ID: ALA3753644

Max Phase: Preclinical

Molecular Formula: C26H19N5O3

Molecular Weight: 449.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(Nc1ccc(Nc2c3ccccc3nc3ccccc23)cc1)Nc1ccc([N+](=O)[O-])cc1

Standard InChI:  InChI=1S/C26H19N5O3/c32-26(29-19-13-15-20(16-14-19)31(33)34)28-18-11-9-17(10-12-18)27-25-21-5-1-3-7-23(21)30-24-8-4-2-6-22(24)25/h1-16H,(H,27,30)(H2,28,29,32)

Standard InChI Key:  FRBICWAQKKWVMX-UHFFFAOYSA-N

Associated Targets(non-human)

gyrB DNA gyrase subunit A/DNA gyrase subunit B (505 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gyrB DNA gyrase subunit B (445 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gyrB DNA gyrase (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gyrA DNA gyrase (39 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 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: 449.47Molecular Weight (Monoisotopic): 449.1488AlogP: 6.68#Rotatable Bonds: 5
Polar Surface Area: 109.19Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 11.06CX Basic pKa: 8.50CX LogP: 6.03CX LogD: 5.00
Aromatic Rings: 5Heavy Atoms: 34QED Weighted: 0.16Np Likeness Score: -1.06

References

1. Medapi B, Meda N, Kulkarni P, Yogeeswari P, Sriram D..  (2016)  Development of acridine derivatives as selective Mycobacterium tuberculosis DNA gyrase inhibitors.,  24  (4): [PMID:26787274] [10.1016/j.bmc.2016.01.011]

Source