(S)-1-(6,7-Dihydroxy-2-naphthoyl)-N-phenylpyrrolidine-2-carboxamide

ID: ALA4878362

PubChem CID: 164626890

Max Phase: Preclinical

Molecular Formula: C22H20N2O4

Molecular Weight: 376.41

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(Nc1ccccc1)[C@@H]1CCCN1C(=O)c1ccc2cc(O)c(O)cc2c1

Standard InChI:  InChI=1S/C22H20N2O4/c25-19-12-14-8-9-15(11-16(14)13-20(19)26)22(28)24-10-4-7-18(24)21(27)23-17-5-2-1-3-6-17/h1-3,5-6,8-9,11-13,18,25-26H,4,7,10H2,(H,23,27)/t18-/m0/s1

Standard InChI Key:  GVTVNGAYGYEBQX-SFHVURJKSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4878362

    ---

Associated Targets(non-human)

NS3 Genome polyprotein (385 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dengue virus type 2 NS3 protein (2214 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

Calculated Properties

Molecular Weight: 376.41Molecular Weight (Monoisotopic): 376.1423AlogP: 3.49#Rotatable Bonds: 3
Polar Surface Area: 89.87Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 9.09CX Basic pKa: CX LogP: 3.18CX LogD: 3.17
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.61Np Likeness Score: -0.97

References

1. Maus H, Barthels F, Hammerschmidt SJ, Kopp K, Millies B, Gellert A, Ruggieri A, Schirmeister T..  (2021)  SAR of novel benzothiazoles targeting an allosteric pocket of DENV and ZIKV NS2B/NS3 proteases.,  47  [PMID:34509861] [10.1016/j.bmc.2021.116392]

Source