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CAS No 9011-97-6 , Cholecystokinin

  • Name: Cholecystokinin
  • Synonyms: 8066-00-0; 9001-71-2;Cholecystokinin;CCRIS 3307; 71710-32-2; LS-182690; 9012-22-0; 9011-97-6;
  • CAS Registry Number:
  • Safety Statements:
    WGK Germany 3
  • Molecular Weight: 3931.41904
  • InchiKey: QFLBZJPOIZFFJQ-UHFFFAOYSA-N
  • InChI: InChI=1S/C166H261N51O52S4/c1-15-84(9)130(159(261)211-116(78-220)154(256)
    206-110(68-125(227)228)150(252)191-97(38-27-54-182-165(176)177)139(241)
    205-112(70-127(231)232)152(254)215-132(88-42-44-91(45-43-88)269-273(266,
    267)268)161(263)197-100(48-58-270-12)135(237)185-75-124(226)190-106(64-
    89-72-184-94-35-21-20-33-92(89)94)146(248)195-101(49-59-271-13)141(243)
    204-111(69-126(229)230)151(253)198-103(133(173)235)63-87-31-18-17-19-32-
    87)213-143(245)98(39-28-55-183-166(178)179)192-147(249)107(65-90-73-180-
    80-187-90)201-153(255)115(77-219)210-157(259)119-41-30-57-217(119)163
    (265)113(71-128(233)234)207-145(247)105(62-82(5)6)200-149(251)109(67-122
    (172)224)203-140(242)99(46-47-120(170)222)193-144(246)104(61-81(3)4)199-
    148(250)108(66-121(171)223)202-138(240)96(36-23-25-52-168)196-158(260)
    129(83(7)8)212-160(262)131(85(10)16-2)214-155(257)117(79-221)208-142
    (244)102(50-60-272-14)194-137(239)95(37-26-53-181-164(174)175)189-123
    (225)74-186-136(238)114(76-218)209-156(258)118-40-29-56-216(118)162(264)
    86(11)188-134(236)93(169)34-22-24-51-167/h17-21,31-33,35,42-45,72-73,
    80-86,93,95-119,129-132,184,218-221H,15-16,22-30,34,36-41,46-71,74-79,
    167-169H2,1-14H3,(H2,170,222)(H2,171,223)(H2,172,224)(H2,173,235)(H,180,
    187)(H,185,237)(H,186,238)(H,188,236)(H,189,225)(H,190,226)(H,191,
    252)(H,192,249)(H,193,246)(H,194,239)(H,195,248)(H,196,260)(H,197,
    263)(H,198,253)(H,199,250)(H,200,251)(H,201,255)(H,202,240)(H,203,
    242)(H,204,243)(H,205,241)(H,206,256)(H,207,247)(H,208,244)(H,209,
    258)(H,210,259)(H,211,261)(H,212,262)(H,213,245)(H,214,257)(H,215,
    254)(H,227,228)(H,229,230)(H,231,232)(H,233,234)(H4,174,175,181)(H4,176,
    177,182)(H4,178,179,183)(H,266,267,268)
  • Molecular Formula: C166H261N51O52S4
  • Molecular Structure:CAS No:9011-97-6 Cholecystokinin

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9011-97-6 Cholecystokinin

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References of Cholecystokinin
Title: Cholecystokinin
CAS Registry Number: 9011-97-6
Synonyms: Pancreozymin; cholecystokinin-pancreozymin; CCK-PZ
Literature References: Polypeptide hormone found in the mammalian gastrointestinal tract and brain. Stimulates pancreatic exocrine secretion and growth. May also play a role in appetite satiation, pain perception, and neuronal transmission. First shown to cause gallbladder contraction: Ivy, Oldberg, Am. J. Physiol. 86, 599 (1928). Discovery of a substance, designated as pancreozymin, which promotes secretion of digestive enzymes by the pancreas: Harper, Raper, J. Physiol. (London) 102, 115 (1943). Identity with pancreozymin: Jorpes et al., Acta Chem. Scand. 18, 2408 (1964). The C-terminal pentapeptide has been shown to be identical to that of gastrin and caerulein: V. Mutt, J. E. Jorpes, Eur. J. Biochem. 6, 156 (1968); eidem, Biochem. J. 125, 57P (1971). Various biologically active, amino-truncated forms have been identified. Cholecystokinin consisting of 33 amino acids (CCK-33) is the predominant gastrointestinal form; CCK-39 and CCK-58 have also been identified. CCK-8 is the predominant CNS form. Identification of CCK in brain: J. J. Vanderhaeghen et al., Nature 257, 604 (1975); G. J. Dockray, ibid. 264, 568 (1976). Distribution and molecular heterogeneity: J. F. Rehfeld, J. Biol. Chem. 253, 4022 (1978). Synthesis of the C-terminal dodecapeptide: M. A. Ondetti et al., J. Am. Chem. Soc. 92, 195 (1970). Synthesis of the N-terminal hexapeptide of porcine CCK-33: Bodanszky et al., J. Org. Chem. 37, 2303 (1972). Cloning and nucleotide sequence of the human cholecystokinin gene: Y. Takahashi et al., Proc. Natl. Acad. Sci. USA 82, 1931 (1985). Total synthesis of porcine CCK-33: Y. Kurano, Chem. Commun. 1987, 323; of human CCK-33: N. Fujii et al., ibid. 1988, 324. Proposed role in suppression of food intake: M. A. Della-Fera, C. A. Baile, Science 206, 471 (1979); C. J. Savory, M. J. Gentle, Experientia 36, 1191 (1980); M. A. Della-Fera et al., Science 212, 687 (1981); in regulation of hypothalamic peptides: S. Itoh et al., Life Sci. 25, 1725 (1979); in modulation of catecholaminergic activity: K. Fuxe et al., Eur. J. Pharmacol. 67, 329 (1980). There is also evidence that CCK acts as a specific antagonist of opiate analgesia: P. L. Faris et al., Science 219, 310 (1983). Reviews: E. Straus, R. S. Yalow, Fed. Proc. 38, 2320-2324 (1979); V. Mutt, Biochem. Soc. Trans. 8, 11-14 (1980); idem, Vitam. Horm. 39, 231-426 (1982). Review of physiology: G. J. Dockray, Br. Med. Bull. 38, 253-258 (1982); of role in appetite satiation and pain perception: G. Stacher, Psychoneuroendocrinology 11, 39-48 (1986). Symposium on neuronal CCK: Ann. N.Y. Acad. Sci. 448, 1-697 (1985).
 
Derivative Type: C-Terminal octapeptide see Sincalide