5-[(Triphenylphosphonio)methyl]-3-hydroxy-4-(hydroxymethyl)-2-methylpyridin-1-ium dichloride

ID: ALA2398203

PubChem CID: 71723320

Max Phase: Preclinical

Molecular Formula: C26H26Cl2NO2P

Molecular Weight: 414.47

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ncc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c(CO)c1O.Cl.[Cl-]

Standard InChI:  InChI=1S/C26H24NO2P.2ClH/c1-20-26(29)25(18-28)21(17-27-20)19-30(22-11-5-2-6-12-22,23-13-7-3-8-14-23)24-15-9-4-10-16-24;;/h2-17,28H,18-19H2,1H3;2*1H

Standard InChI Key:  XFMOORWFDYAVQC-UHFFFAOYSA-N

Molfile:  

     RDKit          2D

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   14.7765   -5.7606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4913   -6.1735    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   16.2077   -5.7602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2049   -4.9296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0617   -6.1726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9178   -4.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6338   -4.9243    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   17.6369   -5.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9249   -6.1613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9276   -6.9855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   18.9617   -2.8195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   18.4290   -5.1333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6432   -5.9283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4377   -6.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0172   -5.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7971   -4.7564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0031   -4.5509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7777   -4.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4909   -4.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4916   -3.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7808   -3.2897    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0651   -4.5256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.5915   -3.6833    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
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M  CHG  2   8   1  32  -1
M  END

Associated Targets(non-human)

Proteus (150 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 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: 414.47Molecular Weight (Monoisotopic): 414.1617AlogP: 4.08#Rotatable Bonds: 6
Polar Surface Area: 53.35Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 9.37CX Basic pKa: 5.52CX LogP: 4.20CX LogD: 4.18
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.47Np Likeness Score: 0.23

References

1. Pugachev MV, Shtyrlin NV, Sysoeva LP, Nikitina EV, Abdullin TI, Iksanova AG, Ilaeva AA, Musin RZ, Berdnikov EA, Shtyrlin YG..  (2013)  Synthesis and antibacterial activity of novel phosphonium salts on the basis of pyridoxine.,  21  (14): [PMID:23683836] [10.1016/j.bmc.2013.04.051]

Source