ZT-12-037-01

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CAS:2328073-61-4
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CAS:2328073-61-4
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CAS:2328073-61-4
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CAS:2328073-61-4
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Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:ZT-12-037-01
CAS:2328073-61-4
Package:1 mL * 10mM (in DMSO);10 mg;100 mg;2 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY

ZT-12-037-01 manufacturers

  • ZT-12-037-01
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  • $30.00 / 1mg
  • 2025-12-05
  • CAS:2328073-61-4
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  • Purity: 99.56%
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ZT-12-037-01 Basic information
Product Name:ZT-12-037-01
Synonyms:ZT-12-037-01;2,4-Quinazolinediamine, N2-cyclopropyl-6,7-dimethoxy-N4-[1-(1-methylethyl)-4-piperidinyl]-;inhibit,ZT 12 037 01,ZT1203701,Ras,Inhibitor;N2-Cyclopropyl-N4-(1-isopropylpiperidin-4-yl)-6,7-dimethoxyquinazoline-2,4-diamine;ZT-12-037-01, 10 mM in DMSO
CAS:2328073-61-4
MF:C21H31N5O2
MW:385.5
EINECS:
Product Categories:
Mol File:2328073-61-4.mol
ZT-12-037-01 Structure
ZT-12-037-01 Chemical Properties
storage temp. 2-8°C(protect from light)
solubility DMSO: 8.33 mg/mL (21.61 mM)
form Solid
color White to off-white
Safety Information
MSDS Information
ZT-12-037-01 Usage And Synthesis
UsesZT-12-037-01 is a STK19-targeted inhibitor, has a high-affinity interaction with STK19 protein and inhibits oncogenic NRAS-driven melanocyte malignant transformation. ZT-12-037-01 is an ATP-competitive inhibitor, inhibiting phosphorylation of NRAS (major isoform of Ras family) with an IC50 of 24 nM[1].
Biological ActivityZT-12-037-01 is an ATP-competitive STK19 inhibitor with IC50 values of 23.96 nM and 27.94 nM for STK19 (WT) and STK19 (D89N), respectively. At a concentration of 1 μM, it is highly selective against a kinase library of 468 kinases.
in vitro

Treatment with ZT-12-037-01 could effectively inhibit NRAS phosphorylation. ZT-12-037-01 is an ATP-competitive inhibitor that potently inhibits melanocytic colony formation, proliferation and tumor formation driven by mutant NRAS-STK19. It's pro-apoptotic activity was significantly enhanced in cells expressing oncogenic NRAS.

in vivo

ZT-12-037-01 is a potent STK19 inhibitor with low toxicity in vivo. In the SK-MEL-2 xenograft model (carrying NRAS.

target< /table>
TargetValue
STK19
(Cell-free assay)
23.96 nM
STK19 (D89N)
(Cell-free assay)
27.94 nM
References[1] Yin C, et al. Pharmacological Targeting of STK19 Inhibits Oncogenic NRAS-Driven Melanomagenesis. Cell. 2019 Feb 21;176(5):1113-1127.e16. DOI:10.1016/j.cell.2019.01.002
ZT-12-037-01 Preparation Products And Raw materials
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