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Paper7247

Phosphonomethyl analogues of hexose phosphates.

Webster D and 2 others. Biochem J, 1976. Cited by 13 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Phosphonomethyl analogues of hexose phosphates. Papers, record 7247. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7247

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Phosphonomethyl analogues of hexose phosphates.
PubMed
Journal
Biochem J
PubMed
Year
1976
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
13
iCite
Relative citation ratio, by iCite
0.54
iCite
Revised in PubMed
2019-05-01
PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Webster DD
2Jondorf WRW R
3Dixon HBH B

Source PubMed

Topics9

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
HexosephosphatesMajor topic
OrganophosphonatesMajor topic
Fructose-Bisphosphatase
Fructose-Bisphosphate Aldolase
Hexoses
Hydroxybutyrates
NAD
NADP
Phosphoenolpyruvate

Source PubMed

References13

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
5239,683The purification of fructose 1,6-diphosphatase from ox liver and its activation by ethylenediaminetetra-acetate.Biochem J1975https://conductscience.org/library/papers/239683PubMed
64,111,619Preparation of triethylenetetramine dihydrochloride for the treatment of Wilson's disease.Lancet1972https://conductscience.org/library/papers/4111619PubMed
74,364,123Rabbit muscle L-glycerol-3-phosphate dehydrogenase. Substrate activity of 3,4-dihydroxybutyl 1-phosphonate and 4-hydroxy-3-oxobutyl 1-phosphonate.Biochim Biophys Acta1974https://conductscience.org/library/papers/4364123PubMed
84,377,103Phosphonomethyl analogues of phosphate ester glycolytic intermediates.Biochem J1974https://conductscience.org/library/papers/4377103PubMed
94,377,104Properties of the phosphonomethyl isosteres of two phosphate ester glycolytic intermediates.Biochem J1974https://conductscience.org/library/papers/4377104PubMed
104,463,959The interaction of the phosphonate analogue of 3-phospho-D-glycerate with phosphoglycerate kinase.Biochem J1974https://conductscience.org/library/papers/4463959PubMed
114,463,960Dehydration of a phosphonate substrate analogue by glycerol 3-phosphate dehydrogenase.Biochem J1974https://conductscience.org/library/papers/4463960PubMed
124,508,150Protein structure, ribonuclease-S and nucleotide interactions.Cold Spring Harb Symp Quant Biol1972https://conductscience.org/library/papers/4508150PubMed
134,590,243Isosteres of natural phosphates. 2. Synthesis of the monosodium salt of 4-hydroxy-3-oxobutyl-1-phosphonic acid, an isostere of dihydroxyacetone phosphate.J Med Chem1974https://conductscience.org/library/papers/4590243PubMed
144,808,457Synthesis of phosphonic acid isosteres of 2-phospho-, 3-phospho-, and 2,3-diphosphoglyceric acid.J Med Chem1974https://conductscience.org/library/papers/4808457PubMed
155,670,802The synthesis of 6'-deoxyhomonucleoside-6'-phosphonic acids.J Am Chem Soc1968https://conductscience.org/library/papers/5670802PubMed
167,238Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase.Biochem J1976https://conductscience.org/library/papers/7238PubMed
17938,490A simplified preparation of 2-hydroxy-4-phosphonobutyric acid.Biochem J1976https://conductscience.org/library/papers/938490PubMed

Cited by8

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 13 citations.

PMIDTitleJournalYearIn PapersSource
7,325,981Dehydrogenation by gluconate 6-phosphate dehydrogenase of an isosteric phosphonate substrate analogue.Biochem J1981https://conductscience.org/library/papers/7325981PubMed
6,615,422The arsonomethyl analogue of 3-phosphoglycerate.Biochem J1983https://conductscience.org/library/papers/6615422PubMed
2,996,505The phosphonomethyl analogue of 3-phosphoglycerate is a potent competitive inhibitor of phosphoglycerate mutases.Biochem J1985https://conductscience.org/library/papers/2996505PubMed
938,490A simplified preparation of 2-hydroxy-4-phosphonobutyric acid.Biochem J1976https://conductscience.org/library/papers/938490PubMed
743,207Phosphonate analogues of aminoacyl adenylates.Biochem J1978https://conductscience.org/library/papers/743207PubMed
417,719Purification and characterization of the class-II D-fructose 1,6-bisphosphate aldolase from Escherichia coli (Crookes' strain).Biochem J1978https://conductscience.org/library/papers/417719PubMed
348,198Novel kinetic and structural properties of the class-I D-fructose 1,6-bisphosphate aldolase from Escherichia coli (Crookes' strain).Biochem J1978https://conductscience.org/library/papers/348198PubMed
204,292An arsenical analogue of adenosine diphosphate.Biochem J1978https://conductscience.org/library/papers/204292PubMed

Genes2

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
G6PD2,539PubTator's text mininghttps://conductscience.org/library/genes/2539NCBI Gene
GPI2,821PubTator's text mininghttps://conductscience.org/library/genes/2821NCBI Gene

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

None in this release

  • Grants
  • Trials
  • Comments and corrections
  • Drugs
  • Data

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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