Carmaphycin A

group of stereoisomers with the chemical formula C₂₅H₄₅N₃O₆S
ChemicalSubstance group_of_stereoisomers Q104246394
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Carmaphycin A

Summary

Carmaphycin An is a group of stereoisomers[1].

Key Facts

  • Carmaphycin A's instance of is recorded as group of stereoisomers[2].
  • Carmaphycin A's canonical SMILES is recorded as CCCCCC(=O)NC(C(=O)NC(CCS+[O-])C(=O)NC(CC(C)C)C(=O)C1(C)CO1)C(C)CS+[O-])C(=O)NC(CC(C)C)C(=O)C1(C)CO1)C(C)C">[3].
  • Carmaphycin A's InChI is recorded as InChI=1S/C25H45N3O6S/c1-8-9-10-11-20(29)28-21(17(4)5)24(32)26-18(12-13-35(7)33)23(31)27-19(14-16(2)3)22(30)25(6)15-34-25/h16-19,21H,8-15H2,1-7H3,(H,26,32)(H,27,31)(H,28,29)/t18-,19-,21-,25+,35?/m0/s1[4].
  • Carmaphycin A's InChIKey is recorded as KLYPRXGLYCCNGZ-PFIKXURKSA-N[5].
  • Carmaphycin A's chemical formula is recorded as C₂₅H₄₅N₃O₆S[6].
  • Carmaphycin A's subclass of is recorded as chemical compound[7].
  • Carmaphycin A's PubChem CID is recorded as 71499515[8].
  • Carmaphycin A's ChEBI ID is recorded as 213693[9].
  • Carmaphycin A's found in taxon is recorded as Symploca[10].
  • Carmaphycin A's isomeric SMILES is recorded as CCCCCC(=O)NC@HC(C)CC@HC(C)C">[11].
  • Carmaphycin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+515.30290716'}[12].
  • Carmaphycin A's SureChEMBL ID is recorded as 29706897[13].
  • Carmaphycin A's DSSTox substance ID is recorded as DTXSID701046274[14].
  • Carmaphycin A's Natural Product Atlas ID is recorded as NPA027451[15].
  • Carmaphycin A's UniChem compound ID is recorded as 34588665[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] . The carmaphycins: new proteasome inhibitors exhibiting an α,β-epoxyketone warhead from a marine cyanobacterium.. 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). Carmaphycin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/carmaphycin-a
MLA “Carmaphycin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/carmaphycin-a.
BibTeX @misc{4ortxyz_carmaphycin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Carmaphycin A}}, year = {2026}, url = {https://4ort.xyz/entity/carmaphycin-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Carmaphycin A — https://4ort.xyz/entity/carmaphycin-a (retrieved 2026-05-03)

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