ID: ALA226661

Max Phase: Preclinical

Molecular Formula: C14H10O2

Molecular Weight: 210.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC1=Cc2cccc3cccc(c23)C1=O

Standard InChI:  InChI=1S/C14H10O2/c1-16-12-8-10-6-2-4-9-5-3-7-11(13(9)10)14(12)15/h2-8H,1H3

Standard InChI Key:  FMZHCYXNNGLTLF-UHFFFAOYSA-N

Associated Targets(non-human)

Pseudocercospora fijiensis (23 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 210.23Molecular Weight (Monoisotopic): 210.0681AlogP: 3.02#Rotatable Bonds: 1
Polar Surface Area: 26.30Molecular Species: NEUTRALHBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.50CX LogD: 2.50
Aromatic Rings: 2Heavy Atoms: 16QED Weighted: 0.72Np Likeness Score: 1.14

References

1. Otálvaro F, Nanclares J, Vásquez LE, Quiñones W, Echeverri F, Arango R, Schneider B..  (2007)  Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijiensis.,  70  (5): [PMID:17428093] [10.1021/np070091e]
2. Hidalgo W, Duque L, Saez J, Arango R, Gil J, Rojano B, Schneider B, Otálvaro F..  (2009)  Structure-activity relationship in the interaction of substituted perinaphthenones with Mycosphaerella fijiensis.,  57  (16): [PMID:19630386] [10.1021/jf901052e]

Source