J-113863 Size:Contact [email protected] for quotation Smiles: CN1C2=CC=C(C=C2OC1=O)N1C=C(C(O)=O)C(=O)N([C@@H]2CCC3C(=CC=CC=32)C(F)(F)F)C1=O

Smiles: CN1C2=CC=C(C=C2OC1=O)N1C=C(C(O)=O)C(=O)N([C@@H]2CCC3C(=CC=CC=32)C(F)(F)F)C1=O

inducing nerve growth factor production in epidermal keratinocytes

Smiles: CC1N=C2C=CC=CN2C(=O)C=1CCN1CC2C3=CC=CC=C3OC=2CC1

high affinity peptidic inhibitor of B cell lymphoma 6 (BCL6)

A-83-01 inhibited the epithelial-to-mesenchymal transition induced by TGF-beta

J-113863 Size:Contact [email protected] for quotation Smiles: CN1C2=CC=C(C=C2OC1=O)N1C=C(C(O)=O)C(=O)N([C@@H]2CCC3C(=CC=CC=32)C(F)(F)F)C1=OJ 113863 is a potent and selective CCR1 (CD18) antagonist with IC50 values of 0. 9 nM and 5. 8 nM for human and mouse CCR1 receptors, respectively. J 113863 is also a potent antagonist of the human CCR3 (IC50 of 0. 58 nM) , but a weak antagonist of the mouse CCR3 (IC50 of 460 nM). J 113863 is inactive against CCR2, CCR4 and CCR5, as well as the LTB4 or TNF receptors. Anti inflammatory effect. Product information CAS Number: 353791 85 2 Molecular