MedKoo Cat#: 528102 | Name: RP-72540

Description:

WARNING: This product is for research use only, not for human or veterinary use.

RP-72540, also known as RPR-102681, is a cholecystokinin B receptor antagonist potentially for the treatment of cocaine abuse. RP 72540 showed selectivity factors in express of 200 for CCKB versus CCKA receptors and also had high affinity for gastrin binding sites in the stomach. Administration of RP-72540 resulted in a dose-dependent inhibition of [3H]pCCK-8 binding in mouse brain homogenate. However, the relative penetration of RP-72540 into the forebrain after peripheral administration was below 0.01%.

Chemical Structure

RP-72540
RP-72540
CAS#139088-45-2

Theoretical Analysis

MedKoo Cat#: 528102

Name: RP-72540

CAS#: 139088-45-2

Chemical Formula: C28H30N4O6

Exact Mass: 518.2165

Molecular Weight: 518.57

Elemental Analysis: C, 64.85; H, 5.83; N, 10.80; O, 18.51

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
RP-72540; RP 72540; RP72540; RPR-102681; RPR 102681; RPR102681
IUPAC/Chemical Name
2-(3-(3-(2-((3-methoxyphenyl)(2-(methyl(phenyl)amino)-2-oxoethyl)amino)-2-oxoethyl)ureido)phenyl)propanoic acid
InChi Key
ZDOYTKRSYALDTJ-UHFFFAOYSA-N
InChi Code
InChI=1S/C28H30N4O6/c1-19(27(35)36)20-9-7-10-21(15-20)30-28(37)29-17-25(33)32(23-13-8-14-24(16-23)38-3)18-26(34)31(2)22-11-5-4-6-12-22/h4-16,19H,17-18H2,1-3H3,(H,35,36)(H2,29,30,37)
SMILES Code
COC1=CC(N(C(CNC(NC2=CC(C(C(O)=O)C)=CC=C2)=O)=O)CC(N(C3=CC=CC=C3)C)=O)=CC=C1
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 518.57 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Bertrand P, Böhme GA, Durieux C, Guyon C, Capet M, Jeantaud B, Boudeau P, Ducos B, Pendley CE, Martin GE, et al. Pharmacological properties of ureido-acetamides, new potent and selective non-peptide CCKB/gastrin receptor antagonists. Eur J Pharmacol. 1994 Sep 12;262(3):233-45. PubMed PMID: 7813588. 2: Jensen RT. CCKB/gastrin receptor antagonists: recent advances and potential uses in gastric secretory disorders. Yale J Biol Med. 1996 May-Jun;69(3):245-59. Review. PubMed PMID: 9165693; PubMed Central PMCID: PMC2589015. 3: Bierkamp C, Kowalski-Chauvel A, Dehez S, Fourmy D, Pradayrol L, Seva C. Gastrin mediated cholecystokinin-2 receptor activation induces loss of cell adhesion and scattering in epithelial MDCK cells. Oncogene. 2002 Oct 31;21(50):7656-70. PubMed PMID: 12400008.