The chemical substance with the name "(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-3-methyl-6-[(4aS,7aR)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yloxy]tetrahydro-2H-pyran-2,3,4,5-tetrol" and CAS number "83889-88-7" is a complex organic compound characterized by multiple stereocenters, indicating its chiral nature. It features a tetrahydropyran core, which is a six-membered ring containing oxygen, and is substituted with various functional groups, including hydroxymethyl and methyl groups. The presence of multiple hydroxyl (-OH) groups suggests that it is a polyol, which can influence its solubility and reactivity. The compound's structure includes a cyclopentane moiety, contributing to its overall three-dimensional conformation and potentially affecting its biological activity. Such compounds often exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The specific stereochemistry and functional groups can significantly impact the compound's interactions with biological systems, including enzyme binding and receptor activity.

(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-3-methyl-6-[(4aS,7aR)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yloxy]tetrahydro-2H-pyran-2,3,4,5-tetrol (non-preferred name)

83889-88-7: The chemical substance with the name "(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-3-methyl-6-[(4aS,7aR)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yloxy]tetrahydro-2H-pyran-2,3,4,5-tetrol" and CAS number "83889-88-7" is a complex organic compound characterized by multiple stereocenters, indicating its chiral nature. It features a tetrahydropyran core, which is a six-membered ring containing oxygen, and is substituted with various functional groups, including hydroxymethyl and methyl groups. The presence of multiple hydroxyl (-OH) groups suggests that it is a polyol, which can influence its solubility and reactivity. The compound's structure includes a cyclopentane moiety, contributing to its overall three-dimensional conformation and potentially affecting its biological activity. Such compounds often exhibit interesting pharmacological properties, making them of interest in medicinal chemistry. The specific stereochemistry and functional groups can significantly impact the compound's interactions with biological systems, including enzyme binding and receptor activity.

<p>Loasaside is an iridoid glycoside.</p>

CAS 83889-88-7

(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-3-methyl-6-[(4aS,7aR)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-1-yloxy]tetrahydro-2H-pyran-2,3,4,5-tetrol (non-preferred name)

Loasaside

Ref: TM-T32831