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ROCK-IN-4
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ROCK-IN-4图片
CAS NO:2488395-07-7

ROCK-IN-4 是一种有效的ROCK抑制剂,能够维持 NO 释放能力。ROCK-IN-4 可逆地解聚 F-肌动蛋白,并抑制人小梁网 (HTM) 细胞的线粒体呼吸。ROCK-IN-4 可用于青光眼或高眼压的研究。
生物活性

ROCK-IN-4 is a potentROCKinhibitor maintaining NO releasing ability. ROCK-IN-4 reversibly depolymerizes F-actin, and suppresses mitochondrial respiration in human trabecular meshwork (HTM) cells. ROCK-IN-4 can be used for glaucoma or ocular hypertension research[1].

体外研究
(In Vitro)

ROCK-IN-4 (RNO-6) (10 μM; 1 h) decreases p-MLC level and induces reversible F-actin depolymerization[1].
ROCK-IN-4 (10 μM; 24 h) involves in cGMP activation, increases cGMP concentration in human trabecular meshwork (HTM) cells[1].
ROCK-IN-4 (10 μM; 1 h) suppresses mitochondrial respiration by releasing NO and remarkably decreases the basal respiration, maximal respiration, and ATP production[1].

Western Blot Analysis[1]

Cell Line:Human trabecular meshwork (HTM) cells
Concentration:10 μM
Incubation Time:1 hour
Result:Inhibited the phosphorylation of MLC, reduced the level of p-MLC.

Immunofluorescence[1]

Cell Line:Human trabecular meshwork (HTM) cells
Concentration:10 μM
Incubation Time:1 hour
Result:Exhibited conspicuous F-actin depolymerization, and after recovery for 4 h, recovered F-actin to the polymerization morphology, indicating a reversible depolymerization effect without permanent damage to cells.
体内研究
(In Vivo)

ROCK-IN-4 (0.26% w/v for 10 μL; o.p. in right eye; single dose) exhibits significant IOP lowering and (0.26% w/v for 10 μL; o.p.; 10 d) exerts visual function and retinal ganglion cell (RGC) protection activities in glaucoma mouse model[1].
ROCK-IN-4 (0.579% w/v for 25 μL; o.p. in left eye; single dose) shows low hyperemic effect and eye irritation in New Zealand White rabbits[1].

Animal Model:Chronic Ocular Hypertension Mouse Model induced by Microbead[1]
Dosage:0.26% (w/v), 10 μL
Administration:Ophthalmic drop; singel dose; administration in right eye 7 days after modeling, and measured IOP prior to and at 1, 2, 3, 4, and 6 h after instillation
Result:Reduced IOP (mmHg) to 3.68 ± 0.5 mmHg (19.9%) and 1.36 ± 0.6 mmHg (7.4%) at 1 and 4 h after instillation, respectively.
Animal Model:New Zealand White rabbits[1]
Dosage:0.579% (w/v); 25 μL
Administration:Ophthalmic drop; singel dose; administration in left eye before and at 1, 2, and 4 h after the first instillation
Result:Showed low side effects in conjunctival hyperemia.
分子量

520.96

Formula

C20H26ClFN4O7S

CAS 号

2488395-07-7

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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