L 692429

L 692429 Suppliers list
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Jinan Yaoyan Pharmaceutical Co., Ltd.  
Tel:
Email: jnyaoyan@163.com
Company Name: Nanjing Meihao Pharmaceutical Technology Co., Ltd.  
Tel: meitaochem@126.com
Email: meitaochem@126.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: Shanghai Dexuan Pharmaceutical Technology Co., Ltd  
Tel: dexuanyiyao@126.com
Email: dexuanyiyao@126.com

L 692429 manufacturers

  • L-692429
  • L-692429 pictures
  • $158.00
  • 2026-04-28
  • CAS:145455-23-8
  • Purity: 99.19%
  • Supply Ability: 10g
  • L-692429
  • L-692429 pictures
  • $158.00
  • 2026-04-28
  • CAS:145455-23-8
  • Purity: 99.19%
  • Supply Ability: 10g
L 692429 Basic information
Product Name:L 692429
Synonyms:L 692429;MK 0751;3-amino-3-methyl-N-[(3R)-2-oxo-1-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-4,5-dihydro-3H-1-benzazepin-3-yl]butanamide;L-692,429 , CID121879;L692429,L 692429;Butanamide, 3-amino-3-methyl-N-[(3R)-2,3,4,5-tetrahydro-2-oxo-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-1H-1-benzazepin-3-yl]-;L-692429 free base;(R)-N-(1-((2'-(2H-Tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-yl)-3-amino-3-methylbutanamide
CAS:145455-23-8
MF:C29H31N7O2
MW:509.611
EINECS:
Product Categories:
Mol File:145455-23-8.mol
L 692429 Structure
L 692429 Chemical Properties
density 1.33±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 50 mg/mL (98.12 mM)
pka4.14±0.10(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
L 692429 Usage And Synthesis
UsesL-692429 (MK-0751) is a benzolactam derivative and a nonpeptidyl growth hormone secretagogue (GHS) agonist. L-692429 binds to G protein-coupled receptor with a Ki of 63 nM[1][2].
in vivo

When tested in anesthetized rats (Wistar rats), L-756867 inhibits L-692429 (100 μg/kg)-stimulated GH secretion in a dose-dependent manner. Complete inhibition is observed at an i.v. dose of 100 μg/kg of L-756867[1].

References[1] Cheng K, et al. Inhibition of L-692,429-stimulated rat growth hormone release by a weak substance P antagonist: L-756,867. J Endocrinol. 1997 Jan;152(1):155-8. DOI:10.1677/joe.0.1520155
[2] Holst B, et al. Nonpeptide and peptide growth hormone secretagogues act both as ghrelin receptor agonist and as positive or negative allosteric modulators of ghrelin signaling. Mol Endocrinol. 2005 Sep;19(9):2400-11. DOI:10.1210/me.2005-0059
[3] Cunha SR, et al. Ghrelin and growth hormone (GH) secretagogues potentiate GH-releasing hormone (GHRH)-induced cyclic adenosine 3',5'-monophosphate production in cells expressing transfected GHRH and GH secretagogue receptors. Endocrinology. 2002 Dec;143(1 DOI:10.1210/en.2002-220670
L 692429 Preparation Products And Raw materials
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