ID: ALA1818498

Max Phase: Preclinical

Molecular Formula: C34H21Cl2F4N3O4

Molecular Weight: 682.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C1O/C(=C\c2ccc(OCC(O)(Cn3cncn3)c3ccc(F)cc3F)cc2)C(c2ccc(F)cc2F)=C1c1ccc(Cl)c(Cl)c1

Standard InChI:  InChI=1S/C34H21Cl2F4N3O4/c35-26-10-3-20(12-27(26)36)31-32(24-8-4-21(37)13-28(24)39)30(47-33(31)44)11-19-1-6-23(7-2-19)46-16-34(45,15-43-18-41-17-42-43)25-9-5-22(38)14-29(25)40/h1-14,17-18,45H,15-16H2/b30-11-

Standard InChI Key:  SUWYCSWRIRASER-OHUIHDMLSA-N

Associated Targets(non-human)

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nakaseomyces glabratus 9108 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pichia kudriavzevii 7448 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida tropicalis 8381 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cryptococcus neoformans 21258 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus niger 16508 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus fumigatus 16427 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium proliferatum 164 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: 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: 682.46Molecular Weight (Monoisotopic): 681.0845AlogP: 7.62#Rotatable Bonds: 9
Polar Surface Area: 86.47Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.44CX Basic pKa: 2.00CX LogP: 7.73CX LogD: 7.73
Aromatic Rings: 5Heavy Atoms: 47QED Weighted: 0.13Np Likeness Score: -0.57

References

1. Borate HB, Sawargave SP, Chavan SP, Chandavarkar MA, Iyer R, Tawte A, Rao D, Deore JV, Kudale AS, Mahajan PS, Kangire GS..  (2011)  Novel hybrids of fluconazole and furanones: design, synthesis and antifungal activity.,  21  (16): [PMID:21757344] [10.1016/j.bmcl.2011.06.022]

Source