ID: ALA4228410

Max Phase: Preclinical

Molecular Formula: C24H34O5

Molecular Weight: 402.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@@H](OC(=O)CC(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C24H34O5/c1-14(25)18-6-7-19-17-5-4-15-12-16(29-22(28)13-21(26)27)8-10-23(15,2)20(17)9-11-24(18,19)3/h4,16-20H,5-13H2,1-3H3,(H,26,27)/t16-,17-,18+,19-,20-,23-,24+/m0/s1

Standard InChI Key:  YCAAYMDCGUBOGP-GGKRXXEVSA-N

Associated Targets(non-human)

Glutamate NMDA receptor; Grin1/Grin2b 1028 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 402.53Molecular Weight (Monoisotopic): 402.2406AlogP: 4.54#Rotatable Bonds: 4
Polar Surface Area: 80.67Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.13CX Basic pKa: CX LogP: 3.91CX LogD: 0.84
Aromatic Rings: 0Heavy Atoms: 29QED Weighted: 0.42Np Likeness Score: 2.28

References

1. Krausova B, Slavikova B, Nekardova M, Hubalkova P, Vyklicky V, Chodounska H, Vyklicky L, Kudova E..  (2018)  Positive Modulators of the N-Methyl-d-aspartate Receptor: Structure-Activity Relationship Study of Steroidal 3-Hemiesters.,  61  (10): [PMID:29708744] [10.1021/acs.jmedchem.8b00255]

Source