(Q27108447)

inferred from InChIKey

mass

420.266445±0 dalton

1 reference

(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

AC1L9BH1 (English)

5 October 2016

1 reference

(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

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

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

1 reference

chemical formula

C₂₈H₃₆O₃

1 reference

AC1L9BH1 (English)

5 October 2016

CC1CC2C(CCC3(C2(CCC4(C3=CC=C5C4=CC(=O)C(=C5C)O)C)C)C)(CC1=O)C

1 reference

AC1L9BH1 (English)

5 October 2016

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

1 reference

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

AC1L9BH1 (English)

5 October 2016

1 reference

Monteverdia laevis

1 reference

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

Gymnosporia nemorosa

1 reference

The chemistry of toxic principles from Maytenus nemerosa

Tripterygium wilfordii

3 references

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

Terpenoids in transformed root culture of Tripterygium wilfordii

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)

Cheiloclinium cognatum

1 reference

Antioxidant phenolic and quinonemethide triterpenes from Cheiloclinium cognatum

Euonymus tingens

1 reference

Tingenone and hydroxytingenone, triterpenoid quinone methides from Euonymus tingens

Elaeodendron croceum

2 references

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

Isolation and identification of poisonous triterpenoids from Elaeodendron croceum.

Catha edulis

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

Glyptopetalum sclerocarpum

1 reference

Quinone-methide triterpenoids from Glyptopetalum sclerocarpum

Kokoona ochracea

2 references

Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea

Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea

Maytenus amazonica

1 reference

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

Maytenus chubutensis

1 reference

Triterpenoid and Phenolic Compounds from Two Chilean 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)

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

Kokoona zeylanica

1 reference

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

Monteverdia retusa

1 reference

Cytotoxic triterpenoids from Maytenus retusa

Hippocratea volubilis

1 reference

Friedelanes and triterpenoid quinone methides from Hippocratea excelsa

Maytenus canariensis

2 references

Antibiotic phenol nor-triterpenes from Maytenus canariensis

Taxonomy and chemotaxonomy of some species of celastraceae

Monteverdia macrocarpa

4 references

Isolation of tingenone and pristimerin 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.

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

Salacia chinensis

3 references

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

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.

Maytenus umbellata

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

Maytenus spinosa

2 references

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

Structure and absolute configuration of triterpene dimers from Maytenus scutioides

Monteverdia catingarum

1 reference

A new antibiotic nortriterpene quinone methide from Maytenus catingarum

Monteverdia aquifolium

1 reference

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

Peritassa campestris

1 reference

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

Maytenus

5 references

Cytotoxic aromatic triterpenes from Maytenus ilicifolia and Maytenus chuchuhuasca

Novel Stereoisomeric Triterpene Dimers, Xuxuarines Aαand Aβ, fromMaytenus chuchuhuasca

Structures of xuxuarines, stereoisomeric triterpene dimers from Maytenus chuchuhuasca

Nine Regioisomeric and Stereoisomeric Triterpene Dimers from Maytenus chuchuhuasca.

Isolation of tingenone and pristimerin from Maytenus chuchuhuasca

Monteverdia spinosa

2 references

Structure and absolute configuration of triterpene dimers from Maytenus scutioides

Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (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

1 reference

WSTYNZDAOAEEKG-QSPBTJQRSA-N

AC1L9BH1 (English)

5 October 2016

2 references

AC1L9BH1 (English)

5 October 2016

ChEBI release 2020-09-01

1 reference

Tingenone (English)

5 October 2016

1 reference

(6bR,8aS,11R,12aR,12bR,14aR)-3-Hydroxy-4,6b,8a,11,12b,14a-hexamethyl-7,8,8a,11,12,12a,12b,13,14,14a-decahydro-2,10(6bH,9H)-picenedione (English)

5 October 2016

2 references

matched by identifier from

AC1L9BH1 (English)

retrieved

5 October 2016

InChIKey

WSTYNZDAOAEEKG-QSPBTJQRSA-N

ChEBI ID

9602

mapping relation type

2 references

matched by identifier from

Tingenone (English)

retrieved

5 October 2016

International Chemical Identifier

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

SureChEMBL ID

SCHEMBL20957664

2 references

matched by identifier from

inferred from InChIKey

InChIKey

WSTYNZDAOAEEKG-QSPBTJQRSA-N

1 reference

0 references

1 reference

Tingenone (English)

5 October 2016

1 reference