Ligas Organometálicas
Subcategorias de "Ligas Organometálicas"
- Ligantes de Buchwald(25 produtos)
- DPEN(4 produtos)
- DPHEN(4 produtos)
- JOSIPHOS(4 produtos)
- Fosfina(486 produtos)
- Porfirinas(73 produtos)
Foram encontrados 2868 produtos para "Ligas Organometálicas".
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CAS:Increases VEGF via heme oxygenase-1 modulation; anti-ulcer agentFórmula:C27H30O6Pureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:450.52 g/molVE 822
CAS:VE 822 is a potent and selective inhibitor of ATR protein kinase, which is derived through chemical synthesis with a high specificity for ATR over related kinases. ATR, or ataxia telangiectasia and Rad3-related kinase, plays a critical role in the cellular response to DNA damage and replication stress. VE 822 achieves its mode of action by interfering with ATR’s catalytic activity, thereby halting the DNA damage response and rendering cancer cells more susceptible to DNA-damaging agents.
Fórmula:C24H25N5O3SPureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:463.55 g/molLicofelone
CAS:Dual COX/5-LO inhibitor; anti-inflammatory; analgesic
Fórmula:C23H22ClNO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:379.88 g/molDilevalol hydrochloride
CAS:Produto ControladoBeta-adrenoceptor antagonist; anti-hypertensiveFórmula:C19H24N2O3·HClPureza:Min. 95%Cor e Forma:SolidPeso molecular:364.87WM 8014
CAS:Selective and potent inhibitor of lysine acetyltransferases KAT6A and KAT6B with IC50 values of 8 nM and 28 nM, respectively. The compound is a reversible competitor of acetyl coenzyme A domain of KAT6A/B enzymes. It inhibits MYST-catalysed histone acetylation and potentiates senescence in vitro and in zebrafish model of hepatocellular carcinoma. The compound opened the door to a new class of cancer therapeutics that could potentially direct the cancer cells in senescence or permanent dormancy.Fórmula:C20H17FN2O3SPureza:Min. 95%Cor e Forma:PowderPeso molecular:384.43 g/mol(+)-Muscarine tosylate
CAS:Muscarinic acetylcholine receptor agonistFórmula:C9H20NO2·C7H7O3SPureza:Min. 95%Cor e Forma:PowderPeso molecular:345.46 g/molBrivanib alaninate
CAS:VEGFR2 a tyrosine kinase receptor inhibitor; antineoplasticFórmula:C22H24FN5O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:441.18123Zotepine
CAS:Produto ControladoAntagonist of dopamine (D2), serotonin (5-HT2A) and histamine H1 receptorsFórmula:C18H18ClNOSPureza:Min. 95%Cor e Forma:PowderPeso molecular:331.86 g/molDAPT
CAS:Inhibitor of proteaseγâsecretase, which allows to modulate of the activity of γâsecretase substrates Notch, E-cadherin, ErbB4, and amyloid precursor protein (APP). The compound can inhibit the growth of tongue carcinoma cells by arresting cell cycle in G0–G1 phase, modulate the activity of Notch1 receptor and Caspase-3 protease and induce apoptosis. It was also demonstrated that this inhibitor reduces the levels of β-amyloid peptide in the brain of mice model for Alzheimer’s disease. This compound also enhances the neuronal differentiation embryonic cells.
Fórmula:C23H26O4N2F2Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:432.46 g/molBafilomycin A1
CAS:Inhibitor of vacuolar-type proton pumpFórmula:C35H58O9Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:622.83 g/molDeslorelin acetate
CAS:Produto ControladoGnRH super-agonist
Fórmula:C66H87N17O14Pureza:Min. 95%Cor e Forma:White Off-White PowderPeso molecular:1341.661848-Deschloro-8-bromo-N-methyl desloratadine
CAS:Antagonist of platelet activating factorFórmula:C20H21BrN2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:369.3 g/molMK 4827
CAS:Inhibitor of PARP1 and PARP2 enzymes
Fórmula:C19H20N4OPureza:Min. 96 Area-%Cor e Forma:White PowderPeso molecular:320.39 g/molLixivaptan
CAS:Selective vasopressin receptor V2 agonistFórmula:C27H21ClFN3O2Pureza:Min. 95%Cor e Forma:Yellow PowderPeso molecular:473.93 g/molTandospirone
CAS:Tandospirone is a psychotropic drug that acts as a selective serotonin receptor partial agonist. It is derived from a synthetic source, specifically targeting the 5-HT1A receptors in the brain. Tandospirone modulates serotonergic neurotransmission by binding to these receptors, which are associated with mood regulation. This action results in the anxiolytic and antidepressant effects observed with the drug.Fórmula:C21H29N5O2Pureza:Min. 95%Peso molecular:383.49 g/molRepSox
CAS:Selective inhibitor of the transforming growth factor beta receptor TGFβ1. RepSox can replace Sox, a transcriptional factor required for cell self-renewal, in reprogramming of adult cells to induced pluripotent stem cells (iPSCs). In the cloned interspecies embryos, RepSox induced expression of pluripotency regulatory genes Oct4 and Nanog, improved viability and developmental potential of embryos in the pre-implantation stage.
Fórmula:C17H13N5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:287.32 g/molRucaparib camsylate
CAS:Inhibitor of poly (ADP-ribose) polymerase enzyme; antineoplasticFórmula:C19H18FN3O•C10H16O4SPureza:Min. 95%Cor e Forma:Off-White To Yellow SolidPeso molecular:555.66 g/molArbutin - Synthetic origin
CAS:Inhibitor of tyrosinase in melanocytes: skin whitener
Fórmula:C12H16O7Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:272.25 g/molLumiracoxib - Bio-X ™
CAS:Produto ControladoLumiracoxib is a COX-2 selective non-steroidal anti-inflammatory drug that is used for the treatment of osteoarthritis. This drug inhibits prostaglandin synthesis via inhibition of COX-2.Fórmula:C15H13ClFNO2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:293.72 g/molFlurbiprofen
CAS:Inhibitor of cytochrome P450; inhibitor of prostaglandin synthesis
Fórmula:C15H13FO2Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:244.26 g/mol
