4-Oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile, with CAS number 22242-96-2, is a heterocyclic compound characterized by its complex bicyclic structure that incorporates both pyrrole and pyrimidine moieties. This compound features a carbonitrile functional group, which contributes to its reactivity and potential applications in medicinal chemistry. The presence of a pentofuranosyl group suggests that it may exhibit properties relevant to nucleoside analogs, potentially influencing its biological activity. The oxo group indicates the presence of a carbonyl functionality, which can participate in various chemical reactions, including condensation and nucleophilic attacks. The dihydro form implies that the compound may exist in a reduced state, affecting its stability and reactivity. Overall, this compound's unique structural features may confer interesting pharmacological properties, making it a candidate for further investigation in drug development and other applications in organic synthesis.

4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile

22242-96-2: 4-Oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile, with CAS number 22242-96-2, is a heterocyclic compound characterized by its complex bicyclic structure that incorporates both pyrrole and pyrimidine moieties. This compound features a carbonitrile functional group, which contributes to its reactivity and potential applications in medicinal chemistry. The presence of a pentofuranosyl group suggests that it may exhibit properties relevant to nucleoside analogs, potentially influencing its biological activity. The oxo group indicates the presence of a carbonyl functionality, which can participate in various chemical reactions, including condensation and nucleophilic attacks. The dihydro form implies that the compound may exist in a reduced state, affecting its stability and reactivity. Overall, this compound's unique structural features may confer interesting pharmacological properties, making it a candidate for further investigation in drug development and other applications in organic synthesis.

<p>Jaspamycin is an antitumor antibiotic, which is a natural product isolated from the bacterium *Streptomyces hygroscopicus*. Its mode of action involves disrupting RNA synthesis by inhibiting nucleic acid chain elongation, thereby impeding cell proliferation and leading to cell death in rapidly dividing cancer cells. This mechanism makes Jaspamycin particularly effective as a chemotherapeutic agent.</p>

Jaspamycin

Jaspamycin (7-CN-7-C-Ino) does not bind with purified human PKARIα.

CAS 22242-96-2

4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile

Jaspamycin

Ref: 3D-XAA24296

Jaspamycin

Ref: TM-T11711