ID: ALA4564023

Max Phase: Preclinical

Molecular Formula: C25H30N4O9S

Molecular Weight: 562.60

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1SCCNCCCN1C(=O)c2cccc3c([N+](=O)[O-])ccc(c23)C1=O

Standard InChI:  InChI=1S/C25H30N4O9S/c1-13(31)27-20-22(33)21(32)18(12-30)38-25(20)39-11-9-26-8-3-10-28-23(34)15-5-2-4-14-17(29(36)37)7-6-16(19(14)15)24(28)35/h2,4-7,18,20-22,25-26,30,32-33H,3,8-12H2,1H3,(H,27,31)/t18-,20-,21-,22-,25+/m1/s1

Standard InChI Key:  JUDDLSSNCHTJBF-QRBWNZBVSA-N

Associated Targets(Human)

Beta-hexosaminidase subunit beta 131 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bifunctional protein NCOAT 460 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 562.60Molecular Weight (Monoisotopic): 562.1733AlogP: 0.00#Rotatable Bonds: 11
Polar Surface Area: 191.57Molecular Species: BASEHBA: 11HBD: 5
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.66CX Basic pKa: 9.87CX LogP: -0.76CX LogD: -3.16
Aromatic Rings: 2Heavy Atoms: 39QED Weighted: 0.11Np Likeness Score: -0.26

References

1. Shen S, Dong L, Chen W, Zeng X, Lu H, Yang Q, Zhang J..  (2018)  Modification of the Thioglycosyl-Naphthalimides as Potent and Selective Human O-GlcNAcase Inhibitors.,  (12): [PMID:30613333] [10.1021/acsmedchemlett.8b00406]

Source