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2,3-Dihydroxy-12-oleanen-28-oic acid

group of stereoisomers with the chemical formula C₃₀H₄₈O₄
ChemicalSubstance group_of_stereoisomers Q104171595
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2,3-Dihydroxy-12-oleanen-28-oic acid

Summary

2,3-Dihydroxy-12-oleanen-28-oic acid is a group of stereoisomers[1].

Key Facts

  • 2,3-Dihydroxy-12-oleanen-28-oic acid's instance of is recorded as group of stereoisomers[2].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's canonical SMILES is recorded as O=C(O)C12CCC(C)(C)CC2C3=CCC4C5(C)CC(O)C(O)C(C)(C)C5CCC4(C)C3(C)CC1[3].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's InChI is recorded as InChI=1S/C30H48O4/c1-25(2)12-14-30(24(33)34)15-13-28(6)18(19(30)16-25)8-9-22-27(5)17-20(31)23(32)26(3,4)21(27)10-11-29(22,28)7/h8,19-23,31-32H,9-17H2,1-7H3,(H,33,34)[4].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's InChIKey is recorded as MDZKJHQSJHYOHJ-UHFFFAOYSA-N[5].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's chemical formula is recorded as C₃₀H₄₈O₄[6].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's subclass of is recorded as oleanane triterpenoid[7].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's PubChem CID is recorded as 3694932[8].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Syncarpha gnaphaloides[9].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Crataegus pinnatifida[10].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Salvia trijuga[11].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Hyptis[12].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Anisomeles[13].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Euonymus nanoides[14].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Gardenia tubifera[15].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Punica[16].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Leucas[17].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Bitter milkwort[18].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Syzygium sandwicense[19].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Perilla frutescens[20].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Eriobotrya japonica[21].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Phytolacca dodecandra[22].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Olea[23].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Rosmarinus officinalis[24].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Lyonia ovalifolia[25].
  • 2,3-Dihydroxy-12-oleanen-28-oic acid's found in taxon is recorded as Olea europaea[26].

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] ↑ . Diterpenes from Leyssera gnaphaloides. wikidata.org.
  9. [10] ↑ . Synergetic effect and structure-activity relationship of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors from Crataegus pinnatifida Bge.. wikidata.org.
  10. [11] ↑ . Terpenoids from Salvia trijuga. wikidata.org.
  11. [12] ↑ . Bioactive 5,6-dihydro-alpha-pyrone derivatives from Hyptis brevipes. wikidata.org.
  12. [13] ↑ . Bioactive cembrane diterpenoids of Anisomeles indica. wikidata.org.
  13. [14] ↑ . Two new sesquiterpene polyesters from the seeds of Euonymus nanoides LOES.. wikidata.org.
  14. [15] ↑ . Pyronane monoterpenoids from the fruit of Gardenia jasminoides. wikidata.org.
  15. [16] ↑ . Medicinal flowers. XXIII. New taraxastane-type triterpene, punicanolic acid, with tumor necrosis factor-alpha inhibitory activity from the flowers of Punica granatum. wikidata.org.
  16. [17] ↑ . Diterpenes from Leucas aspera inhibiting prostaglandin-induced contractions. wikidata.org.
  17. [18] ↑ . Two new triterpenoid saponins isolated from Polygala japonica. wikidata.org.
  18. [19] ↑ . An orsellinic acid glucoside from syzygium aromatica. wikidata.org.
  19. [20] ↑ . Cytotoxic activity of Perilla frutescens var. japonica leaf extract is due to high concentrations of oleanolic and ursolic acids. wikidata.org.
  20. [21] ↑ . Production of bioactive triterpenes by Eriobotrya japonica calli.. wikidata.org.
  21. [22] ↑ . Triterpene aglycones from various Phytolacca dodecandra populations. wikidata.org.
  22. [23] ↑ . Production of triterpene acids by cell suspension cultures of Olea europaea. wikidata.org.
  23. [24] ↑ . Die kohlenwasserstoffe des blattwachses von rosmarinus officinalis. wikidata.org.
  24. [25] ↑ . Studies on the Constituents of Lyonia ovalifolia DRUDE var. elliptica HAND.-MAZZ. X. : On the Constituents of the Flowers. (I). wikidata.org.
  25. [26] ↑ . Assessment of the safety of maslinic acid, a bioactive compound from Olea europaea L.. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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