(6aS,6bS,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione (Q76009779)

(6aS,6bS,8aS,11R,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

1 reference

3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

1 reference

mass

420.266445012 dalton

1 reference

(6aR,6bS,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

stereoisomer of

2 references

(6aS,6bS,8aS,11S,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

inferred from InChIKey

1 reference

1 reference

(6aR,6bS,8aR,11S,12aS,14aS)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

inferred from InChI

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

inferred from InChI

chemical formula

C₂₈H₃₆O₃

0 references

canonical SMILES

O=C1C=C2C(=CC=C3C2(C)CCC4(C)C5CC(C(=O)CC5(C)CCC34C)C)C(=C1O)C

0 references

isomeric SMILES

C[C@@H]1C[C@@H]2[C@@](CC[C@]3([C@]2(CC[C@@]4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C

0 references

2 references

Tripterygium wilfordii

4 references

Terpenoids in transformed root culture of Tripterygium wilfordii

SARS-CoV 3CLpro inhibitory effects of quinone-methide triterpenes from Tripterygium regelii

Studies with tissue cultures of the Chinese herbal plant, Tripterygiumwilfordii. Isolation of metabolites of interest in rheumatoid arthritis, immunosuppression, and male contraceptive activity

A diterpenoid and triterpenes from tissue cultures of Tripterygium wilfordii

Monteverdia aquifolium

2 references

Quantitative determination of maitenin and 22β-hydroxymaitenin in callus ofMaytenus aquifolium (celastraceae) by reverse phase high performance liquid chromatography

Biosynthesis of friedelane and quinonemethide triterpenoids is compartmentalized in Maytenus aquifolium and Salacia campestris

Kokoona ochracea

1 reference

Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea

Kokoona zeylanica

1 reference

Catalytic inhibition of topoisomerase IIalpha by demethylzeylasterone, a 6-oxophenolic triterpenoid from Kokoona zeylanica

Monteverdia krukovii

4 references

Antimitotic quinoid triterpenes from Maytenus chuchuhuasca

Cytotoxic aromatic triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca

Structures of xuxuarines, stereoisomeric triterpene dimers from Maytenus chuchuhuasca

Nine Regioisomeric and Stereoisomeric Triterpene Dimers from Maytenus chuchuhuasca.

Monteverdia retusa

2 references

Cytotoxic triterpenoids from Maytenus retusa

Cytotoxic triterpenoids from Maytenus retusa

Salacia chinensis

3 references

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of New Friedelane- and Norfriedelane-Type Triterpenes and Polyacylated Eudesmane-Type Sesquiterpene from Salacia chinensis Linn. (S. prinoides DC., Hippocrateaceae) and Radical Scavenging Activities of Principal Constituents.

Peritassa campestris

2 references

Evaluation of antioxidant capacity and synergistic associations of quinonemethide triterpenes and phenolic substances from Maytenus ilicifolia (Celastraceae)

Biosynthesis of friedelane and quinonemethide triterpenoids is compartmentalized in Maytenus aquifolium and Salacia campestris

Elaeodendron croceum

2 references

Isolation and identification of poisonous triterpenoids from Elaeodendron croceum.

Flavanoids and triterpenoids from Cassine papillosa and the absolute configuration of 11,11-dimethyl-1,3,8,10-tetra-hydroxy-9-methoxypeltogynan

Elaeodendron balae

2 references

ChemInform Abstract: Terpenoids and Steroids. Part 18. Balaenonol (Ia), Balaenol (Ib) and Isobalaendiol (Ic): Three New 14(15)-Ene-quinone-methide Triterpenoids from Cassine balae.

Studies on terpenoids and steroids - 18 balaenonol, balaenol and isobalaendiol: Three new 14(15)-ene-quinone-methide triterpenoids from cassine balae

Lydenburgia cassinoides

1 reference

Iguesterin, a new quinonoid triterpene from Catha cassinoides

Cheiloclinium cognatum

1 reference

Antioxidant phenolic and quinonemethide triterpenes from Cheiloclinium cognatum

Glyptopetalum sclerocarpum

1 reference

Quinone-methide triterpenoids from Glyptopetalum sclerocarpum

Gymnosporia cassinoides

2 references

Antibiotic phenol nor-triterpenes from Maytenus canariensis

Taxonomy and chemotaxonomy of some species of celastraceae

Monteverdia horrida

1 reference

Triterpenes from Maytenus horrida

Tricerma vitis-idaeum

1 reference

Antiproliferative terpenoids and alkaloids from the roots of Maytenus vitis-idaea and Maytenus spinosa

Salacia petenensis

2 references

Isolation and frontier molecular orbital investigation of bioactive quinone-methide triterpenoids from the bark of Salacia petenensis

The cytotoxic activity of a Salacia liana species from Monteverde, Costa Rica, is due to a high concentration of tingenone.

Kothala himbutu

1 reference

Biogenetically important quinonemethides and other triterpenoid constituents of Salacia reticulata

Tripterygium regelii

1 reference

SARS-CoV 3CLpro inhibitory effects of quinone-methide triterpenes from Tripterygium regelii

Hippocratea volubilis

2 references

Antigiardial activity of triterpenoids from root bark of Hippocratea excelsa

Friedelanes and triterpenoid quinone methides from Hippocratea excelsa

Monteverdia macrocarpa

4 references

Antimitotic quinoid triterpenes from Maytenus chuchuhuasca

Cytotoxic aromatic triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca

Structures of xuxuarines, stereoisomeric triterpene dimers from Maytenus chuchuhuasca

Nine Regioisomeric and Stereoisomeric Triterpene Dimers from Maytenus chuchuhuasca.

Maytenus retusa

1 reference

Cytotoxic triterpenoids from Maytenus retusa

Monteverdia laevis

1 reference

Chuchuhuasha - a drug used in folk medicine in the Amazonian and Andean areas. A chemical study of Maytenus laevis

Monteverdia fugax

1 reference

The chemistry of toxic principles from Maytenus nemerosa

Acanthothamnus aphyllus

1 reference

D: A-friedo-oleanane triterpenes from the roots of Acanthothamnus aphyllus

Maytenus magellanica

1 reference

Magellanin, a New Triterpene Dimer fromMaytenus magellanica(Celastraceae)

Maytenus woodsonii

1 reference

New Phenolic and Quinone-methide Triterpenes fromMaytenusSpecies (Celastraceae)

Maytenus scutioides

2 references

Structure and absolute configuration of triterpene dimers from Maytenus scutioides

Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae)

Maytenus canariensis

2 references

Antibiotic phenol nor-triterpenes from Maytenus canariensis

Taxonomy and chemotaxonomy of some species of celastraceae

Maytenus amazonica

1 reference

Structure of new bioactive triterpenes related to 22-β-hydroxy-tingenone

Monteverdia catingarum

1 reference

A new antibiotic nortriterpene quinone methide from Maytenus catingarum

Maytenus chubutensis

1 reference

Triterpenoid and Phenolic Compounds from Two Chilean Celastraceae

Gymnosporia dryandri

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

Maytenus spinosa

2 references

Structure and absolute configuration of triterpene dimers from Maytenus scutioides

Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae)

Monteverdia spinosa

2 references

Structure and absolute configuration of triterpene dimers from Maytenus scutioides

Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae)

Gymnosporia nemorosa

1 reference

The chemistry of toxic principles from Maytenus nemerosa

Elaeodendron papillosum

1 reference

Flavanoids and triterpenoids from Cassine papillosa and the absolute configuration of 11,11-dimethyl-1,3,8,10-tetra-hydroxy-9-methoxypeltogynan

Monteverdia truncata

1 reference

Quantitative determination for cytotoxic Friedo-nor-oleanane derivatives from five morphological types of Maytenus ilicifolia (Celastraceae) by reverse-phase high-performance liquid chromatography.

Monteverdia amazonica

1 reference

Structure of new bioactive triterpenes related to 22-β-hydroxy-tingenone

Monteverdia ilicifolia

1 reference

Quantitative determination for cytotoxic Friedo-nor-oleanane derivatives from five morphological types of Maytenus ilicifolia (Celastraceae) by reverse-phase high-performance liquid chromatography.

Maytenus umbellata

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

Identifiers

InChI

InChI=1S/C28H36O3/c1-16-13-23-25(3,15-21(16)30)9-11-27(5)22-8-7-18-17(2)24(31)20(29)14-19(18)26(22,4)10-12-28(23,27)6/h7-8,14,16,23,31H,9-13,15H2,1-6H3/t16-,23-,25+,26+,27-,28+/m1/s1

0 references

InChIKey

WSTYNZDAOAEEKG-GWJSGULQSA-N

0 references

CAS Registry Number

50802-21-6

1 reference