74045-97-9

Usage

Uses

Used in Pharmaceutical Industry:
Psorospermin is used as a pharmaceutical agent for its potential therapeutic properties. The specific reasons for its use in this industry are not provided in the materials, but its unique molecular structure suggests that it may have bioactive properties that could be harnessed for medicinal purposes.
Used in Chemical Research:
In the field of chemical research, psorospermin is used as a subject of study for its unique heterotetracyclic structure. Researchers may investigate its chemical properties, potential reactions, and interactions with other compounds to expand the understanding of organic chemistry and potentially discover new applications.
Used in Material Science:
Psorospermin's distinct molecular structure may also find use in material science, where it could be employed as a component in the development of new materials with specific properties. The exact application reason is not provided in the materials, but the compound's unique features suggest potential uses in creating advanced materials with tailored characteristics.

InChI:InChI=1/C19H16O6/c1-19(8-23-19)14-6-10-12(24-14)7-13(22-2)15-16(21)9-4-3-5-11(20)17(9)25-18(10)15/h3-5,7,14,20H,6,8H2,1-2H3/t14-,19-/m1/s1

Upstream product

• 106212-05-9 3',4'-deoxypsorospermin-3',4'-diol 
• 667885-51-0 4-(3,5-bis-benzyloxy-1-methoxy-9-oxo-9H-xanthen-4-yl)-2-methyl-but-2-enoic acid methyl ester 
• 667885-52-1 3,5-Bis-benzyloxy-4-((Z)-4-hydroxy-3-methyl-but-2-enyl)-1-methoxy-xanthen-9-one 
• 667885-53-2 3,5-Bis-benzyloxy-4-((2S,3R)-3-hydroxymethyl-3-methyl-oxiranylmethyl)-1-methoxy-xanthen-9-one 
• 667885-49-6 4-allyl-3,5-bis-benzyloxy-1-methoxy-xanthen-9-one 
• 667885-48-5 4-allyl-3,5-bis-benzyloxy-1-hydroxy-xanthen-9-one 
• 667885-50-9 (3,5-bis-benzyloxy-1-methoxy-9-oxo-9H-xanthen-4-yl)-acetaldehyde 
• 667885-47-4 4-allyl-1,3,5-trihydroxy-xanthen-9-one 
• 106092-49-3 3-(allyloxy)-1,5-dimethoxyxanthone 
• 106092-50-6 4-allyl-1,5-dimethoxy-3-hydroxyxanthone 
• 106092-47-1 3-(allyloxy)-1-hydroxy-5-methoxyxanthone 
• 6563-47-9 1,3-dihydroxy-5-methoxy-9H-xanthen-9-one 
• 1521-38-6 2,3-dimethoxybenzoic acid 
• 108-73-6 3,5-dihydroxyphenol 

Downstream Products

• 74046-00-7 3',4'-deoxy-4'-chloropsorospermin-3'-ol 

Relevant academic research and scientific papers

PSOROSPERMIN AND ANALOGUES

Methods of making chiral psorospermin or its analogues and/or intermediates thereof are provided.

Total synthesis of psorospermin

The xanthone natural product psorospermin was synthesized in 13 steps with an overall yield of 1.7%. This compound shows potent antineoplastic activity in a variety of cancer cell lines.