ID: ALA4224866

Max Phase: Preclinical

Molecular Formula: C24H36O4

Molecular Weight: 388.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[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/C24H36O4/c1-4-15-6-8-19-18-7-5-16-13-17(28-22(27)14-21(25)26)9-11-24(16,3)20(18)10-12-23(15,19)2/h5,15,17-20H,4,6-14H2,1-3H3,(H,25,26)/t15-,17-,18-,19-,20-,23+,24-/m0/s1

Standard InChI Key:  UCCFYXAIFCHSML-ZBLOIMMDSA-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: 388.55Molecular Weight (Monoisotopic): 388.2614AlogP: 5.36#Rotatable Bonds: 4
Polar Surface Area: 63.60Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.13CX Basic pKa: CX LogP: 5.09CX LogD: 2.02
Aromatic Rings: 0Heavy Atoms: 28QED Weighted: 0.40Np Likeness Score: 2.39

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