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CI-1015

  Cat. No.:  DC76508  
Chemical Structure
156672-01-4
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More than 5000 active chemicals with high quality for research!
Field of application
CI-1015 is a potent CCK-B receptor antagonist.
Cas No.: 156672-01-4
Chemical Name: CI-1015
SMILES: O=C(N[C@@](C)(C(N[C@@H]1[C@H](CCCC1)O)=O)CC2=CNC3=C2C=CC=C3)OC45CC6CC(CC(C5)C6)C4
Formula: C29H39N3O4
M.Wt: 493.64
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
MSDS
Cat. No. Product name Field of application
DC28153 Proglumide sodium Proglumide sodium is a nonpeptide and orally active cholecystokinin (CCK)-A/B receptors antagonist. Proglumide sodium selective blocks CCK’s effects in the central nervous system (CNS). Proglumide sodium has ability to inhibit gastric secretion and to protect the gastroduodenal mucosa. Proglumide sodium also has antiepileptic and antioxidant activities.
DC76509 Sut-8701 Sut-8701 is a Cholecystokinin analog that effectively slows the degenerative process of Alzheimer's disease by protecting the integrity of cholinergic neurons in the nucleus basalis.
DC76508 CI-1015 CI-1015 is a potent CCK-B receptor antagonist.
DC76507 A-70874 A-70874 is a tyrosine-free tetrapeptide analog of cholecystokinin (30-33) (CCK-4). A-70874 is an agonist that stimulates pancreatic amylase release and a partial agonist that stimulates pancreatic phosphoinositide decomposition. A-70874 has an IC50 of 4.9 nM for the guinea pig pancreatic CCK receptor. Cholecystokinin (CCK) receptors are divided into CCK-A (digestive tract) and CCK-B (brain). A-70874 has an affinity of 1.6 μM for the CCK-B/gastrin receptor.
DC72187 L-365260 hemihydrate L-365260 hemihydrate is an orally active and selective antagonist of non-peptide gastrin and brain cholecystokinin receptor (CCK-B), with Kis of 1.9 nM and 2.0 nM, respectively. L-365260 hemihydrate interacts in a stereoselective and competitive manner with guinea pig stomach gastrin and brain CCK receptors. L-365260 hemihydrate can enhance Morphine analgesia and prevents Morphine tolerance.
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