LX7101 (hydrochloride) – 1 mg

Brand:
Cayman
CAS:
2319882-48-7
Storage:
-20
UN-No:
De Minimis - 3077 / 9

LX7101 is a potent inhibitor of LIM kinase (LIMK) 1 and 2 and Rho-associated kinase 1 (ROCK-1) and ROCK-2 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 μM. Topical administration (3 μl 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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SKU: 21209 - Category:

Description

A potent inhibitor of LIMK1, LIMK2, ROCK-1, and ROCK-2 kinases (IC50s = 32, 4.3, 69, and 32 nM, respectively); selective, showing no cross reactivity in a panel of binding assays including 78 receptors, at a concentration of 10 μM; topical administration (3 μl of 1 mg/ml solution) to the eye reduces intraocular pressure in a dexamethasone-induced mouse model of glaucoma,


Formal name: 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

Synonyms: 

Molecular weight: 488

CAS: 2319882-48-7

Purity: ≥98%

Formulation: A crystalline solid


Product Type|Biochemicals|Kinase Inhibitors|Other Serine/Threonine Kinases||Product Type|Biochemicals|Kinase Inhibitors|ROCK||Product Type|Biochemicals|Small Molecule Inhibitors|Kinases||Research Area|Neuroscience|Ophthalmology