ID: ALA2398599

Max Phase: Preclinical

Molecular Formula: C11H16N2O6S

Molecular Weight: 304.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC(=O)c1cnc(N[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)s1

Standard InChI:  InChI=1S/C11H16N2O6S/c1-4(15)6-2-12-11(20-6)13-10-9(18)8(17)7(16)5(3-14)19-10/h2,5,7-10,14,16-18H,3H2,1H3,(H,12,13)/t5-,7-,8+,9+,10+/m1/s1

Standard InChI Key:  HACVSHGRHKRNKG-HHCWIIQDSA-N

Associated Targets(non-human)

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Adhesin protein fimH 338 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: 304.32Molecular Weight (Monoisotopic): 304.0729AlogP: -1.44#Rotatable Bonds: 4
Polar Surface Area: 132.14Molecular Species: NEUTRALHBA: 9HBD: 5
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.79CX Basic pKa: 2.24CX LogP: -1.93CX LogD: -2.07
Aromatic Rings: 1Heavy Atoms: 20QED Weighted: 0.43Np Likeness Score: 0.43

References

1. Brument S, Sivignon A, Dumych TI, Moreau N, Roos G, Guérardel Y, Chalopin T, Deniaud D, Bilyy RO, Darfeuille-Michaud A, Bouckaert J, Gouin SG..  (2013)  Thiazolylaminomannosides as potent antiadhesives of type 1 piliated Escherichia coli isolated from Crohn's disease patients.,  56  (13): [PMID:23795713] [10.1021/jm400723n]

Source