ID: ALA5219892

Max Phase: Preclinical

Molecular Formula: C36H47NO4

Molecular Weight: 557.78

Associated Items:

Representations

Canonical SMILES:  CC1(C)C(=O)/C(=C/c2ccncc2)C[C@]2(C)[C@H]3C(=O)C=C4[C@@H]5C[C@@](C)(C(=O)O)CC[C@]5(C)CC[C@@]4(C)[C@]3(C)CC[C@@H]12

Standard InChI:  InChI=1S/C36H47NO4/c1-31(2)27-8-11-36(7)28(34(27,5)20-23(29(31)39)18-22-9-16-37-17-10-22)26(38)19-24-25-21-33(4,30(40)41)13-12-32(25,3)14-15-35(24,36)6/h9-10,16-19,25,27-28H,8,11-15,20-21H2,1-7H3,(H,40,41)/b23-18+/t25-,27-,28+,32+,33-,34-,35+,36+/m0/s1

Standard InChI Key:  RBZWVIXVSRGMFM-GWDIFKJQSA-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: 557.78Molecular Weight (Monoisotopic): 557.3505AlogP: 7.71#Rotatable Bonds: 2
Polar Surface Area: 84.33Molecular Species: ACIDHBA: 4HBD: 1
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.36CX Basic pKa: 5.19CX LogP: 6.56CX LogD: 4.66
Aromatic Rings: 1Heavy Atoms: 41QED Weighted: 0.38Np Likeness Score: 2.20

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