CHEBI:28542 - 2-deoxy-D-ribofuranose 1-phosphate

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ChEBI Name 2-deoxy-D-ribofuranose 1-phosphate
ChEBI ID CHEBI:28542
ChEBI ASCII Name 2-deoxy-D-ribofuranose 1-phosphate
Definition A 2-deoxyribose 1-phosphate with D-ribofuranose as the sugar. An intermediate in the metabolism of pyrimidine.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:1081, CHEBI:19558
Supplier Information
Download Molfile XML SDF
Formula C5H11O7P
Net Charge 0
Average Mass 214.11040
Monoisotopic Mass 214.024
InChI InChI=1S/C5H11O7P/c6-2-4-3(7)1-5(11-4)12-13(8,9)10/h3-7H,1-2H2,(H2,8,9,10)/t3-,4+,5?/m0/s1
InChIKey KBDKAJNTYKVSEK-PYHARJCCSA-N
SMILES OC[C@H]1OC(C[C@@H]1O)OP(O)(O)=O
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542) has functional parent D-ribofuranose (CHEBI:47013)
2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542) has role fundamental metabolite (CHEBI:78675)
2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542) is a 2-deoxyribose 1-phosphate (CHEBI:19564)
2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542) is conjugate acid of 2-deoxy-D-ribofuranose 1-phosphate(2−) (CHEBI:58576)
Incoming 2-deoxy-α-D-ribose 1-phosphate (CHEBI:11563) is a 2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542)
2-deoxy-β-D-ribose 1-phosphate (CHEBI:48460) is a 2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542)
2-deoxy-D-ribofuranose 1-phosphate(2−) (CHEBI:58576) is conjugate base of 2-deoxy-D-ribofuranose 1-phosphate (CHEBI:28542)
IUPAC Name
2-deoxy-D-erythro-pentofuranose 1-(dihydrogen phosphate)
Synonyms Sources
2-deoxy-1-O-phosphono-D-erythro-pentofuranose IUPAC
2-deoxy-1-O-phosphono-D-ribofuranose ChEBI
2-Deoxy-D-ribose 1-phosphate KEGG COMPOUND
Database Links Databases
C00672 KEGG COMPOUND
ECMDB01351 ECMDB
HMDB0001351 HMDB
YMDB00663 YMDB
View more database links
Registry Numbers Types Sources
1285902 Beilstein Registry Number Beilstein
1285902 Reaxys Registry Number Reaxys
17210-42-3 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
11103787 PubMed citation Europe PMC
Last Modified
22 July 2014