ID: ALA2303853

Max Phase: Preclinical

Molecular Formula: C16H27NO12

Molecular Weight: 425.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)[C@@H]1O[C@@H](OC)[C@@H](NC(C)=O)[C@@H](O)[C@@H]1O[C@@H]1O[C@@H](CO)[C@H](O)[C@H](O)[C@@H]1O

Standard InChI:  InChI=1S/C16H27NO12/c1-5(19)17-7-9(21)12(13(14(24)25-2)29-15(7)26-3)28-16-11(23)10(22)8(20)6(4-18)27-16/h6-13,15-16,18,20-23H,4H2,1-3H3,(H,17,19)/t6-,7-,8-,9+,10-,11-,12-,13+,15+,16-/m0/s1

Standard InChI Key:  HECHRIWYXUCCFQ-ZSRWQXKBSA-N

Associated Targets(Human)

Fucosyltransferase 4 41 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase 61 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: 425.39Molecular Weight (Monoisotopic): 425.1533AlogP: -4.42#Rotatable Bonds: 6
Polar Surface Area: 193.47Molecular Species: NEUTRALHBA: 12HBD: 6
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 6#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.88CX Basic pKa: CX LogP: -3.88CX LogD: -3.88
Aromatic Rings: 0Heavy Atoms: 29QED Weighted: 0.22Np Likeness Score: 1.54

References

1. Galan MC, Dodson CS, Venot AP, Boons GJ..  (2004)  Glycosyltransferase activity can be selectively modulated by chemical modifications of acceptor substrates.,  14  (9): [PMID:15081009] [10.1016/j.bmcl.2004.02.024]

Source