CGP 48369

CGP 48369 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:CGP48369
CAS:135689-23-5
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:CGP48369
CAS:135689-23-5
Purity:99.27% Package:1mg;700USD|5mg;1800USD
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Products Intro: Product Name:CGP 48369
CAS:135689-23-5
Purity:98% Remarks:Reach out to us for more information about custom solutions.
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com
Products Intro: Product Name:CGP 48369
CAS:135689-23-5
Purity:97.0% Package:5mg
Company Name: Beijing Jin Ming Biotechnology Co., Ltd.  
Tel: 010-60605840 15801484223;
Email: psaitong@jm-bio.com
Products Intro: Product Name:CGP48369
CAS:135689-23-5
Package:100mg Remarks: 试剂级

CGP 48369 manufacturers

  • CGP48369
  • CGP48369 pictures
  • $700.00 / 1mg
  • 2025-10-27
  • CAS:135689-23-5
  • Min. Order:
  • Purity: 99.27%
  • Supply Ability: 10g
CGP 48369 Basic information
Product Name:CGP 48369
Synonyms:CGP 48369;4(3H)-Pyrimidinone, 2,6-dibutyl-5-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-;CGP-48369,CGP48369
CAS:135689-23-5
MF:C26H30N6O
MW:442.56
EINECS:
Product Categories:
Mol File:135689-23-5.mol
CGP 48369 Structure
CGP 48369 Chemical Properties
Boiling point 653.2±65.0 °C(Predicted)
density 1.22±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka4.17±0.10(Predicted)
Safety Information
MSDS Information
CGP 48369 Usage And Synthesis
UsesCGP48369 is a nonpeptidic angiotensin II receptor antagonist, used for anti-hypertensive research.
in vivo

CGP48369 (10 mg/kg/day p.o.) decreases BP in two-kidney/one-clip renal hypertensive rats for at least 24 h. In arteries with endothelium, contractions induced by AII 3×10-8 M do not differ in untreated spontaneously hypertensive rats (SHR) and WKY. All evoked significantly smaller contractions in SHR treated with CGP 48369 than in the other treated SHR. Antihypertensive treatment with benazepril or nifedipine, and to a lesser extent with CGP 48369, increases the sensitivity (pD2-va1ue) to intraluminal ACh. In arteries without endothelium, sensitivity to NE is identical in all groups, whereas maximal response in CGP 48369-treated SHR and in nifedipine treated SHR is slightly greater as compared with that in WKY[1]. In SHR, antihypertensive therapy with either benazepril HCl, CGP 48369, valsartan, or nifedipine (each 10 mg/kg/d for 8 weeks) significantly increase endothelium-dependent relaxations evoked by acetylcholine[2].

References[1] Dohi Y, et al. Angiotensin blockade or calcium antagonists improve endothelial dysfunction in hypertension: studies in perfused mesenteric resistance arteries. J Cardiovasc Pharmacol. 1994 Sep;24(3):372-9. DOI:10.1097/00005344-199409000-00004
[2] Tschudi MR, et al. Antihypertensive therapy augments endothelium-dependent relaxations in coronary arteries of spontaneously hypertensive rats. Circulation. 1994 May;89(5):2212-8. DOI:10.1161/01.cir.89.5.2212
CGP 48369 Preparation Products And Raw materials
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