1,3-Cyclohexanediol, 2-methylene-5-[(2E)-2-[(1R,3aS,7aR)-octahydro-1-[(1S)-5-hydroxy-1,5-dimethylhexyl]-7a-methyl-4H-inden-4-ylidene]ethylidene]-(1R,3R)- is a complex organic compound characterized by its bicyclic structure and multiple functional groups, including hydroxyl (-OH) groups and a methylene bridge. This compound features a cyclohexane ring, which contributes to its stability and potential for various chemical interactions. The presence of stereocenters indicates that it can exist in multiple stereoisomeric forms, which may influence its biological activity and reactivity. The compound's intricate structure suggests potential applications in fields such as pharmaceuticals, where stereochemistry plays a crucial role in drug efficacy. Additionally, the presence of hydrophobic and hydrophilic regions may affect its solubility and interaction with biological membranes. Overall, this compound exemplifies the complexity often found in organic chemistry, particularly in the design of molecules with specific functional properties.

1,?3-?Cyclohexanediol, 2-?methylene-?5-?[(2E)?-?2-?[(1R,?3aS,?7aR)?-?octahydro-?1-?[(1S)?-?5-?hydroxy-?1,?5-?dimethylhexyl]?-?7a-?methyl-?4H-?inden-?4-?ylidene]?ethylidene]?-?, (1R,?3R)?-

213250-70-5: 1,3-Cyclohexanediol, 2-methylene-5-[(2E)-2-[(1R,3aS,7aR)-octahydro-1-[(1S)-5-hydroxy-1,5-dimethylhexyl]-7a-methyl-4H-inden-4-ylidene]ethylidene]-(1R,3R)- is a complex organic compound characterized by its bicyclic structure and multiple functional groups, including hydroxyl (-OH) groups and a methylene bridge. This compound features a cyclohexane ring, which contributes to its stability and potential for various chemical interactions. The presence of stereocenters indicates that it can exist in multiple stereoisomeric forms, which may influence its biological activity and reactivity. The compound's intricate structure suggests potential applications in fields such as pharmaceuticals, where stereochemistry plays a crucial role in drug efficacy. Additionally, the presence of hydrophobic and hydrophilic regions may affect its solubility and interaction with biological membranes. Overall, this compound exemplifies the complexity often found in organic chemistry, particularly in the design of molecules with specific functional properties.

<p>2MD, a vitamin D-like oral drug, enhances bone mass/strength and lowers IOP by gene regulation.</p>

<p>Agonist of vitamin D receptor in bone</p>

CAS 213250-70-5

1,?3-?Cyclohexanediol, 2-?methylene-?5-?[(2E)?-?2-?[(1R,?3aS,?7aR)?-?octahydro-?1-?[(1S)?-?5-?hydroxy-?1,?5-?dimethylhexyl]?-?7a-?methyl-?4H-?inden-?4-?ylidene]?ethylidene]?-?, (1R,?3R)?-

2MD

Ref: TM-T74736

2MD

Ref: 3D-FM162210