51
7
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T22567 |
AMPK activator
|
Others | Others |
AMPK activator | |||
T60675L |
AMPK activator 2 hydrochloride( 2410961-69-0 Free base)
AMPK activator 2 hydrochloride( 2410961-69-0 Free base) |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator 2 hydrochloride 是一种含氟氯胍衍生物,可上调 AMPK 信号通路并下调 mTOR/4EBP1/p70S6K。AMPK activator 2 hydrochloride 抑制人类癌细胞系 (UMUC3、T24、A549) 的增殖和迁移。 | |||
T62238 |
AMPK activator 4
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator 4 是一种有效且具有选择性的AMPK激活剂,不抑制线粒体复合物 I。AMPK activator 4 选择性地激活肌肉组织中的 AMPK且剂量依赖性地改善正常小鼠的糖耐量,显著降低 db/db 糖尿病小鼠的空腹血糖水平和改善胰岛素抵抗。AMPK activator 4 具有降血糖作用。 | |||
T10069 | AMPK activator 1 | Others | Others |
AMPK activator 1 is an AMPK activator(compound No.1-75, EC50: <0.1μM). | |||
T70862 |
AMPK Activator SC4
|
||
SC4 is a potent, direct AMPK activator. SC4 preferentially activates α2 complexes and stimulates skeletal muscle glucose uptake. | |||
T23734 |
AMPK activator C2
Compound 2,Compound-2,C2 |
||
AMPK activator C2 is an AMPK allosteric activator. | |||
T78791 |
AMPK activator 12
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator 12 是一种 AMPK 激活剂和 GDF15 诱导剂,能提升人肝细胞内GDF15蛋白的表达水平,可用于研究癌症。 | |||
T83127 |
AMPK activator 13
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator13作为AMPK激活剂,通过激活AMPK通路有效抑制3T3-L1细胞的有丝分裂克隆扩增,并增加细胞线粒体耗氧量,适用于肥胖研究。 | |||
T63177 |
AMPK activator 8
|
||
AMPK activator 8 (Compound 2) 是一种 AMP 激活的蛋白激酶 (AMPK) 激活剂,能够作用于 rAMPK α1β1γ1 (EC50: 11 nM)、rAMPK α2β1γ1 (EC50: 27 nM)、rAMPK α1β2γ1 (EC50: 4 nM)、rAMPK α2β2γ1 (EC50: 2 nM)、rAMPK α2β2γ3 (EC50: 4 nM)。AMPK activator 8 能够用于研究 2 型糖尿病。 | |||
T72690 |
AMPK activator 9
|
||
AMPK activator9 (ZM-6) 是一种有效的 AMPK(α2β1γ1) 激活剂,EC50值为 1.1 µM.AMPK activator9 具有研究 2 型糖尿病的潜力。 | |||
T79226 | AMPK activator 11 | Mitochondrial Metabolism | Metabolism |
AMPK activator11 是一种抗肿瘤活性纳米级化合物,有效针对多种CRC。通过激活AMPK及上调OXPHOS(mitochondrial metabolism),该化合物能选择性抑制RKO异种移植物生长,应用于肿瘤和代谢性疾病研究领域。 | |||
T63117 |
AMPK activator 7
|
||
AMPK activator 7 (compound I-3-24) 是一种 AMPK 激活剂 (EC50: 8.8 nM)。AMPK activator 7 能够用于涉及 AMPK 疾病的研究,尤其是 2 型糖尿病、高血糖症、代谢综合征、肥胖症、高胆固醇血症和/或高血压等疾病。 | |||
T62052 |
AMPK activator 6
|
||
AMPK activator 6 (Compound GC) 可降低 HepG2 和 3T3-L1 细胞中的脂质含量并激活AMPK 通路。AMPK activator 6 对血清中甘油三酯 (TG)、总胆固醇 (TC)、低密度脂蛋白-C (LDL-C) 和其他生化指标的增加有显著的抑制作用。AMPK activator 6 在非酒精性脂肪肝(NAFLD)和代谢综合征中有研究价值。 | |||
T70860 |
Banoxantrone
AQ4N |
||
Banoxantrone (AQ4N) 作为一种典型的缺氧选择性细胞毒素。Banoxantrone 可被还原为 AQ4,AQ4 是一种有效的拓扑异构酶 II 抑制剂。Banoxantrone 通过iNOS 依赖机制选择性地杀死缺氧细胞。Banoxantrone 显示出强大的细胞毒性和低氧选择性效应,且能被辐射增强。 | |||
T83125 |
AMPK-α1β1γ1 activator 1
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK-α1β1γ1激活剂1 (M1) 是一个衍生于Indole-3-carcinoma的酰基葡萄糖醛酸代谢AMPK激活剂,专一性地针对人类β1亚型,表现出38.1nM的EC50值。该化合物能够直接结合至人AMPK α1β1γ1亚型,适用于糖尿病肾病的相关研究。 | |||
T60675 |
AMPK activator 2
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator 2 是一种含氟氯胍衍生物,具有潜在的抗癌活性,可上调 AMPK 信号通路并下调 mTOR/4EBP1/p70S6K,对人类癌细胞系 (UMUC3、T24、A549) 的增殖和迁移有抑制作用。 | |||
T9010 |
IMM-H007
|
Others; AMPK | Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling |
IMM-H007 是一种新型降脂剂,可增加 abca1 蛋白的表达。 | |||
T13411 |
ZLN024
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
ZLN024 是有效的 AMPK 变构激活剂,直接激活重组 AMPK α1β1γ1,AMPK α2β1γ1,AMPK α1β2γ1 和 AMPK α2β2γ1 异源三聚体,EC50分别为 0.42 μM,0.95 μM,1.1 μM 和 0.13 μM。 | |||
T2468 |
A-769662
A 769662 |
AMPK; Fatty Acid Synthase | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
A-769662 是一种可逆 AMPK 激活剂,EC50值为 0.8 μM。 | |||
T6854 |
GSK621
|
Apoptosis; AMPK; Autophagy | Apoptosis; Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
GSK621 是一种特异性AMPK 激动剂,对 AML 细胞系的IC50值为13-30 μM。它可诱导自噬和凋亡,还可诱导eiF2α磷酸化。 | |||
T13368 |
YLF-466D
C24 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
YLF-466D (C24) 是一种新型 AMPK 激活剂,可抑制血小板聚集。 | |||
T8432 |
ASP4132
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
ASP4132 是一种口服活性的 AMPK 激活剂,EC50为 18 nM,具有抗癌活性。 | |||
T5187 |
MK-3903
MK 3903 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
MK-3903 是一种有选择性 AMP 激活的蛋白激酶 (AMPK) 激活剂,其EC50值为 8 nM。 | |||
T4427 |
PF-06409577
PF 06409577 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
PF-06409577 是一种具有口服活性的特异性 AMPK 变构激活剂,对α1β1γ1的EC50值为7 nM。 | |||
T16099 |
MK8722
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
MK8722 是一种全身性泛 AMPK 激活剂。 | |||
TQ0028 |
EX229
Compound 991,C991 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
EX229 (C991) 是一种 AMP 活化蛋白激酶 (AMPK) 的有效变构激动剂, 是苯并咪唑衍生物,其对 α1β1γ1、α2β1γ1 和 α1β2γ1 的Kd 值分别为 0.06、0.06 和 0.51 μM。 | |||
T7362 |
O-304
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
O-304 是 AMP 活化蛋白激酶 (AMPK) 的泛激活剂,可通过抑制 pAMPK 的去磷酸化来增加 AMPK 活性,可用于 2 型糖尿病和相关心血管并发症的研究。 | |||
T8526 |
Metformin
甲福明,二甲双胍,1,1-Dimethylbiguanide |
Mitophagy; AMPK; Autophagy | Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Metformin (1,1-Dimethylbiguanide) 是一种 AMPK 激活剂,具有血脑屏障渗透性。Metformin 可通过提高胰岛素敏感性和减少肠道对葡萄糖的吸收来改善血糖控制,常用于 2 型糖尿病的研究。 | |||
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。 | |||
T16156 |
MT 63-78
|
Apoptosis; AMPK; mTOR | Apoptosis; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
MT 63-78 是一种有效的直接AMPK 激活剂,EC50为 25 μM。它诱导细胞有丝分裂阻滞和细胞凋亡,通过抑制脂肪生成和mTORC1途径来阻止前列腺癌的生长,具有抗肿瘤作用。 | |||
T41162 |
ZLN 024 hydrochloride
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
ZLN 024 hydrochloride 是一种 AMPK 变构激活剂,可刺激无活性的 α1 亚基截短 α1 (1-394) 和 α1 (1-335),但不刺激 α1 (1-312)。 | |||
T8532 |
IM156
|
OXPHOS | Apoptosis |
IM156 (HL156A; HL271 acetate) 是衍生自二甲双胍的化合物,是一种强效的,具有口服活性的AMPK 激活剂。IM156 在动物模型中可缓解与年龄相关的认知下降。IM156 是一种有效的氧化磷酸化 (OXPHOS) 抑制剂,可用于实体肿瘤的研究。 | |||
T16342 |
KL1333
NQO1 activator 1 |
NADPH; Mitochondrial Metabolism | Metabolism |
KL1333 (NQO1 activator 1) 是口服NAD+调节剂,与 NAD(P)H: 醌氧化还原酶 1 作为底物反应。它改善线粒体脑肌病、乳酸酸中毒和中风样发作成纤维细胞的能量代谢和线粒体功能障碍。它对顺铂诱导的小鼠耳蜗培养耳毒性的保护作用。 | |||
T20029 |
Buformin hydrochloride
NSC528218,NSC-528218,盐酸丁双胍,NSC 528218 |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Buformin hydrochloride (NSC-528218) 是一种有效的 AMPK 激活剂,是一种双胍类的口服抗糖尿病药物。Buformin 延缓胃肠道对葡萄糖的吸收,增加胰岛素敏感性和葡萄糖对细胞的吸收,并抑制肝脏对葡萄糖的合成。Buformin 也具有抗癌活性,可用于各种癌症研究。 | |||
T11570 |
HL271
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
HL271, a derivative of metformin, is a potent AMPK activator that increases AMPK phosphorylation. HL271 attenuates aging-associated cognitive impairment. | |||
T71051 |
OSU-53
|
||
OSU-53 is an AMPK activator, inhibiting mTOR signaling and autophagy stimulation. OSU-53 also activates mutations in RAS or BRAF. | |||
T71222 |
Metformin glycinate
|
||
Metformin glycinate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T70806 |
Metformin icosapent
|
||
Metformin icosapent is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T10312 |
Ampkinone
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Ampkinone is an indirect AMPK activator. | |||
T73224 |
AMPK-IN-1
|
||
AMPK-IN-1 是一种 AMPK 激活剂 (对亚型α2β2γ1的 EC50为 551 nM)。AMPK-IN-1 可导致 eEF2 的 mTORC1-非依赖性磷酸化。 | |||
T69405 |
Metformin embonate
|
||
Metformin embonate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T24622 |
PF-06679142
PF06679142,PF-6679142,PF6679142,PF 6679142 |
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PF-06679142 is an effective AMPK activator. PF-06679142 exhibited robust activation of AMPK in rat kidneys as well as desirable oral absorption. | |||
T70085 |
IND 1316
|
||
IND 1316 is an activator of AMP-activated protein kinase (AMPK). | |||
T68628 | Plectranthoic Acid | ||
Plectranthoic Acid is an activator of AMPK which induces apoptotic death in prostate cancer cells. | |||
T70885 |
R419
|
||
R419 is an indirect activator of AMPK with potential application as a method of glucose regulation. | |||
T71314 | GL-V9 | ||
GL-V9 is an AMPK activator, protecting against colitis-associated colorectal cancer by limiting NLRP3 inflammasome through autophagy. | |||
T69049 |
Metformin orotate
|
||
Metformin orotate is an AMP-activated protein kinase (AMPK) activator that improves glycemic control by improving insulin sensitivity and decreasing intestinal absorption of glucose. | |||
T69365 |
HMS607P03
|
||
HMS607P03 is an activator of SIRT1 which induces autophagic cell death via the AMPK-mTOR-ULK complex and induces mitophagy by the SIRT1-PINK1-Parkin pathway. HMS607P03 downregulates 14-3-3γ, catalase, profilin-1, and HSP90α. | |||
T78095 |
Demethyleneberberine chloride
|
NF-κB | NF-κB |
Demethyleneberberine chloride是一种具有线粒体靶向性的天然抗氧化剂,能通过抑制NF-κB通路及调节Th细胞平衡来缓解小鼠结肠炎并抑制炎症。此外,作为一种AMPK激活剂,该化合物亦用于非酒精性脂肪性肝病(NAFLD)的研究。 | |||
T81154 |
SIRT1 activator 1
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
SIRT1 activator1(compound 3),作为海洋化合物xyloallenoide a的衍生物,最初从红树林真菌Xylaria sp中分离获得。该化合物在斑马鱼模型中展现了促进血管生成的活性,并且能够通过提升SIRT1的表达水平以及调节AMPK/Akt信号通路,来防护人类内皮祖细胞(hEPC)免受血管老化的影响。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
TN1731 |
Hernandezine
|
TNF; ROS; P-gp; AMPK | Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience; PI3K/Akt/mTOR signaling |
Hernandezine 是 AMPK 激动剂的激动剂,也是癌细胞中 ABCB1 介导的 MDR 的特异性逆转剂。 | |||
T14149 |
AICAR phosphate
AICA Riboside phosphate,Acadesine phosphate |
Mitophagy; NOS; YAP; AMPK | Autophagy; Chromatin/Epigenetic; Immunology/Inflammation; PI3K/Akt/mTOR signaling; Stem Cells |
AICAR phosphate (Acadesine phosphate) 是 AMPK 激活剂且是自噬、YAP 和 mitophagy 抑制剂,也是一种腺苷类似物, 可调节糖代谢和脂代谢,抑制促炎细胞因子和 iNOS 的产生。 | |||
T2854 |
Phillyrin
Forsythin,连翘苷 |
P450; Influenza Virus; AMPK | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Phillyrin (Forsythin) 是从连翘中分离出来的一种天然产物,具有抗甲型流感病毒的活性,以及抗菌和消炎作用。 | |||
T3863 |
Chikusetsusaponin IVa
竹节参皂苷IVa,Calenduloside F,竹节人参皂苷 IVA |
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
Chikusetsusaponin IVa (Calenduloside F) 是一种三萜皂苷中主要的活性成分,是一种蛋白激酶的激活剂,对血栓及一些代谢性疾病具有抵抗作用。 | |||
T10105 |
3α-Hydroxymogrol
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
3α-Hydroxymogrol is a triterpenoid isolated from Siraitia grosvenorii Swingle. It is a potent AMPK activator and enhances AMPK phosphorylation. | |||
TN6069 |
Thalidezine
|
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Thalidezine, a novel AMPK activator, eliminates apoptosis-resistant cancer cells through energy-mediated autophagic cell death, it can inhibit the growth of mouse L1210 cells in vitro. Thalidezine possesses antimicrobial activity against Mycobacterium sme |