34403-63-9 Usage
Type
Chemical compound
Classification
Isoindole derivative
Potential properties
Anti-cancer
Mechanism
Inhibits cell proliferation and induces cell cycle arrest in cancer cells
Target enzyme
Cyclin-dependent kinase 2 (CDK2)
Function
Regulates the cell cycle and promotes cell division
Therapeutic applications
Treatment of various types of cancer
Note
Further research is needed to understand its mechanisms of action and potential side effects
Check Digit Verification of cas no
The CAS Registry Mumber 34403-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34403-63:
(7*3)+(6*4)+(5*4)+(4*0)+(3*3)+(2*6)+(1*3)=89
89 % 10 = 9
So 34403-63-9 is a valid CAS Registry Number.
34403-63-9Relevant articles and documents
Reactions of N-Aminophthalimide With Electrophiles. II. Preparation and Properties of Araldehyde Hydrazones
Hearn, Michael J.,Lucero, Elena R.
, p. 1537 - 1539 (2007/10/02)
N-Aminophthalimide (I) reacted with a variety of aromatic aldehydes to give the related arylideneaminophthalimides (III-X), although typical ketones such as acetone and benzophenone did not under the specific conditions employed.Catalytic reduction of benzylideneaminophthalimide (III) led to N-benzylaminophthalimide (XI), a stable acid-free precursor of benzylhydrazine.
