111
12
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38948 |
MS-PEG4-THP
|
PROTAC Linker | PROTAC |
MS-PEG4-THP 是PEG 类PROTAC linker,可用于合成 PROTAC 分子。 | |||
T40533 |
THP-PEG10-THP
THP-PEG10-THP |
||
THP-PEG10-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39237 |
THP-PEG9-THP
THP-PEG9-THP |
||
THP-PEG9-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T38576 |
Propargyl-PEG1-THP
Propargyl-PEG1-THP |
||
Propargyl-PEG1-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40531 |
THP-PEG10-OH
THP-PEG10-OH |
||
THP-PEG10-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40530 |
Ms-PEG6-THP
Ms-PEG6-THP |
||
Ms-PEG6-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39076 |
Benzyl-PEG8-THP
Benzyl-PEG8-THP |
||
Benzyl-PEG8-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40780 |
THP-PEG9-OH
THP-PEG9-OH |
||
THP-PEG9-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40632 |
MS-PEG12-THP
MS-PEG12-THP |
||
MS-PEG12-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40779 |
Benzyl-PEG9-THP
Benzyl-PEG9-THP |
||
Benzyl-PEG9-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39834 |
Benzyl-PEG6-THP
Benzyl-PEG6-THP |
||
Benzyl-PEG6-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40448 |
MS-PEG3-THP
MS-PEG3-THP |
||
MS-PEG3-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39835 |
Benzyl-PEG7-THP
Benzyl-PEG7-THP |
||
Benzyl-PEG7-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40532 |
MS-PEG10-THP
MS-PEG10-THP |
||
MS-PEG10-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T38426 |
Benzyl-PEG4-THP
Benzyl-PEG4-THP |
||
Benzyl-PEG4-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T38705 |
MS-PEG1-THP
MS-PEG1-THP |
||
MS-PEG1-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39006 |
Bromo-PEG2-THP
Bromo-PEG2-THP |
||
Bromo-PEG2-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T39228 |
Br-PEG4-THP
Br-PEG4-THP |
||
Br-PEG4-THP is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T40444 |
THP-CH3-ethyl propionate
THP-CH3-ethyl propionate |
||
THP-CH3-ethyl propionate is a PROTAC linker composed of alkyl and ether groups. It finds utility in PROTAC synthesis. | |||
T6628 |
Pirarubicin
吡柔比星,Theprubicin,THP |
Topoisomerase; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Microbiology/Virology |
Pirarubicin (Theprubicin) 是一种蒽环类抗生素,是拓扑异构酶 II 抑制剂,可用于各种癌症的研究。 | |||
T9777 |
THP104c
|
Mitochondrial Metabolism | Metabolism |
THP104c 是有效的线粒体分裂抑制剂。 | |||
T34860 | THP-PEG12 | ||
THP-PEG12 is a PEG linker. | |||
T17082 |
THP-PEG4-OH
|
Others | Others |
THP-PEG4-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T18853 |
Tos-PEG4-THP
|
Others | Others |
Tos-PEG4-THP is a polyethylene glycol (PEG) derivative utilized as a linker in the synthesis of PROTAC K-Ras Degrader-1, a potential therapeutic compound for targeted degradation of K-Ras protein [1]. | |||
T17085 |
THP-PEG8-OH
|
Others | Others |
THP-PEG8-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17084 |
THP-PEG6-OH
|
Others | Others |
THP-PEG6-OH is a polyethylene glycol (PEG)-based PROTAC linker, utilized in the synthesis of PROTACs[1]. It is also a non-cleavable three-unit PEG linker for antibody-drug conjugates (ADCs)[2]. | |||
T17087 |
THP-SS-alcohol
|
Others | Others |
THP-SS-alcohol is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18845 |
THP-PEG11-OH
|
Others | Others |
THP-PEG11-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17086 |
THP-PEG8-Tos
|
Others | Others |
THP-PEG8-Tos is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17083 |
THP-PEG5-OH
|
Others | Others |
THP-PEG5-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17081 |
THP-PEG3-OH
|
Others | Others |
THP-PEG3-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. | |||
T17088 | THP-SS-PEG1-Boc | Others | Others |
THP-SS-PEG1-Boc is a cleavable ADC linker comprising a one-unit PEG, commonly employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17089 | THP-SS-PEG1-Tos | Others | Others |
THP-SS-PEG1-Tos is a 1 unit PEG ADC linker that is cleavable. It is employed during the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T18846 |
THP-PEG4-Pyrrolidine(N-Boc)-CH2OH
|
Others | Others |
THP-PEG4-Pyrrolidine(N-Boc)-CH2OH is a polyethylene glycol (PEG) based PROteolysis TArgeting Chimera (PROTAC) linker, employed for the synthesis of PROTAC K-Ras Degrader-1, as documented in reference [1]. | |||
T18847 | THP-PEG4-Pyrrolidine(N-Me)-CH2OH | Others | Others |
THP-PEG4-Pyrrolidine(N-Me)-CH2OH, a PEG-based PROTAC linker, facilitates the synthesis of PROTAC K-Ras Degrader-1[1]. | |||
T17058 |
Tetrahydropyranyldiethyleneglycol
THP-PEG2-OH |
Others | Others |
Tetrahydropyranyldiethyleneglycol is a polyethylene glycol (PEG)-based PROTAC linker utilized in the synthesis of PROTACs[1]. | |||
T67267 |
THP-PEG1-alcohol
|
||
THP-PEG1-alcohol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67267,CAS号为 2162-31-4。 | |||
T11492 |
GSK2983559 free acid
|
Others; RIP kinase | Apoptosis; NF-κB; Others |
GSK2983559 free acid 是一种有效的特异性受体相互作用蛋白 2 (RIP2) 抑制剂。 GSK2983559 free acid 在阻断人类炎症性肠病外植体样品和体内的许多促炎细胞因子反应方面表现出优异的活性。 | |||
T3278 |
Piribedil
EU-4200,Trivastan,ET-495,Trivastal |
Dopamine Receptor; Histone Methyltransferase; Adrenergic Receptor | Chromatin/Epigenetic; GPCR/G Protein; Neuroscience |
Piribedil (Trivastan) 是多巴胺 D2受体激动剂,对 hα1A-肾上腺素受体也显示出拮抗作用。 | |||
T9552 |
BAZ1A-IN-1
|
Epigenetic Reader Domain | Chromatin/Epigenetic |
BAZ1A-IN-1 是BAZ1A(含溴结构域蛋白)抑制剂(Kd:0.52 μM)。它对低表达BAZ1A 的癌细胞表现出弱活性或无活性,但对高表达BAZ1A 的癌细胞系显示出良好的抗生存作用。 | |||
T9016 |
AI-10-47
1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47 |
Others | Others |
AI-10-47 (1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47) 是 CBFβ-RUNX 结合的小分子抑制剂(IC50:3.2 μM)。 | |||
T8531 |
m-3M3FBS
2,4,6-三甲基-N-[3-(三氟甲基)苯基]苯磺酰胺 |
Apoptosis; Phospholipase | Apoptosis; Metabolism |
m-3M3FBS 是一种有效的磷脂酶C 激活剂,刺激人中性粒细胞产生超氧物,上调细胞内钙离子浓度,刺激多种细胞产生磷酸肌醇。它诱导单核细胞白血病细胞凋亡。 | |||
T28178 |
NLRP3-IN-9
INF-4E,INF 4E,INF4E |
NOD | Immunology/Inflammation; NF-κB |
NLRP3-IN-9 (INF-4E) 是 NLRP3 ATPase 和 caspase-1 的抑制剂。 NLRP3-IN-9 通过不可逆地捕获硫醇亲核体发挥作用,以时间和浓度依赖性方式防止 ATP 和尼日利亚菌素触发的人 THP-1 细胞焦亡。 | |||
T60012 |
HS-243
|
IRAK; MAPK; CDK | Cell Cycle/Checkpoint; Immunology/Inflammation; MAPK; NF-κB |
HS-243 是 IRAK-4 和 IRAK-1 的抑制剂,IC50 分别为 20 和 24 nM。 HS-243 显示出抗炎和抗癌活性。 | |||
T6019 |
Volasertib
BI 6727,伏拉塞替 |
Apoptosis; PLK | Apoptosis; Cell Cycle/Checkpoint |
Volasertib (BI 6727) 是一种具有口服活性的高效ATP 竞争性Polo 样激酶 1 抑制剂。它抑制 PLK2 和 PLK3,IC50分别为 5 和 56 nM。它是二氢蝶呤酮衍生物,有抗肿瘤活性,可诱导有丝分裂停滞和细胞凋亡。 | |||
T10384 |
Farudodstat
ASLAN003 |
Apoptosis; Dehydrogenase; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism |
Farudodstat (ASLAN003) 是一种具有口服活性的二氢乳清酸脱氢酶 (DHODH) 抑制剂,对人 DHODH 酶的IC50为 35 nM。它通过激活 AP-1 转录因子来抑制蛋白质合成,可以诱导凋亡,并在急性髓样白血病异种移植小鼠中大大延长其生存期。 | |||
T7162 |
R1487 Hydrochloride
R1487 (Hydrochloride) |
p38 MAPK; Autophagy | Autophagy; MAPK |
R1487 Hydrochloride (R1487(Hydrochloride)) 是一种可口服的高选择性 p38α 抑制剂,对 p38α 和 p38β 的Kd 值分别为 0.2 nM 和 29 nM。 | |||
T8506 |
THPP-1
|
PDE | Metabolism |
THPP-1 是一种 SGC 推荐的化学探针, 是一种口服具有活性的磷酸二酯酶10A 抑制剂,其对人和大鼠的Ki 分别为 1 nM 和 1.3 nM。它的药理学特性良好。 | |||
T24880 | THPN | ||
THPN is a Nur77 agonist. It also induces autophagy in melanoma cell lines. | |||
T24648 |
PK-THPP
|
||
PK-THPP is a channel blocker of TASK-3. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4038 |
Ectoine
THP(B),L-Ectoine,四氢甲基嘧啶羧酸 |
Others; Antibacterial | Microbiology/Virology; Others |
Ectoine (L-Ectoine) 是生活在极其恶劣环境中的细菌所产生的氨基酸衍生物,是一种天然的细胞保护剂。它具有良好的安全性,可研究过敏性鼻炎。它用作渗透调节相容性溶质,可增加皮肤表面的水合作用并稳定脂质层,常用于皮肤护理。 | |||
T2P2870 |
Damascenone
trans-damascenone,Beta-Damascenone,大马烯酮,大马酮 |
Others; NF-κB; Endogenous Metabolite | Metabolism; NF-κB; Others |
Damascenone (trans-damascenone) 是一种 E-和 Z-异构体大马士革酮的混合物,源于 Epipremnum pinnatum 的具有抗炎特性的特性化合物。 | |||
T9218 |
Andrograpanin
19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE,新穿心莲内酯苷元 |
p38 MAPK | MAPK |
Andrograpanin (19-HYDROXY-8(17),13-LABDADIEN-16,15-OLIDE) 是来自穿心莲的一种天然产物,具有抗炎和抗感染活性。 | |||
T6648 |
Rotundine
Gindarine,L-Tetrahydropalmatine,Caseanine,罗通定,(-)-Tetrahydropalmatine |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Rotundine (Gindarine) 是多巴胺D1、D2和D3受体的拮抗剂,IC50值分别为 166、1.4 和 3.3 μM。 它也是5-HT1A 的拮抗剂,IC50值为 370 nM。 | |||
TN1879 |
Lucideric acid A
Lucidenic acid A,赤芝酸A |
MMP; p38 MAPK; JNK | MAPK; Proteases/Proteasome |
Lucideric acid A (Lucidenic acid A) 是分离自灵芝的天然产物,可抑制 PMA 诱导的MMP-9活性,具有抵抗肝癌细胞侵袭的作用。 | |||
T81159 | Sibiricine | ||
Sibiricine(Compound 8),一种从Corydalis crispa药用植物提取的异喹啉类生物碱,对于LPS诱导的THP-1细胞产生的TNF-α显示出显著的抗炎效果。 | |||
TN5593 | Euphohelioscopin A | ||
Euphohelioscopin A, an activator of protein kinase C (PKC), it inhibits proliferation and induces differentiation of the myeloid leukemia cell lines THP-1 and HL-60. Euphohelioscopin A has anti-inflammary activity, it exhibits moderate inhibitory activity | |||
T72742 |
(-)-Pinocembrin
(-)-乔松素 |
||
(-)-Pinocembrin 对 H37Ra 结核分枝杆菌展示了抗菌活性,无论是休眠还是活跃期,其 IC50 值分别为1.11 mg/mL 和 1.21 mg/mL。作为一种抗增殖剂,(-)-Pinocembrin 对于 THP-1、A549、Panc-1、HeLa 和 MCF7 细胞系,IC50 值范围为 1.88 至 11.00 mg/mL。 | |||
T37751 |
Streptazolin
|
||
Streptazolin is a fungal metabolite originally isolated from S. viridochromogenes. It increases NF-κB activity when used at concentrations ranging from 60 to 130 μg/ml, at least in part, via PI3K signaling. Streptazolin enhances TNF-α secretion induced by LPS and enhances IL-8 secretion when used alone or in combination with LPS in THP-1 Blue cells. | |||
TN5238 |
Viscidulin II
|
IL Receptor; TNF | Apoptosis; Immunology/Inflammation |
Viscidulin II can be potential therapeutic agents against P. acnes-induced skin inflammation, it can significantly suppress P. acnes-induced IL-8 and IL-1β production in THP-1 cells, concomitant intradermal injection of viscidulin II with P. acnes can effectively attenuate P. acnes-induced ear swelling, and decrease the production of IL-6 and tumor necrosis factor-α in ear homogenates. | |||
T37442 |
Aspergillin PZ
|
||
Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis (MIC = 20 μM) but not S. aureus, E. coli, or B. cereus (MICs = >20 μM). It is cytotoxic to HL-60 promyelocytic leukemia cells (IC50 = 56.61 μM) but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells (IC50s = >80 μM). | |||
TN3395 |
Alpinone 3-acetate
|
IFNAR | Immunology/Inflammation |
Alpinone 3-acetate 具有抗炎作用,可抑制12-O-tetradecanophenol 13-acetate 所致小鼠耳部水肿模型的炎症反应。Alpinone 3-acetate 是Alpinone 衍生物 。Alpinone 是一种具有活性的天然化合物,来源于向日葵,具有免疫调节和抗病毒活性 。 |