CAS 634589-47-2

3,5,9-Undecatrienoic acid, 2-ethylidene-11-[(1R,5R)-4-hydroxy-4-methyl-2-oxo-6-oxa-3-azabicyclo[3.1.0]hex-1-yl]-4,10-dimethyl-11-oxo-, 1,1-dimethylethyl ester, (2E,3E,5E,9E)-

Description:

3,5,9-Undecatrienoic acid, 2-ethylidene-11-[(1R,5R)-4-hydroxy-4-methyl-2-oxo-6-oxa-3-azabicyclo[3.1.0]hex-1-yl]-4,10-dimethyl-11-oxo-, 1,1-dimethylethyl ester, with CAS number 634589-47-2, is a complex organic compound characterized by its unique structure that includes multiple functional groups and a long carbon chain. This compound features a series of conjugated double bonds, which contribute to its reactivity and potential applications in organic synthesis and materials science. The presence of a bicyclic structure and various substituents, such as hydroxyl and carbonyl groups, suggests that it may exhibit interesting biological activity, possibly as a pharmaceutical or agrochemical agent. Additionally, the ester functional group indicates that it may be involved in esterification reactions, making it useful in the synthesis of other chemical compounds. Its stereochemistry, particularly the (1R,5R) configuration, may also influence its interactions and properties, highlighting the importance of chirality in organic compounds. Overall, this substance represents a fascinating area of study within organic chemistry.

Formula: C₂₄H₃₃NO₆

Synonyms:

• 3,5,9-Undecatrienoic acid, 2-ethylidene-11-[(1R,5R)-4-hydroxy-4-methyl-2-oxo-6-oxa-3-azabicyclo[3.1.0]hex-1-yl]-4,10-dimethyl-11-oxo-, 1,1-dimethylethyl ester, (2E,3E,5E,9E)-

ETB

CAS: 634589-47-2

ETB is a potent inhibitor of Hsp60 chaperone activity. It can impede the chaperone function of both wild-type proteins and the C237A and C447A mutant proteins. ETB binds to Hsp60 at Cys442, and the C442A mutant demonstrates resistance to ETB inhibition.

Formula: C₂₄H₃₃NO₆

Molecular weight: 431.52

Ref: TM-T210270