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Avilamycin C

group of stereoisomers with the chemical formula C₆₁H₉₀Cl₂O₃₂
ChemicalSubstance group_of_stereoisomers Q83097170
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Avilamycin C

Summary

Avilamycin C is a group of stereoisomers[1].

Key Facts

  • Avilamycin C's instance of is recorded as group of stereoisomers[2].
  • Avilamycin C's CAS Registry Number is recorded as 69787-80-0[3].
  • Avilamycin C's canonical SMILES is recorded as COCC1OC(OC2OCC3OC4(OC3C2OC(=O)C(C)C)OC(C)C(O)(C(C)O)C2OCOC24)C(OC)C(O)C1OC1OC(C)C(OC)C(OC2CC3(C)OC4(CC(O)C(OC5CC(O)C(OC(=O)c6c(C)c(Cl)c(O)c(Cl)c6OC)C(C)O5)C(C)O4)OC3C(C)O2)C1O[4].
  • Avilamycin C's InChI is recorded as InChI=1S/C61H90Cl2O32/c1-21(2)53(70)87-49-45-32(92-61(93-45)52-51(78-20-79-52)60(72,27(8)64)28(9)91-61)19-77-56(49)89-57-48(76-14)39(68)44(31(83-57)18-73-11)88-55-40(69)47(43(74-12)24(5)82-55)85-34-17-58(10)50(26(7)81-34)94-59(95-58)16-30(66)42(25(6)90-59)84-33-15-29(65)41(23(4)80-33)86-54(71)35-22(3)36(62)38(67)37(63)46(35)75-13/h21,23-34,39-45,47-52,55-57,64-69,72H,15-20H2,1-14H3/t23-,24-,25-,26-,27?,28-,29-,30-,31-,32+,33+,34+,39+,40-,41-,42-,43+,44-,45-,47-,48+,49-,50-,51-,52-,55+,56+,57+,58-,59?,60+,61-/m1/s1[5].
  • Avilamycin C's InChIKey is recorded as AEIFATUAVHHRBC-GYPCSUJESA-N[6].
  • Avilamycin C's chemical formula is recorded as C₆₁H₉₀Cl₂O₃₂[7].
  • Avilamycin C's subclass of is recorded as chemical compound[8].
  • Avilamycin C's UNII is recorded as GE1D3N476F[9].
  • Avilamycin C's PubChem CID is recorded as 20055307[10].
  • Avilamycin C's isomeric SMILES is recorded as COC[C@H]1OC@@HC@@HC@@H[C@@H]1O[C@@H]1OC@HC@HC@H[C@H]1OC@@HC@@HC@@H[C@@H]1O[C@@H]1OC@HC@H">[11].
  • Avilamycin C's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+1404.4792260799998'}[12].
  • Avilamycin C's SureChEMBL ID is recorded as 6753731[13].
  • Avilamycin C's DSSTox substance ID is recorded as DTXSID60220080[14].
  • Avilamycin C's DSSTOX compound identifier is recorded as DTXCID60142571[15].
  • Avilamycin C's UniChem compound ID is recorded as 32044543[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] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . 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.

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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). Avilamycin C. Retrieved May 3, 2026, from https://4ort.xyz/entity/avilamycin-c
MLA “Avilamycin C.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/avilamycin-c.
BibTeX @misc{4ortxyz_avilamycin-c_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Avilamycin C}}, year = {2026}, url = {https://4ort.xyz/entity/avilamycin-c}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Avilamycin C — https://4ort.xyz/entity/avilamycin-c (retrieved 2026-05-03)

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