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Fasidotril CAS NO 135038-57-2


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CAS No.:135038-57-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Fasidotril is a dual-acting vasopeptidase inhibitor, representing a significant class of compounds in cardiovascular research. Its primary value lies in its ability to simultaneously inhibit both angiotensin-converting enzyme (ACE) and neutral endopeptidase (NEP), offering a unique mechanism for modulating blood pressure and cardiovascular function. This high-purity intermediate is essential for pharmaceutical R&D teams and manufacturers developing next-generation therapeutic agents for hypertension and heart failure.

Application

  • Pharmaceutical Intermediate: Critical raw material for the synthesis of advanced cardiovascular drug candidates.
  • Biochemical Research: Used as a reference standard and tool compound in studies of the renin-angiotensin-aldosterone system (RAAS) and natriuretic peptide system.
  • Mechanism of Action Studies: Employed in preclinical research to investigate the dual inhibition of ACE and NEP enzymes.
  • Process Development: Serves as a key building block in the scale-up and optimization of API (Active Pharmaceutical Ingredient) manufacturing processes.
  • Analytical Standard: Used for method development, validation, and quality control (HPLC, LC-MS) in analytical laboratories.

Basic Information

Product Name Fasidotril
CAS No. 135038-57-2
Molecular Formula C20H28N2O5S
Molecular Weight 408.51 g/mol
Synonyms Fasidotril; (2R,4R)-4-[[(2S)-3-Mercapto-2-methyl-1-oxopropyl]amino]-5-oxo-2-[[(phenylmethoxy)carbonyl]amino]-N,1-pentanedihydroxamic acid; BMS-186716; S 21402; Dual NEP/ACE inhibitor; Vasopeptidase inhibitor; N-(2-Carboxy-1-oxo-3-phenylpropyl)-L-alanyl-L-tyrosine
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Quality Control

Our Fasidotril is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research and development purposes. We provide comprehensive analytical data to support your regulatory and process requirements. A detailed Certificate of Analysis (COA), including purity by HPLC, identification (IR, NMR), and impurity profile, is supplied with each batch and available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation. For long-term storage, consider desiccated conditions.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.