Formamidopyrimidine nucleoside triphosphate (BioCAD00000011197)

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Metabolite Card

Formula: C10H18N5O15P3 (541.0012)
SMILES: NC1=NC(N[C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O)=C(NC=O)C(=O)N1

Synonyms [en]

Formamidopyrimidine nucleoside triphosphate; [[(2~{R},3~{S},4~{R},5~{R})-5-[(2-amino-5-formamido-6-oxo-1~{H}-pyrimidin-4-yl)amino]-3,4-dihydroxy-tetrahydrofuran-2-yl]methoxy-hydroxy-phosphoryl] phosphono hydrogen phosphate; C05922; 4-dihydroxyoxolan-2-ylmethoxy}(hydroxy)phosphoryl)oxy(hydroxy)phosphoryl}oxy)phosphonic acid; 5R)-5-(2-amino-5-formamido-6-oxo-1; ({({(2R

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Formamidopyrimidine nucleoside triphosphate. 数据之源，洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000011197). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Formamidopyrimidine nucleoside triphosphate is involved in folate biosynthesis. Formamidopyrimidine nucleoside triphosphat is created from 2,5-Diaminopyrimidine nucleoside triphosphate by GTP cyclohydrolase I [EC:3.5.4.16].

Entity Information

DBLinks

Other DBLinks
  • PubChem: 440840
  • ChEBI: ChEBI:58104
  • HMDB: HMDB0006822
  • KEGG: C05922
  • Coconut NaturalProduct: CNP0255215.1

Class / Ontology

Metabolic Network
ID EC Number Name
KEGG:R00428 3.5.4.16 GTP 8,9-hydrolase
KEGG:R05046 3.5.4.16 formamidopyrimidine nucleoside triphosphate amidohydrolase
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
PathBank:SMP0120774 Hyperphenylalaninemia Due to DHPR-Deficiency
PathBank:SMP0120552 Hyperphenylalaninemia Due to Guanosine Triphosphate Cyclohydrolase Deficiency
PathBank:SMP0120556 Sepiapterin Reductase Deficiency
PathBank:SMP0000005 Pterine Biosynthesis
PathBank:SMP0000488 Hyperphenylalaninemia Due to 6-Pyruvoyltetrahydropterin Synthase Deficiency (ptps)
PathBank:SMP0087250 Pterine Biosynthesis
PathBank:SMP0087486 Pterine Biosynthesis
PathBank:SMP0120773 Hyperphenylalaninemia Due to 6-Pyruvoyltetrahydropterin Synthase Deficiency (ptps)
PathBank:SMP0120551 DOPA-Responsive Dystonia
PathBank:SMP0120555 Segawa Syndrome
PathBank:SMP0000487 Hyperphenylalaninemia Due to Guanosine Triphosphate Cyclohydrolase Deficiency
PathBank:SMP0000491 Sepiapterin Reductase Deficiency
PathBank:SMP0120772 Hyperphenylalaninemia Due to Guanosine Triphosphate Cyclohydrolase Deficiency
PathBank:SMP0120776 Sepiapterin Reductase Deficiency
PathBank:SMP0120553 Hyperphenylalaninemia Due to 6-Pyruvoyltetrahydropterin Synthase Deficiency (ptps)
PathBank:SMP0000489 Hyperphenylalaninemia Due to DHPR-Deficiency
PathBank:SMP0087404 Pterine Biosynthesis
PathBank:SMP0120771 DOPA-Responsive Dystonia
PathBank:SMP0120775 Segawa Syndrome
PathBank:SMP0120554 Hyperphenylalaninemia Due to DHPR-Deficiency
View All Pathways