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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H34FN7O4
Molecular Weight 479.5483
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LANOPEPDEN

SMILES

[H][C@]12COCCN1CCN(C2)C3=C(F)C(NNC(=O)[C@H](CC4CCCC4)CN(O)C=O)=NC(C)=N3

InChI

InChIKey=SWHNZGMQMGFQGW-MSOLQXFVSA-N
InChI=1S/C22H34FN7O4/c1-15-24-20(19(23)21(25-15)29-7-6-28-8-9-34-13-18(28)12-29)26-27-22(32)17(11-30(33)14-31)10-16-4-2-3-5-16/h14,16-18,33H,2-13H2,1H3,(H,27,32)(H,24,25,26)/t17-,18+/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H34FN7O4
Molecular Weight 479.5483
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

LANOPEPDEN is an inhibitor of peptide deformylase, a bacterial enzyme required for protein maturation. It was in development for the treatment of complicated bacterial skin infection and hospitalized community-acquired pneumonia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Antibiotics in development targeting protein synthesis.
2011 Dec
Determination of disk diffusion and MIC quality control ranges for GSK1322322, a novel peptide deformylase inhibitor.
2011 Nov
Single-dose safety, tolerability, and pharmacokinetics of the antibiotic GSK1322322, a novel peptide deformylase inhibitor.
2013 May
Comparative analysis of the antibacterial activity of a novel peptide deformylase inhibitor, GSK1322322.
2013 May
Patents

Sample Use Guides

Lanopepden (GSK1322322) had an MIC90 of 1 μg/ml against M. catarrhalis and 4 μg/ml against H. influenzae, with 88.8% of beta-lactamase-positive strains showing growth inhibition at that concentration. All S. pneumoniae strains were inhibited by ≤ 4 μg/ml of GSK1322322, with an MIC90 of 2 μg/ml. GSK1322322 was very potent against S. pyogenes strains, with an MIC90 of 0.5 μg/ml, irrespective of their macrolide resistance phenotype. It was also active against S. aureus strains regardless of their susceptibility to methicillin, macrolides, or levofloxacin, with an MIC90 of 4 μg/ml in all cases.
Substance Class Chemical
Created
by admin
on Sat Dec 16 03:01:36 GMT 2023
Edited
by admin
on Sat Dec 16 03:01:36 GMT 2023
Record UNII
12M6KFD07E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LANOPEPDEN
INN   USAN   WHO-DD  
INN   USAN  
Official Name English
lanopepden [INN]
Common Name English
CYCLOPENTANEPROPANOIC ACID, .ALPHA.-((FORMYLHYDROXYAMINO)METHYL)-, 2-(5-FLUORO-6-((9AS)-HEXAHYDROPYRAZINO(2,1-C)(1,4)OXAZIN-8(1H)-YL)-2-METHYL-4-PYRIMIDINYL)HYDRAZIDE, (.ALPHA.R)-
Common Name English
Lanopepden [WHO-DD]
Common Name English
GSK-1322322B
Code English
GSK-322
Code English
LANOPEPDEN [USAN]
Common Name English
GSK1322322
Code English
GSK-1322322
Code English
GSK1322322B
Code English
Code System Code Type Description
USAN
BC-70
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
DRUG BANK
DB11912
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
NCI_THESAURUS
C166453
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
PUBCHEM
52918384
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
CAS
1152107-25-9
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID00151006
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
FDA UNII
12M6KFD07E
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL3301608
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
INN
10045
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
SMS_ID
300000034284
Created by admin on Sat Dec 16 03:01:36 GMT 2023 , Edited by admin on Sat Dec 16 03:01:36 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
EXCRETED UNCHANGED
ORAL ADMINISTRATION
URINE
EXCRETED UNCHANGED
INTRAVENOUS ADMINISTRATION
URINE
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ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Tmax PHARMACOKINETIC ORAL ADMINISTRATION

Biological Half-life PHARMACOKINETIC INTRAVENOUS ADMINISTRATION