(S)-methyl 2-(2-(3-methoxy-1,4-dioxo-1,4-dihydronaphthalen-2-ylthio)acetamido)propanoate

ID: ALA3309421

Chembl Id: CHEMBL3309421

PubChem CID: 118705829

Max Phase: Preclinical

Molecular Formula: C17H17NO6S

Molecular Weight: 363.39

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COC(=O)[C@H](C)NC(=O)CSC1=C(OC)C(=O)c2ccccc2C1=O

Standard InChI:  InChI=1S/C17H17NO6S/c1-9(17(22)24-3)18-12(19)8-25-16-14(21)11-7-5-4-6-10(11)13(20)15(16)23-2/h4-7,9H,8H2,1-3H3,(H,18,19)/t9-/m0/s1

Standard InChI Key:  ZQBRLZFIOGHFNU-VIFPVBQESA-N

Alternative Forms

  1. Parent:

    ALA3309421

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Associated Targets(Human)

HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SAS (201 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 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: 363.39Molecular Weight (Monoisotopic): 363.0777AlogP: 1.33#Rotatable Bonds: 6
Polar Surface Area: 98.77Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 11.72CX Basic pKa: CX LogP: 0.25CX LogD: 0.25
Aromatic Rings: 1Heavy Atoms: 25QED Weighted: 0.76Np Likeness Score: -0.36

References

1. Sreelatha T, Kandhasamy S, Dinesh R, Shruthy S, Shweta S, Mukesh D, Karunagaran D, Balaji R, Mathivanan N, Perumal PT..  (2014)  Synthesis and SAR study of novel anticancer and antimicrobial naphthoquinone amide derivatives.,  24  (15): [PMID:24913712] [10.1016/j.bmcl.2014.04.080]

Source