9606
TAXONOMY
HMDB0015303
HMDB
1.0
Kanamycin
SubPathwayInhibitor
Adenosine triphosphate
AMP
BioCyc
SMILES
NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
C10H14N5O7P
Adenosine monophosphate
347.06308
Pyrophosphate
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
P0A7K6
UniProt
14000-31-8
CAS
59-01-8
CAS
CHEBI:16027
ChEBI
Bacterial Ribosome
SubPathwayInhibition
SubPathwayControl774
SubPathway774Control
InhibitorySubPathwayControl
HMDB0000538
HMDB
SMILES
NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O
ATP
BioCyc
CHEBI:18361
ChEBI
CHEBI:17630
ChEBI
C00002
KEGG Compound
1.0
1.0
559142
ChemSpider
Cytoplasm
SMP0000255
SMPDB
C01822
KEGG Compound
CHEBI:15422
ChEBI
644102
PubChem-compound
Reaction1959
false
Adenosine triphosphate → Adenosine monophosphate + Pyrophosphate
LEFT_TO_RIGHT
6083
PubChem-compound
Homo sapiens
5742
ChemSpider
C00013
KEGG Compound
61-19-8
CAS
SMILES
NC1=C2N=CN([C@@H]3O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]3O)C2=NC=N1
O7P2
Pyrophosphate
173.91193
5957
PubChem-compound
Adenosine monophosphate
C18H36N4O11
Kanamycin
484.23807
Kanamycin inhibits Bacterial Ribosome
InhibitorySubPathway
Kanamycin Action Pathway
5858
ChemSpider
PW000353
PathWhiz
6032
PubChem-compound
5810
ChemSpider
C10H16N5O13P3
Adenosine triphosphate
506.99576
56-65-5
CAS
C00020
KEGG Compound
Bacterial Ribosome
HMDB0000045
HMDB
GO:0005737
GENE ONTOLOGY
PPI
BioCyc