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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H14N6O10S2
Molecular Weight 466.404
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CARUMONAM

SMILES

NC(=O)OC[C@@H]1[C@H](NC(=O)C(=N/OCC(O)=O)\C2=CSC(N)=N2)C(=O)N1S(O)(=O)=O

InChI

InChIKey=UIMOJFJSJSIGLV-JNHMLNOCSA-N
InChI=1S/C12H14N6O10S2/c13-11-15-4(3-29-11)7(17-28-2-6(19)20)9(21)16-8-5(1-27-12(14)23)18(10(8)22)30(24,25)26/h3,5,8H,1-2H2,(H2,13,15)(H2,14,23)(H,16,21)(H,19,20)(H,24,25,26)/b17-7-/t5-,8+/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: https://www.ncbi.nlm.nih.gov/pubmed/4073864 | https://www.ncbi.nlm.nih.gov/pubmed/3065522 | https://www.ncbi.nlm.nih.gov/pubmed/3377459

Carumonam is a monobactam antibacterial agent. It was highly active in vitro against members of the family Enterobacteriaceae, Pseudomonas aeruginosa, and Haemophilus influenzae and weakly active against Streptococcus pneumoniae, but it was not active against Staphylococcus aureus. The excellent activity of carumonam against Gram-negative bacteria is related to its high affinity for their penicillin-binding proteins. It is indicated for the treatment of urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis. Another factor that contributes to the excellent activity of carumonam against Gram-negative bacteria is its resistance to beta-lactamases. Adverse effects of the carumonam were limited to phlebitis at the intravenous infusion site; bloody diarrhea.

Originator

Curator's Comment: # Takeda Chemical Industries, Ltd. http://doi.org/10.1248/cpb.33.3798 | doi:10.7164/antibiotics.36.1421

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Amasulin

Approved Use

It is indicated for the treatment of infections, caused by sensitive bacteria: urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis.
Curative
Amasulin

Approved Use

It is indicated for the treatment of infections, caused by sensitive bacteria: urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis.
Curative
Amasulin

Approved Use

It is indicated for the treatment of infections, caused by sensitive bacteria: urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis.
Curative
Amasulin

Approved Use

It is indicated for the treatment of infections, caused by sensitive bacteria: urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis.
Curative
Amasulin

Approved Use

It is indicated for the treatment of infections, caused by sensitive bacteria: urinary tract infections, chronic respiratory infections, biliary tract infections, peritonitis, sepsis.
PubMed

PubMed

TitleDatePubMed
Comparative epileptogenic properties of two monobactam derivatives in C57, Swiss and DBA/2 mice.
1996 Sep
Patents

Sample Use Guides

The usual dose is 1-2 g daily in two divided doses.
Route of Administration: Other
In Vitro Use Guide
Enterobacteriaceae were highly susceptible to carumonam, 90% of the isolates being inhibited at 0.5 ug/ml.
Name Type Language
CARUMONAM
INN   MI   WHO-DD  
INN  
Official Name English
ACETIC ACID, (((2-((2-(((AMINOCARBONYL)OXY)METHYL)-4-OXO-1-SULFO-3-AZETIDINYL)AMINO)-1-(2-AMINO-4-THIAZOLYL)-2-OXOETHYLIDENE)AMINO)OXY)-, (2S-(2.ALPHA.,3.ALPHA.(Z)))-
Systematic Name English
AMA 1080 FREE ACID
Code English
(Z)-((((2-AMINO-4-THIAZOLYL)(((2S,3S)-2-(HYDROXYMETHYL)-4-OXO-1-SULFO-3-AZETIDINYL)CARBAMOYL)METHYLENE)AMINO)OXY)ACETIC ACID, CARBAMATE (ESTER)
Systematic Name English
CARUMONAM [MI]
Common Name English
Carumonam [WHO-DD]
Common Name English
carumonam [INN]
Common Name English
AMA-1080 FREE ACID
Code English
Classification Tree Code System Code
WHO-ATC J01DF02
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
WHO-VATC QJ01DF02
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
NCI_THESAURUS C260
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
Code System Code Type Description
MERCK INDEX
m3141
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
PRIMARY Merck Index
NCI_THESAURUS
C79879
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DRUG BANK
DB13553
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SMS_ID
100000081331
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PUBCHEM
6540466
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WIKIPEDIA
CARUMONAM
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INN
5508
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PRIMARY
CAS
87638-04-8
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EPA CompTox
DTXSID3048312
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MESH
C044145
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PRIMARY
ChEMBL
CHEMBL1614658
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EVMPD
SUB06152MIG
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CHEBI
55486
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FDA UNII
486890PI06
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
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DRUG CENTRAL
521
Created by admin on Fri Dec 15 16:13:45 GMT 2023 , Edited by admin on Fri Dec 15 16:13:45 GMT 2023
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