ID: ALA5193508

Max Phase: Preclinical

Molecular Formula: C19H23NO2

Molecular Weight: 297.40

Associated Items:

Representations

Canonical SMILES:  Cc1cccc(-c2cc(CC3CCCCC3)n(O)c(=O)c2)c1

Standard InChI:  InChI=1S/C19H23NO2/c1-14-6-5-9-16(10-14)17-12-18(20(22)19(21)13-17)11-15-7-3-2-4-8-15/h5-6,9-10,12-13,15,22H,2-4,7-8,11H2,1H3

Standard InChI Key:  ZNVSSFWNDAZWJM-UHFFFAOYSA-N

Associated Targets(non-human)

Human alphaherpesvirus 2 4932 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Human alphaherpesvirus 1 11089 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vero 26788 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: 297.40Molecular Weight (Monoisotopic): 297.1729AlogP: 4.18#Rotatable Bonds: 3
Polar Surface Area: 42.23Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.78CX Basic pKa: CX LogP: 4.37CX LogD: 3.66
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.86Np Likeness Score: -0.30

References

1. Zangi M, Donald KA, Casals AG, Franson AD, Yu AJ, Marker EM, Woodson ME, Campbell SD, Mottaleb MA, Narayana Hajay Kumar TV, Reddy MS, Raghava Reddy LV, Sadhukhan SK, Griggs DW, Morrison LA, Meyers MJ..  (2022)  Synthetic derivatives of the antifungal drug ciclopirox are active against herpes simplex virus 2.,  238  [PMID:35635945] [10.1016/j.ejmech.2022.114443]

Source