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(Q104169480)
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β-amyrin
group of stereoisomers with the chemical formula C₃₀H₅₀O
beta-amyrenol
amyrin
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Statements
instance of
group of stereoisomers
0 references
subclass of
oleanane triterpenoid
1 reference
inferred from
oleanane triterpenoid
mass
426.38616622
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₃₀H₅₀O
0 references
canonical SMILES
OC1CCC2(C)C(CCC3(C)C2CC=C4C5CC(C)(C)CCC5(C)CCC43C)C1(C)C
0 references
found in taxon
Senecio chionophilus
1 reference
stated in
Constituents of Senecio chionophilus with potential antitubercular activity
Styphnolobium japonicum
1 reference
stated in
Identification of beta-amyrin and sophoradiol 24-hydroxylase by expressed sequence tag mining and functional expression assay
Sophora leachiana
1 reference
stated in
Identification of beta-amyrin and sophoradiol 24-hydroxylase by expressed sequence tag mining and functional expression assay
Sideroxylon rotundifolium
1 reference
stated in
ISOLATION OF ERYTHRODIOL 3–PALMITATE FROMBUMELIA OBTUSIFOLIA
Camellia japonica
1 reference
stated in
Triterpenoids from Camellia japonica and their cytotoxic activity
Pulicaria canariensis
1 reference
stated in
Secondary metabolites from two species of Pulicaria and their cytotoxic activity.
Salacia hainanensis
1 reference
stated in
New triterpenes from Salacia hainanensis Chun et How with α-glucosidase inhibitory activity
Drypetes littoralis
1 reference
stated in
Chemical constituents from Drypetes littoralis
Hippocratea volubilis
2 references
stated in
21beta-Hydroxy-oleanane-type triterpenes from Hippocratea excelsa
stated in
Triterpenoids from Hippocratea excelsa. The Crystal Structure of 29-Hydroxytaraxerol
Trewia nudiflora
1 reference
stated in
The Chemical Constituents from the Callus Culture ofTrewia nudiflora
Phelipanche aegyptiaca
1 reference
stated in
The Alkaloids of Kopsia longiflora Merrill. I. Isolation of the Alkaloids
Gymnosporia cassinoides
1 reference
stated in
Three triterpenes and other terpenoids from Catha cassinoides
Diospyros ferrea
1 reference
stated in
Coumaroyl triterpene lactone, phenolic and naphthalene glycoside from stem bark of Diospyros angustifolia
Zanthoxylum ailanthoides
3 references
stated in
Amides and benzenoids from Zanthoxylum ailanthoides with inhibitory activity on superoxide generation and elastase release by neutrophils
stated in
Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides
stated in
Chemical Constituents from the Root Bark of FormosanZanthoxylum Ailanthoides
Cyrtocarpa
1 reference
stated in
Anti-ulcer activity of Cyrtocarpa procera analogous to that of Amphipterygium adstringens, both assayed on the experimental gastric injury in rats
Cupania americana
1 reference
stated in
Cupaniol, a New branched polyprenol, from Cupania latifolia
Plinia pinnata
1 reference
stated in
5,7,2′,5′-Tetrahydroxydihydroflavonol 3-rhamnoside from Plinia pinnata
Mimusops
1 reference
stated in
107. Extractives from woods. Part III. Extractives from Manilkara bidentata
Sophora flavescens var. flavescens
1 reference
stated in
Identification of beta-amyrin and sophoradiol 24-hydroxylase by expressed sequence tag mining and functional expression assay
Sideritis candicans
1 reference
stated in
New diterpenes from Sideritis candicans
Salacia chinensis
1 reference
stated in
Biological activities of Salacia chinensis originating in Thailand: the quality evaluation guided by alpha-glucosidase inhibitory activity
Tainia bicornis
1 reference
stated in
Cupaniol, a New branched polyprenol, from Cupania latifolia
Zanthoxylum alatum
1 reference
stated in
A new amide from zanthoxylum armatum
Trochodendron aralioides
1 reference
stated in
Isolation and Identification of Betulin, Lupeol, and β-Amyrin from the Bird-lime of Trochodendron aralioides Siebold et Zuccarini
Andaliman
1 reference
stated in
A new amide from zanthoxylum armatum
Tainia latifolia
1 reference
stated in
Cupaniol, a New branched polyprenol, from Cupania latifolia
Identifiers
InChI
InChI=1S/C30H50O/c1-25(2)15-16-27(5)17-18-29(7)20(21(27)19-25)9-10-23-28(6)13-12-24(31)26(3,4)22(28)11-14-30(23,29)8/h9,21-24,31H,10-19H2,1-8H3
0 references
InChIKey
JFSHUTJDVKUMTJ-UHFFFAOYSA-N
0 references
PubChem CID
225689
1 reference
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
UniChem compound ID
64084907
1 reference
stated in
UniChem
Human Metabolome Database ID
HMDB0249098
1 reference
based on heuristic
inferred from InChIKey
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