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| Product | Description | |
|---|---|---|
| Gastrin I (human) | Gastrin I (human) is an endogenous peptide produced by stomach and it acts as a selective CCK2 receptor agonist. Gastrin I stimulates gastric acid secretion in vivo, and increases levels of cytosolic calcium in isolated rabbit stomach parietal cells (EC50 = 11 nM). Group: Pharmaceutical. Alternative Names: Gastrin-17; Little gastrin I; Gastrin I human. CAS No. 10047-33-3. Pack Sizes: 2.5 mg. Product ID: BAT-006092. Molecular formula: C97H124N20O31S. Mole weight: 2098.2. Custom synthesis is available. Send your inquiries for more information. |  London |
| [Leu15]-Gastrin I (human) | A derivative of Gastrin I (human), an endogenous peptide produced by stomach and it acts as a selective CCK2 receptor agonist. Group: Pharmaceutical. Alternative Names: H-DL-Pyr-Gly-DL-Pro-DL-Trp-DL-Leu-DL-Glu-DL-Glu-DL-Glu-DL-Glu-DL-Glu-DL-Ala-DL-Tyr-Gly-DL-Trp-DL-Leu-DL-Asp-DL-Phe-NH2. CAS No. 39024-57-2. Pack Sizes: 5 mg. Product ID: BAT-006204. Molecular formula: C98H126N20O31. Mole weight: 2080.16. Custom synthesis is available. Send your inquiries for more information. | London |
| A 71378 | A 71378 is a high potency, selectivity CCK-A receptors agonist with the IC50 values of 0.4 nM, 300 nM, and 1,200 nM for the pancreatic CCK-A, cortical CCK-B, and gastrin receptor, respectively. Group: Pharmaceutical. Alternative Names: A-71378; Desamino-tyr(SO3H)-nle-gly-trp-nle-(N-methyl)asp-phe-NH2. CAS No. 127902-33-4. Pack Sizes: 1mg;1g;10g. Product ID: 127902-33-4. Molecular formula: C48H62N8O13S. Mole weight: 991.12. Custom synthesis is available. Send your inquiries for more information. | London |
| Antagonist G | Antagonist G is a substance P analog, which is a broad spectrum neuropeptide growth factor antagonist and antiproliferative agent. It was developed for the treatment of small cell lung cancer. It could inhibit neuropeptide-dependent and -independent proliferation of small cell lung cancer in vitro. It also inhibits growth of SCLC xenografts in mice in vivo. It blocks Swiss 3T3 cell growth induced by vasopressin, gastrin-releasing peptide and bradykinin. It activates JNK and stimulates apoptosis. It is an anticancer agent and is resistant to degradation by peptidases. Group: Pharmaceutical. Alternative Names: [Arg6,D-Trp7,9,N-MePhe8]-Substance P(6-11). CAS No. 115150-59-9. Pack Sizes: 1 mg. Product ID: BAT-006104. Molecular formula: C49H66N12O6S. Mole weight: 951.2. Custom synthesis is available. Send your inquiries for more information. | London |
| Bombesin | Bombesin is a neuropeptide with many biological effects such as hormone release, activation of pancreatic enzyme secretion, inhibition of gastric emptying and modulation of gastric acid secretion. It binds to the gastrin-releasing peptide receptor (GRPR) in rat pancreatic acinar cells (Ki = 1.88 nM), and also to frog bombesin receptor subtype 4 (BB4) in CHO cells overexpressing the receptor (Ki = 1.7 nM). Uses: Neurotransmitter agents. Group: Pharmaceutical. Alternative Names: H-Pyr-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2; L-pyroglutamyl-L-glutaminyl-L-arginyl-L-leucyl-glycyl-L-asparagyl-L-glutaminyl-L-tryptophyl-L-alanyl-L-valyl-glycyl-L-histidyl-L-leucyl-L-methioninamide; Glp-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val-Gly-His-Leu-Met-NH2. CAS No. 31362-50-2. Pack Sizes: 10 mg. Product ID: BAT-006169. Molecular formula: C71H110N24O18S. Mole weight: 1619.85. Custom synthesis is available. Send your inquiries for more information. | London |
| GRP (porcine) | GRP (porcine) is a mammalian bombesin-like peptide neurotransmitter that acts as an agonist for the gastrin-releasing peptide receptor (GRPR). It was shown to activate GABAergic interneurons in the amygdala resulting in an increase in GABA release and fear suppression in mice in vivo. Group: Pharmaceutical. Alternative Names: Gastrin Releasing Peptide porcine. CAS No. 74815-57-9. Pack Sizes: 10 mg. Product ID: B2693-032077. Molecular formula: C126H198N38O31S2. Mole weight: 2805.31. Custom synthesis is available. Send your inquiries for more information. | London |
| Z-360 | Z-360 is a selective and orally available 1,5-benzodiazepine-derivative gastrin/cholecystokinin 2 (CCK-2) receptor antagonist with potential antineoplastic activity. Z-360 binds to the gastrin/CCK-2 receptor, thereby preventing receptor activation by gastrin, a peptide hormone frequently associated with the proliferation of gastrointestinal and pancreatic tumor cells. Group: Pharmaceutical. Alternative Names: Z-360; Z 360; Z360; Nastorazepide; 3-[[(3R)-1-cyclohexyl-5-(3,3-dimethyl-2-oxobutyl)-4-oxo-2,3-dihydro-1,5-benzodiazepin-3-yl]carbamoylamino]benzoic acid. CAS No. 209219-38-5. Pack Sizes: 5 mg. Product ID: B0084-462248. Molecular formula: C29H36N4O5. Mole weight: 520.63. Custom synthesis is available. Send your inquiries for more information. | London |
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