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Protactin

group of stereoisomers with the chemical formula C₃₂H₄₈N₆O₈
ChemicalSubstance group_of_stereoisomers Q82906796
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Protactin

Summary

Protactin is a group of stereoisomers[1].

Key Facts

  • Protactin's instance of is recorded as group of stereoisomers[2].
  • Protactin's CAS Registry Number is recorded as 141912-59-6[3].
  • Protactin's canonical SMILES is recorded as C=C(C)C(NC(=O)C(NC(=O)c1ccc(C)c(O)c1N)C(C)O)C(=O)N1C(C)CCC1C(=O)N(C)CC(=O)N(C)C(C=O)C(C)C[4].
  • Protactin's InChI is recorded as InChI=1S/C32H48N6O8/c1-16(2)23(15-39)37(9)24(41)14-36(8)31(45)22-13-11-19(6)38(22)32(46)26(17(3)4)34-30(44)27(20(7)40)35-29(43)21-12-10-18(5)28(42)25(21)33/h10,12,15-16,19-20,22-23,26-27,40,42H,3,11,13-14,33H2,1-2,4-9H3,(H,34,44)(H,35,43)/t19?,20-,22+,23-,26-,27+/m1/s1[5].
  • Protactin's InChIKey is recorded as XZQTTYYQLUHMIZ-ZEVMZUSBSA-N[6].
  • Protactin's chemical formula is recorded as C₃₂H₄₈N₆O₈[7].
  • Protactin's subclass of is recorded as chemical compound[8].
  • Protactin's PubChem CID is recorded as 3081299[9].
  • Protactin's ChEBI ID is recorded as 221294[10].
  • Protactin's found in taxon is recorded as Streptomyces[11].
  • Protactin's isomeric SMILES is recorded as C=C(C)C@@HC(=O)N1C(C)CC[C@H]1C(=O)N(C)CC(=O)N(C)C@HC(C)CC@@HC(=O)N1C(C)CC[C@H]1C(=O)N(C)CC(=O)N(C)C@HC(C)C">[12].
  • Protactin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+644.3533624959999'}[13].
  • Protactin's SureChEMBL ID is recorded as 29396584[14].
  • Protactin's DSSTox substance ID is recorded as DTXSID80931247[15].
  • Protactin's Natural Product Atlas ID is recorded as NPA020638[16].
  • Protactin's DSSTOX compound identifier is recorded as DTXCID601359959[17].
  • Protactin's UniChem compound ID is recorded as 55519209[18].

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] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . Protactin, a new antibiotic metabolite and a possible precursor of the actinomycins. 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] ↑ . 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). Protactin. Retrieved May 3, 2026, from https://4ort.xyz/entity/protactin
MLA “Protactin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/protactin.
BibTeX @misc{4ortxyz_protactin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Protactin}}, year = {2026}, url = {https://4ort.xyz/entity/protactin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Protactin — https://4ort.xyz/entity/protactin (retrieved 2026-05-03)

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