CGP-42112

CAT:
804-HY-12405-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
CGP-42112 - image 1

CGP-42112

  • Description :

    CGP-42112 (CGP-42112A) is a potent Angiotensin-II subtype 2 receptor (AT2 R) agonist[1].
  • Product Name Alternative :

    CGP42112A
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Angiotensin Receptor
  • Type :

    Reference compound
  • Related Pathways :

    GPCR/G Protein
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Neurological Disease; Endocrinology; Cardiovascular Disease
  • Assay Protocol :

    https://www.medchemexpress.com/CGP-42112.html
  • Purity :

    99.84
  • Solubility :

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles :

    CC[C@H](C)[C@@H](C(O)=O)NC([C@H]1N(C([C@H](CC2=CNC=N2)NC([C@H](CCCCNC([C@H](CCCNC(N)=N)NC(OCC3=CC=CC=C3)=O)=O)NC([C@H](CC4=CC=C(C=C4)O)NC(C5=CC=CN=C5)=O)=O)=O)=O)CCC1)=O
  • Molecular Formula :

    C52H69N13O11
  • Molecular Weight :

    1052.19
  • Precautions :

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

    [1]Takekoshi K, et al. Angiotensin-II subtype 2 receptor agonist (CGP-42112) inhibits catecholamine biosynthesis in cultured porcine adrenal medullary chromaffin cells. Biochem Biophys Res Commun. 2000 Jun 7;272 (2) :544-50.|[2]Speth RC. [125I]CGP 42112 binding reveals differences between rat brain and adrenal AT2 receptor binding sites. Regul Pept. 1993 Mar 19;44 (2) :189-97.|[3]Naveri L, et al. Angiotensin II AT2 receptor stimulation extends the upper limit of cerebral blood flow autoregulation: agonist effects of CGP 42112 and PD 123319. J Cereb Blood Flow Metab. 1994 Jan;14 (1) :38-44.|[4]Heemskerk FM, et al. Quantitative autoradiography of angiotensin II AT2 receptors with [125I]CGP 42112. Brain Res. 1995 Apr 17;677 (1) :29-38.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    AT1 Receptor; AT2 Receptor
  • CAS Number :

    [127060-75-7]

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