ID: ALA4226487

Max Phase: Preclinical

Molecular Formula: C24H34O5

Molecular Weight: 402.53

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C24H34O5/c1-23-12-10-16(29-22(28)5-3-4-21(26)27)14-15(23)6-7-17-18-8-9-20(25)24(18,2)13-11-19(17)23/h6,16-19H,3-5,7-14H2,1-2H3,(H,26,27)/t16-,17-,18-,19-,23-,24-/m0/s1

Standard InChI Key:  MMJKXSYYRUPOKG-JVFZSLGPSA-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: 4.69#Rotatable Bonds: 5
Polar Surface Area: 80.67Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.25CX Basic pKa: CX LogP: 4.07CX LogD: 1.07
Aromatic Rings: 0Heavy Atoms: 29QED Weighted: 0.53Np Likeness Score: 1.86

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