ID: ALA2297434

Max Phase: Preclinical

Molecular Formula: C19H19NO3

Molecular Weight: 309.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(CC)c1ccc(C2(O)C(=O)c3ccccc3C2=O)cc1

Standard InChI:  InChI=1S/C19H19NO3/c1-3-20(4-2)14-11-9-13(10-12-14)19(23)17(21)15-7-5-6-8-16(15)18(19)22/h5-12,23H,3-4H2,1-2H3

Standard InChI Key:  QDPSKNLBGDIWJL-UHFFFAOYSA-N

Associated Targets(non-human)

Klebsiella pneumoniae 43867 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vibrio cholerae 1211 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pseudomonas aeruginosa 123386 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus pumilus 984 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Micrococcus luteus 7463 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Shigella dysenteriae 933 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Staphylococcus aureus 210822 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: 309.37Molecular Weight (Monoisotopic): 309.1365AlogP: 2.80#Rotatable Bonds: 4
Polar Surface Area: 57.61Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.57CX Basic pKa: 5.54CX LogP: 3.11CX LogD: 3.10
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.88Np Likeness Score: -0.19

References

1. Sahu KB, Banerjee M, Ghosh S, Maity A, Mondal S, Paira R, Hazra A, Karmakar S, Samanta A, Mondal NB.  (2013)  I2 catalyzed FriedelCrafts alkylation reaction of substituted anilines with ninhydrin: formation of novel products and their antimicrobial evaluation,  22  (4): [10.1007/s00044-012-0202-z]

Source