ID: ALA5203645

Max Phase: Preclinical

Molecular Formula: C13H10O4

Molecular Weight: 230.22

Associated Items:

Representations

Canonical SMILES:  CC(=O)[C@@H]1Cc2cc3ccc(=O)oc3cc2O1

Standard InChI:  InChI=1S/C13H10O4/c1-7(14)10-5-9-4-8-2-3-13(15)17-11(8)6-12(9)16-10/h2-4,6,10H,5H2,1H3/t10-/m0/s1

Standard InChI Key:  SFPYWYBZNZWIPO-JTQLQIEISA-N

Associated Targets(Human)

C8166 1658 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus type 1 reverse transcriptase 18245 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: 230.22Molecular Weight (Monoisotopic): 230.0579AlogP: 1.69#Rotatable Bonds: 1
Polar Surface Area: 56.51Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.69CX LogD: 1.69
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.70Np Likeness Score: 1.12

References

1. Popović-Djordjević J, Quispe C, Giordo R, Kostić A, Katanić Stanković JS, Tsouh Fokou PV, Carbone K, Martorell M, Kumar M, Pintus G, Sharifi-Rad J, Docea AO, Calina D..  (2022)  Natural products and synthetic analogues against HIV: A perspective to develop new potential anti-HIV drugs.,  233  [PMID:35276425] [10.1016/j.ejmech.2022.114217]

Source