(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol

group of stereoisomers with the chemical formula C₂₇H₄₃NO₂
ChemicalSubstance group_of_stereoisomers Q104252966
Press Enter · cited answer in seconds

(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol

Summary

(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol is a group of stereoisomers[1].

Key Facts

  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's instance of is recorded as group of stereoisomers[2].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's canonical SMILES is recorded as OC1CC2=CCC3C(CCC4(C)C3CC5OC6(NCC(C)CC6)C(C)C54)C2(C)CC1[3].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's InChI is recorded as InChI=1S/C27H43NO2/c1-16-7-12-27(28-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(29)8-10-25(18,3)21(20)9-11-26(22,24)4/h5,16-17,19-24,28-29H,6-15H2,1-4H3/t16?,17?,19?,20-,21-,22+,23+,24-,25+,26+,27-/m1/s1[4].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's InChIKey is recorded as KWVISVAMQJWJSZ-FFRUGWTFSA-N[5].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's chemical formula is recorded as C₂₇H₄₃NO₂[6].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's subclass of is recorded as spirosolane alkaloid[7].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's PubChem CID is recorded as 137704740[8].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's found in taxon is recorded as Solanum elaeagnifolium[9].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's found in taxon is recorded as Solanum myriacanthum[10].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's found in taxon is recorded as Solanum umbelliferum[11].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's found in taxon is recorded as Solanum aethiopicum[12].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's found in taxon is recorded as Solanum incanum[13].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's isomeric SMILES is recorded as CC1CC[C@@]2(NC1)O[C@H]1C[C@H]3[C@@H]4CC=C5CC(O)CC[C@]5(C)[C@@H]4CC[C@]3(C)[C@@H]1C2C[14].
  • (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+413.329379616'}[15].

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] . Solasodine Production bySolanum Eleagnifolium cav. in vitroCultures: Influence of Plant Growth Regulators. Age and Inoculum Size. Large-Scale Production. wikidata.org.
  9. [10] . Steroidal Alkaloids and Sapogenins from Roots of SomeSolanumSpecies1. wikidata.org.
  10. [11] . Bioactive steroidal glycosides from Solanum torvum. wikidata.org.
  11. [12] . Selection and characterization of Solanum xanthocarpum cell line with augmented steroid metabolism. wikidata.org.
  12. [13] . The cytotoxic principles of Solanum incanum. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

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). (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol. Retrieved May 3, 2026, from https://4ort.xyz/entity/-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol
MLA “(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol.
BibTeX @misc{4ortxyz_-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol}}, year = {2026}, url = {https://4ort.xyz/entity/-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-ol — https://4ort.xyz/entity/-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/-1s-2s-4s-6r-8s-9s-12r-13r-5-7-9-13-tetramethylspiro-5-oxapentacyclo-10-8-0-02-9-04-8-013-18-icos-18-ene-6-2-piperidine-16-ol · Last refreshed: