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ICI 216,140 (CAS 124001-41-8)

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Alternate Names:
(CH3)2CHCO-His-Trp-Ala-Val-D-Ala-His-Leu-NHCH3
Application:
ICI 216,140 is an effective antagonist of the bombesin/gastrin releasing peptide
CAS Number:
124001-41-8
Purity:
≥95%
Molecular Weight:
916.09
Molecular Formula:
C45H65N13O8
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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ICI 216,140, a selective antagonist of the angiotensin II type 1 (AT1) receptor, has been extensively studied in scientific research for its role in elucidating the renin-angiotensin system (RAS) and its involvement in cardiovascular physiology. By competitively binding to the AT1 receptor, ICI 216,140 effectively blocks the actions of angiotensin II, a key regulator of blood pressure, vascular tone, and fluid-electrolyte balance. Through detailed investigations, researchers have unveiled the signaling pathways modulated by the AT1 receptor and its implications in hypertension, cardiac hypertrophy, and renal function. Additionally, studies utilizing ICI 216,140 have contributed to our understanding of the physiological and pathophysiological roles of angiotensin II in various organ systems, highlighting its significance in cardiovascular homeostasis. Furthermore, the development and refinement of ICI 216,140 as a research tool have paved the way for exploring novel strategies targeting the renin-angiotensin system for the management of cardiovascular diseases. Overall, ICI 216,140 serves as a valuable pharmacological tool in unraveling the complexities of angiotensin II signaling and its potential implications in cardiovascular research.


ICI 216,140 (CAS 124001-41-8) References

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  2. Therapeutic potential of growth factors and their antagonists.  |  Garner, A. 1992. Yale J Biol Med. 65: 715-23; dscussion 737-40. PMID: 1341074
  3. Gastrin-releasing peptide/neuromedin B receptor antagonists PD176252, PD168368, and related analogs are potent agonists of human formyl-peptide receptors.  |  Schepetkin, IA., et al. 2011. Mol Pharmacol. 79: 77-90. PMID: 20943772
  4. N-isobutyryl-His-Trp-Ala-Val-D-Ala-His-Leu-NHMe (ICI 216140) a potent in vivo antaconist analogue of bombesin/gastrin releasing peptide (BN/GRP) derived from the C-terminal sequence lacking the final methionine residue.  |  Camble, R., et al. 1989. Life Sci. 45: 1521-7. PMID: 2555638
  5. Effect of gastrointestinal hormones and synthetic analogues on the growth of pancreatic cancer.  |  Robertson, JF., et al. 1995. Int J Cancer. 63: 69-75. PMID: 7558455
  6. Pharmacological analysis of receptors for bombesin-related peptides on guinea pig gallbladder smooth muscle.  |  Parkman, HP., et al. 1994. Regul Pept. 52: 173-80. PMID: 7800849
  7. Potent gastrin-releasing peptide (GRP) antagonists derived from GRP (19-27) with a C-terminal DPro psi [CH2NH]Phe-NH2 and N-terminal aromatic residues.  |  Leban, JJ., et al. 1994. J Med Chem. 37: 439-45. PMID: 8120863
  8. Two bombesin analogues discriminate between neuromedin B- and bombesin-induced calcium flux in a lung cancer cell line.  |  Ryan, RR., et al. 1993. Peptides. 14: 1231-5. PMID: 8134305
  9. Pharmacological profiles of two bombesin analogues in cells transfected with human neuromedin B receptors.  |  Ryan, RR., et al. 1996. Eur J Pharmacol. 306: 307-14. PMID: 8813645
  10. Peripheral bombesin induces gastric vagal afferent activation in rats.  |  Yoshida-Yoneda, E., et al. 1996. Am J Physiol. 271: R1584-93. PMID: 8997356

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

ICI 216,140, 1 mg

sc-361211
1 mg
$369.00