ID: ALA4281743

Max Phase: Preclinical

Molecular Formula: C23H33FN2O7S2

Molecular Weight: 532.66

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  NC(=O)[C@@H](CCC(=O)O)NC(=O)[C@H]1C[C@@H](O)[C@H](O)[C@H](O)[C@H]1SCCCCSCc1cccc(F)c1

Standard InChI:  InChI=1S/C23H33FN2O7S2/c24-14-5-3-4-13(10-14)12-34-8-1-2-9-35-21-15(11-17(27)19(30)20(21)31)23(33)26-16(22(25)32)6-7-18(28)29/h3-5,10,15-17,19-21,27,30-31H,1-2,6-9,11-12H2,(H2,25,32)(H,26,33)(H,28,29)/t15-,16+,17+,19-,20-,21-/m0/s1

Standard InChI Key:  XWFAZBHVUZVKKN-HWMQIADMSA-N

Associated Targets(Human)

CD209 antigen 101 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: 532.66Molecular Weight (Monoisotopic): 532.1713AlogP: 0.88#Rotatable Bonds: 14
Polar Surface Area: 170.18Molecular Species: ACIDHBA: 8HBD: 6
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 7#RO5 Violations (Lipinski): 2
CX Acidic pKa: 3.90CX Basic pKa: CX LogP: 0.38CX LogD: -2.83
Aromatic Rings: 1Heavy Atoms: 35QED Weighted: 0.19Np Likeness Score: -0.41

References

1. Kiessling LL..  (2018)  Chemistry-driven glycoscience.,  26  (19): [PMID:30297120] [10.1016/j.bmc.2018.09.024]

Source