(3R,4S,5R)-3-hydroxy-5-[(R)-hydroxy(phenyl)methyl]-1-methyl-4-phenylpyrrolidin-2-one
AlkaPlorer ID: AK017409
Synonym: None
IUPAC Name: (3R,4S,5R)-3-hydroxy-5-[(R)-hydroxy(phenyl)methyl]-1-methyl-4-phenylpyrrolidin-2-one
Structure
SMILES: CN1C(=O)[C@H](O)[C@@H](C2=CC=CC=C2)[C@@H]1[C@H](O)C1=CC=CC=C1
InChI: InChI=1S/C18H19NO3/c1-19-15(16(20)13-10-6-3-7-11-13)14(17(21)18(19)22)12-8-4-2-5-9-12/h2-11,14-17,20-21H,1H3/t14-,15+,16+,17+/m0/s1
InChIKey: WGYGSZOQGYRGIP-YLFCFFPRSA-N
Reference
Synthesis and activity in enhancing long-term potentiation (LTP) of clausenamide stereoisomers
PubChem CID: 10149518
LOTUS: LTS0130699
SuperNatural Ⅲ: SN0409985-15
NPASS: NPC90194
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Clausena lansium | Clausena | Rutaceae | Sapindales | Magnoliopsida | Streptophyta | Viridiplantae | Eukaryota |
Properties Information
Molecule Weight: 297.35400000000004
TPSA？: 60.77000000000001
MolLogP？: 1.7052999999999998
Number of H-Donors: 2
Number of H-Acceptors: 3
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|---|---|---|---|---|
| None | NON-PROTEIN TARGET | Activity | -5.3 | % | 10.1016/j.bmcl.2009.03.018 |
| None | NON-PROTEIN TARGET | Activity | 1.1 | % | 10.1016/j.bmcl.2009.03.018 |
| None | NON-PROTEIN TARGET | Activity | 4.7 | % | 10.1016/j.bmcl.2009.03.018 |