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Merck

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SML1069

TH287 盐酸盐

≥98% (HPLC)

同義詞:

6-(2,3-Dichlorophenyl)-N4-methylpyrimidine-2,4-diamine hydrochloride

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經驗公式(希爾表示法):
C11H10Cl2N4 · HCl
CAS 編號:
分子量::
305.59
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
eCl@ss:
32150313
Assay:
≥98% (HPLC)
Form:
powder
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Quality Segment

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 5 mg/mL, clear (warmed)

storage temp.

2-8°C

SMILES string

ClC1=CC=CC(C2=NC(N)=NC(NC)=C2)=C1Cl.Cl

InChI

1S/C11H10Cl2N4.ClH/c1-15-9-5-8(16-11(14)17-9)6-3-2-4-7(12)10(6)13;/h2-5H,1H3,(H3,14,15,16,17);1H

InChI key

YBLIJWDQSUDCJU-UHFFFAOYSA-N

Biochem/physiol Actions

TH287 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1) with an IC50 value of 0.8 nM. 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. TH287 is considered a new target for cancer therapy. TH287 is highly selective towards MTH1, with no relevant inhibition of other members of the nudix protein family. TH287 has been shown to selectively kill a variety of cancer cell lines, but is rapidly metablized, so not as useful for in vivo studies.
TH287 is a potent inhibitor of human 7,8-Dihydro-8-oxoguaninetriphosphatase MTH1 (NUDT1).


警示詞

Danger

危險代碼

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

存儲類別/等級

11 - Combustible Solids

WGK

WGK 3

閃點 (F)

Not applicable

閃點(°C)

Not applicable



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