(Q27135398)

Maytenoic acid (English)

(2S,4aS,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bS)-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid

7 October 2016

stereoisomer of

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(2S,4aS,6aR,6aS,6bS,8aS,9R,12aR,14aS,14bR)-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid

1 reference

1 reference

C₃₀H₄₈O₃

1 reference

Maytenoic acid (English)

7 October 2016

canonical SMILES

CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C

1 reference

Maytenoic acid (English)

7 October 2016

isomeric SMILES

C[C@H]1C(=O)CC[C@@H]2[C@@]1(CC[C@H]3[C@]2(CC[C@@]4([C@@]3(CC[C@@]5([C@H]4C[C@](CC5)(C)C(=O)O)C)C)C)C)C

1 reference

Terpenoids from Tripterygium doianum (Celastraceae)

Maytenoic acid (English)

7 October 2016

2 references

Terpenoids from Tripterygium doianum (Celastraceae)

Gymnosporia diversifolia

2 references

Antitumor agents, 116. Cytotoxic triterpenes from Maytenus diversifolia

Antitumor agents, 116. Cytotoxic triterpenes from Maytenus diversifolia

Salacia chinensis

5 references

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

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.

Celastrus vulcanicola

2 references

Friedelane triterpenes from Celastrus vulcanicola as photosynthetic inhibitors

Friedelane triterpenes from Celastrus vulcanicola as photosynthetic inhibitors

Gymnosporia emarginata

2 references

3-Oxo-friedelan-20α-OIC acid from gymnosporia emarginata

3-Oxo-friedelan-20α-OIC acid from gymnosporia emarginata

Plenckia populnea

2 references

Constituents of the root wood of Austroplenckia populnea var. ovata

Epikatonic acid fromAustroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography

Phyllanthus oxyphyllus

1 reference

A novel 29-nor-3,4-seco-friedelane triterpene and a new guaiane sesquiterpene from the roots of Phyllanthus oxyphyllus

Tripterygium regelii

1 reference

The genus Tripterygium: A phytochemistry and pharmacological review

Celastrus vulcanicolus

1 reference

Friedelane triterpenes from Celastrus vulcanicola as photosynthetic inhibitors

Tripterygium hypoglaucum

2 references

Di- and triterpenoids from Tripterygium hypoglaucum

Terpenoids from Tripterigyum hypoglaucum

Escherichia coli

1 reference

Exploiting exogenous MEP pathway genes to improve the downstream isoprenoid pathway effects and enhance isoprenoid production in Escherichia coli

Tripterygium wilfordii

8 references

Terpenoids from Tripterigyum hypoglaucum

The genus Tripterygium: A phytochemistry and pharmacological review

Di- and triterpenoids from Tripterygium hypoglaucum

Terpenoids from Tripterygium wilfordii.

A novel epoxy-triterpene and nortriterpene from callus cultures of Tripterygium wilfordii

Anti-aids agents, 6. Salaspermic acid, an anti-HIV principle from Tripterygium wilfordii, and the structure-activity correlation with its related compounds

Triterpenoids from Tripterygium wilfordii

Terpenoids from Tripterygium wilfordii

Monteverdia truncata

2 references

Triterpenes from Maytenus horrida

Antitumor Substtance from Higher Plants

Monteverdia ilicifolia

2 references

Triterpenes from Maytenus horrida

Antitumor Substtance from Higher Plants

Identifiers

InChI

InChI=1S/C30H48O3/c1-19-20(31)8-9-21-27(19,4)11-10-22-28(21,5)15-17-30(7)23-18-26(3,24(32)33)13-12-25(23,2)14-16-29(22,30)6/h19,21-23H,8-18H2,1-7H3,(H,32,33)/t19-,21+,22-,23+,25+,26+,27+,28-,29+,30-/m0/s1

1 reference

Maytenoic acid (English)

WHWHDGKOSUKYOV-GDXNDQEESA-N

7 October 2016

InChIKey

2 references

Maytenoic acid (English)

7 October 2016

ChEBI release 2020-09-01

2 references

Polpunonic acid (English)

WHWHDGKOSUKYOV-GDXNDQEESA-N

7 October 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=33600-93-0

1 reference

(2R,4aS,6aR,6bS,8aS,9R,12aS,12bS,14aS,14bR)-2,4a,6a,8a,9,12b,14a-Heptamethyl-10-oxodocosahydro-2-picenecarboxylic acid (English)

7 October 2016

1 reference

Maytenoic acid (English)

7 October 2016

ChEBI ID

66769

mapping relation type

1 reference

Polpunonic acid (English)

7 October 2016

1 reference