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ZT-12-037-01

SKU: orb1301658

Description

Zt-12-037-01 is a potent and ATP-competitive inhibitor of STK19, demonstrating IC50 values of 23.96 nM against the wild-type and 27.94 nM against the D89N mutant. This small molecule is a valuable research tool for investigating STK19 kinase function in biochemical and cellular assays relevant to cancer and dermatological research.

Research Area

Pharmacology & Drug Discovery, Protein Biochemistry, Signal Transduction

Images & Validation

Key Properties

CAS Number2328073-61-4
MW385.5
Purity98.00% (May vary between batches)
FormulaC21H31N5O2
SMILESCOc1cc2nc(NC3CC3)nc(NC3CCN(CC3)C(C)C)c2cc1OC
TargetSerine Protease,Ras
SolubilityDMSO:41 mg/mL (106.36 mM)

Bioactivity

Target IC50
STK19 (WT):23.96 nM |STK19 (D89N):27.94 nM
In Vivo
ZT-12-037-01 as a specific STK19-targeted inhibitor and it effectively blocks oncogenic NRAS-driven melanocyte malignant transformation and melanoma growth in vivo.
In Vitro
ZT-12-037-01 significantly inhibits mutant NRAS-STK19-driven melanocyte colony formation and proliferation.
Animal Research
ZT-12-037-01 (injection subcutaneously; 25-50 mg/kg; once daily; 21 days) inhibits growth of SK-MEL-2 xenograft melanoma and the sections of tumors indicates induction of apoptosis by increasing cleaved caspase-3.

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Inhibitor, inhibit, Ras, Serine Protease, SerineProtease, STK19, ZT 12 037 01, ZT1203701, ZT-12-037-01

Similar Products

  • ZT-12-037-01 [orb1225570]

    >98% (HPLC)

    2328073-61-4

    385.512

    C21H31N5O2

    2 mg, 5 mg, 10 mg, 50 mg, 100 mg, 25 mg, 200 mg, 500 mg, 1 g
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Key Properties

No computed properties available.

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Protocol Information

ZT-12-037-01 (orb1301658)

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Available Sizes

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1 mg
$ 70.00
1 ml x 10 mM (in DMSO)
$ 80.00
5 mg
$ 110.00
10 mg
$ 160.00
25 mg
$ 280.00
50 mg
$ 440.00
100 mg
$ 660.00
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