Tyrphostin A1 Size:Solid 10 mg Smiles: CN1N=CC=C1NC1=NC(=CC=N1)C1C=CN([C@H](CO)C2=CC(F)=C(Cl)C=C2)C(=O)C=1

Smiles: CN1N=CC=C1NC1=NC(=CC=N1)C1C=CN([C@H](CO)C2=CC(F)=C(Cl)C=C2)C(=O)C=1

5-difluorobenzyl)-1H-indazol-3-yl)-4-(4-methylpiperazin-1-yl)-2-((tetrahydro-2H-pyran-4-yl)amino)benzamide

6-fold increase in ATM reporter activity in HEK-293 cells

VR23 was structurally distinct from other known proteasome inhibitors and selectively killed cancer cells by apoptosis

SCH442416 is selective for A2AR (Ki=0

Tyrphostin A1 Size:Solid 10 mg Smiles: CN1N=CC=C1NC1=NC(=CC=N1)C1C=CN([C@H](CO)C2=CC(F)=C(Cl)C=C2)C(=O)C=1Tyrphostin 1 is an EGFR tyrosine kinase inhibitor. Product information CAS Number: 2826 26 8 Molecular Weight: 184. 19 Formula: C11H8N2O Synonym: Tyrphostin 1 AG9 Chemical Name: 2 [(4 methoxyphenyl)methylidene]propanedinitrile Smiles: COC1C=CC(C=C(C#N)C#N)=CC=1 InChiKey: UOHFCPXBKJPCAD UHFFFAOYSA N InChi: InChI=1S C11H8N2O c1 14 11 4 2 9(3 5 11)6 10(7 12)8 13 h2 6H,1H3 Technical Data Appearance: Solid Power Purity: 98% (or refer to the Certificate of