Ligands organométalliques
Sous-catégories appartenant à la catégorie "Ligands organométalliques"
- Ligands de Buchwald(25 produits)
- DPEN(4 produits)
- DPHEN(4 produits)
- JOSIPHOS(4 produits)
- Phosphine(486 produits)
- Porphyrines(73 produits)
2868 produits trouvés pour "Ligands organométalliques".
Sofalcone
CAS :Increases VEGF via heme oxygenase-1 modulation; anti-ulcer agentFormule :C27H30O6Degré de pureté :Min. 95%Couleur et forme :Yellow PowderMasse moléculaire :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.
Formule :C24H25N5O3SDegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :463.55 g/molLicofelone
CAS :Dual COX/5-LO inhibitor; anti-inflammatory; analgesic
Formule :C23H22ClNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :379.88 g/molDilevalol hydrochloride
CAS :Produit contrôléBeta-adrenoceptor antagonist; anti-hypertensiveFormule :C19H24N2O3·HClDegré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :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.Formule :C20H17FN2O3SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :384.43 g/mol(+)-Muscarine tosylate
CAS :Muscarinic acetylcholine receptor agonistFormule :C9H20NO2·C7H7O3SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :345.46 g/molBrivanib alaninate
CAS :VEGFR2 a tyrosine kinase receptor inhibitor; antineoplasticFormule :C22H24FN5O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :441.18123Zotepine
CAS :Produit contrôléAntagonist of dopamine (D2), serotonin (5-HT2A) and histamine H1 receptorsFormule :C18H18ClNOSDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :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.
Formule :C23H26O4N2F2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :432.46 g/molBafilomycin A1
CAS :Inhibitor of vacuolar-type proton pumpFormule :C35H58O9Degré de pureté :Min. 95 Area-%Couleur et forme :White PowderMasse moléculaire :622.83 g/molDeslorelin acetate
CAS :Produit contrôléGnRH super-agonist
Formule :C66H87N17O14Degré de pureté :Min. 95%Couleur et forme :White Off-White PowderMasse moléculaire :1341.661848-Deschloro-8-bromo-N-methyl desloratadine
CAS :Antagonist of platelet activating factorFormule :C20H21BrN2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :369.3 g/molMK 4827
CAS :Inhibitor of PARP1 and PARP2 enzymes
Formule :C19H20N4ODegré de pureté :Min. 96 Area-%Couleur et forme :White PowderMasse moléculaire :320.39 g/molLixivaptan
CAS :Selective vasopressin receptor V2 agonistFormule :C27H21ClFN3O2Degré de pureté :Min. 95%Couleur et forme :Yellow PowderMasse moléculaire :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.Formule :C21H29N5O2Degré de pureté :Min. 95%Masse moléculaire :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.
Formule :C17H13N5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :287.32 g/molRucaparib camsylate
CAS :Inhibitor of poly (ADP-ribose) polymerase enzyme; antineoplasticFormule :C19H18FN3O•C10H16O4SDegré de pureté :Min. 95%Couleur et forme :Off-White To Yellow SolidMasse moléculaire :555.66 g/molArbutin - Synthetic origin
CAS :Inhibitor of tyrosinase in melanocytes: skin whitener
Formule :C12H16O7Degré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :272.25 g/molLumiracoxib - Bio-X ™
CAS :Produit contrôléLumiracoxib 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.Formule :C15H13ClFNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :293.72 g/molFlurbiprofen
CAS :Inhibitor of cytochrome P450; inhibitor of prostaglandin synthesis
Formule :C15H13FO2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :244.26 g/mol
