Dexamethasone-d5

CAT:
804-HY-14648S
Size:
1 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Dexamethasone-d5 - image 1

Dexamethasone-d5

  • Description:

    Dexamethasone-d5 is the deuterium labeled Dexamethasone. Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18 expression on monocytes. Dexamethasone is highly effective in the control of COVID-19 infection. Dexamethasone inhibits production of exosomes containing inflammatory microRNA-155 in lipopolysaccharide-induced macrophage inflammatory responses[1][2].
  • Product Name Alternative:

    Hexadecadrol-d5; Prednisolone F-d5
  • UNSPSC:

    12352211
  • Hazard Statement:

    H315, H317, H319, H334, H335
  • Target:

    Antibiotic; Autophagy; Bacterial; Complement System; Glucocorticoid Receptor; Mitophagy; SARS-CoV
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    Anti-infection; Autophagy; Immunology/Inflammation; Vitamin D Related/Nuclear Receptor
  • Field of Research:

    Cancer; Infection; Endocrinology; Inflammation/Immunology
  • Purity:

    99.23
  • Solubility:

    10 mM in DMSO|DMSO : 250mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles:

    C[C@@]12[C@] (C (C ([2H]) (O) [2H]) =O) (O) [C@H] (C) C[C@@]1 ([H]) [C@]3 ([H]) CC ([2H]) ([2H]) C4=C ([2H]) C (C=C[C@]4 (C) [C@@]3 (F) [C@@H] (O) C2) =O
  • Molecular Formula:

    C22H24D5FO5
  • Molecular Weight:

    397.49
  • Precautions:

    H315, H317, H319, H334, H335
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216. |[2]Rocksén D, et al. Differential anti-inflammatory and anti-oxidative effects of Dexamethasone and N-acetylcysteine in endotoxin-induced lung inflammation. Clin Exp Immunol. 2000 Nov;122 (2) :249-56|[3]LaLone CA, et al. Effects of a glucocorticoid receptor agonist, Dexamethasone, on fathead minnow reproduction, growth, and development. Environ Toxicol Chem. 2012 Mar;31 (3) :611-22.|[4]Heidi Ledford. et al. Coronavirus Breakthrough: Dexamethasone Is First Drug Shown to Save Lives. Nature. 2020 Jun 16.|[5]Yun Chen, et al. Glucocorticoids inhibit production of exosomes containing inflammatory microRNA-155 in lipopolysaccharide-induced macrophage inflammatory responses. Int J Clin Exp Pathol 2018;11 (7) :3391-3397.|[6]Roussel D, et al. Dexamethasone treatment specifically increases the basal proton conductance of rat liver mitochondria. FEBS Lett. 2003 Apr 24;541 (1-3) :75-9.|[7]Ballabh P, et al. Neutrophil and monocyte adhesion molecules in bronchopulmonary dysplasia, and effects of corticosteroids. Arch Dis Child Fetal Neonatal Ed. 2004 Jan;89 (1) :F76-83.|[8]Adcock IM, et al. Ligand-induced differentiation of glucocorticoid receptor (GR) trans-repression and transactivation: preferential targetting of NF-kappaB and lack of I-kappaB involvement. Br J Pharmacol. 1999 Jun;127 (4) :1003-11
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

    -20°C, 3 years (Powder)
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    358731-91-6