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AZD-0364AZD 0364 is a potent and selective ERK2 inhibitor extracted from patent WO2017080979A1, compound example 18, has an IC50 of 0. 6 nM. Product information CAS Number: 2097416 76 5 Molecular Weight: 494. 50 Formula: C24H24F2N8O2 Chemical Name: (6R) 7 [(3,4 difluorophenyl)methyl] 6 (methoxymethyl) 2 {5 methyl 2 [(1 methyl 1H pyrazol 5 yl)amino]pyrimidin 4 yl} 5H,6H,7H,8H imidazo[1,2 a]pyrazin 8 one Smiles:
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AZD-0364 is a potent and selective ERK2 inhibitor extracted from patent WO2017080979A1, compound example 18, has an IC50 of 0.6 nM.

Product information

CAS Number: 2097416-76-5

Molecular Weight: 494.50

Formula: C24H24F2N8O2

Chemical Name: (6R)-7-[(3,4-difluorophenyl)methyl]-6-(methoxymethyl)-2-{5-methyl-2-[(1-methyl-1H-pyrazol-5-yl)amino]pyrimidin-4-yl}-5H,6H,7H,8H-imidazo[1,2-a]pyrazin-8-one

Smiles: CN1N=CC=C1NC1N=C(C2=CN3C[C@H](COC)N(CC4C=C(F)C(F)=CC=4)C(=O)C3=N2)C(C)=CN=1

InChiKey: HVIGNZUDBVLTLU-MRXNPFEDSA-N

InChi: InChI=1S/C24H24F2N8O2/c1-14-9-27-24(30-20-6-7-28-32(20)2)31-21(14)19-12-33-11-16(13-36-3)34(23(35)22(33)29-19)10-15-4-5-17(25)18(26)8-15/h4-9,12,16H,10-11,13H2,1-3H3,(H,27,30,31)/t16-/m1/s1

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO : ≥ 100 mg/mL (202.22 mM).

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

AZD-0364 is measured in the ERK2 mass spectrometry and A375 phospho-p90RSK assays with IC50s of 0.6 nM and 5.7 nM, respectively. AZD-0364 can inhibit the growth of a panel of cancer cell lines (A549, H2122, H2009, and Calu6 cell lines) with KRAS mutations as a monotherapy and this effect is synergistically enhanced by treatment with Selumetinib.

In Vivo:

Tumor growth inhibition by AZD-0364 ethanesulfonic acid (Example 18a) in combination with MEK inhibitor Selumetinib is measured. Studies are performed in the A549 xenograft model. Selumetinib is dosed twice daily (BiD) 8 hours apart and AZD-0364 ethanesulfonic acid is dosed once daily (QD) 4 hours after the first Selumetinib dose. Both compounds are dosed continuously for 3 weeks. Both vehicles are dosed in the vehicle group. Both Selumetinib and AZD-0364 ethanesulfonic acid reduce tumor growth relative to vehicle only control. The combination of Selumetinib and AZD-0364 ethanesulfonic acid results in a reduction in tumor growth.

Products are for research use only. Not for human use.

AZD-0364

Item no : 56117161
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