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1.0 CHEBI:64174 ChEBI HMDB61723 HMDB HMDB00250 HMDB C07624 KEGG Compound Reaction2343 false Abacavir → Carbovir Triphosphate LEFT_TO_RIGHT AMP BioCyc 1.0 1.0 1.0 C10H14N5O7P Adenosine monophosphate 347.06308 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS CHEBI:16027 ChEBI C11H16N5O11P3 Carbovir Triphosphate 487.00592 HMDB15182 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 C00002 KEGG Compound 398566 ChemSpider 1.0 SMILES NC1=NC2=C(N=CN2[C@@H]2C[C@H](CO)C=C2)C(NC2CC2)=N1 559142 ChemSpider HMDB00538 HMDB GO:0005634 GENE ONTOLOGY 452506 PubChem-compound Abacavir Action Pathway Carbovir Triphosphate CHEBI:15422 ChEBI 644102 PubChem-compound Reaction1959 false Adenosine triphosphate → Adenosine monophosphate + Pyrophosphate LEFT_TO_RIGHT 6083 PubChem-compound 5742 ChemSpider 441300 PubChem-compound 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 136470-78-5 CAS 5957 PubChem-compound PW000714 PathWhiz Pyrophosphate Nucleus Adenosine monophosphate HMDB00045 HMDB 5858 ChemSpider SMP00737 SMPDB C10H16N5O13P3 Adenosine triphosphate 506.99576 CHEBI:421707 ChEBI SMILES NC1=NC2=C(N=CN2[C@@H]2C[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C=C2)C(=O)N1 56-65-5 CAS C00020 KEGG Compound 129941-14-6 CAS Adenosine triphosphate C14H18N6O Abacavir 286.1542 Abacavir PPI BioCyc 390063 ChemSpider Abacavir Carbovir Triphosphate ATP ATP AMP PP i Reverse Transcriptase DNA Viral RNA Chain termination
1.0 CHEBI:64174 ChEBI HMDB61723 HMDB HMDB00250 HMDB C07624 KEGG Compound Reaction2343 false Abacavir → Carbovir Triphosphate LEFT_TO_RIGHT AMP BioCyc 1.0 1.0 1.0 C10H14N5O7P Adenosine monophosphate 347.06308 SMILES [O-]P([O-])(=O)OP([O-])([O-])=O 14000-31-8 CAS CHEBI:16027 ChEBI C11H16N5O11P3 Carbovir Triphosphate 487.00592 HMDB15182 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 C00002 KEGG Compound 398566 ChemSpider 1.0 SMILES NC1=NC2=C(N=CN2[C@@H]2C[C@H](CO)C=C2)C(NC2CC2)=N1 559142 ChemSpider HMDB00538 HMDB GO:0005634 GENE ONTOLOGY 452506 PubChem-compound Abacavir Action Pathway Carbovir Triphosphate CHEBI:15422 ChEBI 644102 PubChem-compound Reaction1959 false Adenosine triphosphate → Adenosine monophosphate + Pyrophosphate LEFT_TO_RIGHT 6083 PubChem-compound 5742 ChemSpider 441300 PubChem-compound 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 136470-78-5 CAS 5957 PubChem-compound PW000714 PathWhiz Pyrophosphate Nucleus Adenosine monophosphate HMDB00045 HMDB 5858 ChemSpider http://identifiers.org/smpdb/SMP00737 SMPDB C10H16N5O13P3 Adenosine triphosphate 506.99576 CHEBI:421707 ChEBI SMILES NC1=NC2=C(N=CN2[C@@H]2C[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C=C2)C(=O)N1 56-65-5 CAS C00020 KEGG Compound 129941-14-6 CAS Adenosine triphosphate C14H18N6O Abacavir 286.1542 Abacavir PPI BioCyc 390063 ChemSpider Abacavir Carbovir Triphosphate Adenosine triphosphate Adenosine triphosphate Adenosine monophosphate Pyrophosphate Reverse Transcriptase Created with Snap