LX7101 (hydro<wbr/>chloride)

LX7101 (hydrochloride)

CAT N°: 21209
Price:

From 100.00 85.00

LX7101 is a potent inhibitor of LIM kinase (LIMK) 1 and 2 and Rho-associated kinase 1 (ROCK1) and ROCK2 with IC50 values of 32, 4.3, 69, and 32 nM, respectively.{38221} It is selective, showing no cross reactivity in a panel of binding assays including 78 receptors and transporters and 430 additional kinases, at a concentration of 10 ?M. Topical administration (3 ?l of 1 mg/ml solution) of LX7101 to the eye reduces intraocular pressure in a dexamethasone-induced mouse model of glaucoma.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • N,N-dimethyl-carbamic acid, 3-[[[4-(aminomethyl)-1-(5-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-4-piperidinyl]carbonyl]amino]phenyl ester, monohydrochloride
  • Correlated keywords
    • 1192189-69-7 LX-7101 ROCK1 ROCK2 LIMK1 LIMK2
  • Product Overview:
    LX7101 is a potent inhibitor of LIM kinase (LIMK) 1 and 2 and Rho-associated kinase 1 (ROCK1) and ROCK2 with IC50 values of 32, 4.3, 69, and 32 nM, respectively.{38221} It is selective, showing no cross reactivity in a panel of binding assays including 78 receptors and transporters and 430 additional kinases, at a concentration of 10 ?M. Topical administration (3 ?l of 1 mg/ml solution) of LX7101 to the eye reduces intraocular pressure in a dexamethasone-induced mouse model of glaucoma.

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