Methyl ursolate (Q82123127)

inferred from SMILES

mass

470.37599546 dalton

1 reference

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

inferred from SMILES

stereoisomer of

2 references

inferred from InChIKey

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

1 reference

(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-methyl 10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate

1 reference

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

1 reference

Crepidiastrum chelidoniifolium

chemical formula

C₃₁H₅₀O₃

0 references

canonical SMILES

O=C(OC)C12CCC(C)C(C)C2C3=CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC1

0 references

isomeric SMILES

C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)C)[C@@H]2[C@H]1C)C)C(=O)OC

0 references

found in taxon

1 reference

The inhibition of diacylglycerol acyltransferase by terpenoids from Youngia koidzumiana.

Eriobotrya japonica

3 references

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

Nerium oleander

1 reference

Three new triterpenes from Nerium oleander and biological activity of the isolated compounds

Cunila lythrifolia

1 reference

Triterpenoid acids from Cunila lythrifolia

Eucalyptus globulus

1 reference

Terpenoids and other constituents of Eucalyptus globulus

Eucalyptus perriniana

1 reference

Triterpenoids from Eucalyptus perriniana cultured cells

Hedyotis lawsoniae

1 reference

Studies on the constituents of medicinal and related plants in sri lanka. I. New triterpenes from Hedyotis lawsoniae.

Isodon japonicus

1 reference

Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara

Mallotus repandus

1 reference

Triterpenoids from Mallotus repandus: Three new δ-lactones

Rosa transmorrisonensis

1 reference

Chemical Constituents from the Aerial Part of Rosa Transmorrisonensis

Salvia glutinosa

1 reference

Terpenoids from Salvia glutinosa

Salvia regla

1 reference

Abietane and clerodane diterpenes from Salvia regla

Prunella vulgaris

1 reference

Prunella vulgaris: A Comprehensive Review of Chemical Constituents, Pharmacological Effects and Clinical Applications

Uncaria sinensis

1 reference

Suppression of the SOS-inducing activity of mutagenic heterocyclic amine, Trp-P-1, by triterpenoid from Uncaria sinensis in the Salmonella typhimurium TA1535/pSK1002 Umu test

Combretum indicum

1 reference

A new acylglycosyl sterol from quisqualis fructus

Lepechinia caulescens

1 reference

Di- and triterpenoid acids from Lepechinia caulescens

Musanga cecropioides

1 reference

Kalaic acid, a new ursane-type saponin from Musanga cecropioides

Polylepis australis

1 reference

Oleanolic and ursolic acid derivatives from Polylepis australis

Morus alba

1 reference

Hypoglycemic effect of Egyptian Morus alba root bark extract: effect on diabetes and lipid peroxidation of streptozotocin-induced diabetic rats.

Rhaphiolepis loquata

2 references

11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches

Anti-inflammatory and antitumor-promoting effects of the triterpene acids from the leaves of Eriobotrya japonica

Identifiers

InChI

InChI=1S/C31H50O3/c1-19-11-16-31(26(33)34-8)18-17-29(6)21(25(31)20(19)2)9-10-23-28(5)14-13-24(32)27(3,4)22(28)12-15-30(23,29)7/h9,19-20,22-25,32H,10-18H2,1-8H3/t19-,20+,22+,23-,24+,25+,28+,29-,30-,31+/m1/s1

0 references

0 references

0 references

1 reference

1 reference

NMRShiftDB structure ID

2289

1 reference

10019061

1 reference

DSSTox substance ID

DTXSID60348374

1 reference