89042-35-3 Usage
Core structure
Pyrrolidine-2,5-dione
Core structure
The central part of the molecule is a pyrrolidine-2,5-dione, which is a four-membered ring with two carbonyl groups.
Substituent group
2-[6-(benzyloxy)-3,4-dihydroisoquinolin-1-yl]ethyl
Substituent group
A 2-[6-(benzyloxy)-3,4-dihydroisoquinolin-1-yl]ethyl group is attached to the core structure, adding complexity to the molecule.
Type of molecule
Heterocyclic
Type of molecule
Heterocyclic molecules contain one or more rings with both carbon and heteroatoms (e.g., nitrogen, oxygen, or sulfur).
Potential pharmacological and biological activity
Yes
Potential pharmacological and biological activity
The presence of the pyrrolidine and isoquinoline rings suggests that the molecule may have pharmacological or biological effects.
Possible effects
Central nervous system or other physiological systems
Possible effects
The molecule's structure indicates that it could potentially interact with the central nervous system or other physiological systems.
Presence of rings
Pyrrolidine and isoquinoline rings
Presence of rings
The molecule contains two types of rings a pyrrolidine ring and an isoquinoline ring.
Applications
Medicinal chemistry, drug development, and study of structure-activity relationships of complex organic molecules
Applications
Due to its complex structure and potential pharmacological activity, the molecule may be useful in the fields of medicinal chemistry, drug development, and the study of structure-activity relationships in complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 89042-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,4 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89042-35:
(7*8)+(6*9)+(5*0)+(4*4)+(3*2)+(2*3)+(1*5)=143
143 % 10 = 3
So 89042-35-3 is a valid CAS Registry Number.
89042-35-3Relevant academic research and scientific papers
Diazaestrones and analogs. I. Pharmacological study and synthesis of heterosteroid analogs to establish structure-analgesic activity relationships
Hocquaux,Marcot,Redeuilh,et al.
, p. 319 - 329 (2007/10/02)
With the intention of showing the effect, about pharmacological properties, in replacing two estron asymetric carbon by nitrogen atoms and removal of angular methyl from steroid, stereospecific synthesis of 8,13-diazaestron and several substituted similar compounds was realized from β-1-(succinimidoethyl)-dihydroisoquinolines, precursors of a C open ring synthesis. The splitting of the 2-methoxydiazaestron methyl ester was carried out by mean of binaphthylphosphoric acid, and synthesis of several modified analogs of heterosteroid, was carried out to determine the effect of aromatic ring reduction, lactamic carbonyl reduction, and distance between 8 and 13 nitrogen atoms, about pharmacological activity. Hormonal, spasmolytic and analgesic activities were studied, good results were observed in analgesic activity.
