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Cat. No. Product Name Field of Application Chemical Structure
DCC4118 Pgam1 Inhibitor Kh3 Novel allosteric PGAM1 inhibitor, showing efficacious in multiple preclinical models of pancreatic ductal adenocarcinoma (PDAC), especially with high PGAM1 expression
DCC4119 Pge-2946979 Novel potent matrix metalloproteinase (MMP) inhibitor, targeting MMPs 1, 3, 9, and 13 (24, 18, 1.9, and 1.3 nM, respectively)
DCC4120 Pgmi-004a Glycolytic enzyme phosphoglycerate mutase 1 (PGAM1) inhibitor
DCC4122 pha-680626 Inhibitor of both Bcr-Abl tyrosine kinase and Aurora kinases
DCC4123 Pha-e429 Selective ATP competitive ALK inhibitor
DCC4124 Phagocytosis Inhibitor Inhibitor of phagocytosis, interacting with and inhibiting the activating Fc receptors on macrophages, inhibiting downstream signaling pathways driving Fc-mediated phagocytosis
DCC4125 Phantasmidine Natural nicotinic acetylcholine receptor agonist
DCC4126 Phar-095239 Novel COX-2 inhibitor
DCC4127 Phencyclidine Hydrochloride Inhibitor of NMDA receptors, used as a veterinary anesthetic, and briefly as a general anesthetic for humans
DCC4128 Phen-dc3 Selective ligand of a specific G-quadruplex conformation, interacting with the quadruplex through extensive
DCC4129 phenoxodiol Diacetate Prodrug of phenoxodiol
DCC4130 Phenylarsine Oxide Inhibitor of internalization of cell surface receptors and tyrosine phosphatases, with no effect on tyrosine kinase
DCC4131 phenylmethimazole Blocker of dsRNA-induced IRF3 nuclear translocation and homodimerization; Inhibitor of lipopolysaccharide-mediated Toll-like receptor-4 signaling; Inhibitor of human pancreatic cancer
DCC4132 Phnp-3 Novel selective α-syn ligand, exhibited the promising binding characteristics for α-syn aggregates (Ki = 0.52 nM)
DCC4133 Phoenixin-14 Novel neuropeptide, protecting human brain vascular endothelial cells against oxygen-glucose deprivation/reoxygenation (OGD/R)-induced inflammation and permeability, significantly ameliorating HFD-induced obesity and fatty liver, regulating pituitary gona
DCC4134 Phoenixin-20 Novel GPR173 agonist, promoting osteoblastic differentiation of MC3T3-E1 cells. stimulating mRNAs encoding hypothalamo-pituitary-gonadal hormones
DCC4135 Phomoxanthone A Natural anti-tumor agent, showing strong apoptotic anticancer effects against platinum-resistant solid cancers
DCC4136 Phosphatidylinositol Potent antagonist of (H1N1)pdm09 infection, markedly suppressing cytopathic effects and attenuating viral gene expression in (H1N1)pdm09-infected MDCK cells
DCC4137 phospho-sulindac Sulindac derivative with promising anticancer activities
DCC4138 Phosphotyrosine Inducer of platelet aggregation, playing a role in cellular signal transduction and possibly in cell growth control and carcinogenesis
DCC4139 Photac-i-3 Novel photoswitchable BET bromodomain Degrader (PHOTAC)
DCC4140 Photoazolol-1 Novel potent photoswitchable antagonist for a precise spatiotemporal control of β2-adrenoceptors
DCC4141 Photogbi1 Novel photocontrol inhibitor of the voltage-gated proton channel Hv1
DCC4142 Photo-lenalidomide-acid Functionalized photoswitchable cereblon ligand for Degraders
DCC4143 Photos1p Novel photoswitchable sphingolipid probe, reversibly controlled S1P3-dependent pain hypersensitivity in mice and uniquely suited for the study of S1P biology in cultured cells and in vivo
DCC4144 Photosensitizer Pz I Novel porphyrazine-based photodynamic anti-cancer agent, inducing immunogenic cell death
DCC4145 Photosensitizer Pz Iii Novel porphyrazine-based photodynamic anti-cancer agent, inducing immunogenic cell death
DCC4146 Photosph Novel photoswitchable sphingolipid probe
DCC4147 Phototrexate Novel photoswitchable inhibitor of human dihydrofolate reductase
DCC4148 Phyllospadine Natural flavonoidal alkaloid from the sea-grass Phyllosphadix iwatensis

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