Spleen Tyrosine Kinase (Syk)
Syk is a family of non-receptor cytoplasmic tyrosine kinases that plays a role in transmitting signals from a variety of cell surface receptors including CD74, Fc Receptor, and integrins.
Products Related to Spleen Tyrosine Kinase (Syk)(37)
- GC63429CevidoplenibCAS: 1703788-21-9Purity: >98%
Cevidoplenib (SKI-O-703) is an orally active and selective spleen tyrosine kinase (Syk) inhibitor.
- GC63455Cevidoplenib dimesylateCAS: 2043659-93-2Purity: >98%
Cevidoplenib is an orally available inhibitor of spleen tyrosine kinase (Syk), with potential anti-inflammatory and immunomodulating activities.
- GC64279SovleplenibCAS: 1415792-84-5Purity: >98%
Sovleplenib (HMPL-523) is a highly potent, orally available and selective SYK inhibitor with an IC50 of 25 nM. Anti-tumor activity. Sovleplenib can be used for the research of immune thrombocytopenia (ITP).
- GC64889GSK2646264CAS: 1398695-47-0Purity: >98%
GSK2646264 (Compound 44) is a potent and selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.1.
- GC73424PRT062607 acetateCAS: 1370261-98-5Purity: >99.00%
PRT062607 (P505-15) acetate is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis.
- GC81306PRT-060318 dihydrochlorideCAS: 3032567-93-1Purity: >98.50%
PRT-060318 (PRT318) dihydrochloride is a potent, selective and orally active tyrosine kinase Syk inhibitor with an IC 50 of 3 nM.
- GN10503PiceatannolCAS: 10083-24-6Purity: >98.00%
Piceatannol (3,3′,4,5′-trans-trihydroxystilbene) is a naturally occurring hydroxylated analogue of resveratrol.
- GC11044Fostamatinib (R788)CAS: 901119-35-5Purity: >98.00%
Fostamatinib (R788) is the oral prodrug of the active compound R406, a relatively selective small molecule inhibitor of Syk .
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC63429 | Cevidoplenib | 1703788-21-9 | >98% | |
Cevidoplenib (SKI-O-703) is an orally active and selective spleen tyrosine kinase (Syk) inhibitor. | ||||
| GC63455 | Cevidoplenib dimesylate | 2043659-93-2 | >98% | |
Cevidoplenib is an orally available inhibitor of spleen tyrosine kinase (Syk), with potential anti-inflammatory and immunomodulating activities. | ||||
| GC64279 | Sovleplenib | 1415792-84-5 | >98% | |
Sovleplenib (HMPL-523) is a highly potent, orally available and selective SYK inhibitor with an IC50 of 25 nM. Anti-tumor activity. Sovleplenib can be used for the research of immune thrombocytopenia (ITP). | ||||
| GC64889 | GSK2646264 | 1398695-47-0 | >98% | |
GSK2646264 (Compound 44) is a potent and selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.1. | ||||
| GC68447 | GSK143 dihydrochloride | 2341796-81-2 | >99.00% | |
| GC70810 | ER-27319 | 201010-95-9 | >98.00% | |
ER-27319, an acridone derivative, is a potent and selective SYK inhibitor, and inhibits the tyrosine phosphorylation of SYK and its activity. | ||||
| GC73424 | PRT062607 acetate | 1370261-98-5 | >99.00% | |
PRT062607 (P505-15) acetate is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis. | ||||
| GC79422 | As48 | 1214405-38-5 | >97.50% | |
As48 is a selective TREM2 agonist with a K D value of 12.48 μM in TRIC binding assay. | ||||
| GC81306 | PRT-060318 dihydrochloride | 3032567-93-1 | >98.50% | |
PRT-060318 (PRT318) dihydrochloride is a potent, selective and orally active tyrosine kinase Syk inhibitor with an IC 50 of 3 nM. | ||||
| GC81330 | MRL-SYKi | 1312534-69-2 | >98.50% | |
MRL-SYKi is a chemical probe for gain-of-function variants of spleen tyrosine kinase ( SYK ). | ||||
| GC81443 | E8431 | 2419580-01-9 | >97.00% | |
E8431 is a DCSTAMP antagonist with an IC 50 value of 775.8 nM for osteoclastogenesis. | ||||
| GN10503 | Piceatannol | 10083-24-6 | >98.00% | |
Piceatannol (3,3′,4,5′-trans-trihydroxystilbene) is a naturally occurring hydroxylated analogue of resveratrol. | ||||
| GC11044 | Fostamatinib (R788) | 901119-35-5 | >98.00% | |
Fostamatinib (R788) is the oral prodrug of the active compound R406, a relatively selective small molecule inhibitor of Syk . | ||||
