Cholecystokinin (26-33), CCK8, Non-Sulfated CCK-8

Cholecystokinin (26-33), CCK8, Non-Sulfated CCK-8

For laboratory research purposes only. Not for human or veterinary use.

Cas No: 25679-24-7

Purity: ≥ 95%

Chemical Formula: C49H62N10O13S2

CAT.NO: P400541

Categories: , ,

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Description

Product Name: Cholecystokinin (26-33), CCK8, Non-Sulfated CCK-8

Sequence One Letter Code: DYMGWMDF-NH2

Sequence Three Letter Code: H-Asp-Tyr-Met-Gly-Trp-Met-Asp-Phe-NH2

Cas No: 25679-24-7

Chemical Formula:C49H62N10O13S2

Molecular Weight: 1063.3

Purity: ≥ 95%

Form: Lyophilized

Storage Conditions: - 20 °C

SMILES: CSCC[C@@H](C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)C(=O)[C@H](CC(=O)O)N)NC(=O)CNC(=O)[C@H](CC2=CNC3=CC=CC=C32)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC4=CC=CC=C4)NN

IUPAC: (3S,6S)-3-amino-6-[[(2S)-2-[[2-[[(2S)-2-[[(2S)-2-[[(2S)-3-carboxy-2-[[(2S)-2-hydrazinyl-3-phenylpropanoyl]amino]propanoyl]amino]-4-methylsulfanylbutanoyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]acetyl]amino]-4-methylsulfanylbutanoyl]amino]-7-(4-hydroxyphenyl)-4,5-dioxoheptanoic acid

INCHIKEY: ZBTPHEHKAHBSMT-YRVFCXMDSA-N

INCHI:

InChI=1S/C49H62N10O13S2/c1-73-18-16-34(46(69)56-36(20-28-12-14-30(60)15-13-28)44(67)43(66)32(50)23-41(62)63)54-40(61)26-53-45(68)37(22-29-25-52-33-11-7-6-10-31(29)33)57-47(70)35(17-19-74-2)55-48(71)38(24-42(64)65)58-49(72)39(59-51)21-27-8-4-3-5-9-27/h3-15,25,32,34-39,52,59-60H,16-24,26,50-51H2,1-2H3,(H,53,68)(H,54,61)(H,55,71)(H,56,69)(H,57,70)(H,58,72)(H,62,63)(H,64,65)/t32-,34-,35-,36-,37-,38-,39-/m0/s1

Source / Species: Human, mouse, rat, pig

Conjugation: Unconjugated

Code Nacres: NA.26

Application: Non-sulfated CCK-8 is an octapeptide fragment of cholecystokinin, an important gastrointestinal hormone and neuropeptide involved in digestion, satiety, and gut–brain signaling. CCK regulates pancreatic enzyme secretion, gallbladder contraction, and central appetite control. Although sulfation enhances receptor affinity, the non-sulfated CCK-8 form remains valuable for studying receptor subtype selectivity, peptide–receptor interactions, and signaling dynamics. This peptide is commonly used in neuroscience research, metabolism studies, appetite regulation models, gastrointestinal physiology, and investigations of endocrine communication between the digestive system and central nervous system. 

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