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Methylsulfomycin I

chemical compound
ChemicalSubstance group_of_stereoisomers Q27149221
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Methylsulfomycin I

Summary

Methylsulfomycin I is a group of stereoisomers[1].

Key Facts

  • Methylsulfomycin I's instance of is recorded as group of stereoisomers[2].
  • Methylsulfomycin I's canonical SMILES is recorded as CC=C1C2=NC(=C(O2)C)C(=O)NC(=C)C(=O)NC(=C)C3=NC(=C(O3)C)C4=C(C=CC(=N4)C(=O)NC(=C)C(=O)NC(=C)C(=O)NC(=C)C(=O)N)C5=NC(=CS5)C(=O)NC(C(=O)NC(=CC(C)O)C6=NC(=C(O6)C)C(=O)NC(C7=NC(=CS7)C(=O)N1)OC)C(C)O[3].
  • Methylsulfomycin I's InChI is recorded as InChI=1S/C55H54N16O16S2/c1-13-30-51-69-37(27(10)86-51)48(82)60-23(6)43(77)61-24(7)50-68-36(26(9)85-50)39-29(14-15-31(62-39)44(78)59-22(5)42(76)58-21(4)41(75)57-20(3)40(56)74)54-65-34(17-88-54)46(80)67-35(25(8)73)47(81)64-32(16-19(2)72)52-70-38(28(11)87-52)49(83)71-53(84-12)55-66-33(18-89-55)45(79)63-30/h13-19,25,35,53,72-73H,3-7H2,1-2,8-12H3,(H2,56,74)(H,57,75)(H,58,76)(H,59,78)(H,60,82)(H,61,77)(H,63,79)(H,64,81)(H,67,80)(H,71,83)/b30-13-,32-16-[4].
  • Methylsulfomycin I's InChIKey is recorded as AGPXPIZWMMLJPG-CBZXLTCLSA-N[5].
  • Methylsulfomycin I's chemical formula is recorded as C₅₅H₅₄N₁₆O₁₆S₂[6].
  • Methylsulfomycin I's subclass of is recorded as biogenic cyclopeptide[7].
  • Methylsulfomycin I's subclass of is recorded as thiazole alkaloid[8].
  • Methylsulfomycin I's subclass of is recorded as oxazole alkaloid[9].
  • Methylsulfomycin I's ChemSpider ID is recorded as 10282633[10].
  • Methylsulfomycin I's PubChem CID is recorded as 16147920[11].
  • Methylsulfomycin I's KEGG ID is recorded as C15741[12].
  • Methylsulfomycin I's ChEBI ID is recorded as 80069[13].
  • Methylsulfomycin I's isomeric SMILES is recorded as C/C=C\1/C2=NC(=C(O2)C)C(=O)NC(=C)C(=O)NC(=C)C3=NC(=C(O3)C)C4=C(C=CC(=N4)C(=O)NC(=C)C(=O)NC(=C)C(=O)NC(=C)C(=O)N)C5=NC(=CS5)C(=O)NC(C(=O)N/C(=C\C(C)O)/C6=NC(=C(O6)C)C(=O)NC(C7=NC(=CS7)C(=O)N1)OC)C(C)O[14].
  • Methylsulfomycin I's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+1258.334512'}[15].
  • Methylsulfomycin I's SureChEMBL ID is recorded as 6432310[16].
  • Methylsulfomycin I's Natural Product Atlas ID is recorded as NPA014901[17].
  • Methylsulfomycin I's UniChem compound ID is recorded as 1069945[18].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . PubChem. Retrieved . wikidata.org.
  5. [6] ↑ . PubChem. Retrieved . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Q2311683. Retrieved . wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . ChEBI. Retrieved . wikidata.org.
  12. [13] ↑ . ChEBI. Retrieved . wikidata.org.
  13. [14] ↑ . PubChem. Retrieved . wikidata.org.
  14. [15] ↑ . PubChem. Retrieved . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . 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). Methylsulfomycin I. Retrieved May 3, 2026, from https://4ort.xyz/entity/methylsulfomycin-i
MLA “Methylsulfomycin I.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/methylsulfomycin-i.
BibTeX @misc{4ortxyz_methylsulfomycin-i_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Methylsulfomycin I}}, year = {2026}, url = {https://4ort.xyz/entity/methylsulfomycin-i}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Methylsulfomycin I — https://4ort.xyz/entity/methylsulfomycin-i (retrieved 2026-05-03)

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