Stachybocin B

bioactive natural product
ChemicalSubstance group_of_stereoisomers Q77495677
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Stachybocin B

Summary

Stachybocin B is a group of stereoisomers[1].

Key Facts

  • Stachybocin B's instance of is recorded as group of stereoisomers[2].
  • Stachybocin B's canonical SMILES is recorded as O=C(O)C(N1C(=O)C2=CC(O)=C3C(OC4(C3)C(C)CCC5C(C)(C)C(O)C(O)CC54C)=C2C1)CCCCN6C(=O)C7=CC(O)=C8C(OC9(C8)C(C)CCC%10C(C)(C)C(O)CCC%109C)=C7C6[3].
  • Stachybocin B's InChI is recorded as InChI=1S/C52H70N2O11/c1-26-12-14-38-47(3,4)40(58)16-17-49(38,7)51(26)21-30-35(55)19-28-32(41(30)64-51)24-53(44(28)60)18-10-9-11-34(46(62)63)54-25-33-29(45(54)61)20-36(56)31-22-52(65-42(31)33)27(2)13-15-39-48(5,6)43(59)37(57)23-50(39,52)8/h19-20,26-27,34,37-40,43,55-59H,9-18,21-25H2,1-8H3,(H,62,63)/t26-,27-,34+,37-,38?,39?,40-,43-,49+,50+,51-,52-/m1/s1[4].
  • Stachybocin B's InChIKey is recorded as ZRTGPZGAMCJZNA-CRDDFVEESA-N[5].
  • Stachybocin B's chemical formula is recorded as C₅₂H₇₀N₂O₁₁[6].
  • Stachybocin B's subclass of is recorded as drimane sesquiterpenoid[7].
  • Stachybocin B's subclass of is recorded as isoindole alkaloid[8].
  • Stachybocin B's PubChem CID is recorded as 10509958[9].
  • Stachybocin B's ChEBI ID is recorded as 213479[10].
  • Stachybocin B's found in taxon is recorded as Stachybotrys[11].
  • Stachybocin B's isomeric SMILES is recorded as C[C@@H]1CCC2C(C)(C)C@HC@HC[C@]2(C)[C@@]12Cc1c(O)cc3c(c1O2)CN(C@@HC(=O)O)C3=OC@HC@HC[C@]2(C)[C@@]12Cc1c(O)cc3c(c1O2)CN(C@@HC(=O)O)C">[12].
  • Stachybocin B's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+898.49796106'}[13].
  • Stachybocin B's SureChEMBL ID is recorded as 29711447[14].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000610[15].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000611[16].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000612[17].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000613[18].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000614[19].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000615[20].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000616[21].
  • Stachybocin B's MassBank accession ID is recorded as MSBNK-AAFC-AC000617[22].
  • Stachybocin B's Natural Product Atlas ID is recorded as NPA010350[23].
  • Stachybocin B's UniChem compound ID is recorded as 34015315[24].

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] . PubChem. wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . Stachybocins, Novel Endothelin Receptor Antagonists, Produced by Stachybotrys sp. M6222. I. Taxonomy, Fermentation, Isolation and Characterization.. wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . wikidata.org.
  23. [24] . 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). Stachybocin B. Retrieved May 3, 2026, from https://4ort.xyz/entity/stachybocin-b
MLA “Stachybocin B.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/stachybocin-b.
BibTeX @misc{4ortxyz_stachybocin-b_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Stachybocin B}}, year = {2026}, url = {https://4ort.xyz/entity/stachybocin-b}, note = {Accessed: 2026-05-03}}
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