ID: ALA5220301

Max Phase: Preclinical

Molecular Formula: C38H52O5

Molecular Weight: 588.83

Associated Items:

Representations

Canonical SMILES:  COc1ccc(/C=C2\C[C@]3(C)[C@H]4C(=O)C=C5[C@@H]6C[C@@](C)(C(=O)O)CC[C@]6(C)CC[C@@]5(C)[C@]4(C)CC[C@H]3C(C)(C)[C@H]2O)cc1

Standard InChI:  InChI=1S/C38H52O5/c1-33(2)29-13-14-38(7)30(36(29,5)21-24(31(33)40)19-23-9-11-25(43-8)12-10-23)28(39)20-26-27-22-35(4,32(41)42)16-15-34(27,3)17-18-37(26,38)6/h9-12,19-20,27,29-31,40H,13-18,21-22H2,1-8H3,(H,41,42)/b24-19+/t27-,29-,30+,31-,34+,35-,36-,37+,38+/m0/s1

Standard InChI Key:  ODLCYEZPLLDSMU-OGYTZPOOSA-N

Associated Targets(Human)

NHDF 1164 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 588.83Molecular Weight (Monoisotopic): 588.3815AlogP: 8.11#Rotatable Bonds: 3
Polar Surface Area: 83.83Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.44CX Basic pKa: CX LogP: 7.57CX LogD: 4.72
Aromatic Rings: 1Heavy Atoms: 43QED Weighted: 0.37Np Likeness Score: 2.29

References

1. Kumar A, Archo S, Singh CP, Naikoo SH, Singh B, Kaur S, Tasduq SA..  (2022)  Photoprotective effect of 18β-glycyrrhetinic acid derivatives against ultra violet (UV)-B-Induced skin aging.,  76  [PMID:36167293] [10.1016/j.bmcl.2022.128984]

Source