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Carbomycin A

group of stereoisomers with the chemical formula C₄₂H₆₇NO₁₆
ChemicalSubstance group_of_stereoisomers Q104999908
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Carbomycin A

Summary

Carbomycin An is a group of stereoisomers[1].

Key Facts

  • Carbomycin A's instance of is recorded as group of stereoisomers[2].
  • Carbomycin A's canonical SMILES is recorded as O=CCC1CC(C(=O)C=CC2OC2CC(OC(=O)CC(OC(=O)C)C(OC)C1OC3OC(C)C(OC4OC(C)C(OC(=O)CC(C)C)C(O)(C)C4)C(N(C)C)C3O)C)C[3].
  • Carbomycin A's InChI is recorded as InChI=1S/C42H67NO16/c1-21(2)16-32(47)57-40-25(6)53-34(20-42(40,8)50)58-37-24(5)54-41(36(49)35(37)43(9)10)59-38-27(14-15-44)17-22(3)28(46)12-13-29-30(56-29)18-23(4)52-33(48)19-31(39(38)51-11)55-26(7)45/h12-13,15,21-25,27,29-31,34-41,49-50H,14,16-20H2,1-11H3/b13-12+/t22-,23-,24-,25+,27+,29?,30?,31-,34+,35-,36-,37-,38+,39+,40+,41+,42-/m1/s1[4].
  • Carbomycin A's InChIKey is recorded as FQVHOULQCKDUCY-JXCZFYCESA-N[5].
  • Carbomycin A's chemical formula is recorded as C₄₂H₆₇NO₁₆[6].
  • Carbomycin A's subclass of is recorded as macrolides[7].
  • Carbomycin A's PubChem CID is recorded as 6433412[8].
  • Carbomycin A's ChEBI ID is recorded as 223630[9].
  • Carbomycin A's found in taxon is recorded as Streptomyces thermotolerans[10].
  • Carbomycin A's found in taxon is recorded as Streptomyces halstedii[11].
  • Carbomycin A's isomeric SMILES is recorded as CO[C@@H]1C@@HC@@HCC@@HC(=O)/C=C/C2OC2CC@@HOC(=O)C[C@H]1OC(C)=OC@@HC@@HCC@@HC(=O)/C=C/C2OC2CC@@HOC(">[12].
  • Carbomycin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+841.445985064'}[13].
  • Carbomycin A's SureChEMBL ID is recorded as 140113[14].
  • Carbomycin A's DSSTox substance ID is recorded as DTXSID5046855[15].
  • Carbomycin A's Natural Product Atlas ID is recorded as NPA021071[16].
  • Carbomycin A's UniChem compound ID is recorded as 34751675[17].
  • Carbomycin A's Probes And Drugs ID is recorded as PD014604[18].

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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Production of a hybrid macrolide antibiotic in Streptomyces ambofaciens and Streptomyces lividans by introduction of a cloned carbomycin biosynthetic gene from Streptomyces thermotolerans. wikidata.org.
  10. [11] ↑ . Deltamycins, new macrolide antibiotics. III. Chemical structures. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.
  17. [18] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). Carbomycin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/carbomycin-a
MLA “Carbomycin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carbomycin-a.
BibTeX @misc{4ortxyz_carbomycin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Carbomycin A}}, year = {2026}, url = {https://4ort.xyz/entity/carbomycin-a}, note = {Accessed: 2026-05-03}}
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