Home › Entities › type_of_chemical_entity › rebeccamycin

rebeccamycin

chemical compound
ChemicalSubstance type_of_chemical_entity Q7301989
Press Enter · cited answer in seconds

rebeccamycin

Summary

rebeccamycin is a type of chemical entity[1]. rebeccamycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

Key Facts

  • rebeccamycin's instance of is recorded as type of chemical entity[3].
  • rebeccamycin's chemical structure is recorded as Rebeccamycin.svg[4].
  • rebeccamycin's CAS Registry Number is recorded as 93908-02-2[5].
  • rebeccamycin's canonical SMILES is recorded as COC1C(OC(C(C1O)O)N2C3=C(C=CC=C3Cl)C4=C5C(=C6C7=C(C(=CC=C7)Cl)NC6=C42)C(=O)NC5=O)CO[6].
  • rebeccamycin's InChI is recorded as InChI=1S/C27H21Cl2N3O7/c1-38-24-13(8-33)39-27(23(35)22(24)34)32-20-10(5-3-7-12(20)29)15-17-16(25(36)31-26(17)37)14-9-4-2-6-11(28)18(9)30-19(14)21(15)32/h2-7,13,22-24,27,30,33-35H,8H2,1H3,(H,31,36,37)/t13-,22-,23-,24-,27-/m1/s1[7].
  • rebeccamycin's InChIKey is recorded as QEHOIJJIZXRMAN-QZQSLCQPSA-N[8].
  • rebeccamycin's chemical formula is recorded as C₂₇H₂₁Cl₂N₃O₇[9].
  • rebeccamycin's subclass of is recorded as indolo[2,3-a]carbazole alkaloid[10].
  • rebeccamycin's part of is recorded as demethylrebeccamycin--D-glucose O-methyltransferase activity[11].
  • rebeccamycin's ChEMBL ID is recorded as CHEMBL370100[12].
  • rebeccamycin's Freebase ID is recorded as /m/02pz_1z[13].
  • rebeccamycin's UNII is recorded as Y96MQM21V9[14].
  • rebeccamycin's ChemSpider ID is recorded as 65891[15].
  • rebeccamycin's PubChem CID is recorded as 73110[16].
  • rebeccamycin's ChEBI ID is recorded as 135511[17].
  • rebeccamycin's found in taxon is recorded as Nocardia[18].
  • rebeccamycin's found in taxon is recorded as Lechevalieria aerocolonigenes[19].
  • rebeccamycin's found in taxon is recorded as Streptomyces sanyensis[20].
  • rebeccamycin's found in taxon is recorded as Streptomyces lividans[21].
  • rebeccamycin's DrugBank ID is recorded as DB14729[22].
  • rebeccamycin's Reaxys registry number is recorded as 4732638[23].
  • rebeccamycin's isomeric SMILES is recorded as CO[C@@H]1C@HCOC@HCO">[24].
  • rebeccamycin's mass is recorded as {'unit': 'Q483261', 'amount': '+569.076'}[25].
  • rebeccamycin's NSC number is recorded as 359079[26].
  • rebeccamycin's SureChEMBL ID is recorded as 24695[27].

Why It Matters

rebeccamycin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (5 views/month).[2]

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] ↑ . ChEBI. 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] ↑ . geneontology.org. Retrieved . geneontology.org. Provenance: wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Isolation and structure of rebeccamycin - a new antitumor antibiotic from nocardia aerocoligenes. wikidata.org.
  17. [19] ↑ . The biosynthetic origins of rebeccamycin. wikidata.org.
  18. [20] ↑ . Antiamoebic Activities of Indolocarbazole Metabolites Isolated from Streptomyces sanyensis Cultures. wikidata.org.
  19. [21] ↑ . Mycolic acid-containing bacteria activate heterologous secondary metabolite expression in Streptomyces lividans. wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . ChEBI. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . PubChem. Retrieved . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). rebeccamycin. Retrieved May 3, 2026, from https://4ort.xyz/entity/rebeccamycin
MLA “rebeccamycin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rebeccamycin.
BibTeX @misc{4ortxyz_rebeccamycin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{rebeccamycin}}, year = {2026}, url = {https://4ort.xyz/entity/rebeccamycin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): rebeccamycin — https://4ort.xyz/entity/rebeccamycin (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/rebeccamycin · Last refreshed: