首页工具

登录

搜索结果

Search Results for " rock2 "

47

抑制剂 & 化合物

1

天然产物

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T12747	ROCK2-IN-2	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK2-IN-2 是 ROCK2 的特异性抑制剂（IC50 <1 μM）。
T81261	ROCK2-IN-7	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK2-IN-7是针对ROCK2的激酶抑制剂，能够抑制ROCK2/pSTAT3信号通路。该化合物在治疗银屑病模型中有着明显效果，通过抑制全身免疫激活，从而减轻炎症。
T79832	ROCK2-IN-6	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK2-IN-6 (Comp A) 是一種选择性针对ROCK2的抑制剂，适用于研究ROCK介导的病症、自身免疫性疾病以及炎症。
T73117	ROCK2-IN-5
	ROCK2-IN-5是一种复合型化合物，融合了Rho激酶抑制剂fasudil以及NRF2诱导剂咖啡酸和阿魏酸的结构元素。该化合物展示了优秀的多靶点作用特性和较高的耐受性。ROCK2-IN-5在针对SOD1基因变异型ALS研究中具备应用潜力。
T78205	ROCK2-IN-6 hydrochloride	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK2-IN-6 hydrochloride (Comp A)为一种选择性ROCK2抑制剂，适用于研究ROCK介导的疾病、自身免疫性病症与炎症。
T3518	GSK269962A GSK269962B,GSK 269962,GSK269962A HCl	ROCK; S6 Kinase	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling; Stem Cells
	GSK269962A (GSK269962A HCl) 是一种有效的ROCK 抑制剂，具有抗炎和血管舒张作用。它作用于重组人ROCK1和ROCK2，IC50分别为 1.6 和 4 nM。
T6867	Belumosudil KD025,Rezurock,ROCK inhibitor,SLx-2119	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Belumosudil (Rezurock) 是一种选择性的ROCK2抑制剂，对 ROCK1 和 ROCK2 的IC50值分别为 24 µM 和 105 nM，具有抗纤维化作用。
T13419	ROCK-IN-1	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK-IN-1 是一种高效的 ROCK 抑制剂，对 ROCK2 介导的信号传导有抑制作用，IC50 值为 1.2 nM。ROCK-IN-1 可用于研究神经系统疾病和炎症相关疾病。
T12746	ROCK inhibitor-2	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK inhibitor-2 是一种 ROCK1和 ROCK2的选择性双重抑制剂，IC50值分别为 17 nM 和2 nM。
T15798	LX7101	ROCK; LIM Kinase; PKA	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors
	LX7101是 LIMK 和ROCK2高效抑制剂，对LIMK1/2、ROCK、PKA 的IC50分别为24、1.6、10 和小于1 nM。
T14960	Chroman 1	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Chroman 1 是高效的的ROCK 选择性抑制剂，对 ROCK2 (IC50=1 pM) 的抑制作用强于 ROCK1 (IC50=52 pM) 。它对MRCK 也有抑制作用，IC50为 150 nM。
T22037	AS 1892802	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	AS 1892802是一种强效和选择性的ROCK 抑制剂。AS 1892802 用于人ROCK2、大鼠ROCK2和人ROCK1的 IC50值分别为52nM、57nM 和122nM。AS 1892802的镇痛作用起效速度与曲马多和双氯芬酸的起效速度一样快。
TQ0187	SR-3677	ROCK; Autophagy	Autophagy; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	SR-3677 是一种有效且特异性的 ROCK2 抑制剂，IC50值为3 nM。
T7301	BDP5290	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	BDP5290 是一种有效 ROCK 和 MRCK 抑制剂，对 ROCK1、ROCK2、MRCKα 和 MRCKβ 的 IC50 分别为 5、50 、10 和 100 nM。
T1898	RKI-1447 RKI1447	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	RKI-1447 是一种高效的ROCK1和ROCK2的小分子抑制剂，IC50值分别为14.5和6.2 nM。
T4276L	Hydroxyfasudil Hydroxy-Fasudil,HA-1100,羟基法舒地尔	ROCK; PKA	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells; Tyrosine Kinase/Adaptors
	Hydroxyfasudil (Hydroxy-Fasudil) 是一种ROCK 抑制剂，对ROCK1和ROCK2的IC50分别为 0.73 和 0.72 μM。
T12721	Rho-Kinase-IN-1	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Rho-Kinase-IN-1 是一种 ROCK 抑制剂，对 ROCK1 和 ROCK2 的 Kis 分别为 30.5 nM 和 3.9 nM。 Rho-Kinase-IN-1 可用于细胞过度增殖、重塑、水肿和炎症疾病的研究。
T23308	SAR407899 hydrochloride 6-(哌啶-4-氧基)异喹啉-1(2H)-酮盐酸盐	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	SAR407899 hydrochloride 是一种选择性，ATP 竞争性的ROCK 抑制剂，对人和大鼠ROCK2的Ki 值分别为 36 和 41 nM，对ROCK2的IC50值为 135 nM。
TQ0319	Ripasudil K-115,瑞舒地尔盐酸二水合物,Ripasudil hydrochloride dihydrate	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Ripasudil (Ripasudil hydrochloride dihydrate) 是一种 ROCK 特异性抑制剂，能够抑制 ROCK1和 ROCK2的活性，IC50值分别为 51 和 19 nM。
T69665	Zelasudil
	Zelasudil 是一种 Rho 相关 (ROCK) 激酶抑制剂。Zelasudil 具有 ROCK2结合亲和力。
T60924	Verosudil AR-12286	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Verosudil (AR-12286) 是一种高效的 Rho 激酶 (ROCK) 抑制剂，对 ROCK1 和 ROCK2 的 Ki 分别为 2 和 2 nM。AR-12286 可逆转类固醇诱导的小鼠眼内压，可通过增加眼房水通过小梁网流出来减缓眼压。
T4276	Hydroxyfasudil Hydrochloride Hydroxyfasudil (HA-1100) HCl,羟基法舒地尔盐酸盐,RHO-激酶抑制剂,HA 1100 hydrochloride	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Hydroxyfasudil Hydrochloride (HA 1100 hydrochloride) 是一种ROCK 抑制剂，对ROCK1和ROCK2的IC50值分别为 0.73 和 0.72 μM。
T1606	Fasudil HA-1077,AT877,法舒地尔	ROCK; Serine/threonin kinase; Calcium Channel; PKA; PKC; Autophagy	Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; Membrane transporter/Ion channel; Metabolism; Stem Cells; Tyrosine Kinase/Adaptors
	Fasudil (HA-1077) 是一种非特异性 RhoA/ROCK 抑制剂，也是 Ca2+通道拮抗剂和血管扩张剂。它对蛋白激酶有抑制作用，ROCK1 的 Ki 值为 0.33 μM，ROCK2 和 PKA、PKC、PKG 的 IC50值分别 0.158 μM 和 4.58 μM、12.30 μM、1.650 μM。
T16855	SB-772077B dihydrochloride	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	SB-772077B dihydrochloride is an aminofurazan-based Rho kinase inhibitor (IC50s: 5.6 nM and 6 nM toward ROCK1 and ROCK2, respectively).
T39555	Belumosudil mesylate SLx-2119mesylate,KD025 mesylate
	Belumosudil mesylate (KD025 mesylate) is a selective inhibitor of ROCK2 with IC 50 s of 105 nM and 24 μM for ROCK2 and ROCK1, respectively. Anti-fibrotic properties.
T39944	HSD1590
	HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.
T79077	ROCK-IN-6	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK-IN-6为一有效的ROCK2抑制剂，其IC50值为2.19 nM。该化合物具备用于研究青光眼及视网膜疾病的潜力。
T70024	BA-1049
	BA-1049 is a selective ROCK2 inhibitor.
T74808	THK01
	THK01 是一种有效的 ROCK2抑制剂，对 ROCK2和 ROCK1的 IC50值分别为 5.7 和 923 nM。THK01 通过 ROCK2-STAT3 信号通路抑制乳腺癌转移。THK01 可用于乳腺癌研究。
T7391	SAR407899	ROCK; Rho	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	SAR407899 是一种选择性的 ATP 竞争性ROCK 抑制剂，对ROCK-2的IC50值为 135 nM，对人和大鼠ROCK-2的Ki 值分别为 36 和 41 nM。它是 Rho 激酶抑制剂，有效抑制 endothelin-1 诱导的肾阻力动脉收缩。
T2633	GSK429286A RHO-15	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	GSK429286A (RHO-15) 是一种选择性ROCK1/2抑制剂，IC50值为14 和 63 nM。
T39519	GSK269962A hydrochloride GSK 269962 hydrochloride
	GSK269962A hydrochloride (GSK 269962 hydrochloride) is a highly potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.6 nM and 4 nM, respectively, for recombinant human isoforms. This compound exhibits both anti-inflammatory and vasodilatory properties.
T61497	Rho-Kinase-IN-2
	Rho-Kinase-IN-2 (Compound 23) is an orally active and selective inhibitor of Rho Kinase (ROCK), which can penetrate the central nervous system (CNS). It exhibits a high affinity for ROCK2 with an inhibition constant (IC50) of 3 nM. This compound is of potential interest for further investigations in the field of Huntington's disease research [1].
T26821	BIPM
	BIPM is a potent inhibitor of Rho-associated protein kinase 2 (ROCK2). Exposure of SH-SY5Y cells to BIPM led to significant changes in cell migration, actin stress fibers and neurite length. BIPM significantly inhibits phosphorylation of cofilin, a regula
T61905	RKI-1447 dihydrochloride
	RKI 1447 dihydrochloride 是一种有效的，选择性的 ROCK 抑制剂（ROCK1 IC50=14.5 nM，ROCK2 IC50 = 6.2 nM）。RKI 1447 dihydrochloride 对结直肠癌细胞的生长具有抑制作用，并促进其凋亡。
T63506	Chroman 1 dihydrochloride
	Chroman 1 dihydrochloride 是选择性的 ROCK 高效抑制剂，对 ROCK2 (IC50: 1 pM) 的作用比 ROCK1 (IC50: 52 pM) 更强，也能够抑制 MRCK 的活性 (IC50: 150 nM)。
T14989	CMPD101	ROCK; GRK; PKC	Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; GPCR/G Protein; Stem Cells
	CMPD101 是膜透性的 GRK2/3高选择性小分子抑制剂，IC50分别为 18 nM 和 5.4 nM。它针对 GRK1、GRK5 ROCK-2 和 PKCα 的选择性较小，IC50值分别为 3.1 μM，2.3 μM，1.4 μM 和 8.1 μM，可研究心衰疾病。
TQ0110	ROCK-IN-2 TC-S 7001,Azaindole 1	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	ROCK-IN-2 (Azaindole 1) 是一种选择性，ATP-竞争型的ROCK 抑制剂，对ROCK-1和ROCK-2的IC50值分别为 0.6 和 1.1 nM。
T61382	Fasudil dihydrochloride
	Fasudil dihydrochloride, also known as HA-1077 and AT877, is a nonspecific inhibitor of RhoA/ROCK. It exhibits inhibitory effects on protein kinases, including ROCK1 with a Ki value of 0.33 μM, as well as ROCK2, PKA, PKC, and PKG with IC 50 values of 0.158 μM, 4.58 μM, 12.30 μM, and 1.650 μM, respectively. Additionally, Fasudil dihydrochloride demonstrates potent Ca 2+ channel blocking activity and acts as a vasodilator [1] [2] [3].
T1725	Y-27632 dihydrochloride 反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐,Y-27632 2HCl	ROCK; Apoptosis	Apoptosis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	Y-27632 dihydrochloride (Y-27632 2HCl) 是一种 ROCK-I 和 ROCK-II 抑制剂，具有口服有效性、ATP 竞争性。Y-27632 dihydrochloride 还抑制分离诱导的小鼠前列腺干或祖细胞凋亡。
T7552	H-1152	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	H-1152 是一种膜通透的选择性ROCK 抑制剂，Ki 为 1.6 nM，对ROCK2的IC50为 12 nM。
T7492	Ripasudil free base K-115 (free base)	ROCK; Antibacterial	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Microbiology/Virology; Stem Cells
	Ripasudil free base (K-115 (free base)) 是一种ROCK 特异性抑制剂，能够抑制ROCK1和ROCK2的活性，IC50值分别为 51 和 19 nM。
T71119	Netarsudil free base
	Netarsudil, also known as AR-11324, is a Rho-associated protein kinase inhibitor. Netarsudil is potential useful for treating glaucoma and/or reducing intraocular pressure. Netarsudil Increases Outflow Facility in Human Eyes Through Multiple Mechanisms. Netarsudil inhibited kinases ROCK1 and ROCK2 with a Ki of 1 nM each, disrupted actin stress fibers and focal adhesions in TM cells with IC50s of 79 and 16 nM, respectively, and blocked the profibrotic effects of TGF-β2 in HTM cells. Netarsudi...
T2482	AT13148	ROCK; SGK; Akt; PKA; S6 Kinase	Cell Cycle/Checkpoint; Cytoskeletal Signaling; MAPK; Metabolism; PI3K/Akt/mTOR signaling; Stem Cells; Tyrosine Kinase/Adaptors
	AT13148 是一种 ATP 竞争性 AGC 激酶口服抑制剂，能够抑制 Akt1/Akt2/Akt3、p70S6K、PKA 和 ROCKI/ROCKII 的活性，IC50值分别为 38/402/50、8、3 和 6 nM/4 nM。
T35328	H-1152 dihydrochloride H-1152 2HCl,H-1152 dihydrochloride	ROCK	Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells
	H-1152 dihydrochloride (H-1152 2HCl) 是 Rho 相关蛋白激酶 (ROCK) 的特异性抑制剂，IC50 为 12 nM，Ki 为 1.6 nM。 H-1152 dihydrochloride 抑制 PKA、PKC、PKG、Aurora A 和 CaMKII，IC50 值分别为 3.03 μM、5.68 μM、0.360 μM、0.745 μM 和 0.180 μM。
T27089	CRT0066854 CRT0066854 HCl,CRT-0066854 HCl,CRT 0066854,CRT-0066854
	CRT-0066854 is a PKCι and PKCζ inhibitor. CRT0066854 was able to restore polarized morphogenesis in the dysplastic H-Ras spheroids.
T15428	Uprosertib hydrochloride GSK2141795 (hydrochloride)	Others	Others
	Uprosertib hydrochloride is a potent and selective inhibitor of pan-Akt (IC50: 180/328/38 nM for Akt1/Akt2/Akt3, respectively).

化合物

Cat.No: T12747

Target: ROCK

Cat.No: T81261

Target: ROCK

Cat.No: T79832

Target: ROCK

Cat.No: T73117

ROCK2-IN-6 hydrochloride

Cat.No: T78205

Target: ROCK

Cat.No: T3518

Synonym: GSK269962B,GSK 269962,GSK269962A HCl

Target: ROCK, S6 Kinase

Cat.No: T6867

Synonym: KD025,Rezurock,ROCK inhibitor,SLx-2119

Target: ROCK

Cat.No: T13419

Target: ROCK

ROCK inhibitor-2

Cat.No: T12746

Target: ROCK

Cat.No: T15798

Target: ROCK, LIM Kinase, PKA

Cat.No: T14960

Target: ROCK

Cat.No: T22037

Target: ROCK

Cat.No: TQ0187

Target: ROCK, Autophagy

Cat.No: T7301

Target: ROCK

Cat.No: T1898

Synonym: RKI1447

Target: ROCK

Cat.No: T4276L

Synonym: Hydroxy-Fasudil,HA-1100,羟基法舒地尔

Target: ROCK, PKA

Rho-Kinase-IN-1

Cat.No: T12721

Target: ROCK

SAR407899 hydrochloride

Cat.No: T23308

Synonym: 6-(哌啶-4-氧基)异喹啉-1(2H)-酮盐酸盐

Target: ROCK

Cat.No: TQ0319

Synonym: K-115,瑞舒地尔盐酸二水合物,Ripasudil hydrochloride dihydrate

Target: ROCK

Cat.No: T69665

Cat.No: T60924

Synonym: AR-12286

Target: ROCK

Hydroxyfasudil Hydrochloride

Cat.No: T4276

Synonym: Hydroxyfasudil (HA-1100) HCl,羟基法舒地尔盐酸盐,RHO-激酶抑制剂,HA 1100 hydrochloride

Target: ROCK

Cat.No: T1606

Synonym: HA-1077,AT877,法舒地尔

Target: ROCK, Serine/threonin kinase, Calcium Channel, PKA, PKC, Autophagy

SB-772077B dihydrochloride

Cat.No: T16855

Target: ROCK

Belumosudil mesylate

Cat.No: T39555

Synonym: SLx-2119mesylate,KD025 mesylate

Cat.No: T39944

Cat.No: T79077

Target: ROCK

Cat.No: T70024

Cat.No: T74808

Cat.No: T7391

Target: ROCK, Rho

Cat.No: T2633

Synonym: RHO-15

Target: ROCK

GSK269962A hydrochloride

Cat.No: T39519

Synonym: GSK 269962 hydrochloride

Rho-Kinase-IN-2

Cat.No: T61497

Cat.No: T26821

RKI-1447 dihydrochloride

Cat.No: T61905

Chroman 1 dihydrochloride

Cat.No: T63506

Cat.No: T14989

Target: ROCK, GRK, PKC

Cat.No: TQ0110

Synonym: TC-S 7001,Azaindole 1

Target: ROCK

Fasudil dihydrochloride

Cat.No: T61382

Y-27632 dihydrochloride

Cat.No: T1725

Synonym: 反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐,Y-27632 2HCl

Target: ROCK, Apoptosis

Cat.No: T7552

Target: ROCK

Ripasudil free base

Cat.No: T7492

Synonym: K-115 (free base)

Target: ROCK, Antibacterial

Netarsudil free base

Cat.No: T71119

Cat.No: T2482

Target: ROCK, SGK, Akt, PKA, S6 Kinase

H-1152 dihydrochloride

Cat.No: T35328

Synonym: H-1152 2HCl,H-1152 dihydrochloride

Target: ROCK

Cat.No: T27089

Synonym: CRT0066854 HCl,CRT-0066854 HCl,CRT 0066854,CRT-0066854

Uprosertib hydrochloride

Cat.No: T15428

Synonym: GSK2141795 (hydrochloride)

Target: Others

Cat. No.	Product Name	Target	Signaling Pathways
TN1985	Neoprzewaquinone A	ROCK; Pim; STAT	Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; JAK/STAT signaling; Stem Cells
	Neoprzewaquinone A (NEO) 是 S. miltiorrhiza 的活性成分，通过靶向 PIM1 阻断 ROCK2/STAT3 通路来抑制乳腺癌细胞迁移并促进平滑肌松弛。

天然产物

Neoprzewaquinone A

Cat.No: TN1985

Target: ROCK, Pim, STAT

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼