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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:51758 - azidocillin
Main
ChEBI Ontology
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ChEBI Name
azidocillin
ChEBI ID
CHEBI:51758
Stars
This entity has been manually annotated by the ChEBI Team.
Supplier Information
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SDF
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Formula
C16H17N5O4S
Net Charge
0
Average Mass
375.40348
Monoisotopic Mass
375.10013
InChI
InChI=1S/C16H17N5O4S/c1-
16(2)
11(15(24)
25)
21-
13(23)
10(14(21)
26-
16)
18-
12(22)
9(19-
20-
17)
8-
6-
4-
3-
5-
7-
8/h3-
7,9-
11,14H,1-
2H3,(H,18,22)
(H,24,25)
/t9-
,10-
,11+,14-
/m1/s1
InChIKey
ODFHGIPNGIAMDK-NJBDSQKTSA-N
SMILES
[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N=[N+]=[N-])c1ccccc1)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
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
penicillin
)
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
(via
heterocyclic antibiotic
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
azidocillin (
CHEBI:51758
)
is a
penicillin (
CHEBI:17334
)
azidocillin (
CHEBI:51758
)
is conjugate acid of
azidocillin(1−) (
CHEBI:51762
)
Incoming
azidocillin(1−) (
CHEBI:51762
)
is conjugate base of
azidocillin (
CHEBI:51758
)
azidocilloyl group (
CHEBI:58977
)
is substituent group from
azidocillin (
CHEBI:51758
)
IUPAC Name
2,2-dimethyl-6β-[(2
R
)-2-azido-2-phenylacetamido]penam-3α-carboxylic acid
INNs
Sources
azidocilina
ChemIDplus
azidocilline
ChemIDplus
Synonyms
Sources
(2
S
,5
R
,6
R
)-
6-
{[(2
R
)-
2-
azido-
2-
phenylacetyl]amino}-
3,3-
dimethyl-
7-
oxo-
4-
thia-
1-
azabicyclo[3.2.0]heptane-
2-
carboxylic acid
IUPAC
azidocillin
ChemIDplus
azidocillinum
ChemIDplus
D
-(−)-(α-azidobenzyl)penicillin
ChemIDplus
Manual Xrefs
Databases
273
DrugCentral
DB08795
DrugBank
GB940488
Patent
US3293242
Patent
View more database links
Registry Number
Type
Source
17243-38-8
CAS Registry Number
ChemIDplus
Last Modified
22 February 2017