找到约 31 条 “HAT-IN-8” 相关结果 （用时 0.108 秒）
| 目录号 | 产品名称 | 中文名称 | 靶点 |
|---|---|---|---|
M5944
|
Ruxolitinib phosphate | 鲁索利替尼磷酸盐 | JAK |
| INCB018424 phosphate; INCB 018424 phosphate; INCB-018424 phosphate; Ruxolitinib | |||
| Ruxolitinib(INCB018424)磷酸盐是一种高活性JAK1和2选择性抑制剂，IC50分别为3.3 nM和2.8 nM，比对JAK3的抑制性高130倍以上。可用于斑秃的相关研究。 | |||
| M39080 | Lysophosphatidylcholine 18:2 | Lysophosphatidylcholine 18:2 | Metabolite/Endogenous Metabolite |
| Lysophosphatidylcholine 18:2 (1-Linoleoyl-2-Hydroxy-sn-glycero-3-PC)，一种溶血磷脂，是一种从胰岛素抵抗 (IR) 多囊卵巢综合征 (PCOS) 中发现的潜在生物标志物。低血浆 Lysophosphatidylcholine 18:2 还可以预测糖耐量受损、胰岛素抵抗、2 型糖尿病、冠心病和记忆障碍。 | |||
| M41238 | HAT-IN-8 | HAT-IN-8 | Parasite |
| HAT-IN-8 是一种可穿透血脑屏障的 T. brucei 抑制剂 (EC50: 0.18 μM)。 | |||
| M2510
|
Chloroquine diphosphate | 磷酸氯喹 | Autophagy |
| Chloroquine Phosphate | |||
| Chloroquine diphosphate（磷酸氯喹）是Chloroquine的磷酸盐形式，同时也是一种疟原虫抑制剂，IC50值为0.2812 ng/mL。此外，Chloroquine diphosphate也是细胞自噬（autophagy）的抑制剂，并具有抗癌活性。 | |||
M5315
|
Baricitinib phosphate | 磷酸巴瑞克替尼 | JAK |
| INCB028050; LY3009104 | |||
| Baricitinib phosphate(INCB 028050; LY 3009104)是JAK和JAK2选择性抑制剂，IC50分别为5.9 nM和5.7 nM，比对JAK3 和Tyk2的抑制性强70倍和10倍，而对c-Met和Chk2无活性。可用于活动性类风湿关节炎和斑秃的相关研究。 | |||
| M40771
|
Recombinant Human CTLA-4 Protein (HEK293, C-6His) | 重组人CTLA-4蛋白 (HEK293, C-6His) | Cytokines and Growth Factors |
| Cytotoxic T-lymphocyte-associated antigen 4 | |||
| Cytotoxic Tlymphocyte 4(CTLA-4,CD152), is a type I transmembrane T cell inhibitory molecule that is a member of the Ig superfamily. CTLA4 transmits an inhibitory signal to T cells, whereas CD28 transmits a stimulatory signal. | |||
| M40772
|
Recombinant Human CTLA-4 Protein (HEK293, C-Flag) | 重组人CTLA-4蛋白 (HEK293, C-Flag) | Cytokines and Growth Factors |
| Cytotoxic T-lymphocyte-associated antigen 4 | |||
| Cytotoxic Tlymphocyte 4(CTLA-4,CD152), is a type I transmembrane T cell inhibitory molecule that is a member of the Ig superfamily. CTLA4 transmits an inhibitory signal to T cells, whereas CD28 transmits a stimulatory signal. | |||
| M8403 | VU0405601 | VU0405601 | Others |
| VU0405601 is a hERG (the human Ether-à-go-go-Related Gene) agonist that increased the IC50 of dofetilide from 38. | |||
| M8557 | CS1 | CS1 | Others |
| CS1 is a selective and potent inhibitor of topoisomerase IIα (TopoIIα) that potently inhibits a proliferation of cancer cell lines including MDA-MB-231 and A548 cells, with less toxicity than etoposide. | |||
| M8624 | HPB | HPB | Others |
| HPB is a cell-permeable, non-cytotoxic N-hydroxybenzamide derivative that acts as a HDAC6-selective deacetylase inhibitor (IC50 = 31/376/677/842/1133 nM against HDAC6/8/10/1/7, >2 μM against HDAC2/3/4/11/9/5). | |||
| M8629 | Cbz-B3A | Cbz-B3A | Others |
| Cbz-B3A is a potent and selective inhibitor of mTORC1 signaling that inhibits the phosphorylation of eIF4E binding protein 1 (4EBP1) and blocks 68% of translation. | |||
| M8635 | Displurigen | Displurigen | Others |
| Displurigen is a cell-permeable, phenylthiochromen-4-one derived compound that disrupts the pluripotency of human embryonic stem cells by targeting HSPA8/HSC70 and affects its binding to Oct4. | |||
| M8835 | UA62784 | UA62784 | Others |
| Studies have also reported that UA62784 associates with tubulin at or near the colchicine-binding sites in cells and functions as a cytotoxic, microtubule inhibitor. | |||
| M10822
|
GNE-781 | GNE-781 | Epigenetic Reader Domain |
| GNE-781 (compound 19) 是一种高效的、口服活性的、选择性的 bromodomain 抑制剂对cyclic adenosine monophosphate response element binding protein (CBP) 的IC50值为0.94 nM (in TR-FRET assay)。GNE-781 还抑制 BRET 和 BRD4(1)，IC50分别为6.2 nM和5100 nM。 GNE-781 具有抗肿瘤活性。 | |||
| M20644 | TH34 | TH34 | HDAC |
| TH34 is a HDAC inhibitor that shows pronounced selectivity for HDACs 6, 8 and 10 over HDACs 1, 2 and 3. In a NanoBRET assay, TH34 strongly binds HDAC6, 8 and 10 with low-micromolar IC50 concentrations (HDAC6: 4.6 µM, HDAC8: 1.9 µM, HDAC10: 7.7 µM). | |||
| M20704 | SR18662 | SR18662 | Others |
| SR18662 is an optimized compund based on ML264 that inhibits Krüppel-like factor 5 (KLF5) with IC50 of 4.4 nM. SR18662 reduces the viability of multiple colorectal cancer cell lines. SR18662 induces apoptosis. | |||
| M20734 | (E/Z)-BCI | (E/Z)-BCI | Phosphatase |
| BCI, NSC 150117 | |||
| (E/Z)-BCI (BCI, NSC 150117) is an inhibitor of dual specific phosphatase 1/6 (DUSP1/DUSP6) and mitogen-activated protein kinase with EC50 of 13.3 μM and 8.0 μM for DUSP6 and DUSP1 in cells, respectively. (E)-BCI induces apoptosis via generation of reactive oxygen species (ROS) and activation of intrinsic mitochondrial pathway in H1299 lung cancer cells. | |||
| M20752 | PZ-2891 | PZ-2891 | Others |
| PZ-2891 is a selective, orally active and brain-penetrant pantothenate kinase (PANK) modulator that acts as an orthosteric inhibitor at high concentrations and an allosteric activator at lower sub-saturating concentrations. PZ-2891 inhibits PANK with IC50 of 40.2 nM, 0.7 nM and 1.3 nM for hPANK1β, hPANK2, and hPANK3, respectively. | |||
| M20753 | TBOPP | TBOPP | Others |
| TBOPP is a selective inhibitor of dedicator of cytokinesis (DOCK1, Dock180) that inhibits DOCK1-mediated Rac activation with IC50 of 8.4 μM. TBOPP binds to the DOCK1 DHR-2 domain with Kd of 7.1 μM. TBOPP exhibits anti-tumor activity. | |||
| M20775 | SEC inhibitor KL-1 | SEC inhibitor KL-1 | Others |
| KL-1 | |||
| SEC inhibitor KL-1 (KL-1) is a potent and selective inhibitor of super elongation complex (SEC) that disrupts the interaction between the SEC scaffolding protein AFF4 and P-TEFb, resulting in impaired release of Pol II from promoter-proximal pause sites and a reduced average rate of processive transcription elongation. KL-1 exhibits an dose-dependent inhibitory effect on AFF4-CCNT1 interaction with Ki of 3.48 μM. | |||
| M20820
|
Gly-Phe β-naphthylamide | Gly-Phe β-naphthylamide | Others |
| Gly-Phe beta-naphthylamide | |||
| Gly-Phe β-naphthylamide (Gly-Phe beta-naphthylamide) is a substrate of cathepsin C that accumulates within the lysosome. Gly-Phe-β-naphthylamide can inhibit the cathepsin-dependent activation of caspase-8. | |||
| M20836 | Indirubin-3′-oxime | Indirubin-3′-oxime | GSK-3 |
| IDR3O, I3O | |||
| Indirubin-3′-oxime (IDR3O, I3O) is an indirubin analogue that shows favorable inhibitory activity targeting GSK-3β and CDKs. Indirubin-3′-oxime also inhibits JNKs with IC50s of 0.8 μM, 1.4 μM, and 1.0 μM for JNK1, JNK2, and JNK3, respectively. Indirubin-3′-oxime activates Wnt/β-catenin signaling and inhibits adipocyte differentiation and obesity. | |||
| M20838 | Fluorofenidone | Fluorofenidone | Others |
| AKF-PD | |||
| Fluorofenidone (AKF-PD) inhibits nicotinamide adenine dinucleotide phosphate oxidase (NADPH oxidase, NOX) via PI3K/Akt pathway in the pathogenesis of renal interstitial fibrosis. Fluorofenidone also attenuates BLM-induced pulmonary inflammation and fibrosis through suppressing the activation of NALP3 inflammasome and the IL-1β/IL-1R1/MyD88/NF-κB signalling pathway. | |||
| M21671
|
Recombinant Mouse/Rat VEGF-C Protein (HEK293, aa 108-223, His Tag) | 重组小鼠/大鼠VEGF-C蛋白 (HEK293, aa 108-223, His Tag) | Cytokines and Growth Factors |
| Vascular endothelial growth factor C | |||
| Recombinant Mouse/Rat VEGF-C Protein is a dimeric glycoprotein, as a ligand for two receptors, VEGFR-3 (Flt4), and VEGFR-2. VEGF-C may function in angiogenesis of the venous and lymphatic vascular systems during embryogenesis. Measured in a cell proliferation assay using human umbilical vein endothelial cells (HUVEC), the ED50 for this effect is typically 0.1-0.8 μg/mL. | |||
| M25536
|
Recombinant Human CXCL13/BCA-1 (E. coli) | 重组人CXCL13/BCA-1蛋白 (E. coli) | Cytokines and Growth Factors |
| CXC chemokine BLC; Small-inducible cytokine B13 | |||
| CXCL13, also known as B-lymphocyte chemoattractant (BLC), is a CXC chemokine that is constitutively expressed in secondary lymphoid organs. Recombinant human CXCL13 is a single non-glycosylated polypeptide chain containing 87 amino acids and mature human BCA-1 shares 64 % amino acid sequence similarity with the murine protein and 23–34 % amino acid sequence identity with other known CXC chemokines. Determined by a chemotaxis bioassay using human B cells, the biological activity is in a concentration range of 1.0-10 ng/ml. | |||
| M30139
|
2-Methylthioadenosine diphosphate trisodium | 2-Methylthioadenosine diphosphate trisodium | P2 Receptor |
| 2-Methylthio-ADP trisodium | |||
| 2-Methylthioadenosine diphosphate trisodium (2-Methylthio-ADP trisodium) 是一种有效的嘌呤能 P2Y 受体激动剂，对人 P2Y13、小鼠 P2Y13 和人 P2Y12 的 EC50 分别为 19、6.2 和 5 nM。2-Methylthioadenosine diphosphate trisodium 对人 P2Y1 和大鼠 P2Y6 的 pEC50 分别为 8.29 和 5.75。 | |||
| M40606
|
Recombinant Human C5a Protein (E.coli) | 重组人补体C5a (E.coli) | Cytokines and Growth Factors |
| Complement C5; C5a anaphylatoxin | |||
| Human Complement 5a (C5a) is an enzymatically generated glycoprotein that belongs to a family of structurally and functionally related proteins known as anaphylatoxins. Recombinant Human C5a expressed the target gene encoding Thr678-Arg751. | |||
| M40919
|
Recombinant Human GSTM2 Protein (E. coli, His Tag) | 重组人GSTM2蛋白 (E. coli, His Tag) | Cytokines and Growth Factors |
| Glutathione S-transferase Mu 2; GST class-mu 2 | |||
| Glutathione S-transferase Mu 2, also known as GST class-mu 2, GSTM2-2, and GSTM2, is a cytoplasm protein that belongs to the GST superfamily and Mu family. A DNA sequence encoding the native human GSTM2 (Met 1-Lys 218) was expressed, with a polyhistide tag at the N-terminus. | |||
| M40927
|
Recombinant Mouse IL-1RL2 Protein (HEK293, C-6His) | 重组小鼠 IL-1RL2蛋白 (HEK293, C-6His) | Cytokines and Growth Factors |
| Interleukin-1 Receptor-like 2; IL-36 receptor | |||
| Interleukin-1 receptor-like 2 is a protein that in humans is encoded by the IL1RL2 gene, belongs to the interleukin-1 receptor family. IL1RL2 is the receptor for interleukin-36. Recombinant Mouse Interleukin-1 Receptor-like 2 expressed the target gene encoding Asp22-Arg338(Ala158Val) with a 6His tag at the C-terminus. | |||
| M43397 | Leniolisib phosphate | Leniolisib phosphate | PI3K |
| Leniolisib (CDZ173) phosphate 是一种首创的(first-in-class)，高效的，选择性的 PI3Kδ 抑制剂，其IC50值为11 nM。Leniolisib对PI3K-δ的选择性高于PI3K-α（28 倍）、PI3K-β（43 倍）和PI3K-γ（257 倍）。在细胞测定中，Leniolisib降低了pAKT通路活性并抑制了B细胞和T细胞亚群的增殖和激活。 | |||
| M58788
|
Recombinant Human Menin (E.Coli/BV) | 重组人Menin (E.Coli/BV) | Target Proteins |
| Essential component of a MLL/SET1 histone methyltransferase (HMT) complex, a complex that specifically methylates 'Lys-4' of histone H3 (H3K4). Functions as a transcriptional regulator. Binds to the TERT promoter and represses telomerase expression. Plays a role in TGFB1-mediated inhibition of cell-proliferation, possibly regulating SMAD3 transcriptional activity. Represses JUND-mediated transcriptional activation on AP1 sites, as well as that mediated by NFKB subunit RELA. Positively regulates HOXC8 and HOXC6 gene expression. May be involved in normal hematopoiesis through the activation of HOXA9 expression (By similarity). | |||
