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Merck
CN

B1636

五肽胃泌素

≥95% (HPLC), powder, CCK2 receptor agonist

别名:

五肽促胃酸激素, 五肽胃泌素, N-t-Boc-β-Ala-Trp-Met-Asp-Phe酰胺

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关于此项目

经验公式(希尔记法):
C37H49N7O9S
化学文摘社编号:
分子量:
767.89
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
226-889-7
MDL number:
Assay:
≥95% (HPLC)
Form:
powder
Quality level:
Storage condition:
(Keep container tightly closed in a dry and well-ventilated place.)
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产品名称

五肽胃泌素, ≥95% (HPLC), powder

Quality Level

assay

≥95% (HPLC)

form

powder

storage condition

(Keep container tightly closed in a dry and well-ventilated place.)

color

white to off-white

solubility

DMF: 20 mg/mL, clear, colorless to faint yellow or tan

storage temp.

−20°C

SMILES string

CSCCC(NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CCNC(=O)OC(C)(C)C)C(=O)NC(CC(O)=O)C(=O)NC(Cc3ccccc3)C(N)=O

InChI

1S/C37H49N7O9S/c1-37(2,3)53-36(52)39-16-14-30(45)41-28(19-23-21-40-25-13-9-8-12-24(23)25)34(50)42-26(15-17-54-4)33(49)44-29(20-31(46)47)35(51)43-27(32(38)48)18-22-10-6-5-7-11-22/h5-13,21,26-29,40H,14-20H2,1-4H3,(H2,38,48)(H,39,52)(H,41,45)(H,42,50)(H,43,51)(H,44,49)(H,46,47)

InChI key

NEYNJQRKHLUJRU-UHFFFAOYSA-N

Gene Information

General description

适合研究领域:免疫学 & 细胞因子

Application

五肽胃泌素已被用于双向调节杏仁核外侧核(LA)的活力。在AR42J大鼠胰腺细胞系中,可阻断胆囊收缩素2受体(CCK2R)激动剂抑制受体与Ga-DOTA-MGS5的结合,进行细胞摄取和受体结合研究。

Biochem/physiol Actions

五肽胃泌素为人工合成的胃泌素类似物,肽链羧基末端五肽的结构与天然胃泌素一样。可作为胆囊收缩素-2(CCK2)受体/胆囊收缩素-B(CCKB)受体的激动剂。五肽胃泌素可促进胃蛋白酶和胃酸分泌,适合用于胃酸分泌功能检查。五肽胃泌素具有惊恐和焦虑作用,会导致惊恐症(PD)患者的惊恐发作。


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存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Y Keto et al.
Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society, 24(2), 147-153 (2011-11-10)
Gastroduodenal acidification has been reported to aggravate upper abdominal discomfort and pain that are symptoms suffered by functional dyspepsia (FD) patients. Delayed gastric emptying and hypersensitivity to gastric distension (GD) contribute importantly to the pathophysiology of FD. In the present
L Singh et al.
Proceedings of the National Academy of Sciences of the United States of America, 88(4), 1130-1133 (1991-02-15)
The effect of neuropeptide cholecystokinin (CCK) receptor agonists and antagonists was examined in the rat elevated X-maze model of anxiety. The selective CCK-B receptor antagonists CI-988 (PD 134308) and L-365,260 produced anxiolytic-like effects, whereas MK-329, a CCK-A receptor antagonist, was
T D Barrett et al.
British journal of pharmacology, 166(5), 1684-1693 (2012-02-04)
JNJ-26070109 [(R)4-bromo-N-[1-(2,4-difluoro-phenyl)-ethyl]-2-(quinoxaline-5-sulfonylamino)-benzamide] is a novel antagonist at cholecystokinin CCK(2) receptors with good pharmacokinetic properties and represents a novel mechanism for the treatment of gastro-oesophageal reflux disease (GORD). The purpose of the present study was to determine whether chronic treatment with



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货号GTIN
B1636-100MG04061832674551
B1636-25MG04061833426265