Poststatin

group of stereoisomers with the chemical formula C₂₆H₄₇N₅O₇
ChemicalSubstance group_of_stereoisomers Q82903732
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Poststatin

Summary

Poststatin is a group of stereoisomers[1].

Key Facts

  • Poststatin's instance of is recorded as group of stereoisomers[2].
  • Poststatin's CAS Registry Number is recorded as 135219-43-1[3].
  • Poststatin's canonical SMILES is recorded as O=C(NC(C(=O)N(C(=O)C(N)C(C)CC(=O)C(N)C(C)C)C(C(=O)O)C(C)C)CC(C)C)C(=O)C(N)CC[4].
  • Poststatin's InChI is recorded as InChI=1S/C26H47N5O7/c1-9-16(27)22(33)23(34)30-17(10-12(2)3)24(35)31(21(14(6)7)26(37)38)25(36)20(29)15(8)11-18(32)19(28)13(4)5/h12-17,19-21H,9-11,27-29H2,1-8H3,(H,30,34)(H,37,38)/t15?,16-,17+,19-,20-,21-/m0/s1[5].
  • Poststatin's InChIKey is recorded as UNPBSZUDTFBULK-CZCKBYKRSA-N[6].
  • Poststatin's chemical formula is recorded as C₂₆H₄₇N₅O₇[7].
  • Poststatin's subclass of is recorded as 2,6-dimethyloctane monoterpenoid[8].
  • Poststatin's Guide to Pharmacology Ligand ID is recorded as 10967[9].
  • Poststatin's PubChem CID is recorded as 164380[10].
  • Poststatin's ChEBI ID is recorded as 221382[11].
  • Poststatin's found in taxon is recorded as Streptomyces viridochromogenes[12].
  • Poststatin's isomeric SMILES is recorded as CCC@HC(=O)C(=O)NC@HC(=O)N(C(=O)C@@HC(C)CC(=O)C@@HC(C)C)C@HC(C)CC@HC(=O)C(=O)NC@HC(=O)N(C(=O)C@@HC(C)CC(=O)C@@HC(C)C)C@HC(C)C">[13].
  • Poststatin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+541.347548844'}[14].
  • Poststatin's SureChEMBL ID is recorded as 29614571[15].
  • Poststatin's DSSTox substance ID is recorded as DTXSID10928908[16].
  • Poststatin's Natural Product Atlas ID is recorded as NPA020653[17].
  • Poststatin's DSSTOX compound identifier is recorded as DTXCID501357667[18].
  • Poststatin's UniChem compound ID is recorded as 51278341[19].
  • Poststatin's Probes And Drugs ID is recorded as PD131921[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] . PubChem. Retrieved . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . Poststatin, a new inhibitor of prolyl endopeptidase, produced by Streptomyces viridochromogenes MH534-30F3. I. Taxonomy, production, isolation, physico-chemical properties and biological activities.. wikidata.org.
  12. [13] . 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). Poststatin. Retrieved May 3, 2026, from https://4ort.xyz/entity/poststatin
MLA “Poststatin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/poststatin.
BibTeX @misc{4ortxyz_poststatin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Poststatin}}, year = {2026}, url = {https://4ort.xyz/entity/poststatin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Poststatin — https://4ort.xyz/entity/poststatin (retrieved 2026-05-03)

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