Aprepitant

CAT:
804-HY-10052-01
Size:
5 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
Aprepitant - image 1

Aprepitant

  • Description :

    Aprepitant (MK-0869) is a selective and high-affinity neurokinin 1 receptor antagonist with a Kd of 86 pM.
  • Product Name Alternative :

    MK-0869; MK-869; L-754030
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Antibiotic; Bacterial; HIV; Neurokinin Receptor
  • Type :

    Reference compound
  • Related Pathways :

    Anti-infection; GPCR/G Protein; Neuronal Signaling
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Neurological Disease; Endocrinology; Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/Aprepitant.html
  • Purity :

    99.82
  • Solubility :

    DMSO : 50 mg/mL (ultrasonic)
  • Smiles :

    O=C1NC(CN2[C@H]([C@@H](O[C@@H](C3=CC(C(F)(F)F)=CC(C(F)(F)F)=C3)C)OCC2)C4=CC=C(F)C=C4)=NN1
  • Molecular Formula :

    C23H21F7N4O3
  • Molecular Weight :

    534.43
  • Precautions :

    H302, H315, H319, H335
  • References & Citations :

    [1]Martinez AN, et al. Aprepitant limits in vivo neuroinflammatory responses in a rhesus model of Lyme neuroborreliosis. J Neuroinflammation. 2017 Feb 15;14 (1) :37.|[2]Bayati S, et al. Inhibition of tachykinin NK1 receptor using aprepitant induces apoptotic cell death and G1 arrest through Akt/p53 axis in pre-B acute lymphoblastic leukemia cells. Eur J Pharmacol. 2016 Nov 15;791:274-283.|[3]Mannangatti P, et al. Differential effects of aprepitant, a clinically used neurokinin-1 receptor antagonist on the expression of conditioned psychostimulant versus opioid reward. Psychopharmacology (Berl) . 2017 Feb;234 (4) :695-705.|[4]Barrett JS, et al. Pharmacologic rationale for the NK1R antagonist, aprepitant as adjunctive therapy in HIV. J Transl Med. 2016 May 26;14 (1) :148.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    4°C (Powder, protect from light)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • CAS Number :

    [170729-80-3]

Featured Selection

Popular Products

Discover our most sought-after biotechnology products, trusted by researchers worldwide