85233-38-1 Usage
Uses
Used in Pharmaceutical Research:
2,3,4,10-tetrahydro-3,3-dimethyl-10-phenylpyrimido[1,2-a]indol-10-ol is used as a research compound for exploring its potential pharmacological properties. Its unique structure suggests that it may have applications in the development of new drugs, particularly in the treatment of various health conditions.
Used in Drug Development:
2,3,4,10-tetrahydro-3,3-dimethyl-10-phenylpyrimido[1,2-a]indol-10-ol is used as a candidate molecule in the process of drug development. Its potential biological activity and pharmacological properties make it a promising candidate for further investigation and optimization to create effective therapeutic agents.
Further research is needed to fully explore the potential of 2,3,4,10-tetrahydro-3,3-dimethyl-10-phenylpyrimido[1,2-a]indol-10-ol in the field of pharmaceuticals and medicine, as its current applications are primarily limited to research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 85233-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,3 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85233-38:
(7*8)+(6*5)+(5*2)+(4*3)+(3*3)+(2*3)+(1*8)=131
131 % 10 = 1
So 85233-38-1 is a valid CAS Registry Number.
85233-38-1Relevant academic research and scientific papers
Oral Hypoglycemic Agents. Pyrimidoindoles and Related Compounds
Cliffe, Ian A.,Lien, Eric L.,Mansell, Howard L.,Steiner, Kurt E.,Todd, Richard S.,et al.
, p. 1169 - 1175 (2007/10/02)
A series of pyrimidoindoles were synthesized and studied for their hypoglycemic activity following oral administration at standard dose of 100 mg/kg to fed rats.The effect of 10-alkoxyalkyl, 10-alkyl, 10-aryl, and 3,3-dialkyl substitution on the activity of 10-hydroxypyrimidoindoles was investigated.Relative potencies of a number of the most active compounds were defined by three-point dose-response studies.The most potent compounds were those with either 3,3-dimethyl substituents, compounds 21, 22, and 38, or 3,3-spirocyclohexane substituents, compounds 39 and 49. 10-Aminopyrimidoindoles were in general less active than the 10-hydroxy analogues, and potency was further decreased by derivatizing the 10-amino group.The most potent 10-amino derivatives were 57 and 58.
