1592
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T28996 |
TP-064
TP 064 |
Histone Methyltransferase | Chromatin/Epigenetic |
TP-064 是选择性蛋白精氨酸甲基转移酶 4 抑制剂 ,IC50小于10 nM,具有抗癌活性。它抑制 BAF155 和 MED12 的二甲基化,IC50为 340 和 43 nM。它对于 PRMT6 的 IC50为 1.3 μM。 | |||
T9250 |
TP-4748
|
Others | Others |
TP-4748 是一种生化物质。 | |||
T22440 |
TP-353
EOS-61973 |
CDK | Cell Cycle/Checkpoint |
TP-353 (EOS-61973) 是一种 CDK7 抑制剂。 | |||
T4523 |
TP-3654
|
Pim | Chromatin/Epigenetic; JAK/STAT signaling |
TP3654是一种Pim 激酶抑制剂,对Pim-1和Pim-3的Ki 值分别为5和42 nM。 | |||
T9254 |
TP-2857
TAP2857 |
Antibacterial | Microbiology/Virology |
TP-2857 (TAP2857) 是一种有效的抗菌剂。 | |||
T13189 |
TP-10
|
PDE | Metabolism |
TP-10 是 PDE10A 对其他 PDE 的特异性抑制剂,IC50 为 0.8 nM。 | |||
T24897 |
TP0427736
TP427736,TP-0427736,TP-427736 |
TGF-beta/Smad | Stem Cells |
TP0427736 是一种有效的选择性 ALK5 抑制剂,IC50 为 2.72 nM,比对 ALK3 的抑制作用高 300 倍。 TP0427736 可降低人外根鞘细胞中 TGF-β 诱导的生长抑制,并延长小鼠毛囊中的生长期。 | |||
T2469 |
TP808
TP-808,TP 808 |
Others | Others |
TP808是一种高度通用的中间体,可用于多种四环素类抗生素的构建。 | |||
T11227L |
Eravacycline dihydrochloride
TP-434-046,TP-434 dihydrochloride |
Antibacterial | Microbiology/Virology |
Eravacycline dihydrochloride (TP-434-046) 是一种有效的广谱抗菌剂,可对抗六种大肠杆菌(MIC:0.125-0.25 mg/L)。 | |||
T62525 |
TP-16
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
TP-16是一种新型高效且具有选择性的 EP4 拮抗剂,可阻断IMCs的功能,增强细胞毒性T细胞介导的体内肿瘤消除。 | |||
T34907 |
TP-238
TP 238 |
||
TP-238 是一种有效的,选择性的CECR2/BPTF 双重探针,IC50值分别为 30 nM 和 350 nM。TP-238 还抑制BRD9,pIC50为 5.9,并且对其他 338 激酶的活性较低。 | |||
T28998 |
TP-680
TP 680 |
||
TP-680 is a antagonist of cholecystokininA receptor. | |||
T24896 |
TP 9201
TP-9201,TP9201 |
||
TP 9201 is a platelet integrin alphaIIbbeta3 antagonist. It is a synthetic RGD-containing cyclic peptide. | |||
T39486 |
TP-472N
|
||
TP-472N serves as a negative control probe for TP-472, which is a specific and effective BRD7/9 probe. | |||
TQ0120 |
CDDO-Im
RTA-403,CDDO-Imidazolide,TP-235 |
Others; Ferroptosis; Nrf2; PPAR | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Others |
CDDO-Im (TP-235) 是一种 Nrf2和 PPAR 的激活剂,对 PPARα 和 PPARγ 的 Ki 分别为232 nM 和 344 nM。 | |||
T23466 |
TP003
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
TP003是一种新型的非选择性GABAA 受体苯二氮卓位点激动剂,对α1β2γ2、α2β3γ2、α3β3γ2、α5β2γ2 的具有亲和力,其EC50 分别20.3、10.6、3.24、5.64 nM。 TP003 通过 α2GABAA 受体从而具有抗焦虑活性,也有部分抗惊厥活性。 | |||
T41110 |
EFdA-TP
|
||
EFdA-TP, a highly potent nucleoside reverse transcriptase (RT) inhibitor, exerts its inhibitory effect on RT-catalyzed DNA synthesis through both immediate and delayed chain termination mechanisms, commonly referred to as ICT and DCT, respectively. Additionally, EFdA-TP demonstrates its efficacy in inhibiting HIV-1 RT through multiple pathways. | |||
T68535 | TP-051 | ||
TP-051 is a FFAR1 agonist. | |||
T34866 |
Thymocartin
Thymocartinum,TP 4,Thymopoietin II (32-35),RGH 0206 |
||
Thymocartin (RGH 0206) 是天然存在胸腺因子 (胸腺生成素) 的 32-35 片段。Thymocartin 可用于研究免疫缺陷病。 | |||
T68869 |
TP-110
|
||
TP-110 is a new proteasome inhibitor, which shows potent growth inhibition in various tumor cell lines. Treatment with TP-110 for 24 h in vitro induced apoptosis in multiple myeloma cell line RPMI8226. TP-110 reduced the intrinsic inhibitor of apoptosis proteins (IAPs), cIAP-1 and XIAP, that suppress executioner caspases. | |||
T5392 |
TP0463518
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
TP0463518 是缺氧诱导因子脯氨酰羟化酶抑制剂,能够作用于人 PHD2(Ki= 5.3 nM)。它还抑制人PHD1/PHD3,IC50分别为 18 和 63 nM,以及猴 PHD2(IC50=22 nM)。 | |||
T41202 | TP 472N | ||
TP 472N is a negative control forTP 472. Inactive against other bromodomains (>20μM against BRD9). | |||
T40120 |
FNC-TP
|
||
FNC-TP, the intracellular active form of FNC, is a potent nucleoside reverse transcriptase inhibitor (NRTI) with broad-spectrum antiviral activity against HIV, HBV, and HCV. | |||
T2005 |
Dubermatinib
TP0903 |
Apoptosis; TAM Receptor | Apoptosis; Tyrosine Kinase/Adaptors |
Dubermatinib (TP0903) 是一种具有高效性和选择性的 Axl 受体酪氨酸激酶抑制剂,IC50值为27 nM。 | |||
T11227L1 |
Eravacycline HCl
Eravacycline HCL(1207283-85-9 Free bse),TP-434 HCl |
Antibiotic | Microbiology/Virology |
Eravacycline HCl (TP-434 HCl) 是一种具有广谱抗菌活性的强效抗生素。 | |||
T13190 |
TP-472
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
TP-472 is a selective inhibitor of BRD9 (Kd: 33 nM). | |||
T34908 |
TP-422
TP422 |
||
TP-422 is a negative control for TP-238. | |||
T28997 |
TP-271
TP271 |
||
TP-271, a tetracyclines antibiotic, is used potentially for the treatment of community-acquired bacterial pneumonia (CABP). | |||
T13188 |
TP-004
|
Others | Others |
TP-004 is a potent and reversible methionine aminopeptidase 2 (MetAP2) inhibitor (IC50: 6 nM). | |||
T35649 | EFdA-TP tetraammonium | ||
EFdA-TP tetraammonium is an influential nucleoside reverse transcriptase (RT) inhibitor that effectively prevents RT-mediated DNA synthesis by acting as an immediate or delayed chain terminator (ICT or DCT). Additionally, EFdA-TP tetraammonium exhibits multiple mechanisms of inhibiting HIV-1 RT[1]. | |||
T70429 |
TP-6076
|
||
TP-6076 is a fluorocycline antibiotic, inhibiting bacterial protein synthesis, exhibiting great antimicrobial activity against carbapenem-resistant A. baumannii. | |||
T40055 |
TP-238 hydrochloride
|
||
TP-238 hydrochloride is a highly potent and selective dual CECR2/BPTF probe, demonstrating IC50 values of 30 nM and 350 nM, respectively. It additionally exerts inhibitory effects on BRD9, with a pIC50 value of 5.9, while displaying lower activity against 338 other kinases. | |||
T6165 |
Bardoxolone Methyl
RTA 402,CDDO Methyl ester,TP-155,甲基巴多索隆,NSC 713200 |
Apoptosis; IκB/IKK; Ferroptosis; Nrf2; Autophagy | Apoptosis; Autophagy; Immunology/Inflammation; NF-κB |
Bardoxolone Methyl (TP-155) 是一种合成的三萜类化合物,作为 Nrf2通路的激活剂和 NF-κB 途径的抑制剂,具有潜在的抗肿瘤和抗炎活性。 | |||
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). | |||
T71979 |
TP-S1-68
|
||
TP-S1-68 is a Type-I inhibitor of TIE-2. | |||
T20515 |
Selank
TP-7,TP7,TP 7 |
||
Selank is a synthetic analog of tuftsin. | |||
T19588 |
TP748
2-苄氧基恶唑 |
Others | Others |
TP748 是一种异恶唑,也是合成四环素的关键中间体。 | |||
T26301 |
Tyropeptin A-4
TP 101,TP-101,TP101 |
||
Tyropeptin A-4 is used as a proteasome inhibitor. | |||
T11227 |
Eravacycline
TP-434 |
Antibacterial | Microbiology/Virology |
Eravacycline (TP-434) 是一种有效的广谱抗菌剂。 | |||
T29431 |
4'-Azidothymidine 5'-triphosphate
Adrt TP,Adrt-TP,AdrtTP |
||
4'-Azidothymidine 5'-triphosphate exerts selectively action on both reverse transcriptase of human immunodeficiency virus type 1 and human DNA polymerases alpha and beta. | |||
T39104 |
Itacnosertib
Itacnosertib,TP-0184 |
||
Itacnosertib (TP-0184) is a chemical compound that acts as an inhibitor of JAK2, ACVR1 (ALK2), and ALK5, as indicated in WO2014151871. | |||
T26209 |
Splenotritin
TP 3,Thymopoietin tripeptide,TP3,TP-3 |
||
Splenotritin is used as an antimicrobial peptide. | |||
T73491 | TP-050 | ||
TP-050 是一种口服有效的选择性 NMDAR 激动剂,抑制 GluN2A 和 GluN2D 的 EC50值分别为 0.51 μM 和 9.6 µM。TP-050 可穿过血脑屏障 (BBB)。TP-050 诱导海马区的长期增益效应 (LTP),增强神经元信号传输。 | |||
T6446L |
Clevudine triphosphate
L-FMAU-TP |
||
Clevudine triphosphate is a TTP analog that is able to inhibit protein priming independently of the deoxynucleoside triphosphate substrate. | |||
T75351 | TP-TRFS | ||
TP-TRFS 是高度选择性的一个硫氧还蛋白还原酶 (TrxR) 双光子荧光探针。 | |||
T63701 | TP-5801 | ||
TP-5801 是口服具有活力的非受体酪氨酸激酶 (TNK1) 抑制剂,IC50 值为 1.40 nM,具有抗肿瘤作用。 | |||
T77775 |
TP-1454
|
||
TP-1454是一种针对PKM2的激活剂,其生化测定的AC50为10 Nm。它可通过作用于T调节细胞来调控肿瘤的免疫反应。 | |||
T73374 | TP-030-1 | ||
TP-030-1 是 RIPK1的抑制剂。TP-030-1 抑制 hRIPK1 的 Ki 值为 3.9 nM,抑制 mRIPK1 的 IC50值为 4.2 μM。TP-030-1 可用于炎症性疾病和神经退行性疾病的研究。 | |||
T78147 |
TP-5801 TFA
|
Others | Others |
TP-5801 TFA为口服活性非受体酪氨酸激酶(TNK1)抑制剂(IC50=1.40 nM),展现抗肿瘤活性。 | |||
T40088 |
TP0586352
|
||
TP0586352 is a potent inhibitor of LpxC, exhibiting efficacy against carbapenem-resistant strains of Klebsiella pneumoniae without inducing cardiovascular risks. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2598 |
Thymopentin
TP5,胸腺五肽 |
Estrogen/progestogen Receptor; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Thymopentin (TP5) 是主要由胸腺皮质和髓质上皮细胞分泌的生物特性肽。它能促使自人类胚胎干细胞产生 T 细胞群。它是有效免疫调节剂,具有很短的血浆半衰期(30 秒)。 | |||
T1352 |
ATP disodium salt
Adenosine 5'-triphosphate disodium salt,三磷酸腺苷二钠,ATP,ATP disodium,腺苷-5'-三磷酸二钠盐,Adetide,Adenosine-Triphosphate,Disodium adenosine triphosphate |
P2X Receptor; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Neuroscience |
ATP disodium salt (Adenosine-Triphosphate) 是体内能量储存的重要物质,为代谢提供能量,同时在细胞中作为辅酶发挥作用。Adenosine 5'-triphosphate disodium salt 也是免疫和炎症中重要的内源性信号分子。 | |||
T38427 |
dUTP trisodium
2'-Deoxyuridine-5'-triphosphate trisodium salt,Deoxyuridine triphosphate |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
dUTP trisodium (Deoxyuridine triphosphate) 是在 5'-位具有三磷酸基团的脱氧尿苷磷酸盐,可用于 PCR。 | |||
T64980 |
ATP disodium trihydrate
Adenosine-5'-triphosphate disodium trihydrate |
Endogenous Metabolite | Metabolism |
ATP disodium trihydrate (Adenosine-5'-triphosphate disodium trihydrate) 是体内能量储存和代谢的重要物质,是免疫和炎症中重要的内源性信号分子,可为机体代谢提供能量,同时在细胞中作为辅酶发挥作用。 | |||
T2812 |
ATP disodium salt hydrate
ATP disodium,ATP disodium salt,Adenosine disodium triphosphate,三磷酸腺苷二钠盐 |
Others; Endogenous Metabolite | Metabolism; Others |
ATP disodium salt hydrate (Adenosine disodium triphosphate) 是体内能量储存和代谢的重要物质,为代谢提供能量,同时在细胞中作为辅酶发挥作用。同时,它是也是免疫和炎症中重要的内源性信号分子。 | |||
T20089 |
ATP
Atipi,ATP disodium salt hydrate,Triphosphoric acid adenosine ester,Ara-ATP,Triphosphaden,Adenosine triphosphate;Ara-ATP,Adenosine triphosphate |
Endogenous Metabolite | Metabolism |
ATP (Adenosine triphosphate) 可为细胞提供能量,参与整体能量平衡,维持细胞内稳态。ATP 可以通过与特异性嘌呤能受体的相互作用充当细胞外信号分子,以介导神经传递、炎症、细胞凋亡和骨重塑等多种过程。 | |||
T73073 |
PTP1B-IN-21
|
||
PTP1B-IN-21 是蛋白酪氨酸磷酸酶 1B (PTP1B) 的选择性抑制剂 (IC50=1.56 μM),抑制力超出高度同源 T 细胞蛋白酪氨酸磷酸酶 (TCPTP;IC50>100 μM),PTP1B 是抑制 2 型糖尿病的重要靶点。 | |||
T40526 |
ATP dipotassium
腺苷三磷酸二钾盐,Adenosine5'-triphosphatedipotassium |
||
ATP dipotassium (Adenosine 5'-triphosphate dipotassium) is a vital compound involved in energy storage and metabolism within living organisms. It plays a crucial role in supplying metabolic energy for driving pumps and acts as a coenzyme in cellular processes. Additionally, ATP dipotassium functions as a significant endogenous signaling molecule contributing to immunity and inflammation. | |||
T73072 |
PTP1B-IN-20
|
||
PTP1B-IN-20 是蛋白酪氨酸磷酸酶 1B (PTP1B) 的选择性抑制剂 (IC50=1.05 μM),抑制力超出高度同源 T 细胞蛋白酪氨酸磷酸酶 (TCPTP;IC50=78.0 μM),PTP1B 是抑制 2 型糖尿病的重要靶点。 | |||
T10021 |
1-Methylxanthine
|
Endogenous Metabolite | Metabolism |
1-Methylxanthine 是咖啡因衍生物,是咖啡因和茶碱 (1,3-二甲基黄嘌呤,TP) 在人体尿代谢产物,能够提高肿瘤细胞的放射敏感性。 |