Date published: 2025-9-15

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Devazepide (CAS 103420-77-5)

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Alternate Names:
MK 329
Application:
Devazepide is a potent CCK (cholecystokinin) inhibitor
CAS Number:
103420-77-5
Purity:
≥98%
Molecular Weight:
408.46
Molecular Formula:
C25H20N4O2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
Available in US only.
* Refer to Certificate of Analysis for lot specific data.

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Devazepide, a novel synthetic peptide, has emerged as useful in scientific research. Its applications span various in vivo and in vitro experiments, showcasing its effectiveness in numerous biological activities and yielding biochemical and physiological effects. As a non-peptide antagonist of CCK (cholecystokinin) receptors, Devazepide interacts with CCK, a neuroendocrine peptide known for its involvement in cell growth, proliferation, and other vital functions. Notably, Devazepide has demonstrated the induction of apoptosis in Ewing tumor growth studies and has shown an inability to reverse the blocking effect of IL-1β in rat studies. Moreover, it has been reported to inhibit the growth of HT29-S-B6 cells and impact their morphology. Devazepide exerts diverse biochemical and physiological effects, including the modulation of hormone levels like cortisol and testosterone, as well as neurotransmitters such as serotonin and dopamine. While the exact mechanism of action remains incompletely understood, it is postulated that Devazepide may function as an agonist at specific receptors within the body. Additionally, its interaction with other proteins and enzymes in the body likely contributes to the modulation of their activity.


Devazepide (CAS 103420-77-5) References

  1. Devazepide reversed effect of sincalide against morphine on rat jejunal activities.  |  Xu, MY., et al. 1999. Zhongguo Yao Li Xue Bao. 20: 419-22. PMID: 10678088
  2. [The associative behaviour of methylglucamine salts of the dicarboxylic acid dianilides of 3-carboxy-2,4,6-triiodoaniline in aqueous solutions (author's transl)].  |  Miklautz, H. and Riemann, J. 1975. Arch Pharm (Weinheim). 308: 760-8. PMID: 1200792
  3. Devazepide antagonizes the inhibitory effect of cholecystokinin on intake in sham-feeding rats.  |  Melville, LD., et al. 1992. Pharmacol Biochem Behav. 43: 975-7. PMID: 1448494
  4. Devazepide fails to reverse the inhibitory effect of interleukin-1beta on food intake in female rats.  |  Butera, PC., et al. 2004. Physiol Behav. 82: 777-83. PMID: 15451641
  5. Devazepide, a nonpeptide antagonist of CCK receptors, induces apoptosis and inhibits Ewing tumor growth.  |  Carrillo, J., et al. 2009. Anticancer Drugs. 20: 527-33. PMID: 19407653
  6. The cholecystokinin-1 receptor antagonist devazepide increases cholesterol cholelithogenesis in mice.  |  Wang, HH., et al. 2016. Eur J Clin Invest. 46: 158-69. PMID: 26683129
  7. Devazepide alters meal patterns in lean, but not obese, male Zucker rats.  |  Strohmayer, AJ. and Greenberg, D. 1994. Physiol Behav. 56: 1037-9. PMID: 7824568
  8. [Effect of cholecystokinin and its antagonists lorglumide, devazepide, and L-365,260 on gastrointestinal motility in rats].  |  Wang, SX. 1993. Zhongguo Yao Li Xue Bao. 14: 443-6. PMID: 8010038
  9. Devazepide reverses the anorexic effect of simmondsin in the rat.  |  Cokelaere, MM., et al. 1995. J Endocrinol. 147: 473-7. PMID: 8543917
  10. Devazepide increases food intake in male but not female Zucker rats.  |  Strohmayer, AJ. and Greenberg, D. 1996. Physiol Behav. 60: 273-5. PMID: 8804675
  11. Devazepide-induced hyperplasia in the rat liver and bile ducts.  |  Ohlsson, B., et al. 1996. Eur Surg Res. 28: 299-305. PMID: 8813655
  12. Devazepide (L-364718) inhibits growth and increases expression of tumor markers in HT29-S-B6 cells.  |  Forgue-Lafitte, ME., et al. 1996. C R Acad Sci III. 319: 1133-8. PMID: 9091185
  13. Devazepide attenuates dl-fenfluramine-induced suppression of gastric emptying but not food intake in the 17 h food-deprived rat.  |  Francis, J., et al. 1997. Physiol Behav. 62: 545-50. PMID: 9272662
  14. An evaluation of the influence of devazepide and CCK-8S on the intact and resected rat liver.  |  Ohlsson, B., et al. 1998. Eur Surg Res. 30: 378-84. PMID: 9838229

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Devazepide, 5 mg

sc-203562
5 mg
$245.00
US: Only available in the US

Devazepide, 50 mg

sc-203562A
50 mg
$1030.00
US: Only available in the US