The chemical substance known as 8-(8-chloro-5H-pyrimido[5,4-b]indol-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane, with the CAS number 489402-33-7, is a complex organic compound characterized by its unique structural features. It contains a spirocyclic framework, which is indicative of its potential biological activity. The presence of a pyrimidine and indole moiety suggests that it may interact with biological targets, possibly influencing various biochemical pathways. The chlorine substituent on the pyrimidine ring can enhance lipophilicity and may affect the compound's pharmacokinetic properties. Additionally, the dioxa and azaspiro components contribute to its overall stability and solubility profile. Such compounds are often investigated for their potential therapeutic applications, particularly in the fields of oncology and neurology, due to their ability to modulate specific molecular interactions. However, detailed studies on its biological activity, toxicity, and pharmacological properties would be necessary to fully understand its potential uses in medicinal chemistry.

8-(8-chloro-5H-pyrimido[5,4-b]indol-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane

489402-33-7: The chemical substance known as 8-(8-chloro-5H-pyrimido[5,4-b]indol-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane, with the CAS number 489402-33-7, is a complex organic compound characterized by its unique structural features. It contains a spirocyclic framework, which is indicative of its potential biological activity. The presence of a pyrimidine and indole moiety suggests that it may interact with biological targets, possibly influencing various biochemical pathways. The chlorine substituent on the pyrimidine ring can enhance lipophilicity and may affect the compound's pharmacokinetic properties. Additionally, the dioxa and azaspiro components contribute to its overall stability and solubility profile. Such compounds are often investigated for their potential therapeutic applications, particularly in the fields of oncology and neurology, due to their ability to modulate specific molecular interactions. However, detailed studies on its biological activity, toxicity, and pharmacological properties would be necessary to fully understand its potential uses in medicinal chemistry.

UP158 enhances ATPase activity and stimulates valosin-containing protein (VCP), with an EC50 of 2.57 μM.

CAS 489402-33-7

8-(8-chloro-5H-pyrimido[5,4-b]indol-4-yl)-1,4-dioxa-8-azaspiro[4.5]decane

UP158

Ref: TM-T203467