The chemical substance known as 2H-Pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indole-2-methanol, with the CAS number 167427-23-8, is a complex organic compound characterized by its intricate polycyclic structure. This compound features multiple fused rings, including a pyran and indole moiety, which contribute to its unique chemical properties. It possesses a hydroxymethyl group, indicating potential for hydrogen bonding and reactivity. The stereochemistry is defined by specific chiral centers, which can influence its biological activity and interactions. The presence of multiple methyl groups suggests a degree of hydrophobicity, which may affect its solubility and permeability in biological systems. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or bioactive compounds. Its specific characteristics, such as melting point, boiling point, and reactivity, would require empirical data for precise evaluation.

2H-Pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indole-2-methanol,3,4,4a,4b,5,6,6a,7,12,12b,12c,13,14,14a-tetradecahydro-4-hydroxy-a,a,4a,12b,12c-pentamethyl-, (2S,4R,4aR,4bR,6aS,12bS,12cS,14aS)-

167427-23-8: The chemical substance known as 2H-Pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indole-2-methanol, with the CAS number 167427-23-8, is a complex organic compound characterized by its intricate polycyclic structure. This compound features multiple fused rings, including a pyran and indole moiety, which contribute to its unique chemical properties. It possesses a hydroxymethyl group, indicating potential for hydrogen bonding and reactivity. The stereochemistry is defined by specific chiral centers, which can influence its biological activity and interactions. The presence of multiple methyl groups suggests a degree of hydrophobicity, which may affect its solubility and permeability in biological systems. Overall, this compound's structural complexity and functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or bioactive compounds. Its specific characteristics, such as melting point, boiling point, and reactivity, would require empirical data for precise evaluation.

Terpendole E

<p>Terpendole E is an atypical L5 site inhibitor.</p>

CAS 167427-23-8

2H-Pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indole-2-methanol,3,4,4a,4b,5,6,6a,7,12,12b,12c,13,14,14a-tetradecahydro-4-hydroxy-a,a,4a,12b,12c-pentamethyl-, (2S,4R,4aR,4bR,6aS,12bS,12cS,14aS)-

Terpendole E

Ref: 7W-GL4961

Terpendole E

Ref: TM-T70289