Description

Flavoviridomycin is a specialized antibiotic compound belonging to the pyrrolo[1,4]benzodiazepine family, identified by CAS NO 51668-32-7. This product is valued for its potent biological activity, making it a critical intermediate and research tool in the development of novel therapeutic agents. It is primarily utilized by pharmaceutical R&D departments, biotechnology firms, and academic research institutions focused on microbiology, oncology, and infectious disease studies.

Application

• Pharmaceutical Research & Development: Serves as a key reference standard and active pharmaceutical ingredient (API) intermediate in the discovery of new antibiotics and anticancer drugs.
• Microbiological Studies: Used as a selective agent in research to study bacterial resistance mechanisms and to screen for novel antimicrobial compounds.
• Biochemical Assay Development: Employed in the development and validation of high-throughput screening assays and analytical methods (e.g., HPLC, LC-MS) for potency testing.
• Academic Research: A vital tool for university and institutional labs investigating the structure-activity relationships (SAR) of DNA-binding antibiotics.
• Standards and Controls: Provides a certified reference material for quality control laboratories ensuring the accuracy and consistency of analytical results.

Basic Information

Product Name	Flavoviridomycin
CAS No.	51668-32-7
Molecular Formula	C27H25N3O7
Molecular Weight	503.51 g/mol
Synonyms	Antibiotic DC 92-B; DC 92-B; Flavoviridomycin A; NSC 324553; Pyrrolo[1,4]benzodiazepine antibiotic; 5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one, 7-[(2S)-1,2,3,4-tetrahydro-6,7,8-trimethoxy-2-methyl-1-isoquinolinyl]-; (S)-7-(1,2,3,4-Tetrahydro-6,7,8-trimethoxy-2-methylisoquinolin-1-yl)-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one
EINECS	Contact for details

Quality Control

Our Flavoviridomycin is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identification by spectroscopic methods (IR, NMR), purity assessment by HPLC, and determination of residual solvents and moisture content. A Certificate of Analysis (COA) detailing all test results and specifications is provided with every shipment to ensure traceability and compliance with your research or production standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a desiccated environment to maintain stability and potency.

Specification

Item	Specification
Appearance	Yellow to brownish-yellow powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 3.0%
Residual Solvents (GC)	Meets ICH guidelines
Heavy Metals	≤ 20 ppm

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