(1S,2R)-1-((2R,3R,4S)-3-acetamido-6-(methoxycarbonyl)-4-(3-(2-methoxyphenyl)ureido)-3,4-dihydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate

ID: ALA4171569

Chembl Id: CHEMBL4171569

PubChem CID: 145950499

Max Phase: Preclinical

Molecular Formula: C26H33N3O12

Molecular Weight: 579.56

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COC(=O)C1=C[C@H](NC(=O)Nc2ccccc2OC)[C@@H](NC(C)=O)[C@H]([C@H](OC(C)=O)[C@@H](COC(C)=O)OC(C)=O)O1

Standard InChI:  InChI=1S/C26H33N3O12/c1-13(30)27-22-18(29-26(35)28-17-9-7-8-10-19(17)36-5)11-20(25(34)37-6)41-24(22)23(40-16(4)33)21(39-15(3)32)12-38-14(2)31/h7-11,18,21-24H,12H2,1-6H3,(H,27,30)(H2,28,29,35)/t18-,21+,22+,23+,24+/m0/s1

Standard InChI Key:  PVSIUDJPBMQZDW-PCYHMHGQSA-N

Alternative Forms

  1. Parent:

    ALA4171569

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Associated Targets(non-human)

Hemagglutinin-neuraminidase (36 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

Calculated Properties

Molecular Weight: 579.56Molecular Weight (Monoisotopic): 579.2064AlogP: 0.57#Rotatable Bonds: 11
Polar Surface Area: 193.89Molecular Species: NEUTRALHBA: 12HBD: 3
#RO5 Violations: 2HBA (Lipinski): 15HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.93CX Basic pKa: CX LogP: -0.52CX LogD: -0.52
Aromatic Rings: 1Heavy Atoms: 41QED Weighted: 0.24Np Likeness Score: 0.26

References

1. El-Deeb IM, Guillon P, Dirr L, von Itzstein M..  (2017)  Exploring inhibitor structural features required to engage the 216-loop of human parainfluenza virus type-3 hemagglutinin-neuraminidase.,  (1): [PMID:30108698] [10.1039/C6MD00519E]

Source