novobiocin

chemical compound
ChemicalSubstance type_of_chemical_entity Q1639291
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novobiocin

Summary

novobiocin is a type of chemical entity[1]. novobiocin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • novobiocin's instance of is recorded as type of chemical entity[3].
  • novobiocin's canonical SMILES is recorded as CC1=C(C=CC2=C1OC(=O)C(=C2O)NC(=O)C3=CC(=C(C=C3)O)CC=C(C)C)OC4C(C(C(C(O4)(C)C)OC)OC(=O)N)O[4].
  • novobiocin's chemical formula is recorded as C₃₁H₃₆N₂O₁₁[5].
  • novobiocin is a type of biogenic coumarin[6].
  • novobiocin is part of novobiocin metabolic process[7].
  • novobiocin is part of novobiocin biosynthetic process[8].
  • novobiocin is used for medication[9].
  • novobiocin's Commons category is recorded as Novobiocin[10].
  • novobiocin's found in taxon is recorded as Escherichia coli[11].
  • novobiocin's found in taxon is recorded as Nocardiopsis gilva[12].
  • novobiocin's found in taxon is recorded as Streptomyces[13].
  • novobiocin's found in taxon is recorded as Actinoalloteichus cyanogriseus[14].
  • novobiocin's found in taxon is recorded as Streptomyces niveus[15].
  • novobiocin's found in taxon is recorded as Streptomyces albidoflavus[16].
  • novobiocin's found in taxon is recorded as Streptomyces coelicolor[17].
  • novobiocin's isomeric SMILES is recorded as CC1=C(C=CC2=C1OC(=O)C(=C2O)NC(=O)C3=CC(=C(C=C3)O)CC=C(C)C)O[C@H]4C@@HOC@@HO">[18].
  • novobiocin's mass is recorded as {'unit': 'Q483261', 'amount': '+612.232'}[19].
  • novobiocin's subject has role is recorded as antibiotic[20].
  • novobiocin's subject has role is recorded as enzyme inhibitor[21].
  • novobiocin's subject has role is recorded as DNA polymerase inhibitors[22].
  • novobiocin's stereoisomer of is recorded as [(3R,4S,5R,6S)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate[23].
  • novobiocin's stereoisomer of is recorded as [(3R,4R,5S,6R)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate[24].
  • novobiocin's has active ingredient is recorded as Novobiocin[25].

Why It Matters

novobiocin has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] novobiocin is known by 3 alternative names across languages and contexts.[26]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . PubChem. Retrieved . wikidata.org.
  3. [5] . PubChem. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Gene Ontology release 2019-11-16. wikidata.org.
  6. [8] . Gene Ontology release 2019-11-16. wikidata.org.
  7. [9] . DrugBank. wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.. wikidata.org.
  10. [12] . Isolation and Characterization of New p-Terphenyls with Antifungal, Antibacterial, and Antioxidant Activities from Halophilic Actinomycete Nocardiopsis gilva YIM 90087. wikidata.org.
  11. [13] . Tyrosine derivatives isolated from Streptomyces sp. IFM 10937 in a screening program for TRAIL-resistance-overcoming activity. wikidata.org.
  12. [14] . Studies on the Biosynthesis of Terpenoid Compounds Produced by Actinomycetes. 3. Biosynthesis of the Isoprenoid Side Chain of Novobiocin via the Non-mevalonate Pathway in Streptomyces niveus. wikidata.org.
  13. [15] . Studies on the Biosynthesis of Terpenoid Compounds Produced by Actinomycetes. 3. Biosynthesis of the Isoprenoid Side Chain of Novobiocin via the Non-mevalonate Pathway in Streptomyces niveus. wikidata.org.
  14. [16] . Production of 8'-halogenated and 8'-unsubstituted novobiocin derivatives in genetically engineered streptomyces coelicolor strains.. wikidata.org.
  15. [17] . Production of 8'-halogenated and 8'-unsubstituted novobiocin derivatives in genetically engineered streptomyces coelicolor strains.. wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . Medical Subject Headings. Retrieved . wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . Medical Subject Headings. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [26] . Wikidata aliases. wikidata.org.

📑 Cite this page

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). novobiocin. Retrieved May 3, 2026, from https://4ort.xyz/entity/novobiocin
MLA “novobiocin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/novobiocin.
BibTeX @misc{4ortxyz_novobiocin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{novobiocin}}, year = {2026}, url = {https://4ort.xyz/entity/novobiocin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): novobiocin — https://4ort.xyz/entity/novobiocin (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 5w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of [(3R,4S,5R,6S)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate, [(3R,4R,5S,6R)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate
    Instance of type of chemical entity
    Has use medication
    Part of
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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