AMPK
货号 | 产品名 | CAS号 | 信息 |
---|---|---|---|
FB06261 | ZLN024 | 723249-01-2 | ZLN024 is an AMPK allosteric activator and activates α1β1γ1 and α2β1γ1 by around 2–2.5 fold with an EC50 of about 1–2 μM. |
FB10277 | ZLN024 HCl | 1883548-91-1 | ZLN024 HCl is an AMPK allosteric activator and activates α1β1γ1 and α2β1γ1 by around 2–2.5 fold with an EC50 of about 1–2 μM. |
FB02701 | YLF-466D | 1273323-67-3 | YLF-466D is an allosteric AMPK activator. |
FB02364 | WZ4003 | 1214265-58-3 | WZ4003 is a potent and selective NUAK1/2 inhibitor with IC50 values of 20 and 100 nM, respectively. |
FB10939 | Thalidezine | 18251-36-0 | Thalidezine is an activiator of AMP-activated protein kinase (AMPK). |
FB12627 | PT 1 | 331002-70-1 | PT 1 is a AMP-activated protein kinase (AMPK) activator. |
FB06499 | Phillyrin | 487-41-2 | Phillyrin is a naturally occuring AMPK activity enhancer, isolated and purified from the fruits of Forsythia suspensa. |
FB08173 | Phenformin HCl | 834-28-6 | Phenformin HCl is an AMPK activator which can increase the phosphorylation and activation of AMPKalpha1 and AMPKalpha2. |
FB09957 | PF-06409577 | 1467057-23-3 | PF-06409577 is a potent and selective allosteric activator of AMPK with EC50 value of 7 nM for AMPKα1β1γ1, but >40000 nM for AMPKα1β2γ1. |
FB16048 | O-304 | 1261289-04-6 | O-304 is a first-in-class, orally available pan-AMPK activator, which increases AMPK activity by suppressing the dephosphorylation of pAMPK. O-304 exhibits a great potential as a drug to treat type 2 diabetes (T2D) and associated cardiovascular complications [1][2]. |
FB11538 | ex229 | 1219739-36-2 | Novel AMPK activator, increasing AMPK activity of both AMPKgamma1- and AMPKgamma3-containing complexes in mouse skeletal muscle |
FB01995 | Mogroside IIIE | 88901-37-5 | Mogroside IIIE a naturally occuring cucurbitane glycoside which can attenuate gestational diabetes mellitus through activating of AMPK signaling pathway in mice. |
FB10840 | MK-8722 | 1394371-71-1 | MK-8722 is a potent, direct, allosteric activator of all twelve mammalian AMPK complexes. |
FB03036 | Metformin HCl | 1115-70-4 | Metformin HCl, a widely used anti-diabetic drug has potential efficacy as an anti-cancer drug, decreasing hyperglycemia in hepatocytes primarily by suppressing glucose production by the liver (hepatic gluconeogenesis). |
FB10205 | GSK621 | 1346607-05-3 | In AML cell lines and primary AML samples, GSK621 markedly increases phosphorylation at AMPKα T172, a marker of AMPK activation. |
FB17544 | IM156 | 1422365-93-2 | IM156 is a metformin derivative which has been reported to ameliorate various types of fibrosis and inhibit in vitro and in vivo tumors by inducing AMPK activation more potently than metformin. IM156 treatment impaired the function of virus-specific memory CD8+ T cells, indicating that excessive AMPK activation weakens memory T cell differentiation, thereby suppressing recall immune responses. IM156 activated AMPK in a dose-dependent manner, and produced shortening of the circadian period and enhanced degradation of the clock genes PER2 and CRY1. |
FB09452 | HTH-01-015 | 1613724-42-7 | HTH-01-015 is a selective NUAK1 inhibitor, but not NUAK2, with IC50 of 100 nM, suppressing NUAK1-mediated MYPT1 phosphorylation. |
FB00447 | ETC-1002 | 738606-46-7 | ETC-1002 is an AMPK activator and increase the level of AMPK phosphorylation. |
FB04784 | Dorsomorphin | 866405-64-3 | Dorsomorphin is a selective AMPK inhibitor with Ki value of 109 nM. |
FB08616 | Dorsomorphin 2HCl | 1219168-18-9 | Dorsomorphin 2HCl is a selective AMPK inhibitor with Ki value of 109 nM. |
FB18230 | COH-SR4 | 73439-19-7 | COH-SR4 is an AMPK activator with anticancer properties. It significantly inhibited adipocyte differentiation in a dose-dependent manner in 3T3-L1 cells. It significantly reduced intracellular lipid accumulation and downregulated the expression of key adipogenesis-related transcription factors and lipogenic proteins in differentiating adipocytes. |
FB09404 | Chitosan oligosaccharide COS | 148411-57-8 | Chitosan oligosaccharide (COS) is an oligomer of β-(1→4)-linked D-glucosamine. Chitosan oligosaccharide (COS) activates AMPK and inhibits inflammatory signaling pathways including NF-κB and MAPK pathways. |
FB17192 | ASP4132 Besylate | 1640294-30-9 | ASP4132 is a new type of AMPK activator with EC50 value of 18nM. It showed attractive selective growth inhibition against human cancer cells. |
FB02390 | Ampkinone | 1233082-79-5 | Ampkinone is a small molecule activator of AMPK and stimulates functional activation of AMPK via the phosphorylation at Thr172 in cultured L6 muscle cells with an EC50 value of 4.3 μM, enhancing glucose uptake by 3.2-fold. |
FB12640 | RSVA 405 | 140405-36-3 | AMPK activator; also STAT3 inhibitor |
FB18007 | Amarogentin | 21018-84-8 | Amarogentin is a secoiridoid glycoside that is mainly extracted from Swertia and Gentiana roots. Amarogentin exhibits many biological effects, including anti-oxidative, anti-tumour, and anti-diabetic activities. Amarogentin exerts hepatoprotective and immunomodulatory effects. Amarogentin promotes apoptosis, arrests G2/M cell cycle and downregulates of PI3K/Akt/mTOR signalling pathways. Amarogentin exerts beneficial vasculo-metabolic effect by activating AMPK. |
FB06244 | AICAR Phosphate | 681006-28-0 | AICAR phosphate, is an AMP-activated protein kinase activator, which is used for the treatment of acute lymphoblastic leukemia and may have applications in treating other disorders such as diabetes. |
FB10607 | AICAR | 2627-69-2 | AICAR is an allosteric AMPK activator. |
FB12844 | Adenosine 5'-monophosphate, disodium salt | 4578-31-8 | Adenosine 5'-monophosphate disodium salt is an activator of AMPK and can be used as a substrate of AMP-thymidine kinase, AMP deaminase and 5′-nucleotidase. |
FB05361 | A-769662 | 844499-71-4 | A-769662 is a reverible and allosteric activator of AMPK through inhibiting dephosphorylation of AMPK on Thr-172. |
FB00764 | 1,8-Dihydroxyanthraquinone | 117-10-2 | 1,8-Dihydroxyanthraquinone is a synthetic anthraquinone derivative, currently used as an antioxidant in synthetic lubricants, in the synthesis of antitumor agents, as a fungicide and as an intermediate for making dyes. |