Ligands organométalliques
Dans cette catégorie, vous trouverez un grand nombre de molécules organométalliques utilisées comme ligands dans les biomolécules. Ces ligands organométalliques peuvent être utilisés en chimie organique et en synthèse au laboratoire. Ils jouent un rôle crucial dans la formation de complexes de coordination et la catalyse de diverses réactions chimiques. Chez CymitQuimica, nous offrons une sélection diversifiée de ligands organométalliques de haute qualité pour soutenir vos recherches et besoins industriels.
Sous-catégories appartenant à la catégorie "Ligands organométalliques"
- Ligands de Buchwald(22 produits)
- DPEN(4 produits)
- DPHEN(4 produits)
- JOSIPHOS(4 produits)
- Phosphine(497 produits)
- Porphyrines(75 produits)
2887 produits trouvés pour "Ligands organométalliques"
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Lumateperone tosylate
CAS :<p>5-HT2A receptor antagonist</p>Formule :C24H28FN3O•C7H8O3SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :565.7 g/molCC 292
CAS :<p>Inhibits non-receptor tyrosine kinase BTK; antineoplastic</p>Formule :C22H22FN5O3Degré de pureté :Min. 95%Masse moléculaire :423.44 g/molDroperidol
CAS :Produit contrôlé<p>Droperidol is a butyrophenone derivative, which is an antipsychotic agent and antiemetic medication, sourced from synthetic chemical processes. Its mode of action involves antagonism of dopamine D2 receptors in the central nervous system, particularly in the chemoreceptor trigger zone of the brain, and it also possesses some alpha-adrenergic blocking properties.</p>Formule :C22H22FN3O2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :379.43 g/mol5-Fluorouracil - Bio-X ™
CAS :<p>5-Fluorouracil is a cytotoxic drug that inhibits the synthesis of DNA. It is used in combination therapy to treat cancer and is a pyrimidine analog. This drug inhibits the formation of thymidylate synthase from uracil. As a result, this leads to DNA and RNA synthesis inhibition and cell death.</p>Formule :C4H3FN2O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :130.08 g/mol4-5-(4-Pyridylmethylamino)pyrazolo1,5-apyrimidin-3-ylbenzamide
CAS :<p>Selective inhibitor of the mutated RET variant RETV804M, which is the anticipated drug-resistant RET mutant that can occur in tumours treated with kinase inhibitors. The compound has a biochemical IC50 of 0.02 µM and selectivity for purified RETV804M over purified RET and KDR of 3.7 and 110, respectively. The efficacy of the compound was shown also in cell cultures with IC50 of 4.4 µM, and cell assay selectivity for RETV804M over RET and KDR of 0.89 and 2.3, respectively.</p>Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :344.37 g/molGRL 0617
CAS :<p>A novel non-covalent inhibitor of the PLpro protease from SARS-CoV-2 and SARS-CoV viruses. GRL 0617 inhibits the proteolytic processing of the viral polypeptide. As PLpro also acts as a protease in pathways involved in innate immunity, there are indications that it can promote immunity against the virus.</p>Formule :C20H20N2ODegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :304.39 g/molZileuton- Bio-X ™
CAS :<p>Zileuton is an inhibitor of the 5-lipoxygenase enzyme, thus preventing the leukotrienes LTE4, LDT4, LTB4 and LTC4 from being formed. This in turn reduces inflammation, bronchoconstriction and mucus secretion in the airways. As a result, Zileuton can be used in the treatment and management of asthma and allergic rhinitis. Studies have shown that Zileuton has the potential to reverse dementia-related brain damage.</p>Formule :C11H12N2O2SDegré de pureté :(%) Min. 95%Couleur et forme :PowderMasse moléculaire :236.29 g/molHalofuginone lactate
CAS :<p>Halogenated derivative of febrifugine; coccidiostat</p>Formule :C19H23BrClN3O6Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :504.76 g/molTerlipressin acetate
CAS :Produit contrôlé<p>Vasopressin analog; vasoactive agent</p>Formule :C52H74N16O15S2·C2H4O2Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :1,287.43 g/molOdiparcil
CAS :<p>Dipeptidyl peptidase 4 (DPP4) inhibitor</p>Formule :C15H16O6SDegré de pureté :Min. 99%Couleur et forme :PowderMasse moléculaire :324.35 g/mol17:0-20:4Pi (4) P
CAS :<p>17:0-20:4Pi (4) P is a synthetic phosphoinositide, which is a type of phospholipid. It is typically sourced from laboratory synthesis, often incorporating stable isotopes or specific fatty acid chains to mimic natural compounds found in cell membranes. This product functions primarily as a probe in biochemical experiments, particularly for studying lipid signaling pathways within cells.</p>Formule :C46H88N2O16P2Degré de pureté :Min. 95%Masse moléculaire :987.14 g/molGSK 1904529A
CAS :<p>Inhibitor of IGF1 receptor</p>Formule :C44H47F2N9O5SDegré de pureté :Min. 95%Masse moléculaire :851.33889Fexofenadine HCl - Bio-X ™
CAS :<p>Fexofenadine is a selective histamine-1 receptor antagonist that is used to treat the symptoms of seasonal allergies. It does not cross the blood-brain barrier and carries little-to-no activity at off targets. This drug binds to the inactive form of the H1 receptor and inhibits its activation and downstream effects.</p>Formule :C32H39NO4•HClCouleur et forme :PowderMasse moléculaire :538.12 g/molBaricitinib phosphate
CAS :Produit contrôlé<p>Baricitinib phosphate is a selective Janus kinase (JAK) inhibitor, which is a synthetic product developed through targeted molecular design. Its mode of action involves the inhibition of JAKs, which are intracellular enzymes that transmit cytokine-mediated signals via the JAK-STAT pathway. By blocking these signals, baricitinib phosphate effectively reduces inflammatory responses.</p>Formule :C16H20N7O6PSDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :469.41 g/mol7rh
CAS :Inhibitor of discoidin domain receptor DDR1Formule :C30H29F3N6ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :546.59 g/molFormoterol fumarate dihydrate
CAS :Produit contrôlé<p>beta2-adrenoreceptor agonist; anti-asthmatic</p>Formule :C42H52N4O12·2H2ODegré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :840.91 g/molSD 0006
CAS :<p>SD 0006 is a small-molecule inhibitor, which is synthesized through specialized chemical processes. It functions by selectively inhibiting the cyclooxygenase-2 (COX-2) enzyme, which plays a significant role in the inflammatory pathway. This inhibition reduces the production of pro-inflammatory prostaglandins, ultimately leading to a decrease in inflammation.</p>Formule :C20H20ClN5O2Degré de pureté :Min. 95%Masse moléculaire :397.86 g/molEverolimus
CAS :<p>mTOR kinase inhibitor; rapamycin analog; immunosuppressant</p>Formule :C53H83NO14Degré de pureté :90%Couleur et forme :White Off-White PowderMasse moléculaire :958.23 g/molSertindole
CAS :<p>Antagonist of cardiac potassium channel HERG; anti-psychotic</p>Formule :C24H26ClFN4ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :440.94 g/molLU 005i
CAS :<p>Potent inhibitor of β5i subunit of immunoproteasomes (IC50 = 6.6 nM), selective over β5c subunit (IC50 = 287 nM). The β5i subunit of immunoproteasomes (iCPs) is the chymotrypsin-like active sites that have implications on anti-cancer affects. On the other hand, β5c subunits are found in constitutive proteasomes (cCPs).</p>Formule :C31H46N4O7Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :586.72 g/mol
