ID: ALA5200407

Max Phase: Preclinical

Molecular Formula: C24H30O4

Molecular Weight: 382.50

Associated Items:

Representations

Canonical SMILES:  C=CC(C)(C)c1cc2cc3c(c(CC=C(C)C)c2oc1=O)O[C@H](C(C)(C)O)C3

Standard InChI:  InChI=1S/C24H30O4/c1-8-23(4,5)18-12-15-11-16-13-19(24(6,7)26)27-20(16)17(10-9-14(2)3)21(15)28-22(18)25/h8-9,11-12,19,26H,1,10,13H2,2-7H3/t19-/m0/s1

Standard InChI Key:  GANKRGDTCKPDCH-IBGZPJMESA-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: 382.50Molecular Weight (Monoisotopic): 382.2144AlogP: 4.84#Rotatable Bonds: 5
Polar Surface Area: 59.67Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 5.03CX LogD: 5.03
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.59Np Likeness Score: 2.57

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