Description

Mitemcinal is a synthetic motilin receptor agonist, a compound of significant interest in pharmaceutical research and development. Its primary value lies in its potential to stimulate gastrointestinal motility, making it a key candidate for therapeutic applications. This product is essential for researchers and manufacturers in the pharmaceutical industry, particularly those focused on developing prokinetic agents for treating gastric motility disorders. Mitemcinal CAS NO 154738-42-8 is supplied as a high-purity reference standard and active pharmaceutical ingredient (API) intermediate.

Application

• Pharmaceutical Research & Development: Serves as a critical reference standard and building block in the discovery and development of novel gastroprokinetic drugs.
• Active Pharmaceutical Ingredient (API) Synthesis: Used as a key intermediate in the chemical synthesis of motilin receptor agonist drug candidates.
• Preclinical Studies: Employed in in vitro and in vivo studies to investigate mechanisms of gastric emptying and intestinal motility.
• Analytical Method Development: Utilized as a pure standard for developing and validating HPLC, LC-MS, and other analytical methods for quality control.
• Metabolism and Pharmacokinetics (DMPK) Studies: Acts as a substrate in studies to understand the absorption, distribution, metabolism, and excretion (ADME) profiles of related compounds.

Basic Information

Product Name	Mitemcinal
CAS No.	154738-42-8
Molecular Formula	C32H38N4O4S
Molecular Weight	574.73 g/mol
Synonyms	GM-611; Mitemcinalum; (2S)-N-[(3S,4R)-1-[(2S)-2-[(Methoxycarbonyl)amino]-3-methylbutanoyl]-4-(2-methylpropyl)-2-oxo-3-pyrrolidinyl]-2-[(methylsulfonyl)amino]-3-phenylpropanamide; 3-Phenyl-2-[[(methylsulfonyl)amino]methyl]-N-[(3S,4R)-1-[(2S)-2-[[(methoxycarbonyl)amino]-3-methyl-1-oxobutyl]-4-(2-methylpropyl)-2-oxo-3-pyrrolidinyl]propanamide; Motilin Receptor Agonist GM-611
EINECS	Contact for details

Quality Control

Our Mitemcinal is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and support regulatory filings with detailed documentation. Certificates of Analysis (COA) are available for every lot, confirming compliance with specifications. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability. Keep the container tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤0.5%
Heavy Metals	≤20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.