ID: ALA4558000

Max Phase: Preclinical

Molecular Formula: C27H36N4O7S

Molecular Weight: 560.67

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(C)C)ccc(c23)C1=O

Standard InChI:  InChI=1S/C27H36N4O7S/c1-15(33)29-22-24(35)23(34)20(14-32)38-27(22)39-13-11-28-10-5-12-31-25(36)17-7-4-6-16-19(30(2)3)9-8-18(21(16)17)26(31)37/h4,6-9,20,22-24,27-28,32,34-35H,5,10-14H2,1-3H3,(H,29,33)/t20-,22-,23-,24-,27+/m1/s1

Standard InChI Key:  UBABTXPJHYMGTH-HWGAATHTSA-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: 560.67Molecular Weight (Monoisotopic): 560.2305AlogP: 0.16#Rotatable Bonds: 11
Polar Surface Area: 151.67Molecular Species: BASEHBA: 10HBD: 5
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.66CX Basic pKa: 9.87CX LogP: -0.59CX LogD: -2.99
Aromatic Rings: 2Heavy Atoms: 39QED Weighted: 0.19Np Likeness Score: -0.15

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