ID: ALA4228607

Max Phase: Preclinical

Molecular Formula: C27H42O4

Molecular Weight: 430.63

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C27H42O4/c1-4-18-10-12-22-21-11-9-19-17-20(31-25(30)8-6-5-7-24(28)29)13-15-27(19,3)23(21)14-16-26(18,22)2/h9,18,20-23H,4-8,10-17H2,1-3H3,(H,28,29)/t18-,20-,21-,22-,23-,26+,27-/m0/s1

Standard InChI Key:  SZXFBHIHYFGFQF-FKIHWARDSA-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: 430.63Molecular Weight (Monoisotopic): 430.3083AlogP: 6.53#Rotatable Bonds: 7
Polar Surface Area: 63.60Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.26CX Basic pKa: CX LogP: 5.92CX LogD: 2.92
Aromatic Rings: 0Heavy Atoms: 31QED Weighted: 0.28Np Likeness Score: 2.07

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