
FAK-IN-10
CAS No. 491839-65-7
FAK-IN-10( —— )
Catalog No. M37079 CAS No. 491839-65-7
FAK-IN-10 is an inhibitor of FAK (IC50: 76.3 μM) and demonstrates antitumor activity in MCF-7 and A431 cell lines with IC50 values of 4.23 μM and 0.78 μM, respectively.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 88 | Get Quote |
![]() ![]() |
5MG | 132 | Get Quote |
![]() ![]() |
10MG | 211 | Get Quote |
![]() ![]() |
25MG | 348 | Get Quote |
![]() ![]() |
50MG | 490 | Get Quote |
![]() ![]() |
100MG | 682 | Get Quote |
![]() ![]() |
500MG | 1377 | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameFAK-IN-10
-
NoteResearch use only, not for human use.
-
Brief DescriptionFAK-IN-10 is an inhibitor of FAK (IC50: 76.3 μM) and demonstrates antitumor activity in MCF-7 and A431 cell lines with IC50 values of 4.23 μM and 0.78 μM, respectively.
-
DescriptionFAK-IN-10 is an inhibitor of FAK with an IC50 of 76.3 μM. FAK-IN-10 exhibits antitumor activity against MCF-7 and A431 cell lines with IC50s of 4.23 and 0.78 μM,respectively.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayAngiogenesis
-
TargetFAK
-
RecptorFAK
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number491839-65-7
-
Formula Weight376.23
-
Molecular FormulaC15H10BrN3O2S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 20 mg/mL (53.16 mM; Ultrasonic (<60°C)
-
SMILESO=C(C1=CC=C(Br)C=C1)CSC2=NN=C(O2)C=3C=CN=CC3
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Zhang LR, et al. Synthesis, biological evaluation and molecular docking studies of novel 2-(1,3,4-oxadiazol-2-ylthio)-1-phenylethanone derivatives. Bioorg Med Chem. 2012 Jun 1;20(11):3615-21.?
molnova catalog



related products
-
Alizarin
Alizarin, a red dye derived from the roots of plants of the madder genus, inhibits P450 isoform CYP1A1( IC50 = 6.2 μM), CYP1A2 (IC50 =10.0 μM )and CYP1B1(IC50 = 2.7 μM).
-
GSK-2256098
GSK-2256098 (GTPL-7939) is a potent, selective, reversible and ATP-competitive inhibitor of FAK kinase with Ki of 0.4 nM.
-
FAK-IN-10
FAK-IN-10 is an inhibitor of FAK (IC50: 76.3 μM) and demonstrates antitumor activity in MCF-7 and A431 cell lines with IC50 values of 4.23 μM and 0.78 μM, respectively.