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Details

Stereochemistry ABSOLUTE
Molecular Formula C19H22N8O6S2.H2O4S
Molecular Weight 620.636
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CEFOSELIS SULFATE

SMILES

OS(O)(=O)=O.[H][C@]12SCC(CN3C=CC(=N)N3CCO)=C(N1C(=O)[C@H]2NC(=O)C(=N/OC)\C4=CSC(N)=N4)C(O)=O

InChI

InChIKey=LZOLCSVRFKCSEM-ZQCAECPKSA-N
InChI=1S/C19H22N8O6S2.H2O4S/c1-33-24-12(10-8-35-19(21)22-10)15(29)23-13-16(30)27-14(18(31)32)9(7-34-17(13)27)6-25-3-2-11(20)26(25)4-5-28;1-5(2,3)4/h2-3,8,13,17,20,28H,4-7H2,1H3,(H2,21,22)(H,23,29)(H,31,32);(H2,1,2,3,4)/b20-11?,24-12-;/t13-,17-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C19H22N8O6S2
Molecular Weight 522.558
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: http://psjd.icm.edu.pl/psjd/element/bwmeta1.element.psjd-bcc86349-7720-450f-8027-017dafa5ba9c

Cefoselis sulphate is a new parenteral cephalosporin, which was launched into therapy in Japan on 9 September, 1998, under the brand name Wincef. Cefoselis sulphate, like all the other beta-lactams, exhibits its bactericidal eff ects by binding to penicillinbinding proteins. It has a spectrum of activity that covers aerobic and anaerobic gram-positive and gram-negative bacteria. Cefoselis sulphate has been approved to treat infections caused by Staphylococcus and Pseudomonas especially respiratory and urinary tract infections. The recommended dose of cefoselis is 1 g twice a day as an intravenous infusion. The duration of therapy is from 5 to 14 days. Cefoselis sulfate has a potent antibacterial activity against Gram-positive bacteria involving Staphylococcus, Pneumococcus, and Streptococcus, as well as Gram-negative bacteria involving Pseudomonas, Escherichia coli, Klebsiella, Enterobacter, Serratia, Proteus, Morganella, and Providencia.

Originator

Curator's Comment: Wincef is a new parenteral cephalosporin antibiotic internally generated from Fujisawa's research pipeline.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Wincef

Approved Use

Wincef is indicated to treat a variety of infections with moderate severity or higher caused by cefoselis-susceptible strains such as Staphylococcus and Pseudomonas, including respiratory tract infections and urinary tract infections.

Launch Date

1998
Curative
Wincef

Approved Use

Wincef is indicated to treat a variety of infections with moderate severity or higher caused by cefoselis-susceptible strains such as Staphylococcus and Pseudomonas, including respiratory tract infections and urinary tract infections.

Launch Date

1998
PubMed

PubMed

TitleDatePubMed
Multicenter, double-blind, randomized clinical trial of parenterally administered Cefoselis versus Cefepime for the treatment of acute bacterial infections.
2014
Stability studies of cefoselis sulfate in the solid state.
2015 Oct 10
Patents

Sample Use Guides

1.0 g of for moderate infection or 2.0 g intravenous infusion for severe infection administered at an interval of 12 hours for 7 to 14 days
Route of Administration: Intravenous
In Vitro Use Guide
Cefoselis sulphate inhibited methicillin-susceptible staphylocci at < or = 4 ug/ml. Of 98 isolates of homogenous methicillin-resistant Staphylococcus aureus, 55 (56.1%) were inhibited by 8 ug of FK-037 per ml
Substance Class Chemical
Created
by admin
on Sat Dec 16 06:39:21 GMT 2023
Edited
by admin
on Sat Dec 16 06:39:21 GMT 2023
Record UNII
6EY42207VS
Record Status Validated (UNII)
Record Version
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Name Type Language
CEFOSELIS SULFATE
MI   WHO-DD  
Common Name English
FK 037
Common Name English
5-AMINO-2-(((6R,7R)-7-(((Z)-2-(2-AMINO-4-THIAZOLYL)-2-(METHOXYIMINO)ACETYL)-AMINO)-2-CARBOXY-8-OXO-5-THIA-1-AZABICYCLO(4.2.0)OCT-2-EN-3-YL)METHYL)-1-(2-HYDROXYETHYL)-1H-PYRAZOLIUM HYDROXIDE SULFATE
Common Name English
5-THIA-1-AZABICYCLO(4.2.0)OCT-2-ENE-2-CARBOXYLIC ACID, 7-(((2Z)-2-(2-AMINO-4-THIAZOLYL)-2-(METHOXYIMINO)ACETYL)AMINO)-3-((2,3-DIHYDRO-2-(2-HYDROXYETHYL)-3-IMINO-1H-PYRAZOL-1-YL)METHYL)-8-OXO-, (6R,7R)-, SULFATE (1:1)
Common Name English
FK-037
Common Name English
Cefoselis sulfate [WHO-DD]
Common Name English
CEFOSELIS SULFATE [MI]
Common Name English
CEFOSELIS SULFATE [JAN]
Common Name English
WINSEF
Brand Name English
Code System Code Type Description
CAS
122841-12-7
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
PRIMARY
FDA UNII
6EY42207VS
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
PRIMARY
MERCK INDEX
m3203
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Cefoselis sulfate
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
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EPA CompTox
DTXSID8046795
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
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PUBCHEM
9830519
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
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EVMPD
SUB22069
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
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SMS_ID
100000085393
Created by admin on Sat Dec 16 06:39:21 GMT 2023 , Edited by admin on Sat Dec 16 06:39:21 GMT 2023
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