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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 73 Get Quote
5MG 110 Get Quote
10MG 177 Get Quote
25MG 388 Get Quote
50MG 689 Get Quote
100MG 1278 Get Quote
500MG 2547 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    TC-S 7003
  • Note
    Research use only, not for human use.
  • Brief Description
    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.
  • Description
    Lck 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.
  • In Vitro
    ——
  • In Vivo
    Animal 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.
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    Syk
  • Recptor
    Syk | Src
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    847950-09-8
  • Formula Weight
    530.62
  • Molecular Formula
    C31H30N8O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (188.46 mM; Ultrasonic )
  • SMILES
    O=C1C2=CN=C(N=C2N3C(=NC=4C=CC=CC43)N1C=5C(=CC=CC5C)C)NC6=CC=C(C=C6)N7CCN(C)CC7
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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