ID: ALA4283927

Max Phase: Preclinical

Molecular Formula: C32H25N5O6S

Molecular Weight: 607.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(S(=O)(=O)c2nnn(CCn3c(-c4ccccc4)c(-c4ccccc4)oc3=O)c2-c2ccc([N+](=O)[O-])cc2)cc1

Standard InChI:  InChI=1S/C32H25N5O6S/c1-22-12-18-27(19-13-22)44(41,42)31-29(24-14-16-26(17-15-24)37(39)40)36(34-33-31)21-20-35-28(23-8-4-2-5-9-23)30(43-32(35)38)25-10-6-3-7-11-25/h2-19H,20-21H2,1H3

Standard InChI Key:  UDGWEHQGTYTYHI-UHFFFAOYSA-N

Associated Targets(non-human)

Candida tropicalis 8381 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida albicans 78123 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyberlindnera jadinii 900 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pichia kudriavzevii 7448 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Nakaseomyces glabratus 9108 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Candida parapsilosis 8521 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mucor hiemalis 184 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus fumigatus 16427 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cutaneotrichosporon cutaneum 20 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhizopus arrhizus 810 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: 607.65Molecular Weight (Monoisotopic): 607.1526AlogP: 5.78#Rotatable Bonds: 9
Polar Surface Area: 143.13Molecular Species: NEUTRALHBA: 10HBD: 0
#RO5 Violations: 2HBA (Lipinski): 11HBD (Lipinski): 0#RO5 Violations (Lipinski): 3
CX Acidic pKa: CX Basic pKa: CX LogP: 6.24CX LogD: 6.24
Aromatic Rings: 6Heavy Atoms: 44QED Weighted: 0.15Np Likeness Score: -1.24

References

1. Ramírez-Villalva A, González-Calderón D, Rojas-García RI, González-Romero C, Tamaríz-Mascarúa J, Morales-Rodríguez M, Zavala-Segovia N, Fuentes-Benítes A..  (2017)  Synthesis and antifungal activity of novel oxazolidin-2-one-linked 1,2,3-triazole derivatives.,  (12): [PMID:30108741] [10.1039/C7MD00442G]

Source