Product Name :
AM966
Description:
AM966 is a potent, selective, and orally active LPA(1) receptor antagonist which inhibits lung fibrosis in the mouse bleomycin model. In vitro, AM966 inhibited LPA-stimulated intracellular calcium release from Chinese hamster ovary cells stably expressing human LPA(1) receptors and inhibited LPA-induced chemotaxis of human IMR-90 lung fibroblasts expressing LPA(1) receptors. AM966 reduced lung injury, vascular leakage, inflammation and fibrosis at multiple time points following intratracheal bleomycin instillation. AM966 also decreased lactate dehydrogenase activity and tissue inhibitor of metalloproteinase-1, transforming growth factor beta1, hyaluronan and matrix metalloproteinase-7, in bronchoalveolar lavage fluid.
CAS:
1228690-19-4
Molecular Weight:
490.93
Formula:
C27H23ClN2O5
Chemical Name:
2-{4′-[4-({[(1R)-1-(2-chlorophenyl)ethoxy]carbonyl}amino)-3-methyl-1,2-oxazol-5-yl]-[1,1′-biphenyl]-4-yl}acetic acid
Smiles :
CC1=NOC(=C1NC(=O)O[C@H](C)C1=CC=CC=C1Cl)C1C=CC(=CC=1)C1C=CC(CC(O)=O)=CC=1
InChiKey:
WWQTWEWAPUCDDZ-QGZVFWFLSA-N
InChi :
InChI=1S/C27H23ClN2O5/c1-16-25(29-27(33)34-17(2)22-5-3-4-6-23(22)28)26(35-30-16)21-13-11-20(12-14-21)19-9-7-18(8-10-19)15-24(31)32/h3-14,17H,15H2,1-2H3,(H,29,33)(H,31,32)/t17-/m1/s1
Purity:
≥98% (or refer to the Certificate of Analysis)
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.{{Radotinib} site|{Radotinib} Protein Tyrosine Kinase/RTK|{Radotinib} Biological Activity|{Radotinib} In stock|{Radotinib} custom synthesis|{Radotinib} Autophagy}
Shelf Life:
≥360 days if stored properly.{{Anti-Mouse IFN gamma Antibody} site|{Anti-Mouse IFN gamma Antibody} Immunology/Inflammation|{Anti-Mouse IFN gamma Antibody} Protocol|{Anti-Mouse IFN gamma Antibody} References|{Anti-Mouse IFN gamma Antibody} supplier|{Anti-Mouse IFN gamma Antibody} Epigenetics}
Stock Solution Storage:
0 – 4 oC for 1 month or refer to the Certificate of Analysis.PMID:26760947
Additional information:
AM966 is a potent, selective, and orally active LPA(1) receptor antagonist which inhibits lung fibrosis in the mouse bleomycin model. In vitro, AM966 inhibited LPA-stimulated intracellular calcium release from Chinese hamster ovary cells stably expressing human LPA(1) receptors and inhibited LPA-induced chemotaxis of human IMR-90 lung fibroblasts expressing LPA(1) receptors. AM966 reduced lung injury, vascular leakage, inflammation and fibrosis at multiple time points following intratracheal bleomycin instillation. AM966 also decreased lactate dehydrogenase activity and tissue inhibitor of metalloproteinase-1, transforming growth factor beta1, hyaluronan and matrix metalloproteinase-7, in bronchoalveolar lavage fluid.|Product information|CAS Number: 1228690-19-4|Molecular Weight: 490.93|Formula: C27H23ClN2O5|Chemical Name: 2-{4′-[4-({[(1R)-1-(2-chlorophenyl)ethoxy]carbonyl}amino)-3-methyl-1,2-oxazol-5-yl]-[1,1′-biphenyl]-4-yl}acetic acid|Smiles: CC1=NOC(=C1NC(=O)O[C@H](C)C1=CC=CC=C1Cl)C1C=CC(=CC=1)C1C=CC(CC(O)=O)=CC=1|InChiKey: WWQTWEWAPUCDDZ-QGZVFWFLSA-N|InChi: InChI=1S/C27H23ClN2O5/c1-16-25(29-27(33)34-17(2)22-5-3-4-6-23(22)28)26(35-30-16)21-13-11-20(12-14-21)19-9-7-18(8-10-19)15-24(31)32/h3-14,17H,15H2,1-2H3,(H,29,33)(H,31,32)/t17-/m1/s1|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|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: ≥360 days 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|Products are for research use only. Not for human use.|
