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Detail of "20994-83-6"

  • CAS Number:
  • 20994-83-6
  • Name:
  • Caerulein, 4-desulfo-

  • Molecular Structure:
  • Formula:
  • C58H73 N13 O18 S
  • Molecular Weight:
  • 1272.34
  • Synonyms:
  • Caerulein,4-de(hydrogen sulfate) (8CI); 4-Desulfocaerulein; Caerulein 1.1Y4 (Litoriacitropa); Desulfated caerulein; Desulfated ceruletide

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CAS No.20994-83-6 CAERULEIN (DESULFATED)

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Reference

The effects of gastrin and gastrin analogs on pancreatic acinar cell membrane potential and resistance
The effects of gastrin and gastrin analogs on pancreatic acinar cell membrane potential and resistance. Iwatsuki, N.; Kato, K.; Nishiyama, A. (Sch. Med., Yamagata Univ., Yamagata, Japan). Br. J. Pharmacol., 60(1), 147-54 (English) 1977. CODEN: BJPCBM. DOCUMENT TYPE: Journal CA Section: 2 (Hormone Pharmacology) Cholecystokinin-pancreozymin (I) [9011-97-6], gastrin [9002-76-0], caerulein [17650-98-5], and desulfated caerulein (II) [20994-83-6] stimulated mouse and rat pancreatic acinar cells, with immediate depolarization and a concommitant redn. in input resistance and time const. The depolarization was not abolished by atropine. The gastrin-type secretagog depolarization returned quickly to the resting level, but that evoked by the I-type group was long lasting. The time course and dose-response curve of II was identical with that of gastrin. The activity of gastrin was exerted by the C-terminal tetrapeptide, but caerulein activity depended on the C-terminal heptapeptide, esp. the sulfated tyrosyl residue at position 7. The equiv. sulfated tyrosyl residue in I was probably necessary for max. activity. The relative potencies were caerulein > I > gastrin. Synthetic gastrin was more effective than either tetra- or pentagastrin.
Regulation of the dissociation of [3H]-caerulein from its pancreatic receptors: evidence for negative cooperativity
Regulation of the dissociation of [3H]-caerulein from its pancreatic receptors: evidence for negative cooperativity. Deschodt-Lanckman, Monique; Svoboda, Michal; Camus, Jean C.; Robberecht, Patrick (Fac. Med., Univ. Libre Bruxelles, Brussels, Belg.). INSERM Symp., 3(Horm. Recept. Dig. Tract Physiol., Proc. Int. Symp., 1st), 325-6 (English) 1977. CODEN: INSSDM. DOCUMENT TYPE: Journal CA Section: 2 (Hormone Pharmacology) The rate of dissocn. of 3H-labeled caerulein [17650-98-5] from pancreatic membrane receptors was accelerated in the presence of unlabeled caerulein. Similar effects were caused by pancreozymin C-terminal octapeptide [25126-32-3], BOC-(norleucine8)-(4-10)-caerulein [29129-57-5], desulfated caerulein [20994-83-6], and (11-17)heptagastrin I [30626-80-3]; with their efficiency being proportional to their binding affinities.
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