708
144
5
392
7
Cat. No. | Product Name | ||
---|---|---|---|
L1120 | AMPK靶向分子库 | 80 compounds | |
80 个靶向AMPK 的分子集合,可用于高通量和高内涵筛选; | |||
L1400 | MAPK 抑制剂库 | 365 compounds | |
365 种与MAPK 信号通路相关的生物活性小分子化合物的特有集合,可用于高通量筛选和高内涵筛选; | |||
L4100 | TGF-β/Smad靶点化合物库 | 184 compounds | |
184 个 TGF-β/Smad 靶点相关的小分子化合物的特有集合,用于高通量、高内涵筛选; | |||
L2610 | 神经递质受体化合物库 | 1513 compounds | |
1513 种与神经递质受体相关的化合物,用于高通量、高内涵筛选; | |||
L3800 | NF-κB 通路分子库 | 729 compounds | |
729 个 NF-κB 信号通路相关的小分子化合物的特有集合,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7740 |
Protease-Activated Receptor-4 diTFA
Protease-Activated Receptor-4 diTFA(245443-52-1(free base)) |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-4 diTFA 是蛋白酶激活受体 4 (PAR4) 激动剂。 | |||
TP1628L |
Activated Protein C (390-404), human acetate
Activated Protein C (390-404), human acetate(146340-20-7 Free base) |
APC | Cell Cycle/Checkpoint |
Activated Protein C (390-404), human acetate (Activated Protein C ) 抑制 APC 抗凝活性。 | |||
T7513 |
Protease-Activated Receptor-2, amide
蛋白酶活化的受体-2,酰胺,SLIGKV-NH2,H-丝氨酰亮氨酰异亮氨酰甘氨酰赖氨酰缬氨酰NH2 |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-2, amide (SLIGKV-NH2) 是 PAR2 的激动剂,IC50为 10.4 M。 | |||
T38836L |
Protease-Activated Receptor-1, PAR-1 Agonist acetate
|
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-1, PAR-1 Agonist acetate 是一种选择性蛋白酶激活受体 1 (PAR-1) 激动剂肽。 它对应于 PAR1 栓系配体,可以选择性地模拟凝血酶通过该受体的作用。 | |||
TP1046 |
SLIGRL-NH2
Protease-Activated Receptor-2 Activating Peptide |
Protease-activated Receptor | GPCR/G Protein |
SLIGRL-NH2 (Protease-Activated Receptor-2 Activating Peptide) 为一种蛋白酶激活受体-2 (PAR-2) 激动剂,具有诱导非组胺能性瘙痒的功能。 | |||
T38836 |
Protease-Activated Receptor-1, PAR-1 Agonist
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist, a selective peptide, activates the PAR-1 receptor by mimicking the specific actions of thrombin. It corresponds to the PAR1 tethered ligand, facilitating selective activation of this receptor. | |||
T7380 |
Protease-Activated Receptor-4
蛋白酶活化的受体-4 |
Protease-activated Receptor | GPCR/G Protein |
Protease-Activated Receptor-4 是蛋白酶激活受体 4 激动剂,具有抗血小板治疗。 | |||
T83177 |
Activated A Subunit
|
Others | Others |
Activated A Subunit 适用于合成促进外显子跳跃的寡聚物偶联体。所合成的偶联体与人类抗肌萎缩蛋白基因内特定的序列配对互补,能够有效促进外显子51的跳跃,为肌萎缩疾病研究提供了一种工具。 | |||
TP1628 |
Activated Protein C (390-404), human
|
||
Activated Protein C (390-404), human, a peptide derived from the vitamin K-dependent serine protease, effectively suppresses the anticoagulant activity of APC[1]. | |||
T83175 |
Activated DPG Subunit
|
Others | Others |
Activated DPG Subunit 用于合成可诱导外显子 51 跳跃的外显子跳跃寡聚物偶联物。这些偶联物与人抗肌萎缩蛋白基因中选定的靶位点互补,有助于肌肉萎缩症的研究。 | |||
T36288 |
Protease-Activated Receptor-1, PAR-1 Agonist TFA
|
||
Protease-Activated Receptor-1 (PAR-1) Agonist TFA is a selective peptide that acts as an agonist for the proteinase-activated receptor-1 (PAR-1). Corresponding to the tethered ligand of PAR-1, this compound mimics the actions of thrombin through the PAR-1 receptor[1][2]. | |||
TP1580 |
Activated Protein C (390-404), human TFA
|
||
The peptide region containing residues 390-404 in Activated Protein C (APC) is essential for anticoagulant activity and is available for interaction with antibodies or with other proteins, such as the macromolecular substrates Factors Va or VIIIa. APC reg | |||
T83176 |
Activated C Subunit
|
Others | Others |
Activated C Subunit 用于合成可诱导外显子51跳跃的外显子跳跃寡聚物偶联物。所得寡聚物偶联物与人类抗肌萎缩蛋白基因特定靶位点互补,有助于研究肌肉萎缩症。 | |||
T82526 |
Drotrecogin alfa (activated)
|
Others | Others |
Drotrecogin alfa activated (DrotAA)为重组人活化蛋白C(APC)。该化合物能够抑制由烟雾引起的大鼠肺微血管通透性上升及促炎细胞因子IL-1β水平增加,具有抗凝血与抗炎作用,并促进纤溶过程。Drotrecogin alfa activated主要用于重症脓毒症的实验研究。 | |||
T83173 |
Activated T Subunit
|
Others | Others |
Activated T Subunit 用于合成可诱导外显子51跳跃的外显子跳跃寡聚物偶联物。该寡聚物偶联物与人类抗肌萎缩蛋白基因中选定靶位点互补,适用于肌肉萎缩症研究。 | |||
T83174 |
Activated EG3 Tail
|
Others | Others |
Activated EG3 Tail 适用于合成外显子跳跃寡聚物偶联物。该寡聚物偶联物能与人类抗肌萎缩蛋白基因特定的靶位点匹配,进而诱导外显子 51 的跳跃。此类偶联物对于肌肉萎缩症研究具有重要价值。 | |||
T36289 |
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA
|
||
Protease-Activated Receptor-3 (PAR-3) (1-6), human TFA is a peptide that acts as an agonist for the proteinase-activated receptor (PAR-3)[1]. | |||
T36286 |
Protease-Activated Receptor-3 (PAR-3) (1-6), human
|
||
TFRGAP-amide, human PAR-3-derived tethered ligand sequence which does not activate PAR-3 but rather activates PAR-1 and PAR-2, either in Jurkat or in other PAR-expressing cells. | |||
TP1046L |
PAR-2 Activating Peptide acetate
SLIGRL-NH2 acetate,PAR-2 Activating Peptide acetate(171436-38-7 free base),Protease-Activated Receptor-2 Activating Peptide acetate |
Protease-activated Receptor | GPCR/G Protein |
PAR-2 Activating Peptide acetate (SLIGRL-NH2 acetate)(171436-38-7 free base) 是 Protease-Activated Receptor-2 (PAR-2) 的激动剂。 | |||
T80062 |
Mitogen-activated protein kinase 1
MAPK1 |
NF-κB | NF-κB |
Mitogen-activated protein kinase1 (MAPK1) 能够激活下游的 p38/NF-κB 通路,并调控多种与脓毒症相关的疾病细胞过程。此外,MAPK1 通过磷酸化催化底物蛋白,起到调节底物蛋白活性开关的作用。 | |||
T63382 |
Protease-Activated Receptor-1 antagonist 3
|
Others | Others |
Protease-Activated Receptor-1 antagonist 3 是蛋白酶激活受体 1protease-activated receptor-1 的有效拮抗剂 (IC50: 7 nM)。Protease-Activated Receptor-1 antagonist 3 与 hERG K+通道表现出结合亲和力 (IC50: 9 μM)。 | |||
T14988 |
CMPD1
|
MAPK | MAPK |
CMPD1 是非 ATP 竞争性 p38 MAPK 介导的 MK2磷酸化选择性抑制剂(Ki:330 nM)。 | |||
T74266 |
Protease-Activated Receptor-1 antagonist 2
|
Others | Others |
Protease-Activated Receptor-1 antagonist 2 是一种选择性蛋白酶激活受体-1 (PAR-1) 拮抗剂,口服活性,IC50值为7 nM。该化合物具有优良的药代动力学特性,适用于心血管疾病 (CVD) 如动脉粥样硬化和再狭窄的研究。 | |||
T62507 |
Protease-Activated Receptor-1 antagonist 1
|
Others | Others |
Protease-Activated Receptor-1 antagonist 1 (Compound 13) 是一种蛋白酶激活受体 1 (PAR-1) 拮抗剂,通过 FLIPR 技术得到的 IC50 为 3 nM。Protease-Activated Receptor-1 antagonist 1 能够用于研究血栓性心血管、心肌梗塞和外周动脉疾病。 | |||
T64285 |
Protease-Activated Receptor-1 antagonist 2
|
Others | Others |
Protease-Activated Receptor-1 antagonist 2 是一种选择性的、口服具有活力的蛋白酶激活受体-1 (PAR-1) 拮抗剂 (IC50: 7 nM)。Protease-Activated Receptor-1 antagonist 2 显示出良好的药代动力学特性,能够用于进行心血管疾病 (CVD) 的相关研究(如动脉粥样硬化和再狭窄)。 | |||
T13047 |
Synta66
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Synta66 是一种钙池操纵钙离子通道 Orai 抑制剂,用于神经系统疾病的研究。 | |||
T39516 |
Bocidelpar
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Bocidelpar 是一种有效的过氧化物酶体增殖物激活受体 delta 调节剂,可改善杜兴肌营养不良肌肉细胞中的线粒体生物合成和功能。 | |||
T16501 |
PF-3644022
|
p38 MAPK; Serine Protease; MAPK | MAPK; Proteases/Proteasome |
PF-3644022 是可口服的,具有 ATP 竞争性的MAPKAPK2 (MK2)选择性抑制剂,IC50为 5.2 nM,Ki 为 3 nM。它有效抑制 TNFα 的产生并具有抗炎作用,还抑制 MK3 和 p38 调节/激活激酶,IC50分别为 53 和 5.0 nM。 | |||
T4442 |
MK2-IN-1 hydrochloride
MK2 Inhibitor,MK 25 |
MAPK | MAPK |
MK2-IN-1 hydrochloride (MK 25) 是一种高效的选择性 MAPKAPK2(MK2)激酶抑制剂,其 IC50值为0.11uM。 | |||
T12058 |
MK2-IN-3 hydrate
MK-2 Inhibitor III |
ERK; MAPK; MNK | MAPK |
MK2-IN-3 hydrate (MK-2 Inhibitor III) 是一种口服有活性的、ATP 竞争性的MAPKAP-K2 (MK-2)选择性抑制剂(IC50:0.85 nM)。 | |||
T10885 |
CRAC intermediate 2
|
Others; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Others |
CRAC intermediate 2是CRAC 抑制剂合成的中间体化合物。 | |||
T9034 |
MK2-IN-3
MK2 Inhibitor III |
MAPK | MAPK |
MK2-IN-3 (MK2 Inhibitor III) 是选择性的 MAPKAP-K2 (MK-2)抑制剂(IC50:8.5 nM),能够抑制 U937 细胞及体内 TNFα 的生成。 | |||
T75902 |
SLIGRL-NH2 TFA
Protease-Activated Receptor-2 Activating Peptide TFA |
Others | Others |
SLIGRL-NH2 TFA(Protease-Activated Receptor-2 Activating Peptide TFA)作为PAR-2(蛋白酶激活受体-2)的激动剂,具有高度特异性。 | |||
T10900 |
CUDA
|
PPAR; Epoxide Hydrolase | DNA Damage/DNA Repair; Metabolism |
CUDA 是一种可溶性环氧水解酶抑制剂,对小鼠 sEH 和人 sEH 作用的 IC50分别为 11.1 和 112 nM。它能选择性地上调过氧化物酶体增殖激活受体 PPARα的活性,有用于心血管疾病的研究潜力。 | |||
T24984 |
5J-4
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
5J-4 是一种有效的钙释放激活钙通道 (CRAC) 和钙池操纵性钙内流(SOCE) 阻滞剂。 5J-4 减少 IL-17 的产生并降低 RORα 和 RORγt 的表达。 | |||
T10884 |
CRAC intermediate 1
5-(S)-Fluorowillardiine |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
CRAC intermediate 1是用于CRAC离子通道系列化合物合成的关键中间体,详细信息来自专利WO 2010122089。 | |||
T8476 |
RSVA405
RSVA 405 |
AMPK; STAT; Autophagy | Autophagy; Chromatin/Epigenetic; JAK/STAT signaling; PI3K/Akt/mTOR signaling; Stem Cells |
RSVA405 是一种具有口服活性的AMPK 激活剂,EC50值为 1 μM。它也是一种 STAT3 抑制剂,具有抗炎作用,可研究肥胖症。它通过促进 CaMKKβ 依赖的 AMPK 活化,从而抑制mTOR,并促进自噬以增加 Aβ 的降解。 | |||
T21980 |
PD 198306
|
MEK | MAPK |
PD 198306 是一种具有抗痛觉过敏作用的 MAPK/ERK 激酶 (MEK) 选择性抑制剂。 PD 198306 可降低链脲佐菌素诱导的活性 ERK1 水平升高。 | |||
T2374 |
HTH-01-015
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
HTH-01-015 是一种选择性 NUAK1 抑制剂,IC50为 100 nM。它抑制 NUAK1 的效力比抑制 NUAK2 高 100 倍以上,IC50大于10 μM。 | |||
T6014 |
FRAX597
|
PAK | Cytoskeletal Signaling |
FRAX597 是一种有效的 ATP 竞争性 I 组 PAK 抑制剂,作用于PAK1、2和3,IC50分别为 8、13 和 19 nM。 | |||
T15945 |
MA-0204
|
PPAR | DNA Damage/DNA Repair; Metabolism |
MA-0204 是一种高选择性,可口服的过氧化物酶体增殖物激活受体 δ (PPARδ) 调节剂,对于人,小鼠和大鼠 PPARδ 的 EC50分别为 0.4、7.9 和 10 nM。它有用于 Duchene 肌营养不良症 (DMD) 的研究潜力。 | |||
T1986 |
Atopaxar
E5555,ER-172594-00 |
Protease-activated Receptor | GPCR/G Protein |
Atopaxar (E5555) 是一种高效、可口服的,选择性的,可逆的凝血酶受体蛋白酶激活受体-1 (PAR-1) 拮抗剂。它是一种抗血小板剂,能干扰血小板信号,可用于动脉粥样硬化血栓性疾病的研究。 | |||
T3651 |
YM-58483
YM 58483,BTP2 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
YM-58483 (BTP2) 是一种特异性有效的 CRAC 通道和随后的 Ca2+ 信号抑制剂,可阻断钙池操纵的阳离子内流 (SOCE)。 | |||
T11342L |
G-5555
|
PAK | Cytoskeletal Signaling |
G-5555 是 PAK1有效抑制剂,对 PAK1 和 PAK2 的Ki 值分别为 3.7 nM 和 11 nM。 | |||
T1941 |
GSK3787
|
PPAR | DNA Damage/DNA Repair; Metabolism |
GSK3787 是选择性过氧化物酶体增殖物激活受体 δ (PPARδ) 的一种不可逆拮抗剂,pIC50为 6.6。 | |||
T2674 |
GSK0660
|
PPAR | DNA Damage/DNA Repair; Metabolism |
GSK0660 是 PPARβ/δ 的拮抗剂和反向激动剂,IC50均为155 nM。 | |||
T16429 |
GNE 2861
|
PAK | Cytoskeletal Signaling |
GNE 2861 是一种 PAK 抑制剂,具有 II 组的选择性。它抑制 PAK4、PAK5 和 PAK6 的IC50值分别为7.5、36和126 nM。 | |||
T6840 |
FRAX486
|
PAK | Cytoskeletal Signaling |
FRAX486 是一种有效的 p21 活化激酶 (PAK) 抑制剂,对 PAK1、PAK2、PAK3 和 PAK4 的 IC50 值分别为 14、33、39 和 575 nM。 | |||
T6839 |
FRAX1036
|
PAK | Cytoskeletal Signaling |
FRAX1036 是一种有效的选择性 PAK1 抑制剂,对 PAK1、PAK2 和 PAK4 的 Ki 值分别为 23.3 nM、72.4 nM 和 2.4 μM。 | |||
T1893 |
Parmodulin 2
ML 161 |
Protease-activated Receptor | GPCR/G Protein |
Parmodulin 2 (ML 161) 是一种蛋白酶激活受体 1(PAR1) 变构抑制剂,IC50为 0.26 μM。它是蛋白酶激活受体 1 (PAR1) 介导的血小板活化的抑制剂,可以抑制体外血小板聚集和体内血小板血栓形成。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1693 |
Glabrone
|
Influenza Virus; PPAR | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Glabrone 是从甘草根中分离的一种异黄酮,可与 PPAR-γ 配体结合,具有抗流感活性。 | |||
TN1100 |
Nepodin
|
transporter; COX; AMPK; Parasite | Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling |
Nepodin 是从Rumex crispus 中分离的一种醌氧化还原酶抑制剂,具有抗糖尿病和抗疟疾的作用。。它通过激活 AMPK 刺激 GLUT4 向质膜的转运。 | |||
T3889 |
Platycodin D
|
Prostaglandin Receptor; AMPK | Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; PI3K/Akt/mTOR signaling |
Platycodin D 是从桔梗中分离得到的一种皂苷类天然产物,是AMPKα的激活剂,具有抗肥胖活性。它可刺激 TNF-α 合成或抑制 TNF-α mRNA 的降解。 | |||
TN1828 |
Kahweol
|
Apoptosis; NF-κB; AMPK | Apoptosis; Chromatin/Epigenetic; NF-κB; PI3K/Akt/mTOR signaling |
Kahweol 是小果咖啡的成分之一,可诱导细胞凋亡,具有抗炎、抗血管生成和抗癌活性。它通过激酶的活化抑制的脂肪生成和增加葡萄糖摄取。 | |||
T3867 |
Alpinetin
山姜素,(-)-alpinetin |
BCL; PPAR | Apoptosis; DNA Damage/DNA Repair; Metabolism |
Alpinetin ((-)-alpinetin) 是从草豆蔻中分离得到的一种黄酮类天然产物,能够活化PPAR-γ,具有抗炎、抗菌活性。它通过抑制增殖、调节 Bcl-2 家族和 XIAP 表达、释放细胞色素 c 和激活 caspase 具有很强的抗肝癌和胰腺癌细胞作用。 | |||
T7327 |
7-Methoxyisoflavone
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
7-Methoxyisoflavone 是单磷酸腺苷活化蛋白激酶 (AMPK) 的激活剂,是异黄酮衍生物。 | |||
T3904 |
Gomisin J
|
Calcium Channel; AMPK | Chromatin/Epigenetic; Membrane transporter/Ion channel; Metabolism; PI3K/Akt/mTOR signaling |
Gomisin J 是在五味子中发现的小分子量木脂素,具有血管舒张活性,在非酒精性脂肪性肝病方面有研究潜力。 它通过激活 AMPK、LKB1 和 Ca2+/钙调蛋白依赖性蛋白激酶 II 以及抑制 HepG2 细胞中的胎球蛋白 A 来调节脂肪生成酶和脂肪分解酶以及炎症分子的表达,从而抑制脂质积累。 | |||
T3881 |
Vaccarin
|
Integrin; Akt; PERK; AMPK | Apoptosis; Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Vaccarin 是从王不留行中提取的一种黄酮糖苷,可显著促进伤口愈合以及伤口部位的内皮和成纤维细胞增殖。它通过激活 AMPK 信号通路改善胰岛素抵抗和脂肪变性。 | |||
T4S0800 |
Demethyleneberberine
|
P450; NOS; NF-κB; HIF; AMPK | Angiogenesis; Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
Demethyleneberberine 是从黄连中提取的一种天然产物,是线粒体靶向抗氧化剂。它也可作为AMPK 激活剂,用于非酒精性脂肪性肝病的研究。它通过抑制NF-κB 通路和调节 Th 细胞的平衡来减轻小鼠结肠炎并抑制炎症反应。 | |||
T19500 |
Palmitelaidic Acid
trans-Palmitoleic acid,9-trans-Hexadecenoic acid,软脂酸 |
Glucokinase; AMPK; PPAR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
trans-Palmitelaidic Acid (trans-Palmitoleic acid) 是palmitoleic acid 的反式异构体。Palmitoleic acid 是血清和组织中最丰富的脂肪酸之一。 | |||
T5497 |
AMAROGENTIN
苦杏苷,苦龙胆酯苷 |
Apoptosis; AMPK | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Amarogentin 是要从 Swertia 和 Gentiana 根中提取的裂环烯醚萜苷,有抗氧化、抗肿瘤和抗糖尿病活性,具有保肝和免疫调节作用。它通过激活 AMPK 发挥有益的血管代谢作用。它促进细胞凋亡,阻止 G2/M 细胞周期和下调 PI3K/Akt/mTOR 信号通路。 | |||
T4S2128 |
Bilobetin
白果双黄酮,白果素 |
PKA; PPAR | DNA Damage/DNA Repair; Metabolism; Tyrosine Kinase/Adaptors |
Bilobetin 是银杏的活性成分,可改善胰岛素抵抗,增加肝脏对脂质的吸收和氧化,降低极低密度脂蛋白甘油三酯分泌和血液甘油三酯水平,增强组织中 β-氧化的酶的表达和活性,并减弱甘油三酯及其代谢产物的积累。它还增加了 PPARα的磷酸化,核转位和活性,并伴随着 cAMP 水平和 PKA 活性的升高。 | |||
TN7060 |
Methyl oleanonate
|
PPAR | DNA Damage/DNA Repair; Metabolism |
Methyl oleanonate 是从柃木中分离得到的一种三萜类天然产物,是齐墩果酸衍生物,是一种PPARγ激动剂,具有抗癌作用。 | |||
T0646 |
5-Aminosalicylic Acid
Mesalazine,5-ASA,5-氨基水杨酸,Mesalamine |
NF-κB; Lipoxygenase; COX; Glutathione Peroxidase; Endogenous Metabolite; PAK; PPAR | Cytoskeletal Signaling; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience; NF-κB |
5-Aminosalicylic Acid (5-ASA) 是一种特异性的PPARγ激动剂,还抑制 p21-激活激酶1(PAK1) 和NF-κB,具有抗炎活性。 | |||
T1238 |
Daidzein
大豆素,Isoflavone,黄豆苷元 |
Endogenous Metabolite; PPAR | DNA Damage/DNA Repair; Metabolism |
Daidzein (Isoflavone) 是一种来自大豆的异黄酮提取物,是酪氨酸激酶抑制剂染料木黄酮的无活性类似物,具有抗氧化和植物雌激素特性。 | |||
TN1990 |
Norathyriol
芒果苷元 |
Akt; DNA/RNA Synthesis; AMPK; PPAR | Cell Cycle/Checkpoint; Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
Norathyriol 是来自芒果的芒果苷代谢物,具有抗氧化、抗癌、抗菌和抗炎活性。它以非竞争性方式抑制 α-葡萄糖苷酶,IC50为 3.12 μM。它还抑制PPARα、PPARβ和PPARγ,IC50分别为 92.8、102.4 和 153.5 µM。 | |||
T2985 |
Gypenoside XLIX
绞股蓝皂苷 XLIX,绞股蓝皂苷XLIX |
PPAR | DNA Damage/DNA Repair; Metabolism |
Gypenoside XLIX 是一种达玛烷型糖苷,是绞股蓝的主要成分。它是选择性过氧化物酶体增殖物激活受体 (PPAR)-α激活剂,可抑制细胞因子诱导的血管细胞粘附分子-1 (VCAM-1) 在人体内皮细胞中过度活跃和表达。 | |||
T2879 |
Fisetin
漆黄素,非瑟酮 |
TNF; Sirtuin; PPAR | Apoptosis; Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Fisetin 是在许多水果和蔬菜中发现的一种天然黄酮醇,有抗氧化、抗癌和神经保护作用。 | |||
T2855 |
Icariin
淫羊藿苷,Ieariline,淫羊藿甙 |
PDE; PPAR; Autophagy | Autophagy; DNA Damage/DNA Repair; Metabolism |
Icariin (Ieariline) 是一种黄酮醇苷,可抑制PDE5和PDE4活性,IC50分别为 432 nM 和 73.50 μM。它也是PPARα激活剂。 | |||
T3362 |
Eupatilin
NSC 122413,异泽兰黄素 |
PPAR; Autophagy | Autophagy; DNA Damage/DNA Repair; Metabolism |
Eupatilin (NSC-122413) 是一种从青蒿中提取的黄酮,是一种 PPARα 激动剂,具有药理活性。 | |||
T2S0820 |
Karanjin
干华豆晶 4,水黄皮素 |
Apoptosis; AMPK | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Karanjin 是干花豆中的主要活性呋喃黄酮醇成分,可通过细胞周期阻滞诱导癌细胞死亡,促进细胞凋亡,还通过提高AMPK 的方式诱导骨骼肌细胞 GLUT4 易位。 | |||
TN1018 |
Angeloylgomisin H
当归酰戈米辛 H,当归酰戈米辛H |
PPAR | DNA Damage/DNA Repair; Metabolism |
Angeloylgomisin H 是从五味子中提取的一种木脂素类天然产物。它通过激活PPAR-γ来改善胰岛素刺激的葡萄糖摄取潜力。 | |||
T4S1545 |
Licarin B
(-)-Licarin B,Licarine B,(-)-利卡灵B |
transporter; Antibacterial; PPAR | DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Licarin B (Licarine B) 是来源于肉豆蔻种子的一种天然产物,是 NO 生成抑制剂,可通过激活 IRS-1/PI3K/AKT 通路中的PPARγ和GLUT4 改善胰岛素敏感性。 | |||
T3405 |
[6]-Gingerol
6-Gingerol,gingerol,(S)-(+)-[6]Gingerol,6-姜酚 |
Apoptosis; AMPK | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
[6]-Gingerol ((S)-(+)-[6]Gingerol) 是一种从生姜中分离的活性物质,具有抗癌,抗炎和抗氧化活性。 | |||
T5552 |
Methyl cinnamate
|
Tyrosinase; Antibacterial; AMPK | Chromatin/Epigenetic; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Methyl cinnamate 是花椒的有效成分,也是一种天然香料。它是一种防止食品褐变的酪氨酸酶抑制剂,具有抗菌活性。它通过由 CaMKK2-AMPK 信号途径介导的机制具有抗脂活性。 | |||
T5S0788 |
Oroxin A
木蝴蝶苷A,Baicalein 7-O-glucoside |
PPAR | DNA Damage/DNA Repair; Metabolism |
Oroxin A (Baicalein 7-O-glucoside) 是从黄芩根中提取的一种天然产物,是PPARγ的部分激动剂,可激活 PPARγ 转录。它通过对接 PPARγ 的蛋白配体结合区域起到激活作用。它对 α-葡萄糖苷酶有抑制活性,具有抗氧化能力,可用于癌症研究。 | |||
T2946 |
Tanshinone IIA sulfonate sodium
丹参酮IIA磺酸盐,丹参酮IIA-磺酸钠,Tanshinone IIA sulfonate,Sodium Tanshinone IIA sulfonate,Tanshinone IIA sodium sulfonate,sodium |
CaMK; P450; Calcium Channel | Membrane transporter/Ion channel; Metabolism; Neuroscience |
Tanshinone IIA sulfonate sodium (Tanshinone IIA sodium sulfonate) 是从丹参中提取的丹参酮IIA 的水溶性衍生物,是SOCE 抑制剂,用于心血管疾病的研究。 | |||
TN1911 |
Marein
马里苷,马里甙 |
transporter; Akt; HDAC; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling |
Marein 能通过CaMKK/AMPK/GLUT1促进葡萄糖摄取,IRS/Akt/GSK-3β增加糖原合成,并通过Akt/FoxO1减少糖异生,从而改善 HepG2 细胞中高葡萄糖诱导的胰岛素抵抗。它对甲基乙二醛诱导的 PC12 细胞损伤具有神经保护作用,还有抗氧化、降压、降血脂和抗糖尿病作用。 | |||
TMS2181 |
trans-Zeatin
(E)-Zeatin,玉米素 |
ERK; MEK; Endogenous Metabolite | MAPK; Metabolism |
trans-Zeatin ((E)-Zeatin) 是植物细胞分裂素,可抑制紫外线诱导的MEK/ERK 的活化,在细胞生长、分化和分裂中起着重要的作用。 | |||
T6917 |
Oleuropein
洋橄榄苦甙,橄榄苦苷 |
Apoptosis; Aromatase; ROS; PPAR | Apoptosis; DNA Damage/DNA Repair; Endocrinology/Hormones; Immunology/Inflammation; Metabolism |
Oleuropein 在橄榄叶和油中发现的天然产物,通过 p53 依赖性途径以及 Bax 和 Bcl2基因的调控来诱导乳腺癌细胞凋亡,还抑制芳香化酶。它可通过直接抑制 PPARγ转录活性来发挥抗氧化,抗炎和抗动脉粥样硬化作用。 | |||
TN1499 |
Cimiracemoside C
千层纸素A-7-0-Β-D-葡萄糖醛酸苷,Cimicifugoside M |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Cimiracemoside C (Cimicifugoside M) 是在升麻中发现的一种天然产物,可激活 AMPK 并具有抗糖尿病的潜在活性。 | |||
T5701 |
OPHIOPOGONIN D
麦冬皂苷 D,麦冬皂苷D |
RAAS; Calcium Channel; NF-κB; PPAR | DNA Damage/DNA Repair; Endocrinology/Hormones; Membrane transporter/Ion channel; Metabolism; NF-κB |
Ophiopogonin D 是从麦冬的块茎中分离的一种天然产物,是罕见的天然存在的 C29甾体糖苷。它是一种 CYP2J3 诱导剂,用于炎症和心血管疾病的相关研究。 | |||
T5S1550 |
Cinnamyl alcohol
肉桂醇,肉桂醇;beta-苯丙烯醇,Cinnamic Alcohol,Styryl Carbinol |
PPAR | DNA Damage/DNA Repair; Metabolism |
Cinnamyl alcohol (Styryl Carbinol) 是从板栗花中分离得到的一种活性成分,抑制增加的 PPARγ表达,具有抗肥胖作用。 | |||
T2750 |
Ginkgolide C
银杏内酯C,BN-52022 |
MMP; Sirtuin; Endogenous Metabolite; AMPK | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Ginkgolide C (BN-52022) 是从银杏叶中分离到的一种黄酮类天然产物,可增强体内大鼠的心脏功能,具有减少血小板聚集,改善阿尔兹海默症等作用。 | |||
T0800 |
Danthron
Dantron,1,8-Dihydroxyanthraquinone,1,8-二羟基蒽醌,丹蒽醌,Chrysazin,Antrapurol |
Virus Protease; Antibacterial; AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Danthron (Antrapurol) 是一种从中药 rhubarb 中提取的天然产物,可通过激活 AMPK 来调节葡萄糖和脂质代谢。 | |||
T7030 |
anemarsaponin B
知母皂苷B,知母皂苷 B |
p38 MAPK; NF-κB; MEK; COX; NO Synthase | Immunology/Inflammation; MAPK; Neuroscience; NF-κB |
Anemarsaponin B 是一种甾体皂苷,可降低iNOS 和COX-2的蛋白和 mRNA 水平,减少促炎细胞因子的表达和产生。它通过阻断 IκBα 的磷酸化来抑制NF-κB 的 p65 亚基的核转位,还抑制 MAP 激酶激酶 3/6 (MKK3/6) 和混合谱系激酶 3 的磷酸化。 | |||
T12296 |
Oleoylethanolamide
油酰单乙醇胺,N-Oleoylethanolamide,Oleamide MEA,Oleic acid monoethanolamide |
Endogenous Metabolite; PPAR | DNA Damage/DNA Repair; Metabolism |
Oleoylethanolamide (N-Oleoylethanolamide) 是一种PPAR-α 的高亲和力内源性激动剂,可用于肥胖和动脉硬化的相关研究。 | |||
T1051 |
Retinoic acid
维生素A酸,Vitamin A acid,ATRA,all-trans-Retinoic acid,Tretinoin |
Retinoid Receptor; Endogenous Metabolite; PPAR; Autophagy | Autophagy; DNA Damage/DNA Repair; Metabolism |
Retinoic acid (Tretinoin) 是维生素 A 的代谢产物,是一种视黄酸受体 RAR 的天然激动剂,激动 RARα/β/γ (IC50=14 nM)。Retinoic acid 可以诱导细胞分化、减少细胞增殖和抑制肿瘤发生。 | |||
T2836 |
Isorhamnetin
3-methylquercetin,3'-Methylquercetin,Isorhamnetol,异鼠李素,3'-Methoxyquercetin |
MEK; PI3K; Endogenous Metabolite | MAPK; Metabolism; PI3K/Akt/mTOR signaling |
Isorhamnetin (3-methylquercetin) 是从中草药沙棘中提取的一种类黄酮,可通过抑制MEK1和PI3K 来抑制皮肤癌。 | |||
T3000 |
Magnolol
NSC 293099,厚朴酚,5,5'-Diallyl-2,2'-biphenyldiol |
NF-κB; Retinoid Receptor; Antibacterial; PPAR; p53; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB |
Magnolol (5,5'-Diallyl-2,2'-biphenyldiol) 是RXRα和PPARγ的激动剂,EC50值分别为 10.4 µM 和 17.7 µM。他是从厚朴的树皮中分离得到的一种木脂素。 | |||
T3403 |
Glabridin
光甘草定,Q-100692,KB-289522,LS-176045 |
Reactive Oxygen Species; Tyrosinase; GABA Receptor; Antibacterial; PPAR | DNA Damage/DNA Repair; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome |
Glabridin (KB-289522) 能够结合并激活PPARγ,EC50值为 6115 nM,是一种从Glycyrrhiza glabra 中分到的异黄烷类天然产物。它具有抗炎、抗菌、抗肾炎、抗氧化、抗肿瘤、抗糖尿病、抗骨质疏松、保护神经、保护心血管、清除自由基等作用。 | |||
TN3500 |
beta-Amyrone
β-Amyron,β-香树脂酮 |
COX; AChR; PPAR; Antifection | DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
beta-Amyrone (β-Amyron) 对基孔肯雅病毒复制具有抗真菌活性,EC50 为 86 uM。 beta-Amyrone 通过抑制 COX-2 的表达而具有抗炎活性。 beta-Amyrone 表现出抗α-葡萄糖苷酶抑制活性和中等 AChE 活性。 β-Amyrone 可用于炎症、感染和肥胖等疾病的研究。 | |||
T13265 |
Urolithin B
尿石素B,3-羟基-6H-苯并[C]苯并吡喃-6-酮 |
ERK; NF-κB; Akt; Endogenous Metabolite; JNK; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; MAPK; Metabolism; NF-κB; PI3K/Akt/mTOR signaling |
Urolithin B 是一种 ellagitannins 的肠道微生物代谢产物,具有抗炎和抗氧化作用。它也是骨骼肌质量的调节因子,通过减少 IκBα 的磷酸化和降解来抑制 NF-κB 活性,并抑制 JNK、ERK 和 Akt 的磷酸化,并增强 AMPK 的磷酸化。 | |||
T7939 |
Fingolimod
2-氨基-2-[2-(4-辛基苯基)乙基]-1,3-丙二醇,FTY-720A,FTY-720,芬戈莫德 |
S1P Receptor; PAK; LPL Receptor | Cytoskeletal Signaling; GPCR/G Protein |
Fingolimod (FTY-720A) 是一种 1-磷酸鞘氨醇 (S1P) 拮抗剂,作用于 K562 和 NK 细胞,IC50为 0.033 nM。它还是pak1激活剂和免疫抑制剂。 | |||
T6S0117 |
Avicularin
Fenicularin,扁蓄苷 |
ERK | MAPK |
Avicularin (Fenicularin) 具有抗过敏、抗炎、保肝、抗氧化、抗肿瘤等活性。它能通过调节 NF-κB(p65)、COX-2 和 PPAR-γ 的活性来改善人类肝细胞癌。在 LPS 刺激的 RAW 264.7 巨噬细胞中,它通过抑制 ERK 信号通路产生抗炎活性。 | |||
T4S1173 |
Agrimol B
仙鹤草酚B,仙鹤草酚 B |
Sirtuin; PPAR | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Agrimol B 是从仙鹤草中分离得到的一种多酚衍生物,可抑制脂肪形成,降低PPARγ的表达,诱导SIRT1易位和表达。 | |||
T2S0633 |
Raspberry ketone
Oxyphenalon,Rasketone,Aloenin,4-(4-Hydroxyphenyl)-2-butanone,p-Hydroxybenzyl acetone,Frambinone,覆盆子酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Raspberry ketone (p-Hydroxybenzyl acetone) 是覆盆子中主要的芳香族天然产物,主要用作化妆品的香料和食品增味剂,也可作 PPAR-α激动剂。 | |||
TN1525 |
Convallatoxin
K-毒毛旋花子配质-3-L-鼠李糖甙,铃兰毒苷 |
NF-κB; P-gp; PPAR | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB |
Convallatoxin 是从铃兰分离得到的一种强心苷。它是 P-糖蛋白底物,并识别 Val982 是参与其转运的重要氨基酸。它是配体诱导的 MOR 胞吞作用的增强剂,通过激活PPARγ和抑制NF-κB 改善结肠炎,具有抗炎和抗增殖特性。 | |||
T1633 |
β-Carotene
beta-胡萝卜素,Carotaben,Beta-Carotene,Provitamin A,β-胡萝卜素 |
Apoptosis; ROS; Endogenous Metabolite | Apoptosis; Immunology/Inflammation; Metabolism |
β-Carotene (Provitamin A) 是一种天然存在的视黄醇(维生素 A)前体。它是一种 ROS 调节剂,具有抗氧化和抗炎活性。它可作为抗氧化剂或者促氧化剂,可诱导乳腺癌细胞凋亡,具有抗癌活性。 | |||
T3138 |
Astaxanthin
β-Carotene-4,4'-dione,Ovoester,AstaXin,AstaREAL,trans-Astaxanthin,虾青素 |
Reactive Oxygen Species; PPAR | DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; NF-κB |
Astaxanthin (trans-Astaxanthin) 是可从雨生红球藻等多种海洋生物中提取得到的红色类胡萝卜素,是过氧化物酶体增殖物活化受体γ 的调节剂,具有抗增殖、神经保护作用和抗炎活性。它是一种抗氧化剂,有用于癌症和心血管疾病的研究潜力,作为颜色添加剂用于动物食品中。 | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01578 |
CD166/ALCAM Protein, Human, Recombinant (His)
activated leukocyte cell adhesion molecule,CD166,ME... |
Human | HEK293 Cells |
CD166/ALCAM Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.4 kDa and the accession number is Q13740-1. | |||
TMPY-02575 |
PPAR gamma/PPARG Protein, Human, Recombinant (His & GST)
CIMT1,PPARγ,GLM1,PPARgamma,PPARG1,PPARG2,NR1C3,peroxisome pr... |
Human | Baculovirus Insect Cells |
Peroxisome proliferator-activated receptor gamma (PPARG), a nuclear hormone receptor, plays a critical role in the lipid and glucose homeostasis, adipocyte differentiation, as well as intracellular insulin-signaling events. The peroxisome proliferator-activated receptor gamma (PPARgamma) regulates osteoblast and osteoclast differentiation, and is the molecular target of thiazolidinediones (TZDs), insulin sensitizers that enhance glucose utilization and adipocyte differentiation. Peroxisome proli... | |||
TMPY-04531 |
p38 delta/MAPK13 Protein, Human, Recombinant (GST), Activated in vitro
P38 δ/MAPK13,MAPK13,PRKM13,MAPK-13,p38δ,p38delta,mitogen- |
Human | Baculovirus Insect Cells |
p38 delta/MAPK13 Protein, Human, Recombinant (GST), Activated in vitro is expressed in Baculovirus insect cells with GST tag. The predicted molecular weight is 68.4 kDa and the accession number is O15264. | |||
TMPY-04572 |
MKK4 Protein, Mouse, Recombinant (His & GST)
MKK4,MEK4,PRKMK4,Sek1,JNKK1,Serk1,mitogen-activated... |
Mouse | Baculovirus Insect Cells |
Dual specificity mitogen-activated protein kinase kinase 4, also known as MAP kinase kinase 4, MAPKK4, JNK-activating kinase 1, MAPK/ERK kinase 4, SAPK/ERK kinase 1, c-Jun N-terminal kinase kinase 1, JNKK, and MAP2K4, is a protein that belongs to the protein kinase superfamily, STE Ser/Thr protein kinase family and MAP kinase kinase subfamily. MAP2K4 / JNKK1 is a protein kinase that is a direct activator of MAP kinases in response to various environmental stresses or mitogenic stimuli. MAP2K4 / ... | |||
TMPY-04544 |
MEK2 Protein, Human, Recombinant (GST)
mitogen-activated protein kinase kinase 2,FLJ26075,... |
Human | Baculovirus Insect Cells |
Dual specificity mitogen-activated protein kinase kinase 2, also known as MAP kinase kinase 2, MAPKK2, ERK activator kinase 2, MAPK / ERK kinase 2, MEK2 and MAP2K2, is a member of the protein kinase superfamily, STE Ser/Thr protein kinase family and MAP kinase kinase subfamily. MAP2K2 / MEK2 contains one protein kinase domain. MEK1 and MEK2 (also known as MAP2K1 and MAP2K2, respectively) are evolutionarily conserved, dual-specificity kinases that mediate Erk1 and Erk2 activation during adhesion ... | |||
TMPY-03520 |
CD166/ALCAM Protein, Cynomolgus, Recombinant (His)
activated leukocyte cell adhesion molecule |
Cynomolgus | HEK293 Cells |
CD166/ALCAM Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.3 kDa and the accession number is G7NZQ8. | |||
TMPY-02936 |
CD166/ALCAM Protein, Rat, Recombinant (His)
activated leukocyte cell adhesion molecule |
Rat | HEK293 Cells |
CD166/ALCAM Protein, Rat, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.5 kDa and the accession number is O35112. | |||
TMPY-03912 |
CD166/ALCAM Protein, Rat, Recombinant (hFc)
activated leukocyte cell adhesion molecule |
Rat | HEK293 Cells |
CD166/ALCAM Protein, Rat, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 83.1 kDa and the accession number is O35112. | |||
TMPY-00249 |
CD166/ALCAM Protein, Cynomolgus, Recombinant (hFc)
activated leukocyte cell adhesion molecule |
Cynomolgus | HEK293 Cells |
CD166/ALCAM Protein, Cynomolgus, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 82.9 kDa and the accession number is F7E9U2. | |||
TMPH-02786 |
MAPK14 Protein, Mouse, Recombinant (His & Myc)
Mapk14,Mitogen-activated protein kinase p38 alpha,C... |
Mouse | E. coli |
MAPK14 Protein, Mouse, Recombinant (His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 48.6 kDa and the accession number is P47811. | |||
TMPH-03592 |
Pneumolysin Protein, S. pneumoniae serotype 4, Recombinant (His)
Thiol-activated cytolysin,ply,Pneumolysin |
Streptococcus pneumoniae | P. pastoris (Yeast) |
A cholesterol-dependent toxin that causes cytolysis by forming pores in cholesterol containing host membranes. After binding to target membranes, the protein undergoes a major conformation change, leading to its insertion in the host membrane and formation of an oligomeric pore complex. Cholesterol is required for binding to host membranes, membrane insertion and pore formation; cholesterol binding is mediated by a Thr-Leu pair in the C-terminus. Can be reversibly inactivated by oxidation. Pneum... | |||
TMPY-04425 |
PRAK/MAPKAPK5 Protein, Human, Recombinant (His & GST)
PRAK,MAPKAP-K5,MK-5,mitogen-activated protein kinas... |
Human | Baculovirus Insect Cells |
MAPKAPK5 contains 1 protein kinase domain and belongs to the protein kinase superfamily, CAMK Ser/Thr protein kinase family. MAPKAPK5 has significant sequence homology to mitogen-activated protein kinase (MAPK)-activated protein kinase (MAPKAPK). It is widely distributed. MAPKAPK5 can be phosphorylated by an extracellular-regulated kinase (ERK), and p38 kinase but not by c-jun N-terminal kinase (JNK)in vitro. Recombinant GST-MAPKAPK5 protein can phosphorylate a peptide derived from the regulator... | |||
TMPH-01031 |
CAPN2 Protein, Human, Recombinant (His)
Calpain-2 catalytic subunit,Millimolar-calpain,Calpain-2 lar... |
Human | E. coli |
Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves MYOC at 'Arg-226'. Proteolytically cleaves CPEB3 following neuronal stimulation which abolishes CPEB3 translational repressor activity, leading to translation of CPEB3 target mRNAs. CAPN2 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 82... | |||
TMPH-01029 |
CAPN1 Protein, Human, Recombinant (His)
CANPL1,CAPN1,Calpain-1 catalytic subunit,Micromolar-calpain,... |
Human | E. coli |
Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves CTBP1 at 'Asn-375', 'Gly-387' and 'His-409'. CAPN1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 85.9 kDa and the accession number is P07384. | |||
TMPH-03593 |
Pneumolysin Protein, S. pneumoniae serotype 4, Recombinant (Avi & His)
Thiol-activated cytolysin,Pneumolysin,ply |
Streptococcus pneumoniae | E. coli |
A cholesterol-dependent toxin that causes cytolysis by forming pores in cholesterol containing host membranes. After binding to target membranes, the protein undergoes a major conformation change, leading to its insertion in the host membrane and formation of an oligomeric pore complex. Cholesterol is required for binding to host membranes, membrane insertion and pore formation; cholesterol binding is mediated by a Thr-Leu pair in the C-terminus. Can be reversibly inactivated by oxidation. Pneum... | |||
TMPY-06830 |
PPAR alpha/PPARA Protein, Human, Recombinant (His)
NR1C1,PPARα,peroxisome proliferator-activated recep... |
Human | E. coli |
PPAR alpha/PPARA Protein, Human, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 31.36 kDa and the accession number is Q07869. | |||
TMPY-05484 |
CD166/ALCAM Protein, Human, Recombinant (hFc)
MEMD,activated leukocyte cell adhesion molecule,CD1... |
Human | HEK293 Cells |
CD166/ALCAM Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 82.7 kDa and the accession number is Q13740-1. | |||
TMPY-04378 |
MAPKAPK3 Protein, Human, Recombinant (GST)
mitogen-activated protein kinase-activated... |
Human | Baculovirus Insect Cells |
The MAPKAP kinases are a group of MAP kinase substrates that are themselves kinases. In response to activation, the MAP kinases phosphorylate downstream components on a consensus Pro-X-Ser/Thr-Pro motif. Several kinases that contain this motif have been identified and serve as substrates for the ERK and p38 MAP kinases. Mitogen-activated protein (MAP) kinase-activated protein kinase 3, also known as MAPKAPK-3 and 3pK, is a member of the Ser/Thr protein kinase family. It is widely expressed in hu... | |||
TMPH-01236 |
DFFB Protein, Human, Recombinant (His)
DNA fragmentation factor 40 kDa subunit,Caspase-activate... |
Human | E. coli |
Nuclease that induces DNA fragmentation and chromatin condensation during apoptosis. Degrades naked DNA and induces apoptotic morphology. | |||
TMPY-02710 |
CANT1 Protein, Human, Recombinant (His)
SCAN1,SCAN-1,DBQD,SHAPY,calcium activated nucleotid... |
Human | HEK293 Cells |
CANT1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 38 kDa and the accession number is Q8WVQ1-1. | |||
TMPH-02194 |
TAB2 Protein, Human, Recombinant (His & Myc)
Mitogen-activated protein kinase kinase kinase 7-in... |
Human | Baculovirus Insect Cells |
Adapter required to activate the JNK and NF-kappa-B signaling pathways through the specific recognition of 'Lys-63'-linked polyubiquitin chains by its RanBP2-type zinc finger (NZF). Acts as an adapter linking MAP3K7/TAK1 and TRAF6 to 'Lys-63'-linked polyubiquitin chains. The RanBP2-type zinc finger (NZF) specifically recognizes Lys-63'-linked polyubiquitin chains unanchored or anchored to the substrate proteins such as RIPK1/RIP1: this acts as a scaffold to organize a large signaling complex to ... | |||
TMPH-01250 |
MAP2K3 Protein, Human, Recombinant (His & SUMO)
MAP2K3,MAPK/ERK kinase 3,Dual specificity mitogen-activa... |
Human | E. coli |
Dual specificity kinase. Is activated by cytokines and environmental stress in vivo. Catalyzes the concomitant phosphorylation of a threonine and a tyrosine residue in the MAP kinase p38. Part of a signaling cascade that begins with the activation of the adrenergic receptor ADRA1B and leads to the activation of MAPK14. MAP2K3 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 55.3 kDa and the accession numbe... | |||
TMPH-00420 |
Perfringolysin O Protein, Clostridium perfringens, Recombinant (His & SUMO)
Perfringolysin O,Thiol-activated cytolysin,pfo,Thet... |
C.perfringens | E. coli |
Perfringolysin O Protein, Clostridium perfringens, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 68.7 kDa and the accession number is P0C2E9. | |||
TMPY-06837 |
PPAR alpha/PPARA Protein, Mouse, Recombinant (His)
PPARα,PPAR-alpha,peroxisome proliferator-activated ... |
Mouse | E. coli |
PPAR alpha/PPARA Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with His tag. The predicted molecular weight is 31.49 kDa and the accession number is P23204. | |||
TMPY-02975 |
CANT1 Protein, Human, Recombinant (hFc)
SCAN1,DBQD,SCAN-1,SHAPY,calcium activated nucleotid... |
Human | HEK293 Cells |
CANT1 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 64.3 kDa and the accession number is Q8WVQ1-1. | |||
TMPH-02481 |
PRKAG1 Protein, Mouse, Recombinant (His)
Prkag1,5'-AMP-activated protein kinase subunit gamm... |
Mouse | E. coli |
PRKAG1 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 41.6 kDa and the accession number is O54950. | |||
TMPH-02437 |
5T4/TPBG Protein, Cynomolgus, Recombinant (His & Myc)
TPBG,WAIF1,Wnt-activated inhibitory factor 1,Tropho... |
Cynomolgus | HEK293 Cells |
May function as an inhibitor of Wnt/beta-catenin signaling by indirectly interacting with LRP6 and blocking Wnt3a-dependent LRP6 internalization. 5T4/TPBG Protein, Cynomolgus, Recombinant (His & Myc) is expressed in HEK293 mammalian cells with N-10xHis and C-Myc tag. The predicted molecular weight is 39.9 kDa and the accession number is Q4R8Y9. | |||
TMPH-02436 |
5T4/TPBG Protein, Cynomolgus, Recombinant (E. coli, His & Myc)
TPBG,Trophoblast glycoprotein,Wnt-activated inhibit... |
Cynomolgus | E. coli |
May function as an inhibitor of Wnt/beta-catenin signaling by indirectly interacting with LRP6 and blocking Wnt3a-dependent LRP6 internalization. 5T4/TPBG Protein, Cynomolgus, Recombinant (E. coli, His & Myc) is expressed in E. coli expression system with N-10xHis and C-Myc tag. The predicted molecular weight is 41.9 kDa and the accession number is Q4R8Y9. | |||
TMPY-04569 |
MEK1 Protein, Mouse, Recombinant (His & GST)
MEKK1,mitogen-activated protein kinase kinase 1,Prk... |
Mouse | Baculovirus Insect Cells |
MEK1 Protein, Mouse, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 71.3 kDa and the accession number is P31938. | |||
TMPY-04756 |
MEK1 Protein, Mouse, Recombinant
Prkmk1,MAPKK1,mitogen-activated protein kinase kina... |
Mouse | Baculovirus Insect Cells |
MEK1 Protein, Mouse, Recombinant is expressed in Baculovirus insect cells. The predicted molecular weight is 43.6 kDa and the accession number is P31938. | |||
TMPH-03755 |
Ppard Protein, Human, Recombinant (His)
NUCI,Peroxisome proliferator-activated receptor del... |
Human | E. coli |
Ligand-activated transcription factor. Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Has a preference for poly-unsaturated fatty acids, such as gamma-linoleic acid and eicosapentanoic acid. Once activated by a ligand, the receptor binds to promoter elements of target genes. Regulates the peroxisomal beta-oxidation pathway of fatty acids. Functions as transcription activator for the acyl-CoA oxidase gene. Decreases expression of NPC1L1 once activated by... | |||
TMPH-01030 |
CAPN14 Protein, Human, Recombinant (His & Myc)
Calpain-14,Calcium-activated neutral proteinase 14,... |
Human | Baculovirus Insect Cells |
Calcium-regulated non-lysosomal thiol-protease. CAPN14 Protein, Human, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 78.6 kDa and the accession number is A8MX76. | |||
TMPH-03392 |
5T4/TPBG Protein, Rat, Recombinant (His & SUMO)
Wnt-activated inhibitory factor 1,Trophoblast glyco... |
Rat | E. coli |
May function as an inhibitor of Wnt/beta-catenin signaling by indirectly interacting with LRP6 and blocking Wnt3a-dependent LRP6 internalization. 5T4/TPBG Protein, Rat, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 51.8 kDa and the accession number is Q5PQV5. | |||
TMPH-02480 |
PRKAB1 Protein, Mouse, Recombinant (His)
5'-AMP-activated protein kinase subunit beta-1,Prka... |
Mouse | E. coli |
PRKAB1 Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 36.1 kDa and the accession number is Q9R078. | |||
TMPH-01107 |
Coagulation factor V Protein, Human, Recombinant (His & SUMO)
F5,Activated protein C cofactor,Coagulation factor ... |
Human | E. coli |
Coagulation factor V Protein, Human, Recombinant (His & SUMO) is expressed in E. coli. | |||
TMPH-01279 |
CRACR2B Protein, Human, Recombinant (His)
CRACR2B,EFCAB4A,EF-hand calcium-binding domain-containing pr... |
Human | E. coli |
Plays a role in store-operated Ca(2+) entry (SOCE). | |||
TMPY-01031 |
CD166/ALCAM Protein, Mouse, Recombinant (His & hFc)
CD166,AI853494,MuSC,DM-GRASP,BEN,activated leukocyt... |
Mouse | HEK293 Cells |
CD166/ALCAM Protein, Mouse, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 84.2 kDa and the accession number is Q54AJ5. | |||
TMPY-04412 |
Germinal Center Kinase/MAP4K2 Protein, Human, Recombinant (His & GST)
mitogen-activated protein kinase kinase kinase kina... |
Human | Baculovirus Insect Cells |
Mitogen-activated protein kinase kinase kinase kinase 2, also known as B lymphocyte serine/threonine-protein kinase, Germinal center kinase, MAPK/ERK kinase kinase kinase 2, MEK kinase kinase 2, Rab8-interacting protein, and MAP4K2, is cytoplasm and peripheral membrane protein that belongs to the protein kinase superfamily, STE Ser/Thr protein kinase family and STE2 subfamily. MAP4K2 contains one CNH domain and one protein kinase domain. Although this kinase is found in many tissues, its express... | |||
TMPY-01153 |
CD166/ALCAM Protein, Mouse, Recombinant (His)
MuSC,CD166,SC1,activated leukocyte cell adhesion mo... |
Mouse | HEK293 Cells |
CD166/ALCAM Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 57.7 kDa and the accession number is Q54AJ5. | |||
TMPY-04551 |
p38 delta/MAPK13 Protein, Human, Recombinant (GST)
MAPK13,p38δ,PRKM13,MAPK-13,mitogen-activated protei... |
Human | Baculovirus Insect Cells |
p38 delta/MAPK13 Protein, Human, Recombinant (GST) is expressed in Baculovirus insect cells with GST tag. The predicted molecular weight is 68.4 kDa and the accession number is O15264. | |||
TMPY-04410 |
MAP4K5 Protein, Human, Recombinant (His & GST)
KHS,GCKR,MAPKKKK5,mitogen-activated protein kinase ... |
Human | Baculovirus Insect Cells |
Mitogen-activated protein kinase kinase kinase kinase 5, also known as Kinase homologous to SPS1/STE2, MAPK/ERK kinase kinase kinase 5, MEK kinase kinase 5, and MAP4K5, is a cytoplasm protein that belongs to the protein kinase superfamily, STE Ser/Thr protein kinase family and STE2 subfamily. MAP4K5 is ubiquitously expressed in all tissues examined, with high levels in the ovary, testis, and prostate. It contains one CNH domain and one protein kinase domain. MAP4K5 is highly similar to yeast SPS... | |||
TMPH-03711 |
PPAR gamma Protein, Xenopus laevis, Recombinant (His)
Nuclear receptor subfamily 1 group C member 3,Peroxisome pro... |
Xenopus laevis | E. coli |
Receptor that binds peroxisome proliferators such as hypolipidemic drugs and fatty acids. Once activated by a ligand, the receptor binds to a promoter element in the gene for acyl-CoA oxidase and activates its transcription. It therefore controls the peroxisomal beta-oxidation pathway of fatty acids. Key regulator of adipocyte differentiation and glucose homeostasis. May play a role in the regulation of circadian rhythm. | |||
TMPH-02827 |
PPAR gamma Protein, Mouse, Recombinant (His)
Pparg,Nuclear receptor subfamily 1 group C member 3,Peroxiso... |
Mouse | E. coli |
PPAR gamma Protein, Mouse, Recombinant (His) is expressed in E. coli expression system with N-10xHis tag. The predicted molecular weight is 63.3 kDa and the accession number is P37238. | |||
TMPY-04365 |
MKK6 Protein, Human, Recombinant (S207D, T211D, His & GST)
SAPKK3,mitogen-activated protein kinase kinase 6,MK... |
Human | Baculovirus Insect Cells |
MKK6 Protein, Human, Recombinant (S207D, T211D, His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 65.3 kDa and the accession number is P52564-1. | |||
TMPY-04749 |
MKK6 Protein, Human, Recombinant (S207D, T211D)
MAPKK6,PRKMK6,MKK6,MEK6,mitogen-activated protein k... |
Human | Baculovirus Insect Cells |
MKK6 Protein, Human, Recombinant (S207D, T211D) is expressed in Baculovirus insect cells. The predicted molecular weight is 37.7 kDa and the accession number is P52564-1. | |||
TMPY-04748 |
MKK6 Protein, Human, Recombinant
MKK6,MAPKK6,SAPKK-3,SAPKK3,PRKMK6,MEK6,mitogen-activated... |
Human | Baculovirus Insect Cells |
MKK6 Protein, Human, Recombinant is expressed in Baculovirus insect cells. The predicted molecular weight is 37.6 kDa and the accession number is A8K3Y2. | |||
TMPY-04364 |
MKK6 Protein, Human, Recombinant (His & GST)
MKK6,mitogen-activated protein kinase kinase 6,SAPK... |
Human | Baculovirus Insect Cells |
MKK6 Protein, Human, Recombinant (His & GST) is expressed in Baculovirus insect cells with His and GST tag. The predicted molecular weight is 65.3 kDa and the accession number is P52564-1. | |||
TMPJ-01328 |
ZBP1 Protein, Human, Recombinant (His)
Tumor Stroma and Activated Macrophage Protein DLM,D... |
Human | E. coli |
Z-DNA Binding Protein 1 (ZBP1) is a protein with 2 DRADA repeats. ZBP1 is highly expressed in lymphatic tissues including lymph node, leukocytes, tonsil, bone marrow, and spleen. ZBP1 participates in the detection of viral and bacterial DNA from by the host's innate immune system. It plays a role in host defense against tumors and pathogens. ZBP1 Acts as a cytoplasmic DNA sensor which, when activated, induces the recruitment of TBK1 and IRF3 to its C-terminal region and activates the downstream ... | |||
TMPH-01557 |
ILF2 Protein, Human, Recombinant (GST)
Interleukin enhancer-binding factor 2,ILF2,Nuclear factor of... |
Human | E. coli |
Appears to function predominantly as a heterodimeric complex with ILF3. This complex may regulate transcription of the IL2 gene during T-cell activation. It can also promote the formation of stable DNA-dependent protein kinase holoenzyme complexes on DNA. Essential for the efficient reshuttling of ILF3 (isoform 1 and isoform 2) into the nucleus. ILF2 Protein, Human, Recombinant (GST) is expressed in E. coli expression system with N-GST tag. The predicted molecular weight is 70.1 kDa and the acce... | |||
TMPH-01028 |
KCNMA1 Protein, Human, Recombinant
K(VCA)alpha,Calcium-activated potassium channel sub... |
Human | E. coli |
KCNMA1 Protein, Human, Recombinant is expressed in E. coli expression system. The predicted molecular weight is 17.2 kDa and the accession number is Q12791. | |||
------------------------ 更多 ------------------------ |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10818 |
Ciprofibrate D6
|
Others | Others |
Ciprofibrate D6 is a deuterium-labeled Ciprofibrate. Ciprofibrate is an agonist of peroxisome proliferator-activated receptor. | |||
TMIJ-0523 |
Gliquidone-d6
|
||
Gliquidone-d6 是 Gliquidone 的氘代化合物。Gliquidone 的 CAS 号为 33342-05-1。Gliquidone 是一种磺酰脲类的抗糖尿病药物,可用于2型糖尿病的研究。 | |||
TMIJ-0074 |
Retigabine-d4
|
||
Retigabine-d4 是 Retigabine 的氘代化合物。Retigabine 的 CAS 号为 150812-12-7。Retigabine dihydrochloride 是一种抗惊厥药,用作有治疗经验的成年患者部分性癫痫的辅助治疗。作用机制涉及神经元 K(V)7.2-7.5(以前的 KCNQ2-5)电压激活 K(+) 通道的开放。 | |||
T71306 |
Gemfibrozil-d6
|
||
Gemfibrozil-d6 is intended for use as an internal standard for the quantification of gemfibrozil by GC- or LC-MS. Gemfibrozil is a peroxisome proliferator-activated reporter α and PPARγ agonist. In vivo, gemfibrozil reduces serum total cholesterol, triglyceride, and LDL levels in a rat model of high-cholesterol diet-induced hyperlipidemia. Gemfibrozil reduces atherosclerotic plaque area, superoxide production, and expression of the genes encoding the NF-κB subunit p65 and chemokine (C-C) motif l... | |||
T71305 |
Clofibric Acid-d4
|
||
Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 50 µM in a transactivation assay) and the active metabolite of clofibrate. It is formed from clofibrate by tissue and serum esterases. Dietary administration of clofibric acid (0.067-0.22%) reduces serum cholesterol, phospholipid, and triglyceride levels in rats. It decreases glutamate oxal... | |||
TMID-0242 |
Capecitabine-d11
|
||
Capecitabine-d11 是 Capecitabine 的氘代化合物。Capecitabine 的 CAS 号为 154361-50-9。Capecitabine 是一种可口服的前药,可由胸苷磷酸化酶催化转变为其活性代谢物 Fluorouracil。 | |||
T71303 |
Flufenamic Acid-d4
|
||
Flufenamic acid-d4 is intended for use as an internal standard for the quantification of flufenamic acid by GC- or LC-MS. Flufenamic acid is a non-steroidal anti-inflammatory drug (NSAID) and COX inhibitor (IC50s = 3 and 9.3 µM for human COX-1 and COX-2, respectively). Flufenamic acid inhibits TNF-α-induced increases in COX-2 levels and NF-κB activation in HT-29 colon cancer cells in a concentration-dependent manner. It inhibits calcium influx induced by fMLP or A23187 in human polymorphonuclear... |