Page last updated: 2024-12-04

glycerate 1,3-biphosphate

Description

3-phospho-D-glyceroyl dihydrogen phosphate : The (R)-enantiomer of 3-phosphoglyceroyl dihydrogen phosphate. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID439191
CHEBI ID16001
SCHEMBL ID4360927
MeSH IDM0065509

Synonyms (32)

Synonym
x15 ,
1,3-bisphosphoglyceric acid
(2r)-2-hydroxy-1-oxopropane-1,3-diyl bis(dihydrogen phosphate)
CHEBI:16001
3-phospho-d-glyceroyl dihydrogen phosphate
3-phospho-d-glyceroyl phosphate
1,3-bisphospho-d-glycerate
(r)-2-hydroxy-3-(phosphonooxy)-1-monoanhydride with phosphoric propanoic acid
38168-82-0
C00236
d-glycerate 1,3-diphosphate
1,3-diphosphoglycerate
phosphono (2r)-2-hydroxy-3-phosphonooxypropanoate
SCHEMBL4360927
1,3-biphosphoglycerate
glycerate 1,3-biphosphate
1,3-biphosphoglyceric acid
1,3-bisphosphoglycerate
13-dpg
2-hydroxy-3-(phosphonooxy)-propanoate
1,3-bis-phosphoglycerate
2-hydroxy-3-(phosphonooxy)-propanoic acid
1,3-diphosphateglycerate
glycerate 1,3-diphosphate
2-hydroxy-3-(phosphonooxy)-propanoic acid 1-anhydride with phosphoric acid
2-hydroxy-3-(phosphonooxy)-propanoic acid 1-anhydride with phosphorate
3-phospho-d-glyceroyl-phosphate
3-phosphoglyceroyl-phosphate
(2r)-2-hydroxy-1-oxopropane-1,3-diyl bis[dihydrogen (phosphate)]
Q27098334
1,3-bisphospho-d-glyceric acid
DTXSID101305707
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
Escherichia coli metaboliteAny bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metaboliteAny mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
acyl monophosphateAn organic phosphate ester or anhydride formed by condensation of phosphoric acid with a carboxylic acid.
2,3-bisphosphoglyceric acidA bisphosphoglyceric acid that is glyceric acid carrying two phospho substituents at positions 2 and 3.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (64)

TimeframeStudies, This Drug (%)All Drugs %
pre-199015 (23.44)18.7374
1990's18 (28.13)18.2507
2000's17 (26.56)29.6817
2010's11 (17.19)24.3611
2020's3 (4.69)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews5 (7.69%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other60 (92.31%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
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