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Tiglicamide C

group of stereoisomers with the chemical formula C₄₀H₅₇N₇O₁₃S
ChemicalSubstance group_of_stereoisomers Q104246192
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Tiglicamide C

Summary

Tiglicamide C is a group of stereoisomers[1].

Key Facts

  • Tiglicamide C's instance of is recorded as group of stereoisomers[2].
  • Tiglicamide C's canonical SMILES is recorded as CC=C(C)C(=O)NC(C(=O)NC(Cc1ccc(O)cc1)C(=O)NC1C(=O)NC(C)C(=O)NC(=CC)C(=O)NC(CCC(=O)O)C(=O)NC(CCS+[O-])C(=O)OC1C)C(C)CS+[O-])C(=O)OC1C)C(C)C">[3].
  • Tiglicamide C's InChI is recorded as InChI=1S/C40H57N7O13S/c1-9-21(5)33(51)46-31(20(3)4)38(56)45-29(19-24-11-13-25(48)14-12-24)37(55)47-32-23(7)60-40(58)28(17-18-61(8)59)44-36(54)27(15-16-30(49)50)43-35(53)26(10-2)42-34(52)22(6)41-39(32)57/h9-14,20,22-23,27-29,31-32,48H,15-19H2,1-8H3,(H,41,57)(H,42,52)(H,43,53)(H,44,54)(H,45,56)(H,46,51)(H,47,55)(H,49,50)/b21-9+,26-10-/t22-,23+,27+,28-,29+,31-,32-,61?/m0/s1[4].
  • Tiglicamide C's InChIKey is recorded as LNZZAPVTOPDKIB-RDIOVHBBSA-N[5].
  • Tiglicamide C's chemical formula is recorded as C₄₀H₅₇N₇O₁₃S[6].
  • Tiglicamide C's subclass of is recorded as biogenic cyclopeptide[7].
  • Tiglicamide C's PubChem CID is recorded as 44606682[8].
  • Tiglicamide C's ChEBI ID is recorded as 226491[9].
  • Tiglicamide C's found in taxon is recorded as Lyngbya confervoides[10].
  • Tiglicamide C's isomeric SMILES is recorded as C/C=C1\NC(=O)C@HNC(=O)C@@HC@@HOC(=O)C@HNC(=O)C@@HNC1=OC@HNC(=O)C@@HC@@HOC(=O)C@HNC(=O)C@@HNC1=O">[11].
  • Tiglicamide C's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+875.373505884'}[12].
  • Tiglicamide C's SureChEMBL ID is recorded as 29884767[13].
  • Tiglicamide C's DSSTox substance ID is recorded as DTXSID301046484[14].
  • Tiglicamide C's Natural Product Atlas ID is recorded as NPA017308[15].
  • Tiglicamide C's UniChem compound ID is recorded as 33838220[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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Hapalindole-related alkaloids from the cultured cyanobacterium Fischerella ambigua. 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). Tiglicamide C. Retrieved May 3, 2026, from https://4ort.xyz/entity/tiglicamide-c
MLA “Tiglicamide C.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tiglicamide-c.
BibTeX @misc{4ortxyz_tiglicamide-c_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Tiglicamide C}}, year = {2026}, url = {https://4ort.xyz/entity/tiglicamide-c}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Tiglicamide C — https://4ort.xyz/entity/tiglicamide-c (retrieved 2026-05-03)

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