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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H11N2O6S.Na
Molecular Weight 310.259
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RITIPENEM SODIUM

SMILES

[Na+].[H][C@]12SC(COC(N)=O)=C(N1C(=O)[C@]2([H])[C@@H](C)O)C([O-])=O

InChI

InChIKey=FPLQVCOCYJJHBC-HIQLJADVSA-M
InChI=1S/C10H12N2O6S.Na/c1-3(13)5-7(14)12-6(9(15)16)4(19-8(5)12)2-18-10(11)17;/h3,5,8,13H,2H2,1H3,(H2,11,17)(H,15,16);/q;+1/p-1/t3-,5+,8-;/m1./s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C10H11N2O6S
Molecular Weight 287.269
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
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/10508039 and http://www.genome.jp/dbget-bin/www_bget?dr:D09849

Ritipenem (FCE 22101), a penem antibiotic, penicillin binding protein inhibitor, is potent against both gram-positive and -negative bacteria, and its acetoxymethyl ester (FCE 22891; ritipenem-acoxil) is orally available. Ritipenem is manufactured by Tanabe Seiyaku in the ritipenem acoxil prodrug form, which can be taken orally. It is not FDA approved in the United States.

Approval Year

Targets

Targets

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
A study of the pharmacokinetics and tolerability of ritipenem acoxil in healthy volunteers following multiple oral dosing.
1997 Aug
MEN 10700, a new penem antibiotic: in-vitro activity and its correlation with beta-lactamase stability, PBP affinity and diffusion through the bacterial cell wall.
1998 May
Potent bacteriolytic activity of ritipenem associated with a characteristic profile of affinities for penicillin-binding proteins of Haemophilus influenzae.
1999 Oct
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Can also be used intravenously https://www.ncbi.nlm.nih.gov/pubmed/2732142
Ritipenem-acoxil was orally administered at 200 mg for 14 days
Route of Administration: Oral
In Vitro Use Guide
Ritipenem inhibited Escherichia coli growth with MIC = 1ug/ml
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:06:37 GMT 2023
Edited
by admin
on Sat Dec 16 02:06:37 GMT 2023
Record UNII
5EZT24K3CG
Record Status Validated (UNII)
Record Version
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Name Type Language
RITIPENEM SODIUM
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 3-(((AMINOCARBONYL)OXY)METHYL)-6-((1R)-1-HYDROXYETHYL)-7-OXO-, MONOSODIUM SALT, (5R,6S)-
Common Name English
FCE-22101
Code English
RITIPENEM SODIUM SALT [MI]
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 3-(((AMINOCARBONYL)OXY)METHYL)-6-(1-HYDROXYETHYL)-7-OXO-, MONOSODIUM SALT, (5R-(5.ALPHA.,6.ALPHA.(R*)))-
Common Name English
RITIPENEM SODIUM SALT
MI  
Common Name English
4-THIA-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID, 3-(((AMINOCARBONYL)OXY)METHYL)-6-((1R)-1-HYDROXYETHYL)-7-OXO-, SODIUM SALT (1:1), (5R,6S)-
Common Name English
Code System Code Type Description
MERCK INDEX
m9634
Created by admin on Sat Dec 16 02:06:37 GMT 2023 , Edited by admin on Sat Dec 16 02:06:37 GMT 2023
PRIMARY Merck Index
PUBCHEM
23663950
Created by admin on Sat Dec 16 02:06:37 GMT 2023 , Edited by admin on Sat Dec 16 02:06:37 GMT 2023
PRIMARY
CAS
84845-58-9
Created by admin on Sat Dec 16 02:06:37 GMT 2023 , Edited by admin on Sat Dec 16 02:06:37 GMT 2023
PRIMARY
FDA UNII
5EZT24K3CG
Created by admin on Sat Dec 16 02:06:37 GMT 2023 , Edited by admin on Sat Dec 16 02:06:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID801005118
Created by admin on Sat Dec 16 02:06:37 GMT 2023 , Edited by admin on Sat Dec 16 02:06:37 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE