4331-22-0

Basic information

• Product Name: VERSICOLORINB
• Synonyms: VERSICOLORINB;(3aR)-4,6,8-Trihydroxy-2,3,3aβ,12aβ-tetrahydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione;(3aR,12aS)-2,3,3a,12a-Tetrahydro-4,6,8-trihydroxyanthra[2,3-b]furo[3,2-d]furan-5,10-dione;(-)-2,3,3a,12a-Tetrahydro-4,6,8-trihydroxyanthra[2,3-b]furo[3,2-d]furan-5,10-dione;(3aS,12aR)-2,3,3a,12a-Tetrahydro-4,6,8-trihydroxyanthra[2,3-b]furo[3,2-d]furan-5,10-dione;4,6,8-Trihydroxy-2,3,3aα,5,10,12aα-hexahydroanthra[2,3-b]furo[3,2-d]furan-5,10-dione
• CAS NO: 4331-22-0
• Molecular Formula: C₁₈H₁₂O₇
• Molecular Weight: 340.286
• Mol File: 4331-22-0.mol

Chemical Properties

• Melting Point: 298°C (rough estimate)
• Boiling Point: 396.1°C (rough estimate)
• Appearance: /
• Density: 1.3361 (rough estimate)
• Refractive Index: 1.4790 (estimate)
• CAS DataBase Reference: VERSICOLORINB(CAS DataBase Reference)
• NIST Chemistry Reference: VERSICOLORINB(4331-22-0)
• EPA Substance Registry System: VERSICOLORINB(4331-22-0)

Safety Data

• Hazardous Substances Data: 4331-22-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
VERSICOLORINB is used as a pharmaceutical compound for its potential therapeutic properties. VERSICOLORINB's unique structure allows it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, VERSICOLORINB serves as a valuable compound for studying the properties and behavior of organic heteropentacyclic compounds. Its structure can provide insights into the design and synthesis of new molecules with similar or improved characteristics.
Used in Material Science:
VERSICOLORINB's unique molecular structure may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability or reactivity.
Used in Environmental Applications:
Due to its chemical properties, VERSICOLORINB may be utilized in environmental applications, such as in the development of new methods for pollutant detection or remediation.

Upstream product

• 67-56-1 methanol 

Relevant articles and documents

Quinofuracins A-E, produced by the fungus staphylotrichum boninense PF1444, show p53-dependent growth suppression

Quinofuracins A-E, novel anthraquinone derivatives containing β-d-galactofuranose that were isolated from the fungus Staphylotrichum boninense PF1444, induced p53-dependent cell death in human tumor cells. The structures of quinofuracins A-E, including absolute configurations, were elucidated by extensive spectroscopic analysis and chemical transformation studies. Quinofuracins were classified into three groups according to the aglycone moieties. 5'-Oxoaverantin was present in quinofuracins A-C, whereas averantin and versicolorin B were identified in quinofuracins D and E, respectively. These quinofuracins induced p53-dependent growth suppression in human glioblastoma LNZTA3 cells.