ID: ALA4291068

Max Phase: Preclinical

Molecular Formula: C14H21NO6S2

Molecular Weight: 363.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CS(=O)(=O)N[C@H]1[C@H](OCc2ccccc2)O[C@H](CO)[C@@H](O)[C@@H]1S

Standard InChI:  InChI=1S/C14H21NO6S2/c1-23(18,19)15-11-13(22)12(17)10(7-16)21-14(11)20-8-9-5-3-2-4-6-9/h2-6,10-17,22H,7-8H2,1H3/t10-,11-,12-,13-,14-/m1/s1

Standard InChI Key:  DYFVKGVVTPUASS-DHGKCCLASA-N

Associated Targets(non-human)

Poly-beta-1,6-N-acetyl-D-glucosamine N-deacetylase 23 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Peptidoglycan-N-acetylglucosamine deacetylase 31 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: 363.46Molecular Weight (Monoisotopic): 363.0810AlogP: -0.50#Rotatable Bonds: 6
Polar Surface Area: 105.09Molecular Species: NEUTRALHBA: 7HBD: 4
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.89CX Basic pKa: CX LogP: -0.40CX LogD: -0.51
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.51Np Likeness Score: 0.50

References

1. DiFrancesco BR, Morrison ZA, Nitz M..  (2018)  Monosaccharide inhibitors targeting carbohydrate esterase family 4 de-N-acetylases.,  26  (21): [PMID:30344002] [10.1016/j.bmc.2018.10.008]

Source