
TC-S 7003
CAS No. 847950-09-8
TC-S 7003( —— )
Catalog No. M33407 CAS No. 847950-09-8
TC-S 7003 (Lck Inhibitor) is an orally active, selective and potent lymphocyte kinase (Lck) inhibitor with anti-inflammatory activity, inhibition of Lck, Lyn, Src, and Syk kinases, and inhibition of T-cell proliferation, and may be useful in the study of arthritis.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 73 | Get Quote |
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5MG | 110 | Get Quote |
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10MG | 177 | Get Quote |
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25MG | 388 | Get Quote |
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50MG | 689 | Get Quote |
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100MG | 1278 | Get Quote |
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500MG | 2547 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameTC-S 7003
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NoteResearch use only, not for human use.
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Brief DescriptionTC-S 7003 (Lck Inhibitor) is an orally active, selective and potent lymphocyte kinase (Lck) inhibitor with anti-inflammatory activity, inhibition of Lck, Lyn, Src, and Syk kinases, and inhibition of T-cell proliferation, and may be useful in the study of arthritis.
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DescriptionLck Inhibitor is a potent, orally active Lck (lymphocyte specific kinase) inhibitor with IC50s of 7, 2.1, 4.2 and 200 nM for Lck, Lyn, Src and Syk kinases, respectively. Lck Inhibitor shows >1000-fold selectivity for Lck over MAPK, CDK and RSK family representatives. Lck Inhibitor inhibits T cell proliferation and in vivo models of arthritis.
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In Vitro——
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In VivoAnimal Model:Male Lewis rat (adjuvant-inducedarthritis model) Dosage:0, 30, and 60 mg/kg Administration:P.o.; once daily; from day 9 today 17 Result:Showed a dose-dependent inhibition of arthritis, with an ED50 estimated at 24 mg/kg.Animal Model:Sprague-Dawley Rats Dosage:P.o. (Pharmacokinetic Analysis) Administration:5 mg/kg Result:The Cmax, AUC0-∞, tmax and F% were 82 ng/mL, 862 ng h/mL, and 17%, respectively.
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Synonyms——
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PathwayAngiogenesis
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TargetSyk
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RecptorSyk | Src
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Research Area——
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Indication——
Chemical Information
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CAS Number847950-09-8
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Formula Weight530.62
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Molecular FormulaC31H30N8O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (188.46 mM; Ultrasonic )
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SMILESO=C1C2=CN=C(N=C2N3C(=NC=4C=CC=CC43)N1C=5C(=CC=CC5C)C)NC6=CC=C(C=C6)N7CCN(C)CC7
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Martin, Matthew W.; Newcomb, John; Nunes, Joseph J.; et al. Structure-Based Design of Novel 2-Amino-6-phenyl-pyrimido[5',4':5,6]pyrimido[1,2-a]benzimidazol-5(6H)-ones as Potent and Orally Active Inhibitors of Lymphocyte Specific Kinase (Lck): Synthesis, SAR, and In Vivo Anti-Inflammatory Activity. Journal of Medicinal Chemistry (2008), 51(6), 1637-1648.?
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