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CCK-4_1947-37-1_产品详情
1947-37-1
  • names:

    CCK-4, CCKB receptor agonist

  • CAS号:

    1947-37-1

    MDL Number:
  • MF(分子式): C29H36N6O6S MW(分子量): 596.7
  • EINECS: Reaxys Number:
  • Pubchem ID:446569 Brand:BIOFOUNT
CCK-4
CCK-4, CCKB receptor agonist(1947-37-1)是一种选择性胆囊收缩素 B (CCKB) 受体激动剂,可以增加肥大细胞的分泌活性。CCK-4是一种焦虑剂,在体内和体外都有活性。
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中文别名 CCK-4(1947-37-1);CCKB受体激动剂
英文别名 CCK-4, CCKB receptor agonist(1947-37-1);Tetragastrin; Gastrin tetrapeptide; Cholecystokinin tetrapeptide;
CAS号 1947-37-1
Inchi InChI=1S/C29H36N6O6S/c1-42-12-11-22(33-27(39)20(30)14-18-16-32-21-10-6-5-9-19(18)21)28(40)35-24(15-25(36)37)29(41)34-23(26(31)38)13-17-7-3-2-4-8-17/h2-10,16,20,22-24,32H,11-15,30H2,1H3,(H2,31,38)(H,33,39)(H,34,41)(H,35,40)(H,36,37)/t20-,22-,23-,24-/m0/s1
InchiKey RGYLYUZOGHTBRF-BIHRQFPBSA-N
分子式 Formula C29H36N6O6S
分子量 Molecular Weight 596.7
溶解度Solubility
性状 Solid powder
储藏条件 Storage conditions Store at -20°C. Store under desiccating conditions.
产品说明 CCK-4, CCKB receptor agonist(1947-37-1)是一种选择性胆囊收缩素 B (CCKB) 受体激动剂,可以增加肥大细胞的分泌活性。CCK-4是一种焦虑剂,在体内和体外都有活性。
IntroductionTetragastrin(1947-37-1) is the C-terminal tetrapeptide of gastrin. It is the smallest peptide fragment of gastrin which has the same physiological and pharmacological activity as gastrin.
Application1
Application2
Application3
[1]Tenma T, Yodoya E, Tashima S, Fujita T, Murakami M, Yamamoto A, Muranishi S. Development of new lipophilic derivatives of tetragastrin: physicochemical characteristics and intestinal absorption of acyl-tetragastrin derivatives in rats. Pharm Res. 1993 Oct;10(10):1488-92. PubMed PMID: 8272412.
[2]Komuro Y, Ishihara K, Ohara S, Saigenji K, Hotta K. Effects of tetragastrin on mucus glycoprotein in rat gastric mucosal protection. Gastroenterol Jpn. 1992 Oct;27(5):597-603. PubMed PMID: 1385248.
[3] Tatsuta M, Iishi H, Yamamura H, Taniguchi H. Inhibition by tetragastrin of experimental carcinogenesis in rat colon: effect of wheat bran consumption. Int J Cancer. 1988 Feb 15;41(2):239-42. PubMed PMID: 2828245.
[4] Tatsuta M, Iishi H, Baba M, Taniguchi H. Effect of 6-hydroxydopamine on gastric carcinogenesis and tetragastrin inhibition of gastric carcinogenesis induced by N-methyl-N'-nitro-N-nitrosoguanidine in Wistar rats. Cancer Res. 1989 Aug 1;49(15):4199-203. PubMed PMID: 2501024.
[5] Tatsuta M, Iishi H, Yamamura H, Taniguchi H. Enhancement by propranolol of the inhibitory effect of tetragastrin on gastric carcinogenesis induced by N-methyl-N'-nitro-N-nitrosoguanidine in Wistar rats. Cancer Res. 1987 Jan 1;47(1):111-4. PubMed PMID: 3791197.
6: Setoh K, Murakami M, Araki N, Fujita T, Yamamoto A, Muranishi S. Improvement of transdermal delivery of tetragastrin by lipophilic modification with fatty acids. J Pharm Pharmacol. 1995 Oct;47(10):808-11. PubMed PMID: 8583347.7: Komuro Y, Ishihara K, Kojima Y, Saigenji K, Hotta K. Distinct effects of tetragastrin in rat gastroduodenal mucosa on mucin content and mucosal protective action against histamine-induced injury. Dig Dis Sci. 1998 May;43(5):1050-6. PubMed PMID: 9590421.8: Tatsuta M, Yamamura H, Baba M, Yamamoto R, Iishi H, Taniguchi H. Inhibitory effect of prolonged administration of tetragastrin on experimentally induced intestinal metaplasia in Wistar rats. Cancer. 1988 May 15;61(10):2051-6. PubMed PMID: 3359403.9: Tatsuta M, Iishi H, Yamamura H, Yamamoto R, Taniguchi H. Enhancement by tetragastrin of experimental induction of gastric epithelium in the duodenum. Gut. 1989 Mar;30(3):311-5. PubMed PMID: 2707631; PubMed Central PMCID: PMC1378451.10: Tatsuta M, Iishi H, Baba M, Taniguchi H. Effect of ornithine decarboxylase inhibitor on tetragastrin treatment of gastric carcinogenesis induced by N-methyl-N'-nitro-N-nitrosoguanidine in Wistar rats. Int J Cancer. 1990 Feb 15;45(2):308-11. PubMed PMID: 2105911.1
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