The chemical substance known as "6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2,3,9-trimethyl-4-[4-[(1E)-3-oxo-1-propen-1-yl]phenyl]-, 1,1-dimethylethyl ester, (6S)-" with CAS number 3079093-92-5 is a complex organic compound characterized by its unique structural framework that includes a thieno-triazolo-diazepine core. This compound features multiple functional groups, including an acetic acid moiety and an ester group, which contribute to its chemical reactivity and potential biological activity. The presence of multiple methyl groups and a propenyl substituent on a phenyl ring suggests that it may exhibit significant lipophilicity, potentially influencing its pharmacokinetic properties. The stereochemistry indicated by the (6S) designation suggests specific spatial arrangements that could be crucial for its interaction with biological targets. Overall, this compound may be of interest in medicinal chemistry, particularly for its potential therapeutic applications, although detailed studies would be necessary to elucidate its biological effects and mechanisms of action.

6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2,3,9-trimethyl-4-[4-[(1E)-3-oxo-1-propen-1-yl]phenyl]-, 1,1-dimethylethyl ester, (6S)-

3079093-92-5: The chemical substance known as "6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2,3,9-trimethyl-4-[4-[(1E)-3-oxo-1-propen-1-yl]phenyl]-, 1,1-dimethylethyl ester, (6S)-" with CAS number 3079093-92-5 is a complex organic compound characterized by its unique structural framework that includes a thieno-triazolo-diazepine core. This compound features multiple functional groups, including an acetic acid moiety and an ester group, which contribute to its chemical reactivity and potential biological activity. The presence of multiple methyl groups and a propenyl substituent on a phenyl ring suggests that it may exhibit significant lipophilicity, potentially influencing its pharmacokinetic properties. The stereochemistry indicated by the (6S) designation suggests specific spatial arrangements that could be crucial for its interaction with biological targets. Overall, this compound may be of interest in medicinal chemistry, particularly for its potential therapeutic applications, although detailed studies would be necessary to elucidate its biological effects and mechanisms of action.

TMX1 is a molecular glue degrader targeting BRD4, selectively recruiting the ubiquitin ligase CUL4-DCAF16 complex to BRD4 (BD2.

CAS 3079093-92-5

6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2,3,9-trimethyl-4-[4-[(1E)-3-oxo-1-propen-1-yl]phenyl]-, 1,1-dimethylethyl ester, (6S)-

TMX1

Ref: TM-T75139