U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C18H29N3O5S
Molecular Weight 399.505
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LENAPENEM

SMILES

[H][C@]12[C@@H](C)C(S[C@@H]3CN[C@@]([H])(C3)[C@H](O)CCNC)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(O)=O

InChI

InChIKey=PZLOCBSBEUDCPF-YJIVIRPOSA-N
InChI=1S/C18H29N3O5S/c1-8-14-13(9(2)22)17(24)21(14)15(18(25)26)16(8)27-10-6-11(20-7-10)12(23)4-5-19-3/h8-14,19-20,22-23H,4-7H2,1-3H3,(H,25,26)/t8-,9-,10+,11+,12-,13-,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula C18H29N3O5S
Molecular Weight 399.505
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including, https://www.ncbi.nlm.nih.gov/pubmed/9099223

Lenapenem is an anti-bacterial agent that was tested in late 90's in phase II clinical trials against bacterial infections. Lenapenem was shown to be active against both Gram-positive and Gram-negative bacteria and exerted its therapeutic effect by inhibiting penicillin binding proteins. The development of the drug was terminated due to the safety reason.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Mechanism of enhanced antipseudomonal activity of BO-2727, a new injectable 1-beta-methyl carbapenem.
1995 Mar
In vitro and in vivo evaluation of BO-2727 against imipenem- and/or meropenem-resistant Pseudomonas aeruginosa.
1997 Feb
Patents

Patents

Sample Use Guides

Unknown
Route of Administration: Intravenous
In Vitro Use Guide
Lenapenam was tested against different strains of bacteria. The MIC50 values were: 0.1 ug/ml (Staphylococcus aureus, methicillin susceptibl), 0.05 ug/ml (Staphylococcus epidermidis), <0.006 ug/ml (Streptococcus pyogenes), 0.025 ug/ml (Streptococcus pneumoniae), 0.05 ug/ml (E.coli, Kiebsiella pneumoniae, Enterobacter cloacae), 0.012 ug/ml (Branhamella catarrhalis), etc.
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:39:21 GMT 2023
Edited
by admin
on Fri Dec 15 16:39:21 GMT 2023
Record UNII
D6NBQ3H12U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LENAPENEM
INN  
INN  
Official Name English
(+)-(4R,5S,6S)-6-((R)-1-HYDROXYETHYL)-3-(((3S,5S)-5-((R)-1-HYDROXY-3-(METHYLAMINO)PROPYL)-3-PYRROLIDINYL)THIO)-4-METHYL-7-OXO-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID
Systematic Name English
lenapenem [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C260
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID701031259
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
WIKIPEDIA
Lenapenem
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
SMS_ID
100000082569
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104796
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
INN
7384
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
FDA UNII
D6NBQ3H12U
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
NCI_THESAURUS
C81662
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
CAS
149951-16-6
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
PUBCHEM
216262
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
EVMPD
SUB08431MIG
Created by admin on Fri Dec 15 16:39:21 GMT 2023 , Edited by admin on Fri Dec 15 16:39:21 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY