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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H21ClN2O3
Molecular Weight 420.888
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RO-41-3290

SMILES

O[C@H]1CCN(C1)C(=O)C2=C3N(CCC4=C3C=C(Cl)C=C4)C(=O)C(=C2)C5=CC=CC=C5

InChI

InChIKey=ASOBQUGZPVVXJT-SFHVURJKSA-N
InChI=1S/C24H21ClN2O3/c25-17-7-6-16-8-11-27-22(19(16)12-17)21(23(29)26-10-9-18(28)14-26)13-20(24(27)30)15-4-2-1-3-5-15/h1-7,12-13,18,28H,8-11,14H2/t18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H21ClN2O3
Molecular Weight 420.888
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 02:53:18 GMT 2023
Edited
by admin
on Sat Dec 16 02:53:18 GMT 2023
Record UNII
EIR1Q66583
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RO-41-3290
Common Name English
RO41-3290
Code English
10-CHLORO-1-((3S)-3-HYDROXYPYRROLIDINE-1-CARBONYL)-3-PHENYL-6,7-DIHYDROBENZO(A)QUINOLIZIN-4-ONE
Systematic Name English
3-PYRROLIDINOL, 1-((10-CHLORO-6,7-DIHYDRO-4-OXO-3-PHENYL-4H-BENZO(A)QUINOLIZIN-1-YL)CARBONYL)-, (3S)-
Systematic Name English
3-PYRROLIDINOL, 1-((10-CHLORO-6,7-DIHYDRO-4-OXO-3-PHENYL-4H-BENZO(A)QUINOLIZIN-1-YL)CARBONYL)-, (S)-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
LIREQUINIL
Created by admin on Sat Dec 16 02:53:18 GMT 2023 , Edited by admin on Sat Dec 16 02:53:18 GMT 2023
PRIMARY
CAS
143943-72-0
Created by admin on Sat Dec 16 02:53:18 GMT 2023 , Edited by admin on Sat Dec 16 02:53:18 GMT 2023
PRIMARY
FDA UNII
EIR1Q66583
Created by admin on Sat Dec 16 02:53:18 GMT 2023 , Edited by admin on Sat Dec 16 02:53:18 GMT 2023
PRIMARY
PUBCHEM
14770131
Created by admin on Sat Dec 16 02:53:18 GMT 2023 , Edited by admin on Sat Dec 16 02:53:18 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
Ro 41-3290 induced moderate, dose-independent effects, which were most pronounced at 4 h after intake. Long-term memory, as assessed by a word learning and recall test, was not clearly affected by any drug. The pharmacokinetics of Ro 41-3290 were dose proportional with an elimination half-life of approximately 8 h. The relatively slow absorption of Ro 41-3290 (t(max) approximately 2.5 h) and the concentration-effect time delay do not make it a good candidate to replace its parent compound Ro 41-3696 as an investigational hypnotic.