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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:53705 - amoxicilloyl group
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ChEBI Ontology
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ChEBI Name
amoxicilloyl group
ChEBI ID
CHEBI:53705
Definition
A penicilloyl group formed from nucleophilic cleavage of the β-lactam ring of amoxicillin.
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This entity has been manually annotated by the ChEBI Team.
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Formula
C16H20N3O5S
Net Charge
0
Average Mass
381.44700
Monoisotopic Mass
366.11237
SMILES
N1[C@H](C(S[C@]1([H])[C@H](NC([C@@H](C2=CC=C(C=C2)O)N)=O)C(=O)*)(C)C)C(O)=O
Roles Classification
Biological Role
(s):
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
allergen
A chemical compound, or part thereof, which causes the onset of an allergic reaction by interacting with any of the molecular pathways involved in an allergy.
(via
penicilloyl group allergen
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
amoxicilloyl group (
CHEBI:53705
)
has role
antibacterial agent (
CHEBI:33282
)
amoxicilloyl group (
CHEBI:53705
)
is a
penicilloyl group (
CHEBI:88224
)
amoxicilloyl group (
CHEBI:53705
)
is a
penicilloyl group allergen (
CHEBI:88223
)
amoxicilloyl group (
CHEBI:53705
)
is a
univalent carboacyl group (
CHEBI:27207
)
amoxicilloyl group (
CHEBI:53705
)
is substituent group from
amoxicillin (
CHEBI:2676
)
Incoming
amoxicilloyl-
L
-lysine (
CHEBI:139366
)
has part
amoxicilloyl group (
CHEBI:53705
)
amoxicilloyl-benzylamine (
CHEBI:55440
)
has part
amoxicilloyl group (
CHEBI:53705
)
IUPAC Name
(2
R
)-
2-
{[(2
R
)-
2-
amino-
2-
(4-
hydroxyphenyl)acetyl]amino}-
2-
[(2
R
,4
S
)-
4-
carboxy-
5,5-
dimethyl-
1,3-
thiazolidin-
2-
yl]acetyl
Synonyms
Sources
AMO
ChEBI
amoxicilloyl
ChEBI
AXO
ChEBI
Citations
Types
Sources
16033609
PubMed citation
Europe PMC
2438963
PubMed citation
Europe PMC
Last Modified
29 March 2019