ID: ALA3038258

Max Phase: Preclinical

Molecular Formula: C16H23N5Na3O18P3

Molecular Weight: 669.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C[C@@H]1O[C@H](OP(=O)([O-])OP(=O)([O-])OP(=O)([O-])OC[C@H]2O[C@@H](n3cnc4c(O)nc(N)nc43)[C@H](O)[C@@H]2O)[C@H](O)[C@@H](O)[C@@H]1O.[Na+].[Na+].[Na+]

Standard InChI:  InChI=1S/C16H26N5O18P3.3Na/c1-4-7(22)9(24)11(26)15(35-4)37-41(30,31)39-42(32,33)38-40(28,29)34-2-5-8(23)10(25)14(36-5)21-3-18-6-12(21)19-16(17)20-13(6)27;;;/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H,32,33)(H3,17,19,20,27);;;/q;3*+1/p-3/t4-,5+,7+,8+,9-,10+,11+,14+,15+;;;/m0.../s1

Standard InChI Key:  WLMDSGQDMCFYTO-KVNJRFESSA-K

Associated Targets(Human)

Galactoside 3(4)-L-fucosyltransferase 5 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fucosyltransferase 6 19 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: 669.32Molecular Weight (Monoisotopic): 669.0486AlogP: -3.07#Rotatable Bonds: 10
Polar Surface Area: 358.28Molecular Species: ACIDHBA: 20HBD: 10
#RO5 Violations: 3HBA (Lipinski): 23HBD (Lipinski): 11#RO5 Violations (Lipinski): 3
CX Acidic pKa: 0.88CX Basic pKa: 0.61CX LogP: -4.29CX LogD: -10.79
Aromatic Rings: 2Heavy Atoms: 42QED Weighted: 0.11Np Likeness Score: 1.21

References

1. Baisch G, Ohrlein R, Katopodis A.  (1996)  Enzymatic fucosylations with purine-diphosphate-fucoses (PDP-Fucoses),  (24): [10.1016/S0960-894X(96)00543-4]

Source