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4-CDP-2-C-methyl-D-erythritol

chemical compound
ChemicalSubstance group_of_stereoisomers Q2715091
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4-CDP-2-C-methyl-D-erythritol

Summary

4-CDP-2-C-methyl-D-erythritol is a group of stereoisomers[1]. 4-CDP-2-C-methyl-D-erythritol draws 1 Wikipedia views per month (group_of_stereoisomers category, ranking #217 of 1,063).[2]

Key Facts

  • 4-CDP-2-C-methyl-D-erythritol's instance of is recorded as group of stereoisomers[3].
  • 4-CDP-2-C-methyl-D-erythritol's chemical structure is recorded as 4-diphosphocytidyl-2-C-methylerythritol.png[4].
  • 4-CDP-2-C-methyl-D-erythritol's CAS Registry Number is recorded as 263016-94-0[5].
  • 4-CDP-2-C-methyl-D-erythritol's canonical SMILES is recorded as CC(CO)(C(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=CC(=NC2=O)N)O)O)O)O[6].
  • 4-CDP-2-C-methyl-D-erythritol's InChI is recorded as InChI=1S/C14H25N3O14P2/c1-14(23,6-18)8(19)5-29-33(26,27)31-32(24,25)28-4-7-10(20)11(21)12(30-7)17-3-2-9(15)16-13(17)22/h2-3,7-8,10-12,18-21,23H,4-6H2,1H3,(H,24,25)(H,26,27)(H2,15,16,22)/t7-,8-,10-,11-,12-,14+/m1/s1[7].
  • 4-CDP-2-C-methyl-D-erythritol's InChIKey is recorded as YFAUKWZNPVBCFF-XHIBXCGHSA-N[8].
  • 4-CDP-2-C-methyl-D-erythritol's chemical formula is recorded as C₁₄H₂₅N₃O₁₄P₂[9].
  • 4-CDP-2-C-methyl-D-erythritol's subclass of is recorded as pyrimidine nucleotide[10].
  • 4-CDP-2-C-methyl-D-erythritol's ChEMBL ID is recorded as CHEMBL1231708[11].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 2V2Z[12].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 3PYE[13].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 1U40[14].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 1INI[15].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 3Q80[16].
  • 4-CDP-2-C-methyl-D-erythritol's PDB structure ID is recorded as 1OJ4[17].
  • 4-CDP-2-C-methyl-D-erythritol's Freebase ID is recorded as /m/047skqh[18].
  • 4-CDP-2-C-methyl-D-erythritol's UNII is recorded as FB44VKC5JD[19].
  • 4-CDP-2-C-methyl-D-erythritol's ChemSpider ID is recorded as 391471[20].
  • 4-CDP-2-C-methyl-D-erythritol's PubChem CID is recorded as 443199[21].
  • 4-CDP-2-C-methyl-D-erythritol's KEGG ID is recorded as C11435[22].
  • 4-CDP-2-C-methyl-D-erythritol's ChEBI ID is recorded as 16578[23].
  • 4-CDP-2-C-methyl-D-erythritol's found in taxon is recorded as Arabidopsis thaliana[24].
  • 4-CDP-2-C-methyl-D-erythritol's found in taxon is recorded as Pseudomonas aeruginosa[25].
  • 4-CDP-2-C-methyl-D-erythritol's found in taxon is recorded as Asparagus officinalis[26].
  • 4-CDP-2-C-methyl-D-erythritol's DrugBank ID is recorded as DB03687[27].

Why It Matters

4-CDP-2-C-methyl-D-erythritol draws 1 Wikipedia views per month (group_of_stereoisomers category, ranking #217 of 1,063).[2] 4-CDP-2-C-methyl-D-erythritol has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] 4-CDP-2-C-methyl-D-erythritol is known by 4 alternative names across languages and contexts.[29]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  11. [13] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  12. [14] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  13. [15] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  14. [16] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  15. [17] ↑ . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] ↑ . Freebase Data Dumps. wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Q2311683. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . Antisense and chemical suppression of the nonmevalonate pathway affects ent-kaurene biosynthesis in Arabidopsis. wikidata.org.
  23. [25] ↑ . Characterization of the Mycobacterium tuberculosis 4-diphosphocytidyl-2-C-methyl-D-erythritol synthase: potential for drug development. wikidata.org.
  24. [26] ↑ . Transcriptome analysis of Asparagus officinalis reveals genes involved in the biosynthesis of rutin and protodioscin. wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . Wikidata aliases. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). 4-CDP-2-C-methyl-D-erythritol. Retrieved May 3, 2026, from https://4ort.xyz/entity/4-cdp-2-c-methyl-d-erythritol
MLA “4-CDP-2-C-methyl-D-erythritol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/4-cdp-2-c-methyl-d-erythritol.
BibTeX @misc{4ortxyz_4-cdp-2-c-methyl-d-erythritol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{4-CDP-2-C-methyl-D-erythritol}}, year = {2026}, url = {https://4ort.xyz/entity/4-cdp-2-c-methyl-d-erythritol}, note = {Accessed: 2026-05-03}}
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