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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9732 | VY-3-135 | Fatty Acid Synthase | |
VY-3-135 is a metastasis inhibitor and an acetyl-CoA synthetase 2 (ACSS2) modulator. | |||
TN3131 | 5-O-Cinnamoylquinic acid | Others | |
5-O-Cinnamoylquinic acid is a nature product. | |||
T14980 | CLK-IN-T3 | DYRK , CDK | |
CLK-IN-T3 is an inhibitor of CLK1, CLK2, and CLK3 with IC50s of 0.67, 15, and 110 nM. CLK-IN-T3 exhibits anti-cancer activity. | |||
T7504 | Necrostatin 2 racemate | Necrostatin-2 racemate | RIP kinase |
Necrostatin 2 racemate (Necrostatin-2 racemate) is an potent and specific inhibitor of RIPK1. | |||
T23588 | 9-CP-Ade Mesylate | 9-Cyclopentyladenine monomethanesulfonate,9 CP Ade Mesylate,9CPAde Mesylate | AChR |
9-CP-Ade Mesylate (9 CP Ade Mesylate) is a cell-permeable, stable and non-competitive inhibitor of adenylate cyclase. | |||
T60084 | FINO2 | Ferroptosis | |
FINO2 is a potent ferroptosis-inducing compound that inhibits GPX4 activity. It functions as a stable oxidant, effectively oxidizing ferrous iron and demonstrating stability across varying pH levels. Furthermore, FINO2 i... | |||
T15196 | EC23 | BASF-46928,AGN 190205 | Others |
EC23 (AGN 190205) is a stable synthetic retinoid analogue. It is also induces neuronal differentiation. | |||
T15140 | DLinDMA | Others | |
DLinDMA, as a benchmark, is a key stable nucleic acid lipid particleslipid component. | |||
T8753 | LX-2761 intermediate | Others | |
LX-2761 intermediate is a synthetic intermediate of LX-2761, a chemically stable and potent SGLT1/2 inhibitor. | |||
T19651 | Isoflurane | HSDB-8057,Forane,HSDB 8057,HSDB8057,Terrell | Others |
Isoflurane (Forane) is a stable, non-explosive inhalation anesthetic that has been reported to induce caspase-3 activation. | |||
T13362 | XY101 | ROR | |
XY101 is a selective, metabolically stable and orally available agonist of RORγ inverse(IC50 of 30 nM and a Kd of 380 nM). | |||
T12808 | S-Nitroso-N-acetyl-DL-penicillamine | SNAP | NO Synthase |
S-Nitroso-N-acetyl-DL-penicillamine (SNAP) acts as a stable inhibitor of platelet aggregation, is a nitric oxide donor and . | |||
T4172 | Methoxy-PMS | 1-Methoxyphenazine methosulfate,1-Methoxy PMS | Reactive Oxygen Species |
Methoxy-PMS (1-Methoxyphenazine methosulfate) is stable electron-transport mediator between NAD(P)H and tetrazolium dyes, can induce active oxygen formation. | |||
T40423 | L48H37 | ||
L48H37 is a chemically stable analog of Curcumin. It exhibits potent inhibitory properties against myeloid differentiation protein 2 (MD2), acting as a specific inhibitor. Its mechanism involves inhibiting the interactio... | |||
T6268 | Ceftiofur hydrochloride | Ceftiofur HCl,U-67279A,Excenel hydrochloride | Antibacterial , Antibiotic |
Ceftiofur hydrochloride (U-67279A) is the hydrochloride salt form of ceftiofur, a semisynthetic, beta-lactamase-stable, broad-spectrum, third-generation cephalosporin with antibacterial activity. | |||
T66932 | Ferrozine monosodium salt | Autophagy | |
Ferrozine monosodium salt is a dye that reacts with divalent iron to form a stable magenta complex that can be used for the spectrophotometric determination of iron. | |||
T3053 | CZC-25146 | CHEMBL2397014 | LRRK2 |
CZC-25146 (CHEMBL2397014) is an effective, specific and metabolically stable LRRK2 inhibitor with IC50 of 4.76/6.87 nM for wild-type LRRK2(Leucine-rich repeat kinase-2) and G2019S LRRK2, respectively. | |||
T6411 | Biapenem | CLI 86815,Biapenern,Omegacin,L 627,LJC 10627 | Antibacterial , Antibiotic |
Biapenem (CLI 86815) is a 1-beta-methylcarbapenem antibiotic with a wide range of antibacterial activity. Biapenem has similar antibacterial activity to that of imipenem, but is more stable against human renal dehydropep... | |||
T18964 | Dabsyl chloride | DABS-Cl | Others |
Dabsyl chloride (DABS-Cl) is an amine derivatizing agent and able to give rise to stable products that can be easily monitored spectrophotometrically at 460 nm. | |||
T40437L | Caloxin 2A1 acetate | Proton pump | |
Caloxin 2A1 acetate is an inhibitor of extracellular plasma membrane Ca2+-ATPase (PMCA) peptide. Caloxin 2A1 acetate inhibits Ca2+-dependent formation of the 140-kDa acid-stable acylphosphate. |