Compounds > achromobactin
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achromobactin

Description

achromobactin: isolated from Erwinia chrysanthemi; structure in first source [MeSH]

achromobactin : A citrate siderophore possessing four carboxylate groups suitable for iron coordination. [CHeBI]

Cross-References

ID SourceID
PubMed CID50909799
CHEBI ID61346
MeSH IDM0370163

Synonyms (4)

Synonym
achromobactin
1-[1-carboxylato-3-({(3r)-3-carboxylato-5-[2-(2-carboxylato-2-hydroxy-5-oxopyrrolidin-1-yl)ethoxy]-3-hydroxy-5-oxopentanoyl}amino)propyl]-2-hydroxy-5-oxopyrrolidine-2-carboxylate
CHEBI:61346
Q27131050

Roles (1)

RoleDescription
siderophoreAny of low-molecular-mass iron(III)-chelating compounds produced by microorganisms for the purpose of the transport and sequestration of iron.

Drug Classes (1)

ClassDescription
tetracarboxylic acid anionAny anion of a tetracarboxylic acid formed by deprotonation of one or more carboxy groups.

Research

Studies (11)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (45.45)29.6817
2010's5 (45.45)24.3611
2020's1 (9.09)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (8.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other11 (91.67%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
deferoxamine
0
acyclic desferrioxaminebacterial metabolite;
ferroptosis inhibitor;
iron chelator;
siderophore		00low000000
enterobactin
0
catechols;
crown compound;
macrotriolide;
polyphenol		bacterial metabolite;
siderophore		00low000000
aerobactin
0
L-lysine derivativeEscherichia coli metabolite;
siderophore;
virulence factor		00low000000
chrysobactin
0
catechols;
dipeptide;
monocarboxylic acid;
primary alcohol;
primary amino compound		bacterial metabolite;
siderophore		00low000000
deferrioxamine e
0
cyclic desferrioxamine;
cyclic hydroxamic acid;
macrocycle		antineoplastic agent;
bacterial metabolite;
marine metabolite;
siderophore		00low000000
vibriobactin
0
1,3-oxazoles;
secondary carboxamide		siderophore00low000000
pyochelin
0
monocarboxylic acid;
phenols;
thiazolidines		metabolite;
siderophore		00low000000
yersiniabactin
0
monocarboxylic acid;
phenols;
secondary alcohol;
thiazolidines		bacterial metabolite;
siderophore		00low000000
rhodotorulic acid
0
2,5-diketopiperazines;
hydroxamic acid;
L-ornithine derivative		fungal metabolite;
siderophore		00low000000
schizokinen
0
2-hydroxy carboxylic acid;
hydroxamic acid		bacterial metabolite;
siderophore		00low000000
coelichelin
0
formamides;
hydroxamic acid;
tetrapeptide		bacterial metabolite;
siderophore		00low000000
myxochelin b
0
benzamides;
catechols		bacterial metabolite;
siderophore		00low000000
vibrioferrin
0
carboxylic ester;
N-acyl hemiaminal;
pyrrolidin-2-ones;
tertiary alcohol;
tricarboxylic acid		marine metabolite;
siderophore		00low000000
vanchrobactin
0
catechols;
dipeptide;
guanidines;
monocarboxylic acid;
primary alcohol;
triol		bacterial metabolite;
marine metabolite;
siderophore		00low000000
n(alpha)-acetylfusarinines
0
2,5-diketopiperazines;
acetamides;
carboxylic ester;
homoallylic alcohol;
hydroxamic acid;
primary alcohol		siderophore00low000000
staphyloferrin b
0
oxo carboxylic acid;
tertiary alcohol;
tricarboxylic acid amide;
tricarboxylic acid		bacterial metabolite;
siderophore		00low000000
quinolobactin
0
aromatic ether;
monohydroxyquinoline;
phenols;
quinolinemonocarboxylic acid		bacterial metabolite;
siderophore		00low000000
staphyloferrin a
0
D-ornithine derivative;
pentacarboxylic acid;
tertiary alcohol;
tricarboxylic acid amide		bacterial metabolite;
siderophore		00low000000
cefiderocol
0
carboxylic acid;
cephalosporin		antibacterial drug;
siderophore		00low000000
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
citric acid, anhydrous
2
tricarboxylic acidantimicrobial agent;
chelator;
food acidity regulator;
fundamental metabolite		2009201114.0medium000110
trimethylenediamine
1
alkane-alpha,omega-diaminehuman metabolite;
mouse metabolite;
reagent		2009200915.0low000100
2,4-diaminobutyric acid
1
diamino acid;
gamma-amino acid;
non-proteinogenic alpha-amino acid		2009200915.0low000100
ethanolamine
1
ethanolamines;
primary alcohol;
primary amine		Escherichia coli metabolite;
human metabolite;
mouse metabolite		2009200915.0low000100
deferoxamine
1
acyclic desferrioxaminebacterial metabolite;
ferroptosis inhibitor;
iron chelator;
siderophore		2005200519.0low000100
ethylenediamine
1
alkane-alpha,omega-diamineGABA agonist2009200915.0low000100
streptonigrin
1
pyridines;
quinolone		antimicrobial agent;
antineoplastic agent		2009200915.0low000100
serine
1
L-alpha-amino acid;
proteinogenic amino acid;
serine family amino acid;
serine zwitterion;
serine		algal metabolite;
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite		2011201113.0low000010
copper gluconate
1
organic molecular entity2002200222.0low000100
aerobactin
1
L-lysine derivativeEscherichia coli metabolite;
siderophore;
virulence factor		2005200519.0low000100
chrysobactin
2
catechols;
dipeptide;
monocarboxylic acid;
primary alcohol;
primary amino compound		bacterial metabolite;
siderophore		2002200918.5high000200
2-oxo-3-deoxygalactonic acid
1
hexonic acid;
ketoaldonic acid		Escherichia coli metabolite2002200222.0low000100
pectins
1
D-galactopyranuronic acid2002200222.0low000100
pyoverdin
3
2009201114.0medium000210
vibrioferrin
1
carboxylic ester;
N-acyl hemiaminal;
pyrrolidin-2-ones;
tertiary alcohol;
tricarboxylic acid		marine metabolite;
siderophore		2005200519.0low000100
alcaligin
1
cyclic hydroxamic acid2005200519.0low000100
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020