ID: ALA4224980

Max Phase: Preclinical

Molecular Formula: C28H44O4

Molecular Weight: 444.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[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/C28H44O4/c1-4-19-11-13-23-22-12-10-20-18-21(32-26(31)9-7-5-6-8-25(29)30)14-16-28(20,3)24(22)15-17-27(19,23)2/h10,19,21-24H,4-9,11-18H2,1-3H3,(H,29,30)/t19-,21-,22-,23-,24-,27+,28-/m0/s1

Standard InChI Key:  JBIIKDKNHKRHAP-WLYBTZAXSA-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: 444.66Molecular Weight (Monoisotopic): 444.3240AlogP: 6.92#Rotatable Bonds: 8
Polar Surface Area: 63.60Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.11CX Basic pKa: CX LogP: 6.36CX LogD: 3.27
Aromatic Rings: 0Heavy Atoms: 32QED Weighted: 0.25Np Likeness Score: 2.03

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