubts about the cancer-killing ability of MTH1 inhibition.2,3Conversely, TH588 has been also shown to decrease osteosarcoma cell viability, impair cell cycle, and increase apoptosis via an MTH1-dependent pathway.4
UsesTH 588 acts as a novel potent and selective permeable inhibitor of the nudix hydrolase MTH1 protein. It acts as a good tool to show the non-oncogene addiction concept to anti-cancer treatments.
Biochem/physiol ActionsTH588 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 5 nM and good metabolic stability. MTH1 hydrolyzes oxidized purine nucleoside triphosphates that might otherwise be incorporated into DNA/RNA and contribute to DNA damage. MTH1 removal of oxidized nucleotides that result from increased levels of reactive oxygen species (ROS) in fast-proliferating cancer cells helps protect cancer cells from proliferative stress and prevent cancer cell death. TH588 is considered a new target for cancer therapy. TH588 is highly selective towards MTH1, with no relevant inhibition of other members of the nudix protein family or a panel of 87 enzymes, GPCRs, kinases, ion channels and transporter. TH588 has been shown to selectively kill a variety of cancer cell lines and with in vivo activity shown for TH588 in SW480 colorectal and MCF7 breast tumour xenografts.
in vivo

TH588 (30 mg/kg; s.c.; once daily for 35 days) reduces tumour growth in SW480 xenograft cancer model[1].

Animal Model:5-6 weeks female SCID mice (SW480 xenograft cancer model)[1]
Dosage:30 mg/kg
Administration:Subcutaneous injection; once daily for 35 days
Result:Reduced tumour growth in SW480 xenograft cancer model.
storageStore at -20°C
References[1] HELGE GAD. MTH1 inhibition eradicates cancer by preventing sanitation of the dNTP pool[J]. Nature, 2014, 508 7495: 215-221. DOI:10.1038/nature13181
[2] ALESSIA PETROCCHI. Identification of potent and selective MTH1 inhibitors[J]. Bioorganic & Medicinal Chemistry Letters, 2016, 26 6: Pages 1503-1507. DOI:10.1016/j.bmcl.2016.02.026
[3] JASON G. KETTLE*. Potent and Selective Inhibitors of MTH1 Probe Its Role in Cancer Cell Survival[J]. Journal of Medicinal Chemistry, 2016, 59 6: 2346-2361. DOI:10.1021/acs.jmedchem.5b01760
[4] BRICE MOUKENGUE. TH1579, MTH1 inhibitor, delays tumour growth and inhibits metastases development in osteosarcoma model.[J]. EBioMedicine, 2020, 53: 102704. DOI:10.1016/j.ebiom.2020.102704
TH588 Preparation Products And Raw materials
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