GS-9667

CAT:
804-HY-19842-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
GS-9667 - image 1

GS-9667

  • Description:

    GS-9667 (CVT 3619), a novel N6-5'-substituted adenosine analog, is a selective, partial agonist of the A1 adenosine receptor (A1AdoR) . GS-9667 binds to adipocyte membranes with high (KH=14 nM) and low (KL=5.4 μM) affinities. GS-9667 reduces cyclic AMP content and release of nonesterified fatty acids from epididymal adipocytes with IC50 values of 6 nM and 44 nM, respectively. GS-9667 inhibits lipolysis and has the potential for Type 2 diabetes (T2DM) and dyslipidemia via lowering of free fatty acids (FFA) [1][2].
  • Product Name Alternative:

    CVT 3619
  • UNSPSC:

    12352005
  • Target:

    Adenosine Receptor
  • Type:

    Reference compound
  • Related Pathways:

    GPCR/G Protein
  • Applications:

    Metabolism-sugar/lipid metabolism
  • Field of Research:

    Metabolic Disease; Cardiovascular Disease
  • Assay Protocol:

    https://www.medchemexpress.com/gs-9667.html
  • Purity:

    98.08
  • Solubility:

    DMSO : 125 mg/mL (ultrasonic)
  • Smiles:

    O[C@H]1[C@@H] (O[C@@H] ([C@H]1O) CSC2=C (C=CC=C2) F) N3C4=NC=NC (N[C@H]5[C@@H] (CCC5) O) =C4N=C3
  • Molecular Formula:

    C21H24FN5O4S
  • Molecular Weight:

    461.51
  • References & Citations:

    [1]Marjan Fatholahi, et al. A novel partial agonist of the A (1) -adenosine receptor and evidence of receptor homogeneity in adipocytes. J Pharmacol Exp Ther. 2006 May;317 (2) :676-84. |[2]Peter M Staehr, et al. Reduction of free fatty acids, safety, and pharmacokinetics of oral GS-9667, an A (1) adenosine receptor partial agonist. J Clin Pharmacol. 2013 Apr;53 (4) :385-92.
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

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

    Reference compound1
  • Clinical Information:

    Phase 1
  • CAS Number:

    618380-90-8