The chemical substance known as "6H-2-Benzopyran-6-one, 5-chloro-7,8-dihydro-7-hydroxy-3-[(1E,3S,4R)-4-hydroxy-3-methyl-1-penten-1-yl]-7-methyl-8-[(3E)-3-methyl-2-oxo-3-penten-1-yl]-, (7S,8S)-" with CAS number 1319729-88-8 is a complex organic compound characterized by its multi-ring structure, which includes a benzopyran moiety. This compound features several functional groups, including hydroxyl (-OH) groups and a chloro (-Cl) substituent, contributing to its potential reactivity and biological activity. The presence of multiple chiral centers indicates that it may exist in different stereoisomeric forms, which can influence its pharmacological properties. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of bioactive agents. Its intricate arrangement of substituents may also impart unique physical and chemical properties, such as solubility and stability, which are critical for its use in various chemical and pharmaceutical applications. Further studies would be necessary to fully elucidate its properties and potential uses.

6H-2-Benzopyran-6-one, 5-chloro-7,8-dihydro-7-hydroxy-3-[(1E,3S,4R)-4-hydroxy-3-methyl-1-penten-1-yl]-7-methyl-8-[(3E)-3-methyl-2-oxo-3-penten-1-yl]-, (7S,8S)-

1319729-88-8: The chemical substance known as "6H-2-Benzopyran-6-one, 5-chloro-7,8-dihydro-7-hydroxy-3-[(1E,3S,4R)-4-hydroxy-3-methyl-1-penten-1-yl]-7-methyl-8-[(3E)-3-methyl-2-oxo-3-penten-1-yl]-, (7S,8S)-" with CAS number 1319729-88-8 is a complex organic compound characterized by its multi-ring structure, which includes a benzopyran moiety. This compound features several functional groups, including hydroxyl (-OH) groups and a chloro (-Cl) substituent, contributing to its potential reactivity and biological activity. The presence of multiple chiral centers indicates that it may exist in different stereoisomeric forms, which can influence its pharmacological properties. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of bioactive agents. Its intricate arrangement of substituents may also impart unique physical and chemical properties, such as solubility and stability, which are critical for its use in various chemical and pharmaceutical applications. Further studies would be necessary to fully elucidate its properties and potential uses.

<p>11-epi-Chaetomugilin I, from Chaetomium globosum, has cytotoxic effects against P388, HL-60, L1210 leukemia, and KB carcinoma cells.</p>

CAS 1319729-88-8

6H-2-Benzopyran-6-one, 5-chloro-7,8-dihydro-7-hydroxy-3-[(1E,3S,4R)-4-hydroxy-3-methyl-1-penten-1-yl]-7-methyl-8-[(3E)-3-methyl-2-oxo-3-penten-1-yl]-, (7S,8S)-

11-epi-Chaetomugilin I

Ref: TM-T75453