MedKoo Cat#: 528823 | Name: Itriglumide

Description:

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

Itriglumide is a CCK2 receptor antagonist potentially for the treatment of peptic ulcers, dyspepsia, and gastroesophageal reflux disease (GERD).

Chemical Structure

Itriglumide
Itriglumide
CAS#201605-51-8

Theoretical Analysis

MedKoo Cat#: 528823

Name: Itriglumide

CAS#: 201605-51-8

Chemical Formula: C33H38N2O4

Exact Mass: 526.2832

Molecular Weight: 526.68

Elemental Analysis: C, 75.26; H, 7.27; N, 5.32; O, 12.15

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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Related CAS #
No Data
Synonym
CR-2945; CR2945; CR 2945
IUPAC/Chemical Name
(R)-5-((2,4-dimethyl-6-(8-azaspiro[4.5]decane-8-carbonyl)phenyl)amino)-3-(naphthalen-1-yl)-5-oxopentanoic acid
InChi Key
MFOOVZCXWVAWOV-RUZDIDTESA-N
InChi Code
InChI=1S/C33H38N2O4/c1-22-18-23(2)31(28(19-22)32(39)35-16-14-33(15-17-35)12-5-6-13-33)34-29(36)20-25(21-30(37)38)27-11-7-9-24-8-3-4-10-26(24)27/h3-4,7-11,18-19,25H,5-6,12-17,20-21H2,1-2H3,(H,34,36)(H,37,38)/t25-/m1/s1
SMILES Code
O=C(O)C[C@H](C1=C2C=CC=CC2=CC=C1)CC(NC3=C(C)C=C(C)C=C3C(N(CC4)CCC54CCCC5)=O)=O
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 526.68 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: Ekström J, Cevik Aras H. Parasympathetic non-adrenergic, non-cholinergic transmission in rat parotid glands: effects of cholecystokinin-A and -B receptor antagonists on the secretory response. Regul Pept. 2008 Feb 7;146(1-3):278-84. Epub 2007 Oct 22. PubMed PMID: 18006087. 2: Danzer M, Jocic M, Samberger C, Painsipp E, Bock E, Pabst MA, Crailsheim K, Schicho R, Lippe IT, Holzer P. Stomach-brain communication by vagal afferents in response to luminal acid backdiffusion, gastrin, and gastric acid secretion. Am J Physiol Gastrointest Liver Physiol. 2004 Mar;286(3):G403-11. Epub 2003 Oct 30. PubMed PMID: 14592947. 3: Cevik Aras H, Ekström J. Pentagastrin-induced protein synthesis in the parotid gland of the anaesthetized rat, and its dependence on CCK-A and -B receptors and nitric oxide generation. Exp Physiol. 2006 Jul;91(4):673-9. Epub 2006 Mar 23. PubMed PMID: 16556659. 4: Aras HC, Ekström J. Cholecystokinin- and gastrin-induced protein and amylase secretion from the parotid gland of the anaesthetized rat. Regul Pept. 2006 May 15;134(2-3):89-96. Epub 2006 Mar 2. PubMed PMID: 16515811. 5: Lehmann F, Hildebrand P, Beglinger C. New molecular targets for treatment of peptic ulcer disease. Drugs. 2003;63(17):1785-97. Review. PubMed PMID: 12921485.