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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H15NO5S3
Molecular Weight 349.446
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULOPENEM

SMILES

[H][C@]12SC(S[C@H]3CC[S@@+]([O-])C3)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C(O)=O

InChI

InChIKey=FLSUCZWOEMTFAQ-PRBGKLEPSA-N
InChI=1S/C12H15NO5S3/c1-5(14)7-9(15)13-8(11(16)17)12(20-10(7)13)19-6-2-3-21(18)4-6/h5-7,10,14H,2-4H2,1H3,(H,16,17)/t5-,6+,7+,10-,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H15NO5S3
Molecular Weight 349.446
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Sulopenem is a thiolanylthiopenem derivative patented by American multinational pharmaceutical corporation Pfizer Inc as an antibiotic with broad-spectrum antibacterial activity against most gram-positive and gram-negative bacteria. Sulopenem showed concentration-dependent bactericidal activities against Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Acinetobacter calcoaceticus. Morphological observation using a phase-contrast microscope revealed that sulopenem induced spherical cell formation with E. coli and K. pneumoniae at lower concentrations and bacteriolysis at higher concentrations. Therapeutic efficacies of sulopenem against systemic infections in mice were almost equal to those of imipenem against Streptococcus pneumoniae.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative antipneumococcal activities of sulopenem and other drugs.
2009 Jun
Patents

Patents

Sample Use Guides

10-min intravenous infusion of 1 g
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:51:05 GMT 2023
Edited
by admin
on Fri Dec 15 15:51:05 GMT 2023
Record UNII
XX514BJ1XW
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULOPENEM
INN   USAN  
USAN   INN  
Official Name English
sulopenem [INN]
Common Name English
CP-70429
Code English
(5R,6S)-6-((1R)-1-HYDROXYETHYL)-7-OXO-3-(((1R,3S)-1-OXOTETRAHYDRO-1H-1.LAMBA.(SUP 4)-THIOPHEN-3-YL)SULFANYL)-4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 6-(1-HYDROXYETHYL)-7-OXO-3-((TETRAHYDRO-3-THIENYL)THIO)-, S-OXIDE, (5R-(3(1R*,3S*),5.ALPHA.,6.ALPHA.(R*)))-
Common Name English
CP-70,429
Code English
(5R,6S)-6-[(1R)-1-Hydroxyethyl]-7-oxo-3-[[(3S)-tetrahydro-3-thienyl]thio]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid, (R)-S-oxide
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 6-((1R)-1-HYDROXYETHYL)-7-OXO-3-(((1R,3S)-TETRAHYDRO-1-OXIDO-3-THIENYL)THIO)-, (5R,6S)-
Common Name English
SULOPENEM [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C260
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
Code System Code Type Description
SMS_ID
100000082956
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
INN
7028
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
NCI_THESAURUS
C84189
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
PUBCHEM
9950244
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
EVMPD
SUB10754MIG
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
USAN
EE-1
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
ChEMBL
CHEMBL2029184
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
FDA UNII
XX514BJ1XW
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
DRUG BANK
DB15284
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
CAS
120788-07-0
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID20869656
Created by admin on Fri Dec 15 15:51:05 GMT 2023 , Edited by admin on Fri Dec 15 15:51:05 GMT 2023
PRIMARY
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