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thiazomycin A

chemical compound
ChemicalSubstance group_of_stereoisomers Q104400716
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thiazomycin A

Summary

thiazomycin An is a group of stereoisomers[1].

Key Facts

  • thiazomycin A's instance of is recorded as group of stereoisomers[2].
  • thiazomycin A's canonical SMILES is recorded as C=C(NC(=O)c1csc(-c2nc3c(cc2O)-c2nc(cs2)C(=O)NC(C(C)O)C(=O)NC(=C(C)OC)c2nc(cs2)C(=O)NC2c4nc(cs4)C(=O)NC(COC(=O)c4c5c6c(cccc6n4O)COC(=O)C(OC4CC6(C)OC(C)N(C)C6C(C)O4)C2OC5)c2nc-3cs2)n1)C(N)=O[3].
  • thiazomycin A's InChI is recorded as InChI=1S/C62H60N14O18S5/c1-22(49(63)79)64-50(80)32-19-98-58(69-32)43-37(78)12-28-42(71-43)31-17-96-56(66-31)30-16-91-60(85)45-29-15-89-46(47(61(86)90-14-27-10-9-11-36(39(27)29)76(45)87)93-38-13-62(6)48(25(4)92-38)75(7)26(5)94-62)44(59-70-33(20-99-59)51(81)65-30)74-53(83)35-21-97-57(68-35)41(24(3)88-8)73-54(84)40(23(2)77)72-52(82)34-18-95-55(28)67-34/h9-12,17-21,23,25-26,30,38,40,44,46-48,77-78,87H,1,13-16H2,2-8H3,(H2,63,79)(H,64,80)(H,65,81)(H,72,82)(H,73,84)(H,74,83)/b41-24+/t23-,25+,26?,30+,38+,40+,44+,46+,47+,48-,62+/m1/s1[4].
  • thiazomycin A's InChIKey is recorded as LPGAAUZJQIRAAG-CAYKKMKNSA-N[5].
  • thiazomycin A's chemical formula is recorded as C₆₂H₆₀N₁₄O₁₈S₅[6].
  • thiazomycin A's subclass of is recorded as thiazole alkaloid[7].
  • thiazomycin A's subclass of is recorded as biogenic cyclopeptide[8].
  • thiazomycin A's ChEMBL ID is recorded as CHEMBL500817[9].
  • thiazomycin A's Guide to Pharmacology Ligand ID is recorded as 10990[10].
  • thiazomycin A's PubChem CID is recorded as 16155032[11].
  • thiazomycin A's ChEBI ID is recorded as 215362[12].
  • thiazomycin A's found in taxon is recorded as Actinokineospora fastidiosa[13].
  • thiazomycin A's isomeric SMILES is recorded as C=C(NC(=O)c1csc(-c2nc3c(cc2O)-c2nc(cs2)C(=O)NC@@HC(=O)N/C(=C(\C)OC)c2nc(cs2)C(=O)N[C@@H]2c4nc(cs4)C(=O)NC@@Hc2nc-3cs2)n1)C(N)=OC@@HC(=O)N/C(=C(\C)OC)c2nc(cs2)C(=O)N[C@@H]2c4nc(cs4)C(=O)N[C@@H](COC(=O)c4c5c6c(cccc6n4O)COC(=O)[C@">[14].
  • thiazomycin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+1448.28135608'}[15].
  • thiazomycin A's SureChEMBL ID is recorded as 14192133[16].
  • thiazomycin A's SureChEMBL ID is recorded as 30358499[17].
  • thiazomycin A's Natural Product Atlas ID is recorded as NPA019485[18].
  • thiazomycin A's UniChem compound ID is recorded as 382744[19].
  • thiazomycin A's Probes And Drugs ID is recorded as PD131830[20].

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] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [10] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . Isolation and structure elucidation of thiazomycin- a potent thiazolyl peptide antibiotic from Amycolatopsis fastidiosa. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . UniChem. wikidata.org.
  19. [20] ↑ . 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). thiazomycin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/thiazomycin-a
MLA “thiazomycin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/thiazomycin-a.
BibTeX @misc{4ortxyz_thiazomycin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{thiazomycin A}}, year = {2026}, url = {https://4ort.xyz/entity/thiazomycin-a}, note = {Accessed: 2026-05-03}}
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