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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5402 |
DDR1-IN-2
DDR1 inhibitor 7rh |
Discoidin Domain Receptor (DDR) | Tyrosine Kinase/Adaptors |
DDR1-IN-2 (DDR1 inhibitor 7rh) 是盘状结构域受体 1 抑制剂 (IC50:13.1 nM),对 DDR2 的抑制作用相对较弱 (IC50:203 nM)。 | |||
T3337 |
Ddr1-In-1
|
Discoidin Domain Receptor (DDR) | Tyrosine Kinase/Adaptors |
DDR1-IN-1 是一种特异性的 DDR1 受体酪氨酸激酶抑制剂,选择性是 DDR2 的 3 倍左右。 | |||
T40061 |
DDR1-IN-6
DDR1-IN-6 |
||
DDR1-IN-6 is a potent and selective inhibitor of Discoidin Domain Receptor family member 1 (DDR1), exhibiting remarkable inhibitory activity at an IC50 of 9.72 nM. It effectively suppresses the auto-phosphorylation of DDR1b (Y513) with an IC50 value of 9.7 nM. Furthermore, DDR1-IN-6 displays strong anti-cancer activity. | |||
T40062 |
DDR1-IN-5
DDR1-IN-5 |
||
DDR1-IN-5 is a potent and selective inhibitor of the Discoidin Domain Receptor family, member 1 (DDR1). It effectively inhibits the phosphorylation of DDR1b (Y513) with an IC 50 value of 4.1 nM. Furthermore, DDR1-IN-5 demonstrates remarkable anti-cancer activity. Its inhibitory potency against DDR1 (IC 50 = 7.36 nM) makes it a promising compound for targeted therapy in cancer treatment. | |||
T39572 |
DDR1-IN-4
DDR1-IN-4 |
||
DDR1-IN-4 (Compound 2.45) is a highly potent inhibitor that selectively targets Discoidin Domain Receptor 1 (DDR1) autophosphorylation. This compound demonstrates exceptional efficacy with IC50 values of 29 nM and 1.9 μM for DDR1 and DDR2, respectively. | |||
T70202 |
DDR1-IN-1 dihydrochloride
|
||
DDR1-IN-1 dihydrochloride 是 DDR1受体酪氨酸激酶抑制剂,IC50值为105 nM,而对 DDR2的 IC50为413 nM。 | |||
T79811 |
DDR1/2 inhibitor-2
|
||
DDR1/2 inhibitor-2 (Example 31),作为一种DDR1/DDR2抑制剂,其IC50值小于100 nM,适用于癌症和纤维化疾病的研究领域。 | |||
T70201 |
S 16020-2
|
||
S 16020-2 is an olivacine derivative, and DNA topoisomerase II inhibitor endowed with a remarkable antitumor activity against various experimental tumors. | |||
T4646 |
TA-02
|
p38 MAPK; Autophagy | Autophagy; MAPK |
TA02 是一种Adezmapimod 类似物,是p38 MAPK 的抑制剂,其IC50值为 20 nM。它和Adezmapimod、SB 202190 具有相似的心源活性,可抑制 TGFBR-2。 | |||
T4349 |
Sitravatinib
MG516,MGCD516 |
Discoidin Domain Receptor (DDR); VEGFR; FLT; Trk receptor; TAM Receptor; c-Kit; Ephrin Receptor | Angiogenesis; Tyrosine Kinase/Adaptors |
Sitravatinib (MGCD516) 是一种有口服活性的受体酪氨酸激酶抑制剂。它单独使用即具有有效的抗肿瘤功效,且通过促进抗肿瘤免疫微环境增强了 PD-1 阻断的活性。 | |||
T10984 |
DDR-TRK-1
|
Discoidin Domain Receptor (DDR) | Tyrosine Kinase/Adaptors |
DDR-TRK-1 是 DDR1的一个选择性抑制剂,其 IC50 值为 9.4 nM。DDR-TRK-1 也抑制 TRK 激酶家族。 | |||
T7862 |
VU6015929
|
Discoidin Domain Receptor (DDR) | Tyrosine Kinase/Adaptors |
VU6015929 是一种活性双盘状结构域受体 1/2 (DDR1/2) 的抑制剂(IC50 分别为 4.67 nM 和 7.39 nM)。 | |||
T10985 |
DDR Inhibitor
|
Discoidin Domain Receptor (DDR) | Tyrosine Kinase/Adaptors |
DDR Inhibitor 是一种高效的盘状结构域受体 (discoidin domain receptor) 抑制剂,对 DDR2 的 IC50 值为 3.3 nM,在浓度为 1.5 nM 时,对 DDR1 有 53% 的抑制作用。 | |||
T60805 |
JNK3 inhibitor-2
|
||
JNK3 inhibitor-2 是一种有效的选择性JNK3抑制剂。JNK3 inhibitor-2 对 JNK1、JNK2、 JNK3的IC50值分别为 >100, >100, 0.25 μM。JNK3 inhibitor-2也抑制 DDR1 和 EGFR (T790M, L858R)。 | |||
T12925 |
Sitravatinib malate
MGCD516 malate,MG-516 malate |
TAM Receptor | Tyrosine Kinase/Adaptors |
Sitravatinib malate is an orally bioavailable receptor inhibitor of tyrosine kinase (RTK) (IC50s of 1.5 nM, 2 nM, 2 nM, 5 nM, 6 nM, 6 nM, 8 nM, 0.5 nM, 29 nM, 5 nM, and 9 nM for Axl, MER, VEGFR3, VEGFR2, VEGFR1, KIT, FLT3, DDR2, DDR1, TRKA, TRKB, respectively.) , shows potent single-agent antitumor efficacy and enhances the activity of PD-1 blockade through promoting an antitumor immune microenvironment. | |||
T15808 |
Merestinib dihydrochloride
LY2801653 dihydrochloride |
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Merestinib dihydrochloride is an effective and orally bioavailable c-Met inhibitor (Ki=2 nM). It has anti-tumor activities and also has potent activity against MST1R (IC50=11 nM), FLT3 (IC50=7 nM), AXL (IC50=2 nM), MERTK (IC50=10 nM), TEK (IC50=63 nM), RO | |||
T10801 |
CHMFL-ABL/KIT-155
CHMFL-ABL-KIT-155 |
c-Kit | Tyrosine Kinase/Adaptors |
CHMFL-ABL/KIT-155 is a highly potent and orally active type II ABL/c-KIT dual kinase inhibitor (IC50s: 46 nM/75 nM). It arrests cell cycle progression and induces apoptosis. |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01289 |
DDR1 Protein, Human, Recombinant (His)
RTK6,DDR,TRKE,PTK3,NTRK4,NEP,PTK3A,MCK10,E... |
Human | HEK293 Cells |
DDR1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 45.7 kDa and the accession number is A0A024RCQ1. | |||
TMPH-01297 |
DDR1 Protein, Human, Recombinant (aa 21-417, His)
EDDR1,MCK-10,Epithelial discoidin... |
Human | HEK293 Cells |
Tyrosine kinase that functions as cell surface receptor for fibrillar collagen and regulates cell attachment to the extracellular matrix, remodeling of the extracellular matrix, cell migration, differentiation, survival and cell proliferation. Collagen binding triggers a signaling pathway that involves SRC and leads to the activation of MAP kinases. Regulates remodeling of the extracellular matrix by up-regulation of the matrix metalloproteinases MMP2, MMP7 and MMP9, and thereby facilitates cell... | |||
TMPY-03313 |
DDR1 Protein, Rat, Recombinant (His)
discoidin domain receptor tyrosine kinase 1,Drd... |
Rat | HEK293 Cells |
DDR1 Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 45.3 kDa and the accession number is Q6MG19. | |||
TMPY-02310 |
DDR1 Protein, Mouse, Recombinant (His)
CD167a,discoidin domain receptor tyrosine kinase |
Mouse | HEK293 Cells |
DDR1 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 45.4 kDa and the accession number is Q03146-1. | |||
TMPY-04442 |
DDR1 Protein, Mouse, Recombinant (His & GST)
6030432F18,Nep,Cak,AI323681,CD167... |
Mouse | Baculovirus Insect Cells |
DDR1 Protein, Mouse, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 75.8kDa and the accession number is Q03146-2. | |||
TMPY-03541 |
DDR1 Protein, Rat, Recombinant (hFc)
Drd1,Cak,discoidin domain receptor tyrosine kinase ... |
Rat | HEK293 Cells |
DDR1 Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 70.9 kDa and the accession number is Q6MG19. | |||
TMPY-02506 |
DDR1 Protein, Mouse, Recombinant (hFc)
AI323681,CD167a,Nep,Cak,PTK3A,6030432F... |
Mouse | HEK293 Cells |
DDR1 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 71 kDa and the accession number is Q03146-1. | |||
TMPY-04382 |
DDR1 Protein, Human, Recombinant (aa 444-913, His & GST)
discoidin domain receptor tyrosine kinase 1,NEP,TRK... |
Human | Baculovirus Insect Cells |
DDR1 Protein, Human, Recombinant (aa 444-913, His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 80 kDa and the accession number is Q08345-1. |