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Pachysandrine A

group of stereoisomers with the chemical formula C₃₃H₅₀N₂O₃
ChemicalSubstance group_of_stereoisomers Q82977056
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Pachysandrine A

Summary

Pachysandrine An is a group of stereoisomers[1].

Key Facts

  • Pachysandrine A's instance of is recorded as group of stereoisomers[2].
  • Pachysandrine A's CAS Registry Number is recorded as 6879-28-3[3].
  • Pachysandrine A's canonical SMILES is recorded as O=C(OC1C(N(C(=O)C=2C=CC=CC2)C)CCC3(C)C1CCC4C5CCC(C(N(C)C)C)C5(C)CCC43)C[4].
  • Pachysandrine A's InChI is recorded as InChI=1S/C33H50N2O3/c1-21(34(5)6)25-15-16-26-24-13-14-28-30(38-22(2)36)29(35(7)31(37)23-11-9-8-10-12-23)18-20-33(28,4)27(24)17-19-32(25,26)3/h8-12,21,24-30H,13-20H2,1-7H3/t21?,24?,25-,26?,27?,28+,29?,30-,32-,33-/m1/s1[5].
  • Pachysandrine A's InChIKey is recorded as ZQUSGHWWSCAMAR-BIVHXRCOSA-N[6].
  • Pachysandrine A's chemical formula is recorded as C₃₃H₅₀N₂O₃[7].
  • Pachysandrine A's subclass of is recorded as [(4R,10R,13S)-3-[benzoyl(methyl)amino]-17-[1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate[8].
  • Pachysandrine A's PubChem CID is recorded as 201813[9].
  • Pachysandrine A's found in taxon is recorded as Pachysandra terminalis[10].
  • Pachysandrine A's isomeric SMILES is recorded as CC(=O)O[C@H]1C(N(C)C(=O)c2ccccc2)CC[C@]2(C)C3CC[C@@]4(C)C(CC[C@@H]4C(C)N(C)C)C3CC[C@@H]12[11].
  • Pachysandrine A's KNApSAcK ID is recorded as C00062695[12].
  • Pachysandrine A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+522.38214346'}[13].
  • Pachysandrine A's DSSTox substance ID is recorded as DTXSID20988497[14].
  • Pachysandrine A's DSSTOX compound identifier is recorded as DTXCID601415638[15].
  • Pachysandrine A's UniChem compound ID is recorded as 67870526[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] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Studies on the alkaloids of pachysandra terminalis sieb. et zucc. (3). : Systematic separation and characterization of alkaloids.. 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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APA 4ort.xyz Knowledge Graph. (2026). Pachysandrine A. Retrieved May 3, 2026, from https://4ort.xyz/entity/pachysandrine-a
MLA “Pachysandrine A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pachysandrine-a.
BibTeX @misc{4ortxyz_pachysandrine-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Pachysandrine A}}, year = {2026}, url = {https://4ort.xyz/entity/pachysandrine-a}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Pachysandrine A — https://4ort.xyz/entity/pachysandrine-a (retrieved 2026-05-03)

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