ID: ALA4473153

Max Phase: Preclinical

Molecular Formula: C27H21NO5

Molecular Weight: 439.47

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(/C=C/c1ccccc1)c1ccc(OCc2cc(-c3ccc4c(c3)OCCO4)no2)cc1

Standard InChI:  InChI=1S/C27H21NO5/c29-25(12-6-19-4-2-1-3-5-19)20-7-10-22(11-8-20)32-18-23-17-24(28-33-23)21-9-13-26-27(16-21)31-15-14-30-26/h1-13,16-17H,14-15,18H2/b12-6+

Standard InChI Key:  FSZNGACEZPGHHC-WUXMJOGZSA-N

Associated Targets(non-human)

Tyrosinase 438 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

B16-F10 4610 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Tyrosinase 3884 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 439.47Molecular Weight (Monoisotopic): 439.1420AlogP: 5.59#Rotatable Bonds: 7
Polar Surface Area: 70.79Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.29CX LogD: 5.29
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.28Np Likeness Score: -0.87

References

1. Niu C, Yin L, Nie LF, Dou J, Zhao JY, Li G, Aisa HA..  (2016)  Synthesis and bioactivity of novel isoxazole chalcone derivatives on tyrosinase and melanin synthesis in murine B16 cells for the treatment of vitiligo.,  24  (21): [PMID:27622747] [10.1016/j.bmc.2016.08.066]

Source