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TGF-β / Smad

TGF-β / Smad

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SR 3677 dihydrochloride

Catalog No. A12674
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ROCK 抑制剂

SR 3677 dihydrochloride是一种有效的选择性Rho激酶抑制剂（ROCK-II和ROCK-I的IC50值分别为3和56 nM）。了解更多

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Hydroxyfasudil hydrochloride

Catalog No. A15119
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ROCK 抑制剂

Hydroxyfasudil hydrochloride是法舒地尔的代谢产物，是一种有效的Rho激酶抑制剂和血管舒张剂。了解更多

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Hydroxyfasudil

Catalog No. A15118
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ROCK 抑制剂

Hydroxyfasudil是法舒地尔的代谢产物，是有效的Rho激酶抑制剂和血管舒张剂。了解更多

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Narciclasine

Catalog No. A15178
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ROCK activator

Narciclasine是Rho/Rho激酶/ LIM激酶/ cofilin信号通路激活剂。了解更多

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ROCK inhibitor

Catalog No. A15225
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ROCK 抑制剂

ROCK inhibitor是人类ROCK-1和ROCK-2同工酶的高效抑制剂，IC50值分别为0.6和1.1 nM。了解更多

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- Nina Seidelmann, .et al. Human platelet lysate as a replacement for fetal bovine serum in human corneal stromal keratocyte and fibroblast culture, J Cell Mol Med, 2021, Oct;25(20):9647-9659 PMID: 34486211
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ROCK inhibitor-1

Catalog No. A15226
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ROCK 抑制剂

N/A 了解更多

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LX7101

Catalog No. A16211
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LIMK2 抑制剂

LX7101是基于吡咯并嘧啶的局部递送的LIM域激酶2（LIMK2）抑制剂，LIM域激酶2是与眼内压调节相关的激酶。了解更多

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Ripasudil

Catalog No. A15888
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ROCK inhibitor

Ripasudil (K-115) is potent ROCK inhibitor with IC50 of 51 nM and 19 nM for ROCK1 and ROCK2, respectively, used for the treatment of glaucoma and ocular hypertension. 了解更多

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SAR407899 HCl

Catalog No. A15921
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ROCK 抑制剂

SAR407899是一种有效且选择性的Rho激酶抑制剂，具有良好的抗高血压活性。了解更多

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SLx-2119 (KD025)

Catalog No. A15239
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ROCK2 抑制剂

SLx-2119 (KD025)是ROCK2的小分子和选择性抑制剂，IC50为105 nM。在ROCK1上的选择性> 200倍（IC50 = 24 uM）。了解更多

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Glycyl-H 1152 2HCl

Catalog No. A13659
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ROCK 抑制剂

Glycyl-H 1152 2HCl是一种选择性有效的ROCK抑制剂（ROCKII，Aurora A，CAMKII，PKG，PKA和PKC的IC50值分别为0.0118、2.35、2.57、3.26，> 10和> 10 uM。）了解更多

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H-1152 dihydrochloride

Catalog No. A15102
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ROCK 抑制剂

H-1152 dihydrochloride是一种异喹啉磺酰胺衍生物，是Rho激酶的一种更特异，更强且可透过膜的抑制剂，Ki值为1.6 nM，但对其他丝氨酸/苏氨酸激酶的抑制作用较弱。了解更多

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H-1152

Catalog No. A15101
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ROCK 抑制剂

H-1152是一种异喹啉磺酰胺衍生物，是Rho激酶的一种更特异，更强且可透过膜的抑制剂，Ki值为1.6 nM，但对其他丝氨酸/苏氨酸激酶的抑制作用较差。了解更多

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chroman 1

Catalog No. A15045
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ROCK 抑制剂

Chroman 1 是一种高效且选择性的ROCK II抑制剂。了解更多

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RKI-1447

Catalog No. A13067
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ROCK1/ROCK2 抑制剂

RKI-1447是Rho相关ROCK激酶的有效抑制剂，在乳腺癌中具有抗侵袭和抗肿瘤活性。了解更多

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Y-33075

Catalog No. A11610
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ROCK 抑制剂

Y-33075是ROCK（Rho相关的卷曲螺旋形成蛋白激酶）抑制剂。了解更多

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HA-1077 dihydrochloride

Catalog No. A13785
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ROCK 抑制剂

HA-1077 dihydrochloride通过充当细胞内Ca2+拮抗剂来抑制血管平滑肌收缩。了解更多

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Fasudil HCl (HA-1077)

Catalog No. A10381
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ROCK 抑制剂

Fasudil HCl (HA-1077)是一种环状核苷酸依赖性蛋白激酶抑制剂和Rho相关激酶抑制剂（IC50 = 10.7μM）。了解更多

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- Chengyu Xiang, .et al. Fasudil Ameliorates Osteoporosis Following Myocardial Infarction by Regulating Cardiac Calcitonin Secretion, J Cardiovasc Transl Res, 2022, May 12 PMID: 35551627
- Yeonmi Lee, .et al. Haploidy in somatic cells is induced by mature oocytes in mice, Commun Biol, 2022, Jan 25;5(1):95 PMID: 35079104
- Jiwan Choi, .et al. Efficient hepatic differentiation and regeneration potential under xeno-free conditions using mass-producible amnion-derived mesenchymal stem cells, Stem Cell Res Ther, 2021, Nov 12;12(1):569
- Jee Myung Yang, .et al. Long-term effects of human induced pluripotent stem cell-derived retinal cell transplantation in Pde6b knockout rats, Exp Mol Med, 2021, Apr;53(4):631-642 PMID: 33828232
- Jooyoung Lee, .et al. Hepatogenic Potential and Liver Regeneration Effect of Human Liver-derived Mesenchymal-Like Stem Cells, Cells, 2020, Jun; 9(6): 1521 PMID: 32580448
- Kumar M, .et al. Fasudil hydrochloride ameliorates memory deficits in rat model of streptozotocin-induced Alzheimer's disease: Involvement of PI3-kinase, eNOS and NFκB, Behav Brain Res, 2018, Oct 1;351:4-16 PMID: 29807069
- Wei J, .et al. Inhibition of RHO Kinase by Fasudil Attenuates Ischemic Lung Injury After Cardiac Arrest in Rats, Shock, 2018, Dec;50(6):706-713 PMID: 29283979
- Hofni A, .et al. Fasudil ameliorates endothelial dysfunction in streptozotocin-induced diabetic rats: a possible role of Rho kinase, Naunyn Schmiedebergs Arch Pharmacol, 2017, Aug;390(8):801-811 PMID: 28493050
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GSK 269962

Catalog No. A12348
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ROCK 抑制剂

GSK 269962是一种强效Rho激酶(ROCK)抑制剂(重组人ROCK1和ROCK2的IC50值分别为1.6和4 nM)。了解更多

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- Praneeth Siripurapu, .et al. Two independent but synchronized Gβγ subunit-controlled pathways are essential for trailing-edge retraction during macrophage migration, J Biol Chem, 2017, Oct 20; 292(42): 17482-17495 PMID: 28864771
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GSK429286A

Catalog No. A10441
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ROCK 抑制剂

GSK429286A是含有蛋白激酶(ROCK)的Rho相关卷曲螺旋的细胞渗透性选择性小分子抑制剂。了解更多

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Thiazovivin

Catalog No. A10928
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ROCK 抑制剂

Thiazovivin是一种Rho相关激酶（ROCK）的选择性抑制剂。了解更多

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RKI-1313

Catalog No. A10899
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ROCK 抑制剂

RKI-1313是RKI-1447的阴性对照，RKI-1447是Rho相关的ROCK激酶的有效抑制剂，在乳腺癌中具有抗侵袭和抗肿瘤活性。了解更多

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BMS-5

Catalog No. A12839
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LIMK 抑制剂

BMS-5是一种有效的LIMK抑制剂，对LIMK1和LIMK2的IC50分别为7 nM和8 nM。了解更多

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BDP5290

Catalog No. A16966
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ROCK and MRCK 抑制剂

BDP5290是ROCK和MRCK的有效抑制剂，对ROCK1，ROCK2，MRCKα和MRCKβ的IC50分别为5 nM，50 nM，10 nM和100 nM。了解更多

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R-10015

Catalog No. A18806
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LIMK inhibitor

R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent and selective inhibitor of LIM domain kinase (LIMK) and binds to the ATP-binding pocket, with an IC50 of 38 nM for human LIMK1. 了解更多

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ROCK inhibitor-2

Catalog No. A18912
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ROCK1/ROCK2 inhibitor

ROCK inhibitor-2 is a selective dual ROCK1 and ROCK2 inhibitor with IC50s of 17 nM and 2 nM, respectively. 了解更多

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T56-LIMKi

Catalog No. A12266
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LIMK2 inhibitor

T56-LIMKi is a selective inhibitor of LIMK2; inhibits the growth of Panc-1 cells with an IC50 of 35.2 μM. 了解更多

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Y-33075 dihydrochloride

Catalog No. A11611
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ROCK inhibitor

Y-33075 dihydrochloride is a selective ROCK inhibitor with an IC50 of 3.6 nM. 了解更多

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Y-27632

Catalog No. A21448
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ROCK-I/ROCK-II inhibitor

Y-27632 is an ATP-competitive inhibitor of ROCK-I and ROCK-II, with Ki of 220 nM and 300 nM for ROCK-I and ROCK-II, respectively. 了解更多

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- Renata Santos, .et al. Generation of inflammation-responsive astrocytes from glial progenitors derived from human pluripotent stem cells, STAR Protoc, 2022, Mar 17;3(2):101261 PMID: 35313707
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Fasudil

Catalog No. A21628
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ROCK inhibitor

Fasudil (HA-1077; AT877), is a nonspecific ROCK inhibitor and also has inhibitory effect on protein kinases. 了解更多

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BMS-3

Catalog No. A20999
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LIMK inhibitor

BMS-3 is a potent LIMK inhibitor with IC50s of 5 nM and 6 nM for LIMK1 and LIMK2, respectively. 了解更多

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Y-27632 2HCl

Catalog No. A11001
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ROCK 抑制剂

Y-27632是一种Rho相关的线圈激酶（ROCK）抑制剂，可提高人类胚胎干细胞（hESCs）的克隆效率。比对其他激酶包括PKC，cAMP依赖性蛋白激酶，MLCK和PAK的作用强200多倍。了解更多

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- Sergio Pedraza-Arevalo, .et al. Differentiation of beta-like cells from human induced pluripotent stem cell-derived pancreatic progenitor organoids, STAR Protoc, 2022, Aug 30;3(3):101656 PMID: 36092820
- Ji-Hyun Lee, .et al. p57Kip2 imposes the reserve stem cell state of gastric chief cells, Cell Stem Cell, 2022, May 5; 29(5): 826-839 PMID: 35523142
- Adam Pietrobon, .et al. Renal organoid modeling of tuberous sclerosis complex reveals lesion features arise from diverse developmental processes, Cell Rep, 2022, Jul 5;40(1):111048 PMID: 35793620
- Sarkawt Hamad, .et al. High-efficient serum-free differentiation of endothelial cells from human iPS cells, Stem Cell Res Ther, 2022, Jun 11;13(1):251 PMID: 35690874
- Stasia Krishtul, .et al. Development of a bioactive microencapsulation platform incorporating decellularized extracellular matrix to entrap human induced pluripotent stem cells for versatile biomedical applications, Polym Adv Technol, 2022, 33( 11): 3842-3852
- Peter T Ruane, .et al. Trophectoderm differentiation to invasive syncytiotrophoblast is promoted by endometrial epithelial cells during human embryo implantation, Hum Reprod, 2022, Apr 1;37(4):777-792 PMID: 35079788
- Takayuki Miyoshi, .et al. Successful induction of human chemically induced liver progenitors with small molecules from damaged liver, J Gastroenterol, 2022, Jun;57(6):441-452 PMID: 35294680
- Ana-Maria Cujba, .et al. An HNF1α truncation associated with maturity-onset diabetes of the young impairs pancreatic progenitor differentiation by antagonizing HNF1β function, Cell Rep, 2022, Mar 1;38(9):110425 PMID: 35235779
- Dan Zhao, .et al. From crypts to enteroids: establishment and characterization of avian intestinal organoids, Poult Sci, 2022, Mar; 101(3): 101642 PMID: 35016046
- Antigoni Gogolou, .et al. Generating Enteric Nervous System Progenitors from Human Pluripotent Stem Cells, Curr Protoc, 2021, Jun;1(6):e137 PMID: 34102038
- Tiago De Oliveira, .et al. Effects of the Novel PFKFB3 Inhibitor KAN0438757 on Colorectal Cancer Cells and Its Systemic Toxicity Evaluation In Vivo, Cancers (Basel), 2021, Mar 2;S2451-9456(21)00095-7 PMID: 33671096
- Denise Muller, .et al. Functional apoptosis profiling identifies MCL-1 and BCL-xL as prognostic markers and therapeutic targets in advanced thymomas and thymic carcinomas, BMC Med, 2021, Nov 16;19(1):300 PMID: 34781947
- Ayumi Horikawa, .et al. A simple method of hiPSCs differentiation into insulin-producing cells is improved with vitamin C and RepSox, PloS one, 2021, Jul 12;16(7):e0254373 PMID: 34252142
- Hayato Mizuta, .et al. Gilteritinib overcomes lorlatinib resistance in ALK-rearranged cancer, Nat Commun, 2021, Feb 24;12(1):1261 PMID: 33627640
- Scott Bell, .et al. Lesch-Nyhan disease causes impaired energy metabolism and reduced developmental potential in midbrain dopaminergic cells, Stem Cell Reports, 2021, Jul 13;16(7):1749-1762 PMID: 34214487
- Shenyang Li, .et al. Effect of porcine corneal stromal extract on keratocytes from SMILE-derived lenticules, J Cell Mol Med, 2020, Dec 20;25(2):1207-1220 PMID: 33342057
- Takao FUCHIGAMI, .et al. Ameloblastoma cell lines derived from different subtypes demonstrate distinct developmental patterns in a novel animal experimental model, J Appl Oral Sci, 2020, 28: e20190558 PMID: 32348439
- Jing-Yu Lin, .et al. In vitro expansion of pancreatic islet clusters facilitated by hormones and chemicals, Cell Discov, 2020, 6: 20 PMID: 32284878
- Yu Huang, .et al. Development of Bifunctional Three-Dimensional Cysts from Chemically Induced Liver Progenitors, Stem Cells Int, 2019, 2019: 3975689 PMID: 31565060
- XinYan, .et al. Establishment of CSUASOi001-A, a non-integrated induced pluripotent stem cell line from urine-derived cells of a Chinese patient carrying RS1 gene mutation, Stem Cell Res, 2019, May 17 PMID: 31141763
- Daniela F. Duarte Campos, .et al. Corneal bioprinting utilizing collagen?\based bioinks and primary human keratocytes, J Biomed Mater Res A, 2019, April 22 PMID: 31012205
- Scott Bell, .et al. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons, Am J Hum Genet, 2019, May 2;104(5):815-834 PMID: 31031012
- Ooi J, .et al. Unbiased Profiling of Isogenic Huntington Disease hPSC-Derived CNS and Peripheral Cells Reveals Strong Cell-Type Specificity of CAG Length Effects, Cell Rep, 2019, Feb 26;26(9):2494-2508 PMID: 30811996
- Scott Bell, .et al. Disruption of GRIN2B Impairs Differentiation in Human Neurons, Stem Cell Reports, 2018, Jul 10; 11(1):183-196 PMID: 29937144
- Christina Zarouchlioti, .et al. Antisense Therapy for a Common Corneal Dystrophy Ameliorates TCF4 Repeat Expansion-Mediated Toxicity, Am J Hum Genet, 2018, Apr 5; 102(4): 528-539 PMID: 29526280
- Ai Takemoto, .et al. A critical role of platelet TGF-β release in podoplanin-mediated tumour invasion and metastasis, Sci Rep, 2017, 7: 42186 PMID: 28176852
- Scott Bell, .et al. A Rapid Pipeline to Model Rare Neurodevelopmental Disorders with Simultaneous CRISPR/Cas9 Gene Editing, Stem Cells Transl Med, 2017, Mar; 6(3): 886-896 PMID: 28170165
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A-674563

Catalog No. A11034
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Akt 抑制剂

A-674563是一种B/Akt抑制剂，IC50为14 nM，并且还显示出对PKA和CDK2的抑制活性，IC50分别为16和46 nM。了解更多

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- Kobayashi T, .et al. A-674563 increases chondrocyte marker expression in cultured chondrocytes by inhibiting Sox9 degradation, Biochem Biophys Res Commun, 2018, Jan 1;495(1):1468-1475 PMID: 29196261
- Lin Xu, .et al. Concurrent targeting Akt and sphingosine kinase 1 by A-674563 in acute myeloid leukemia cells, Biochem Biophys Res Commun, 2016, Apr 15;472(4):662-8 PMID: 26920060
- Zou Y, .et al. Pre-clinical assessment of A-674563 as an anti-melanoma agent, Biochem Biophys Res Commun, 2016, Aug 12;477(1):1-8 PMID: 26970307
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H 89 2HCl

Catalog No. A11935
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PKA 抑制剂

H 89 dihydrochloride是一种可渗透细胞的，选择性的，可逆的，具有ATP竞争性的有效蛋白激酶抑制剂。了解更多

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- Guo Q, .et al. Antineuropathic pain actions of Wu-tou decoction resulted from the increase of neurotrophic factor and decrease of CCR5 expression in primary rat glial cells, Biomed Pharmacother, 2020, Mar;123:109812 PMID: 31945696
- Y Kaibori, .et al. EphA2 phosphorylation at Ser897 by the Cdk1/MEK/ERK/RSK pathway regulates M-phase progression via maintenance of cortical rigidity, the FASEB Journal, 2019, Jan 22:fj201801519RR PMID: 30668924
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AT13148

Catalog No. A12464
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multi-AGC kinase 抑制剂

AT13148是一种新型多AGC激酶抑制剂，具有强大的药效和抗肿瘤活性，与其他AKT抑制剂相比，具有独特的作用机理。了解更多

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AT7867 2HCl

Catalog No. A15006
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Akt 抑制剂

AT7867 dihydrochloride是一种有效的ATP竞争性Akt1/2/3和p70S6K/PKA抑制剂，IC50分别为32 nM/17 nM/47 nM和85 nM/20 nM，在AGC激酶家族之外几乎没有活性。了解更多

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8-Bromo-cAMP

Catalog No. A15910
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protein kinase A activator

8-Bromo-cAMP是细胞可透过的环AMP（cAMP）类似物和PKA激活剂。了解更多

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KT 5720

Catalog No. A16016
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PKA 抑制剂

KT5720 是一种能透过细胞的、有效的、特异性的、可逆的、ATP 竞争性的蛋白酶 K (PKA) 的抑制剂，其 Ki 值为 60 nM。了解更多

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PKI 14-22 amide, myristoylated

Catalog No. A16031
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PKA 抑制剂

PKI 14-22 amide, myristoylated是有用的热稳定的cAMP依赖性蛋白激酶抑制剂。这通常用于体外研究细胞系统中的PKA。了解更多

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- Dao-Lai Zhang, .et al. Gq activity- and β-arrestin-1 scaffolding-mediated ADGRG2/CFTR coupling are required for male fertility, eLife, 2018, 7: e33432 PMID: 29393851
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cGMP Dependent Kinase Inhibitor Peptid

Catalog No. A16052
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PKG/PKA 抑制剂

cGMP Dependent Kinase Inhibitor Peptid是一种特定的cGKI（环GMP依赖性蛋白激酶）抑制剂。数据表明，它不阻断完整组蛋白的环状GMP依赖性蛋白激酶磷酸化，已被用于研究恶性疟原虫。了解更多

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CCG215022

Catalog No. A16189
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GRK2/5 抑制剂

CCG215022是有效的GRK2和GRK5抑制剂。CCG215022对GRK2和GRK5均表现出纳摩尔IC50值，对其他紧密相关的激酶（如GRK1和PKA）具有良好的选择性。了解更多

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Synaptamide

Catalog No. A16222
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Synaptamide是通过PKA/CREB激活起作用的NSC神经源性分化的有效介体。了解更多

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A-3 Hydrochloride

Catalog No. A13584
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PKA, PKG, Casein Kinase I and II 抑制剂

A-3 Hydrochloride是PKA（cAMP依赖性蛋白激酶，Ki =4.3μM）和cGMP依赖性蛋白激酶，Ki =3.8μM，PKC（蛋白激酶C，Ki =47μM），酪蛋白激酶I和II的抑制剂，和MLCK（肌球蛋白轻链激酶）（Ki =7.4μM）。了解更多

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PKA inhibitor fragment (6-22) amide

Catalog No. A14868
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PKA 抑制剂

PKA inhibitor fragment (6-22) amide是一种合成肽，可作为蛋白激酶抑制剂。了解更多

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Dibutyryl-cAMP

Catalog No. A15914
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PKA activator

Dibutyryl-cAMP是模仿内源性cAMP的作用的细胞渗透性PKA激活剂。了解更多

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6-Bnz-cAMP sodium salt

Catalog No. A16017
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PKA-selective activator

6-Bnz-cAMP sodium salt是PKA选择性激活剂。它调节PKA依赖性信号传导途径。了解更多

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cAMPS-Rp, triethylammonium salt

Catalog No. A16028
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reversible PKA 抑制剂

cAMPS-Rp,triethylammonium salt是PKA（蛋白激酶A）（Ki = 11 uM）的细胞渗透性和可逆抑制剂.Rp-cAMPS耐磷酸二酯酶水解，相对于ATP不具竞争力。了解更多

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LY317615 (Enzastaurin)

Catalog No. A10356
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PKCβ 抑制剂

LY317615（Enzastaurin）是一种有效的，选择性的PKCβ抑制剂，具有抗增殖活性（IC50 =?6 nM）。了解更多

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Daphnetin

Catalog No. A10286
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EGFR, PKA,PKC 抑制剂

Daphnetin是一种香豆素类似物，可作为几种蛋白激酶的抑制剂。它在体外抑制EGFR激酶（IC50 = 7.67 ?M），PKA（IC50 = 9.33 ?M）和PKC（IC50 = 25 ?M）。蜂胶对EGFR激酶的抑制作用与ATP竞争，对肽底物没有竞争性。还可以用作有效的抗氧化剂和抗疟疾剂。了解更多

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Quercetin (Sophoretin)

Catalog No. A10766
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MAO-B 抑制剂

Quercetin (Sophoretin)抑制许多酶系统，包括酪氨酸蛋白激酶，磷脂酶A2，磷酸二酯酶，线粒体ATPase，PI 3-激酶和蛋白激酶C。了解更多

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