AS1949490 structure
|
Common Name | AS1949490 | ||
|---|---|---|---|---|
| CAS Number | 1203680-76-5 | Molecular Weight | 371.88 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C20H18ClNO2S | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | N/A | |
| Symbol |
GHS07 |
Signal Word | Warning | |
Use of AS1949490AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM. AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. |
| Name | 3-[(4-Chlorobenzyl)oxy]-N-[(1S)-1-phenylethyl]-2-thiophenecarboxa mide |
|---|---|
| Synonym | More Synonyms |
| Description | AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM. AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 620 nM (SHIP-2)[1]. |
| References |
| Molecular Formula | C20H18ClNO2S |
|---|---|
| Molecular Weight | 371.88 |
| Exact Mass | 371.07500 |
| PSA | 70.06000 |
| LogP | 6.04630 |
| 3-[(4-Chlorophenyl)methoxy]-N-[(1S)-1-phenylethyl]- 2-thiophenecarboxamide AS 1949490 |