CAS 53342-16-8

(3S,9S,14aR)-9-benzyl-6,6-dimethyl-3-{6-[(2S)-oxiran-2-yl]-6-oxohexyl}decahydropyrrolo[1,2-a][1,4,7,10]tetraazacyclododecine-1,4,7,10-tetrone

Description:

The chemical substance with the name "(3S,9S,14aR)-9-benzyl-6,6-dimethyl-3-{6-[(2S)-oxiran-2-yl]-6-oxohexyl}decahydropyrrolo[1,2-a][1,4,7,10]tetraazacyclododecine-1,4,7,10-tetrone" and CAS number 53342-16-8 is a complex organic compound characterized by its multi-cyclic structure and the presence of multiple functional groups. It features a decahydropyrrolo framework, which is indicative of its potential biological activity. The presence of a benzyl group and an epoxide (oxirane) suggests reactivity and potential interactions with biological systems. The compound also contains several ketone functionalities, which may contribute to its chemical reactivity and stability. Its stereochemistry, denoted by the specific configurations at various chiral centers, is crucial for its biological activity and interaction with enzymes or receptors. Overall, this compound's intricate structure and functional groups suggest it may have applications in medicinal chemistry or as a synthetic intermediate in organic synthesis. Further studies would be necessary to elucidate its specific properties and potential uses.

Formula: C₂₈H₃₈N₄O₆

InChI: InChI=1/C28H38N4O6/c1-28(2)27(37)30-20(16-18-10-5-3-6-11-18)26(36)32-15-9-13-21(32)25(35)29-19(24(34)31-28)12-7-4-8-14-22(33)23-17-38-23/h3,5-6,10-11,19-21,23H,4,7-9,12-17H2,1-2H3,(H,29,35)(H,30,37)(H,31,34)/t19-,20-,21+,23-/m0/s1

Chlamydocin

CAS: 53342-16-8

Formula: C₂₈H₃₈N₄O₆

Purity: 93.74%

Color and Shape: Brown oily solid

Molecular weight: 527.0

Ref: 8R-AD0009

Chlamydocin

CAS: 53342-16-8

Chlamydocin

Formula: C₂₈H₃₈N₄O₆

Purity: By hplc: 97.48% (Typical Value in Batch COA)

Color and Shape: brown oily solid

Molecular weight: 526.62g/mol

Ref: 54-BIBR1026

Chlamydocin

CAS: 53342-16-8

Chlamydocin is a potent histone deacetylase inhibitor, which is a secondary metabolite derived from microbial sources, specifically fungi of the genus Diheterospora. Its mode of action involves the inhibition of histone deacetylases (HDACs), which are enzymes that remove acetyl groups from histone proteins. This deacetylation affects chromatin structure, influencing gene expression by modulating the accessibility of transcriptional machinery to the DNA.

Formula: C₂₈H₃₈N₄O₆

Purity: Min. 95%

Molecular weight: 526.60 g/mol

Ref: 3D-DCA34216