ID: ALA4225172

Max Phase: Preclinical

Molecular Formula: C25H36O5

Molecular Weight: 416.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@]12CC[C@H](OC(=O)CCCCC(=O)O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12

Standard InChI:  InChI=1S/C25H36O5/c1-24-13-11-17(30-23(29)6-4-3-5-22(27)28)15-16(24)7-8-18-19-9-10-21(26)25(19,2)14-12-20(18)24/h7,17-20H,3-6,8-15H2,1-2H3,(H,27,28)/t17-,18-,19-,20-,24-,25-/m0/s1

Standard InChI Key:  DRNFCPQEVRMNJH-DFRSGRCKSA-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: 416.56Molecular Weight (Monoisotopic): 416.2563AlogP: 5.08#Rotatable Bonds: 6
Polar Surface Area: 80.67Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.26CX Basic pKa: CX LogP: 4.52CX LogD: 1.53
Aromatic Rings: 0Heavy Atoms: 30QED Weighted: 0.37Np Likeness Score: 1.83

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