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Cat. No. | Product Name | Target | Signaling Pathways |
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T10283 |
ALK-IN-5
|
ALK | Angiogenesis; Tyrosine Kinase/Adaptors |
ALK-IN-5 is a potent, selective, and brain-penetrant inhibitor of anaplastic lymphoma kinase (ALK, IC50: 2.9 nM). | |||
T3031 |
A 83-01
ALK5 Inhibitor IV,A8301 |
ALK; TGF-beta/Smad | Angiogenesis; Stem Cells; Tyrosine Kinase/Adaptors |
A 83-01 (ALK5 Inhibitor IV) 是一种 TGF-βI 型受体 ALK5、ALK4 和 ALK7 的抑制剂 (IC50=12/45/7.5 nM)。A 83-01 可促进小鼠成纤维细胞重编程为 iPSCs。A 83-01 可用于类器官培养。 | |||
T22560 |
ALK5 Inhibitor II (hydrochloride)
|
Others | Others |
ALK5 Inhibitor II is an ALK5 inhibitor. IC50: 4, 18, and 23 nM for ALK5 autophosphorylation, TGF-β cellular assay, and ALK5 binding in HepG2 cells, respectively. | |||
T67699L |
ALK/ROS1 inhibitor 2e HCL
(R)-1-(2-((2-methoxy-4-(piperazin-1-yl)phenyl)amino)pyridin-4-yl)-N-(4-(trifluoromethoxy)benzyl)piperidine-3-carboxamide hydrochloride(2365497-12-5 Free base) |
Apoptosis | Apoptosis |
ALK/ROS1 inhibitor 2e HCL 具有抗凋亡、抗增殖和抗肿瘤活性。 | |||
T62546 |
ALK5-IN-27
|
||
ALK5-IN-27 (Compound EX-04) 是一种 ALK-5 的有效抑制剂 (IC50≤10 nM)。ALK5-IN-27 对 ALK-2 也具有抑制作用。 | |||
T62393 |
ALK5-IN-25
|
||
ALK5-IN-25 (compound EX-02) 是一种 ALK-5 的有效抑制剂 (IC50<10 nM),也能够抑制 ALK-2。ALK5-IN-25 能够用于研究癌症。 | |||
T62302 | ALK5-IN-28 | ||
ALK5-IN-28 是一种 ALK-5 的选择性抑制剂,其 IC50≤10 nM,可以抑制 TGF-β 诱导的 SMAD 信号传导。ALK5-IN-28 具有抑制体内肿瘤生长的潜力。ALK5-IN-28 能够用于研究增殖性疾病(如癌症、纤维化疾病、系统性硬化症)。 | |||
T62116 |
ALK5-IN-33
|
||
ALK5-IN-33 (Compound EX-10) 是一种口服具有活性的、选择性的 ALK-5 抑制剂 (IC50≤10 nM)。 | |||
T62117 | ALK5-IN-34 | ||
ALK5-IN-34 是一种选择性的、口服具有活力的激活素受体样激酶 (ALK) 抑制剂。ALK5-IN-34 能够抑制激活素受体样激酶的活性 (IC50≤10 nM),也能够抑制肿瘤生长。ALK5-IN-34 能够用于研究癌症等增殖性疾病。 | |||
T79020 | ALK2-IN-5 | ||
ALK2-IN-5为一种吡唑并嘧啶化合物,具有抑制ALK2及FGFR活性的作用。该抑制剂常用于癌症等疾病的研究,这些疾病与ALK2及/或FGFR的活性有关。 | |||
T62395 |
ALK5-IN-32
|
||
ALK5-IN-32 是一种 ALK-5 的选择性抑制剂 (10 nM<IC50<100 nM),对 TGF-β 诱导的 SMAD 信号传导也具有抑制作用。ALK5-IN-31 具有抑制体内肿瘤生长的潜力。ALK5-IN-31 可用于研究增殖性疾病(如癌症、纤维化疾病、系统性硬化症)。 | |||
T62394 | ALK5-IN-31 | ||
ALK5-IN-31 是一种 ALK-5 的选择性抑制剂 (IC50≤10 nM),对 TGF-β 诱导的 SMAD 信号传导也具有抑制作用。ALK5-IN-31 具有抑制体内肿瘤生长的潜力。ALK5-IN-31 可用于研究增殖性疾病(如癌症、纤维化疾病、系统性硬化症)。 | |||
T62613 |
ALK5-IN-26
|
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ALK5-IN-26 (EX-22) 是一种 ALK(Activin receptor-like kinase) 的抑制剂。ALK5-IN-26 对 ALK5 (IC50≤1 nM) 具有抑制作用。ALK5-IN-26 能够用于研究癌症。 | |||
T63114 |
ALK5-IN-7
|
||
ALK5-IN-7 是一种 ALK5 的有效抑制剂。转化生长因子 β (TGF-β) 是一种多功能细胞因子,能够利用细胞表面的复杂受体信号通路,通过自分泌、旁分泌和内分泌的方式参与调控细胞增殖、分化和凋亡。ALK5-IN-7 具有潜力进行 TGF-β 相关疾病和病症的研究(包括但不限于肿瘤、纤维化疾病、炎症性疾病、自身免疫性疾病等)。 | |||
T63498 | ALK5-IN-6 | ||
ALK5-IN-6 是 ALK5 的有效抑制剂。 ALK5-IN-6 具有潜力进行 TGF-β 相关疾病和病症的研究,包括但不限于肿瘤、炎症性疾病、纤维化疾病、自身免疫性疾病等。其中转化生长因子 β (TGF-β) 是一种多功能细胞因子,通过细胞表面的复杂受体信号通路以自分泌、旁分泌和内分泌的方式参与调控细胞增殖、分化和凋亡。 | |||
T64051 | ALK5-IN-9 | ||
ALK5-IN-9 是一种有效的、口服具有活力的 TGFβRI (ALK5) 抑制剂。ALK5-IN-9 能够抑制 ALK5 自磷酸化 (IC50: 25 nM) 并抑制 NIH3T3 细胞活性 (IC50: 74.6 nM)。ALK5-IN-9 具有良好的药代动力学特征,能够改善 hERG 抑制。ALK5-IN-9 对癌症疾病表现出研究潜能。 | |||
T61203 |
ALK5-IN-8
|
||
ALK5-IN-8 is a highly effective inhibitor of TGFβRI (ALK5). It hinders the phosphorylation of ALK5 on downstream signaling proteins (Smad2 or Smad3) by obstructing the interaction between TGFβRI and ligands. Consequently, it disrupts or prevents TGF-β signaling. ALK5-IN-8 shows promise in the study of diverse diseases associated with ALK5-mediated pathways[1]. | |||
T62614 |
ALK5-IN-29
|
||
ALK5-IN-29 是一种激活素受体样激酶 (ALK) 的选择性抑制剂。 ALK5-IN-29 对激活素受体样激酶的活性具有抑制作用 (IC50≤10 nM)。AALK5-IN-29 能够抑制肿瘤生长,可以用于研究癌症等增殖性疾病。 | |||
T62615 |
ALK5-IN-30
|
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ALK5-IN-30 (EX-07) 是一种 ALK 的有效抑制剂,其对 ALK5 (IC50< 10 nM) 和 TGFβ-R1 (IC50< 10 nM) 具有抑制作用。 | |||
T3041 |
ALK inhibitor 2
|
FAK; ALK | Angiogenesis; Cytoskeletal Signaling; Tyrosine Kinase/Adaptors |
ALK inhibitor 2 是嘧啶类 ALK 的有效抑制剂。它是一种睾丸特异性丝氨酸/苏氨酸激酶 2 (TSSK2;IC50=37 nM) 和粘着斑激酶 (FAK;IC50=5 nM) 抑制剂。 | |||
T3678 |
Entrectinib
RXDX-101,恩曲替尼,NMS-E628 |
Trk receptor; ROS; ALK; Autophagy; ROS Kinase | Angiogenesis; Autophagy; Immunology/Inflammation; Tyrosine Kinase/Adaptors |
Entrectinib (RXDX-101) 是一种可口服的 Trk、ROS1和 ALK 抑制剂,具有抗肿瘤和中枢神经活性,抑制 TrkA、TrkB、TrkC、ROS1 和 ALK 的 IC50值分别为 1、3、5、12 和 7 nM。 | |||
T68537 |
CEP-14513
|
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CEP-14513 is a potent ALK inhibitor. CEP-14513 displayed potent ALK inhibitory activity in both in vitro enzymatic assay (IC50 = 5 nM) and cell-based assays of ALK tyrosine phosphorylation (IC50 = 30 nM). | |||
T61443 | Trk-IN-7 | ||
Trk-IN-7 (compound I-6) is a highly potent inhibitor of TRK, exhibiting IC50 values ranging from 0.25-10 nM for TRKA, TRKB, and TRKC, respectively. In addition, Trk-IN-7 demonstrates notable inhibition against EML4-ALK (IC50 <15 nM), as well as ALK G1202R, ALK C1156Y, ALK R1275Q, ALK F1174L, ALK L1197M, and ALK G1269A (IC50 = 5-50 nM) [1]. | |||
T13139 |
TP-008
TGFβRI-IN-2 |
Others | Others |
TGFβRI-IN-2 is a selective, potent and orally active inhibitor of (Activin-Like Kinase 5) ALK 5(pIC50 and pEC50 values of 7.6 and 6.63, respectively). |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-05771 |
ALK-5 Protein, Human, Recombinant (hFc)
AAT5,SKR4,TGFR-1,LDS1,transforming growth factor, b... |
Human | HEK293 Cells |
ALK-5 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 36.87 kDa and the accession number is P36897-1. | |||
TMPY-01358 |
ALK-5 Protein, Human, Recombinant (His & hFc)
tβR-I,ALK5,AAT5,TGFR-1,LDS2A,LDS1... |
Human | HEK293 Cells |
ALK-5 Protein, Human, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 38.1 kDa and the accession number is P36897-1. | |||
TMPK-00305 |
TGFBR1 Protein, Human, Recombinant (mFc & Avi)
tbetaR-I,TGFβRI,TGFbetaRI,LDS2A,ALK-5,TGF-... |
Human | HEK293 Cells |
transforming growth factor beta receptor 1 (TGFBR1), a key stimulator of tumor proliferation and metastasis, was a direct target of miR‑98‑5p. miR‑98‑5p overexpression resulted in the downregulation of TGFBR1 and the suppression of the viability, proliferation, migration and invasion of A549 and H1299 cells. TGFBR1 Protein, Human, Recombinant (mFc & Avi) is expressed in HEK293 mammalian cells with C-mFc-Avi tag. The predicted molecular weight is 38.2 kDa and the accession number is P36897-1. | |||
TMPY-04366 |
ALK-5 Protein, Human, Recombinant (aa 200-503, His & GST)
LDS1,ALK-5,LDS2A,AAT5,SKR4,transf... |
Human | Baculovirus Insect Cells |
ALK-5 Protein, Human, Recombinant (aa 200-503, His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 62.6 kDa and the accession number is P36897-1. | |||
TMPJ-01178 |
TGFBR1 Protein, Mouse, Recombinant (hFc)
ALK-5,ALK-5ALK<... |
Mouse | HEK293 Cells |
TGF-beta RI, also called ALK-5, is an approximately 55 kDa type I transmembrane serine/threonine receptor kinase. In the presence of TGF-beta, TGF-beta RI forms a complex with, and is phosphorylated by, TGF-beta RII. Phosphorylated TGF-beta RI can then transiently bind and phosphorylate Smad2 and Smad3. TGF-beta functions as a tumor suppressor by inhibiting the cell cycle in the G1 phase. Administration of TGF-beta is able to protect against mammary tumor development in transgenic mouse models i... | |||
TMPK-00306 |
TGFBR1 Protein, Human, Recombinant (mFc & Avi), Biotinylated
TGFbetaRI,TGFBR1,ALK-5,SKR4,LDS2A,TGFB1R1,... |
Human | HEK293 Cells |
transforming growth factor beta receptor 1 (TGFBR1), a key stimulator of tumor proliferation and metastasis, was a direct target of miR‑98‑5p. miR‑98‑5p overexpression resulted in the downregulation of TGFBR1 and the suppression of the viability, proliferation, migration and invasion of A549 and H1299 cells. TGFBR1 Protein, Human, Recombinant (mFc & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-mFc-Avi tag. The predicted molecular weight is 38.2 kDa and the accession number is... | |||
TMPY-05485 |
BMPR1A/ALK-3 Protein, Human, Recombinant (hFc)
ACVRLK3,SKR5,10q23del,CD292,bone morphogenetic prot... |
Human | HEK293 Cells |
BMPR1A/ALK-3 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 40.9 kDa and the accession number is P36894. | |||
TMPY-01764 |
BMPR1A/ALK-3 Protein, Human, Recombinant (His)
bone morphogenetic protein receptor, type IA,ALK3,A... |
Human | HEK293 Cells |
BMPR1A/ALK-3 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 15.7 kDa and the accession number is P36894. | |||
TMPJ-00325 |
BMPR1A/ALK-3 Protein, Human, Recombinant (hFc & His)
BMP Type-1A Receptor,Bone Morphogenetic Protein Receptor Typ... |
Human | HEK293 Cells |
Bone Morphogenetic Protein Receptor Type-1A (BMPR1A) belongs to the TKL Ser/Thr protein kinase family and TGFB receptor subfamily, including the type I receptors BMPR1A and BMPR1B and the type II receptor BMPR2. BMPR1A is a single-pass type I membrane protein and highly expressed in skeletal muscle. BMPR1A contains one GS domain and one protein protein kinase domain. BMPR1A is necessary for the extracellular matrix depostition by osteoblasts. BMPR1A can activate SMAD transcriptional regulators, ... | |||
TMPY-05308 |
CD45 Protein, Human, Recombinant (aa 1-529, His)
GP180,B220,L-CA,protein tyrosine phosphatase, receptor type,... |
Human | HEK293 Cells |
CD45 Protein, Human, Recombinant (aa 1-529, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.4 kDa and the accession number is P08575-5. | |||
TMPY-05387 |
SLAMF7 Protein, Human, Recombinant (hFc)
SLAM family member 7,19A,SLAM7,CS1,CD319,CRACC |
Human | HEK293 Cells |
SLAMF7 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 49.1 kDa and the accession number is Q9NQ25-5. | |||
TMPY-04318 |
GRIK2 Protein, Human, Recombinant (hFc)
GLUR6,EAA4,MRT6,GLR6,glutamate receptor, ionotropic, kainate... |
Human | HEK293 Cells |
GRIK2 (Glutamate Ionotropic Receptor Kainate Type Subunit 2, also known as GluR6) is a Protein Coding gene. The GRIK2 (one of the kainate receptors) gene resides in a genetic linkage region (6q21) associated with bipolar disorder (BPD). The gene coding for GRIK2 has been suggested as a candidate gene for autism based on its localization in the autism-specific region on chromosome 6q21 and the involvement of receptor protein in cognitive functions like learning and memory. GRIK2 belongs to the gl... | |||
TMPY-05547 |
SLAMF7 Protein, Human, Recombinant (hFc), Biotinylated
CS1,SLAM7,CD319,SLAM family member 7,CRACC,19A |
Human | HEK293 Cells |
SLAMF7 Protein, Human, Recombinant (hFc), Biotinylated is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 49.1 kDa and the accession number is Q9NQ25-5. | |||
TMPJ-00854 |
ETS1 Protein, Human, Recombinant (His)
V-ets Erythroblastosis Virus E26 Oncogene Homolog 1 (Avian),... |
Human | E. coli |
ETS1 Protein (ETS1) is a nuclear protein that belongs to the ETS family. Members of this family recognize the core consensus DNA sequence GGAA/T in target genes. Proteins function either as transcriptional activators or repressors of numerous genes. They are involved in stem cell development, cell senescence and death, and tumorigenesis. ETS1 is a transcription factor, containing one ETS DNA-binding domain and one PNT (pointed) domain. it has been shown to interact with TTRAP, UBE2I and Death As... | |||
TMPY-05498 |
SR-BI/SCARB1 Protein, Human, Recombinant (hFc)
HDLQTL6,SR-BI,SRB1,CD36L1,CLA-1,CLA1,scavenger receptor clas... |
Human | HEK293 Cells |
SR-BI/SCARB1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 73.4 kDa and the accession number is Q8WTV0-5. | |||
TMPK-01357 |
SIRP alpha V5 Protein, Human, Recombinant (His & Avi)
MFR,PTPNS1,P84,BIT,MYD-1,MYD1,SHPS-1,SIRPA,SIRP α,SIRP α V |
Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal. | |||
TMPK-01363 |
SIRP alpha V5 Protein, Human, Recombinant (His & Avi), Biotinylated
SIRP alpha,MFR,PTPNS1,SIRP α V5,P84,SHPS-1,BIT,CD17... |
Human | HEK293 Cells |
Signal regulatory protein α (SIRPα) is a regulatory membrane glycoprotein from SIRP family expressed mainly by myeloid cells and also by stem cells or neurons.SIRPα acts as inhibitory receptor and interacts with a broadly expressed transmembrane protein CD47 also called the "don´t eat me" signal.Cancer cells highly expressed CD47 that activate SIRP α and inhibit macrophage-mediated destruction. SIRP alpha V5 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian c... |