Home › Entities › group_of_stereoisomers › capomycin

capomycin

group of stereoisomers
ChemicalSubstance group_of_stereoisomers Q105161321
Press Enter · cited answer in seconds

capomycin

Summary

capomycin is a group of stereoisomers[1].

Key Facts

  • capomycin's instance of is recorded as group of stereoisomers[2].
  • capomycin's chemical structure is recorded as Capoamycin.svg[3].
  • capomycin's canonical SMILES is recorded as O=C(OC1C(O)CC(OC1C)C2=CC=C3C(=O)C4=C(C=CC5(O)CC(=CC(=O)C45O)C)C(=O)C3=C2O)C=CC=CCCCCC[4].
  • capomycin's InChI is recorded as InChI=1S/C35H38O10/c1-4-5-6-7-8-9-10-11-27(38)45-33-20(3)44-25(17-24(33)36)21-12-13-22-28(30(21)39)31(40)23-14-15-34(42)18-19(2)16-26(37)35(34,43)29(23)32(22)41/h8-16,20,24-25,33,36,39,42-43H,4-7,17-18H2,1-3H3/b9-8+,11-10+[5].
  • capomycin's InChIKey is recorded as MCNOFFKXBMHLAD-BNFZFUHLSA-N[6].
  • capomycin's chemical formula is recorded as C₃₅H₃₈O₁₀[7].
  • capomycin's subclass of is recorded as benzo[a]anthracene polyketide[8].
  • capomycin's PubChem CID is recorded as 6438788[9].
  • capomycin's ChEBI ID is recorded as 222618[10].
  • capomycin's found in taxon is recorded as Streptomyces capoamus[11].
  • capomycin's isomeric SMILES is recorded as CCCCC/C=C/C=C/C(=O)OC1C(O)CC(c2ccc3c(c2O)C(=O)C2=C(C3=O)C3(O)C(=O)C=C(C)CC3(O)C=C2)OC1C[12].
  • capomycin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+618.246497416'}[13].
  • capomycin's SureChEMBL ID is recorded as 29551306[14].
  • capomycin's Natural Product Atlas ID is recorded as NPA020880[15].
  • capomycin's UniChem compound ID is recorded as 60180957[16].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . Capoamycin, a new isotetracenone antibiotic.. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). capomycin. Retrieved May 3, 2026, from https://4ort.xyz/entity/capomycin
MLA “capomycin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/capomycin.
BibTeX @misc{4ortxyz_capomycin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{capomycin}}, year = {2026}, url = {https://4ort.xyz/entity/capomycin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): capomycin — https://4ort.xyz/entity/capomycin (retrieved 2026-05-03)

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