ID: ALA4227806

Max Phase: Preclinical

Molecular Formula: C28H42O5

Molecular Weight: 458.64

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)CCCCCC(=O)O)CC[C@]4(C)[C@H]3CC[C@]12C

Standard InChI:  InChI=1S/C28H42O5/c1-18(29)22-11-12-23-21-10-9-19-17-20(33-26(32)8-6-4-5-7-25(30)31)13-15-27(19,2)24(21)14-16-28(22,23)3/h9,20-24H,4-8,10-17H2,1-3H3,(H,30,31)/t20-,21-,22+,23-,24-,27-,28+/m0/s1

Standard InChI Key:  DGBDRVWGIGJKKS-IZQLZLHJSA-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: 458.64Molecular Weight (Monoisotopic): 458.3032AlogP: 6.10#Rotatable Bonds: 8
Polar Surface Area: 80.67Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.11CX Basic pKa: CX LogP: 5.18CX LogD: 2.09
Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.27Np Likeness Score: 1.94

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