Paper7238
Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase.
Adams PR and 3 others. Biochem J, 1976. Cited by 12 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase. Papers, record 7238. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7238
Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Dehydrogenation of the phosphonate analogue of glucose 6-phosphate by glucose 6-phosphate dehydrogenase.
- PubMed
Topics7
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Deoxy Sugars | Major topic |
| Glucosephosphate Dehydrogenase | Major topic |
| Heptoses | Major topic |
| Glucosephosphates | |
| Hydrogen-Ion Concentration | |
| Kinetics | |
| Organophosphonates |
Source PubMed
References6
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 2 | 4,364,123 | Rabbit muscle L-glycerol-3-phosphate dehydrogenase. Substrate activity of 3,4-dihydroxybutyl 1-phosphonate and 4-hydroxy-3-oxobutyl 1-phosphonate. | Biochim Biophys Acta | 1974 | https://conductscience.org/library/papers/4364123 | PubMed |
| 3 | 4,377,103 | Phosphonomethyl analogues of phosphate ester glycolytic intermediates. | Biochem J | 1974 | https://conductscience.org/library/papers/4377103 | PubMed |
| 4 | 4,377,104 | Properties of the phosphonomethyl isosteres of two phosphate ester glycolytic intermediates. | Biochem J | 1974 | https://conductscience.org/library/papers/4377104 | PubMed |
| 5 | 4,463,959 | The interaction of the phosphonate analogue of 3-phospho-D-glycerate with phosphoglycerate kinase. | Biochem J | 1974 | https://conductscience.org/library/papers/4463959 | PubMed |
| 6 | 4,463,960 | Dehydration of a phosphonate substrate analogue by glycerol 3-phosphate dehydrogenase. | Biochem J | 1974 | https://conductscience.org/library/papers/4463960 | PubMed |
| 7 | 5,670,802 | The synthesis of 6'-deoxyhomonucleoside-6'-phosphonic acids. | J Am Chem Soc | 1968 | https://conductscience.org/library/papers/5670802 | PubMed |
Cited by3
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 12 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 7,325,982 | An improved synthesis of 6,7-dideoxy-alpha-D-gluco-heptose 7-phosphonic acid. | Biochem J | 1981 | https://conductscience.org/library/papers/7325982 | PubMed |
| 7,325,981 | Dehydrogenation by gluconate 6-phosphate dehydrogenase of an isosteric phosphonate substrate analogue. | Biochem J | 1981 | https://conductscience.org/library/papers/7325981 | PubMed |
| 7,247 | Phosphonomethyl analogues of hexose phosphates. | Biochem J | 1976 | https://conductscience.org/library/papers/7247 | PubMed |
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- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
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- 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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