Temocapril

CAT:
804-HY-100713-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Temocapril - image 1

Temocapril

  • Description :

    Temocapril is an orally active angiotensin-converting enzyme (ACE) inhibitor. Temocapril can be used for the research of hypertension, congestive heart failure, acute myocardial infarction, insulin resistance, and renal diseases[1][2].
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Angiotensin-converting Enzyme (ACE)
  • Type :

    Reference compound
  • Related Pathways :

    Metabolic Enzyme/Protease
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Cardiovascular Disease
  • Assay Protocol :

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

    98.14
  • Solubility :

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

    O=C(O)CN1C[C@@H](C2=CC=CS2)SC[C@H](N[C@H](C(OCC)=O)CCC3=CC=CC=C3)C1=O
  • Molecular Formula :

    C23H28N2O5S2
  • Molecular Weight :

    476.61
  • Precautions :

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

    [1]Fukami T, et al. In vitro evaluation of inhibitory effects of antidiabetic and antihyperlipidemic drugs on human carboxylesterase activities. Drug Metab Dispos. 2010 Dec;38 (12) :2173-8.|[2]Kawasaki H, et al. Angiotensin inhibits neurotransmission of calcitonin gene-related peptide-containing vasodilator nerves in mesenteric artery of spontaneously hypertensive rats. J Pharmacol Exp Ther. 1998 Feb;284 (2) :508-15. |[3]Yuan Z, et al. Temocapril treatment ameliorates autoimmune myocarditis associated with enhanced cardiomyocyte thioredoxin expression. Cardiovasc Res. 2002 Aug 1;55 (2) :320-8.|[4]Ohnishi K, et al. Angiotensin-converting enzyme inhibitor does not suppress renal angiotensin II levels in angiotensin I-infused rats. J Pharmacol Sci. 2013;122 (2) :103-8.
  • Shipping Conditions :

    Blue Ice
  • Storage Conditions :

    -20°C (Powder, protect from light)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • CAS Number :

    [111902-57-9]

Featured Selection

Popular Products

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