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Search Results for " spleen "

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Compounds

Cat No. Product Name Synonyms Targets
T36582 Glucocerebrosides (Gaucher's spleen)
Glucocerebrosides are formed by the tethering of glucose to a ceramide by glucosylceramide synthase. They are present in neuronal and non-neuronal mammalian tissues and are found at low quantities in a large number of pl...
T16776 RO9021 Syk
RO9021 is an orally bioavailable, novel ATP-competitive SYK inhibitor (average IC50: 5.6 nM).
T39437 Cevidoplenib dimesylate Syk
Cevidoplenib dimesylate is an inhibitor of spleen tyrosine kinase (Syk), possessing anti-inflammatory and immunomodulating properties.
T6101 Entospletinib GS-9973 Syk
Entospletinib (GS-9973) (IC50= 7.7 nM)is a specific Syk inhibitor, which is orally bioavailable.
T11824LL Lanraplenib GS-9876 Syk
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases. Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI ...
T4209 TAK-659 hydrochloride TAK-659 VEGFR , FLT , Tyrosine Kinases , JAK , Syk
TAK-659 hydrochloride (TAK-659) is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
T14331 Gusacitinib ASN-002 JAK , Syk
Gusacitinib (ASN-002) (ASN-002) is spleen tyrosine kinase (SYK) and janus kinase (JAK) inhibitor (IC50: 5-46 nM).
T6594 MNS Syk , Src , p97
MNS is a tyrosine kinases inhibitor, inhibits Syk, Src, p97 with IC50 of 2.5 μM, 29.3 μM and 1.7 μM, respectively.
T4348 Syk Inhibitor II 5-HT Receptor , Syk
Syk inhibitor II, a cell-permeable, ATP-competitive, pyrimidine-carboxamide compound, selectively and reversibly inhibits Syk (IC50 = 41 nM).
T0610 Piceatannol trans-Piceatannol,Astringenin Apoptosis , Serine/threonin kinase , PKA , Syk , PKC , Autophagy
Piceatannol (Astringenin) is an anti-inflammatory, immunomodulatory and antiproliferative agent. It inhibits p56lck and syk protein tyrosine kinases and inhibits NF-κB activation and gene expression of TNF-induced. It is...
T6115 Fostamatinib R788 FLT , Syk , Monoamine Transporter , Adenosine Receptor
Fostamatinib (R788)(IC50 of 41 nM), which is a prodrug of the active metabolite R406, is a Syk inhibitor. It does not work on Lyn.
T3185 R112 (E)-Elafibranor Syk
R112 ((E)-Elafibranor) is an ATP-competitive inhibitor of Syk kinase.
T2487 Cerdulatinib PRT2070,PRT062070 Tyrosine Kinases , JAK , Syk
Cerdulatinib (PRT2070) is an novel oral dual Syk/JAK inhibitor.
T6174 R406 R-406 besylate Apoptosis , FLT , Syk
R406 (R-406 besylate) is an effective Syk inhibitor (IC50: 41 nM) and shows no effects on Lyn.
T2467 R406 free base R406 (free base) Apoptosis , FLT , Syk
R406 free base (R406 (free base)) is a potent Syk inhibitor.
T2696 PRT062607 hydrochloride PRT062607 (P505-15, BIIB057) HCl,P505-15 Hydrochloride MLK , Syk , Src
PRT062607 hydrochloride (P505-15 Hydrochloride) is a selective inhibitor of Syk (IC50: 1 nM). It displays at least 80-fold selectivity for Syk over other kinases.
T6957 PRT-060318 P142-76,PRT318,PRT-060318 2HCl Syk
PRT-060318 (P142-76) is a novel selective inhibitor of the Syk tyrosine kinase, as an approach to HIT treatment.
T6776 BAY 61-3606 dihydrochloride BAY 61-3606,BAY-61-3606 dihydrochloride Apoptosis , Syk
BAY 61-3606 dihydrochloride (BAY 61-3606) is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
T4263 BAY 61-3606 Syk inhibitor IV Apoptosis , Syk
BAY 61-3606 (Syk inhibitor IV) is a potent, ATP-competitive, reversible, and highly selective inhibitor of Syk tyrosine kinase activity (Ki= 7.5 nM), exhibiting no inhibitory effect against Btk, Fyn, Itk, Lyn, and Src.
T2605 Fostamatinib Disodium Tamatinib Fosdium,R788(Disodium),R788 Disodium,R788 (Fostamatinib) Disodium FLT , Syk
Fostamatinib Disodium (R788 Disodium) is an orally available Syk kinase inhibitor with potential anti-inflammatory and immunomodulating activities.
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