N-Hydroxy-3-(pyridin-4-yl)acrylamide Hydrochloride

ID: ALA5208488

PubChem CID: 168297495

Max Phase: Preclinical

Molecular Formula: C8H9ClN2O2

Molecular Weight: 164.16

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cl.O=C(/C=C/c1ccncc1)NO

Standard InChI:  InChI=1S/C8H8N2O2.ClH/c11-8(10-12)2-1-7-3-5-9-6-4-7;/h1-6,12H,(H,10,11);1H/b2-1+;

Standard InChI Key:  LAOJAJJYEJRIHJ-TYYBGVCCSA-N

Molfile:  

     RDKit          2D

 13 12  0  0  0  0  0  0  0  0999 V2000
    2.4139   -1.4987    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.0703    1.2370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0703    0.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7846   -0.0002    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4991    0.4120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3558   -0.0002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3585    0.4120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0730   -0.0002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0730   -0.8253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7829   -1.2370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4991   -0.8290    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4991   -0.0008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7847    0.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0
  3  4  1  0
  4  5  1  0
  6  3  1  0
  7  6  2  0
  8  7  1  0
  9  8  2  0
 10  9  1  0
 11 10  2  0
 12 11  1  0
 13 12  2  0
  8 13  1  0
M  END

Associated Targets(non-human)

Mycobacteroides abscessus (2066 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium marinum (465 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 164.16Molecular Weight (Monoisotopic): 164.0586AlogP: 0.60#Rotatable Bonds: 2
Polar Surface Area: 62.22Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 9.55CX Basic pKa: 5.10CX LogP: 0.11CX LogD: 0.10
Aromatic Rings: 1Heavy Atoms: 12QED Weighted: 0.38Np Likeness Score: -0.24

References

1. Mavrikaki V, Pagonis A, Poncin I, Mallick I, Canaan S, Magrioti V, Cavalier JF..  (2022)  Design, synthesis and antibacterial activity against pathogenic mycobacteria of conjugated hydroxamic acids, hydrazides and O-alkyl/O-acyl protected hydroxamic derivatives.,  64  [PMID:35307568] [10.1016/j.bmcl.2022.128692]

Source