6-[(Triphenylphosphonio)methyl]-9-acetoxy-3,3,8-trimethyl-1,5-dihydro-[1,3]dioxepino[5,6-c]pyridin chloride

ID: ALA2398191

PubChem CID: 71723459

Max Phase: Preclinical

Molecular Formula: C32H33ClNO4P

Molecular Weight: 526.59

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)Oc1c(C)nc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c2c1COC(C)(C)OC2.[Cl-]

Standard InChI:  InChI=1S/C32H33NO4P.ClH/c1-23-31(37-24(2)34)29-21-36-32(3,4)35-20-28(29)30(33-23)22-38(25-14-8-5-9-15-25,26-16-10-6-11-17-26)27-18-12-7-13-19-27;/h5-19H,20-22H2,1-4H3;1H/q+1;/p-1

Standard InChI Key:  DCTAZWRMSUFSOS-UHFFFAOYSA-M

Molfile:  

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M  CHG  2   1  -1   8   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: 526.59Molecular Weight (Monoisotopic): 526.2142AlogP: 5.59#Rotatable Bonds: 6
Polar Surface Area: 57.65Molecular Species: NEUTRALHBA: 5HBD:
#RO5 Violations: 2HBA (Lipinski): 5HBD (Lipinski): #RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 2.75CX LogP: 4.91CX LogD: 4.91
Aromatic Rings: 4Heavy Atoms: 38QED Weighted: 0.24Np 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