9606
TAXONOMY
7481-89-2
CAS
AMP
BioCyc
1.0
Zalcitabine
1.0
Reaction2346
false
Zalcitabine → Dideoxycytidine 5'-Triphosphate
LEFT_TO_RIGHT
SMILES
NC1=NC(=O)N(C=C1)[C@H]1CC[C@@H](CO)O1
C10H14N5O7P
Adenosine monophosphate
347.06308
HMDB0000250
HMDB
SMILES
[O-]P([O-])(=O)OP([O-])([O-])=O
14000-31-8
CAS
CHEBI:16027
ChEBI
1.0
C9H16N3O12P3
Dideoxycytidine 5'-Triphosphate
450.9947
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
HMDB0015078
HMDB
106431
ChemSpider
C00002
KEGG Compound
119119
PubChem-compound
1.0
559142
ChemSpider
HMDB0061726
HMDB
GO:0005634
GENE ONTOLOGY
PW000723
PathWhiz
SMP0000746
SMPDB
1.0
CHEBI:15422
ChEBI
644102
PubChem-compound
Reaction1959
false
Adenosine triphosphate → Adenosine monophosphate + Pyrophosphate
LEFT_TO_RIGHT
6083
PubChem-compound
Homo sapiens
C07207
KEGG Compound
5742
ChemSpider
22498
ChemSpider
Dideoxycytidine 5'-Triphosphate
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
24066
PubChem-compound
5957
PubChem-compound
Pyrophosphate
Nucleus
C9H13N3O3
Zalcitabine
211.09569
Adenosine monophosphate
5858
ChemSpider
SMILES
[H][C@@]1(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)CC[C@@]([H])(O1)N1C=CC(=N)N=C1O
C10H16N5O13P3
Adenosine triphosphate
506.99576
CHEBI:10101
ChEBI
56-65-5
CAS
C00020
KEGG Compound
Adenosine triphosphate
HMDB0000045
HMDB
PPI
BioCyc
Zalcitabine Action Pathway