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                                Fasudil Hydrochloride | MedChemExpress
                                英文名稱:HA-1077 Hydrochloride; AT-877 Hydrochloride總訪問:140
                                國產(chǎn)/進(jìn)口:進(jìn)口半年訪問:19
                                產(chǎn)地/品牌:Medchemexpress (MCE)產(chǎn)品類別:生化試劑
                                規(guī)       格:10 mM * 1 mL; 100 mg 最后更新:2025-2-13
                                貨       號:HY-10341
                                CAS   號:105628-07-7
                                參考報價:605; 550; 770; 1252
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                                Fasudil Hydrochloride

                                CAS No. : 105628-07-7

                                MCE 國際站:Fasudil Hydrochloride

                                產(chǎn)品活性:Fasudil Hydrochloride (HA-1077 Hydrochloride; AT877 Hydrochloride) 是一種非特異性 ROCK 抑制劑,對蛋白激酶也有抑制作用,ROCK1 的 Ki 值為 0.33 μM,ROCK2 和 PKA,PKC,PKG 的 IC50 值分別 0.158 μM 和 4.58 μM,12.30 μM,1.650 μM。Fasudil Hydrochloride 也是一種有效的 Ca2+ 通道拮抗劑和血管擴(kuò)張劑。

                                研究領(lǐng)域:Cell Cycle/DNA Damage  |  Stem Cell/Wnt  |  Cytoskeleton  |  TGF-beta/Smad  |  Neuronal Signaling  |  Membrane Transporter/Ion Channel  |  Autophagy  |  Protein Tyrosine Kinase/RTK  |  Epigenetics  |  Anti-infection

                                作用靶點(diǎn):ROCK  |  Calcium Channel  |  Autophagy  |  PKA  |  PKC  |  HIV

                                In Vitro: Fasudil Hydrochloride (100 μM) inhibits cell spreading, the formation of stress fibers, and expression of α-SMA with concomitant suppression of cell growth in rat HSCs and human HSC-derived TWNT-4 cells.
                                Fasudil Hydrochloride (50-100 μM; 24 hours) inhibits the LPA-induced phosphorylation of ERK1/2, JNK, and p38 detected by western blotting in rat HSCs and human HSC-derived TWNT-4 cells.
                                Fasudil Hydrochloride (25-100 μM; 24 hours) suppresses transcription of collagen and TIMP, stimulates transcription of MMP-1 in human HSC-derived TWNT-4 cells.

                                In Vivo: Fasudil (30 μg) increases CBF by 50% via intra-coronary injection to dogs. Fasudil (0.01, 0.03, 0.1 and 0.3 mg/kg, bolus, i.v.) decreases MBP and increases HR, VBF, CBF, RBF, and FBF. Fasudil (1.0 ng/mL) increases cardiac output. Fasudil via i.v. produces a significant fall in MBP, left ventricular systolic pressure and total peripheral resistance with an increase in HR and cardiac output, but without obvious effect on right atrial pressure, dP/dt or left ventricular minute work in dogs. Fasudil exhibits protectable effects on cardiovascular disease and reduces the activation of JNK and attenuates mitochondrial-nuclear translocation of AIF under ischemic injury. Fasudil (100 mg/kg/day, p.o.) significantly reduces incidence and mean maximum clinical score of EAE in SJL/J mice immunized with PLP p139-151. Fasudil inhibits the proliferative response of splenocytes to the antigen in mice. Fasudil decreases inflammation, demyelination, axonal loss and APP positivein spinal cord of Fasudil-treated mice via p.o. administration.

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