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(Q104195794)
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English
Lup-20(29)-en-28-oic acid, 3beta-hydroxy-
group of stereoisomers with the chemical formula C₃₀H₄₈O₃
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Statements
instance of
group of stereoisomers
0 references
subclass of
lupane
1 reference
inferred from
lupane
mass
456.360345396
dalton
1 reference
based on heuristic
inferred from SMILES
chemical formula
C₃₀H₄₈O₃
0 references
canonical SMILES
O=C(O)C12CCC(C(=C)C)C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CC1
0 references
found in taxon
Vismia guineensis
1 reference
stated in
New prenylated anthraquinones and xanthones from Vismia guineensis
Mimosa invisa
1 reference
stated in
5-deoxyflavones with cytotoxic activity from Mimosa diplotricha
Pulsatilla chinensis
2 references
stated in
Three New Triterpenoids from Pulsatilla chinensis (Bunge) Regel and Their Cytotoxic Activities
stated in
Pulsatilloside C from the roots of Pulsatilla chinensis
Alnus hirsuta
1 reference
stated in
Inhibition of diacylglycerol acyltransferase by betulinic acid from Alnus hirsuta
Tridax procumbens
1 reference
stated in
Two new flavones from Tridax procumbens Linn.
Dolomiaea costus
1 reference
stated in
Isolation of betulinic acid, its methyl ester and guaiane sesquiterpenoids with protein tyrosine phosphatase 1B inhibitory activity from the roots of Saussurea lappa C.B.Clarke.
Alphitonia incana
1 reference
stated in
Flavonol Glycosides and Cytotoxic Triterpenoids fromAlphitonia Philippinensis
Alphitonia philippinensis
1 reference
stated in
Flavonol Glycosides and Cytotoxic Triterpenoids fromAlphitonia Philippinensis
Eugenia myrcianthes
1 reference
stated in
Constituents of Eugenia sandwicensis with potential cancer chemopreventive activity.
Ajania nubigena
1 reference
stated in
Identification of antioxidant phenolic compounds in feverfew (Tanacetum parthenium) by HPLC-ESI-MS/MS and NMR
Betula utilis
1 reference
stated in
Polyprenols of Wood and Leaf Tissue of the Silver Birch, Betula verrucosa
Rosa rugosa
2 references
stated in
Microbial transformation of dihydrosarsasapogenin with Mycobacterium sp
stated in
Alkyl chromone and other compounds from Clusia nemorosa
Jasminum grandiflorum
1 reference
stated in
Two new flavanone glycosides of Jasminum lanceolarium and their anti-oxidant activities
Eucalyptus flocktoniae
1 reference
stated in
Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves
alpenrose
1 reference
stated in
Terpenoids of Rhododendron japonicum
Garcinia hombroniana
2 references
stated in
Phenolic compounds from the fruit of Garcinia dulcis.
stated in
Cytotoxic prenylated xanthones from the young fruit of Garcinia mangostana
Syzygium claviflorum
2 references
stated in
Syzygium cumini (L.) Skeels: a review of its phytochemical constituents and traditional uses
stated in
Terpenoids of Syzygium formosanum
Acacia acuminata
1 reference
stated in
Cytotoxic lupane-type triterpenoids from Acacia mellifera.
Salvia prionitis
1 reference
stated in
New Triterpenoids from Salvia nicolsoniana
Rhododendron maximum
1 reference
stated in
Terpenoids of Rhododendron japonicum
Salvia miltiorrhiza
1 reference
stated in
New Triterpenoids from Salvia nicolsoniana
Isodon japonicus
1 reference
stated in
Cytotoxic constituents of Isodon rubescens var. lushiensis.
Corymbia citriodora
1 reference
stated in
Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves
Rhododendron arboreum
1 reference
stated in
Terpenoids of Rhododendron japonicum
Euphorbia segetalis
1 reference
stated in
Chemical Constituents of the Roots of Euphorbia micractina
Salvia nubicola
1 reference
stated in
New Triterpenoids from Salvia nicolsoniana
Salvia coulteri
1 reference
stated in
New Triterpenoids from Salvia nicolsoniana
Sida cordifolia
2 references
stated in
alpha-Glucosidase inhibitory constituents from stem bark of Terminalia superba (Combretaceae).
stated in
alpha-Glucosidase inhibitory activity of triterpenoids from Cichorium intybus
Euphorbia polygonifolia
1 reference
stated in
Chemical Constituents of the Roots of Euphorbia micractina
Ruta microcarpa
1 reference
stated in
Four aromatic derivatives from Ruta angustifolia
Acacia salicina
1 reference
stated in
Cytotoxic lupane-type triterpenoids from Acacia mellifera.
Viscum angulatum
1 reference
stated in
The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum
Oxytropis altaica
1 reference
stated in
Betulinic acid and sterols from Astragalus altaicus
Pongamia glabra
2 references
stated in
Constituents of the stem bark of Pongamia pinnata with the potential to induce quinone reductase
stated in
A chromenoflavanone and two caffeic esters fromPongamia glabra
Vismia guianensis
1 reference
stated in
2-Isoprenylemodin and 5,5′-dimethoxysesamin from vismia guaramirangae
Zizyphus vulgaris
1 reference
stated in
Triterpenoid saponins from the bark of Zizyphus joazeiro
Garcinia dulcis
1 reference
stated in
Cytotoxic prenylated xanthones from the young fruit of Garcinia mangostana
Melaleuca leucadendra
1 reference
stated in
Neutral triterpenoids from Melaleuca leucadendron
Ziziphus jujuba
1 reference
stated in
Ceanothane- and lupane-type triterpenes with antiplasmodial and antimycobacterial activities from Ziziphus cambodiana
Diospyros maritima
1 reference
stated in
Two new lupane-type triterpenes from diospyros maritima
Syzygium cumini
1 reference
stated in
Terpenoids of Syzygium formosanum
Viscum album
1 reference
stated in
The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum
Ternstroemia gymnanthera
1 reference
stated in
Extractives of the Ternstroemiaceae. I. The occurrence of betulic acid in Ternstroemia cherryi (Bail.) and T. merrilliana Kobuski
Ternstroemia cherryi
1 reference
stated in
Ursane- and oleanane-type triterpenes from Ternstroemia gymnanthera callus tissues
Syzygium formosanum
1 reference
stated in
Syzygium cumini (L.) Skeels: a review of its phytochemical constituents and traditional uses
Garcinia hanburyi
2 references
stated in
Cytotoxic prenylated xanthones from the young fruit of Garcinia mangostana
stated in
Phenolic compounds from the fruit of Garcinia dulcis.
Ternstroemia merrilliana
1 reference
stated in
Ursane- and oleanane-type triterpenes from Ternstroemia gymnanthera callus tissues
Alphitonia zizyphoides
1 reference
stated in
Constituents of Alphitonia Species. III. Alphitexolide, a New Triterpene, and Other Extractives
Catharanthus roseus
1 reference
stated in
Flavonoid glucosides from the hairy roots of Catharanthus roseus.
Eucalyptus camaldulensis
2 references
stated in
Spasmolytic constituents from Eucalyptus camaldulensis var. obtusa leaves
stated in
Triterpenoids fromEucalyptus camaldulensisDehnh. Tissue Cultures
Ziziphus jujuba var. spinosa
1 reference
stated in
Ceanothane- and lupane-type triterpenes with antiplasmodial and antimycobacterial activities from Ziziphus cambodiana
Morus mongolica var. yunnanensis
1 reference
stated in
Bioactive constituents of Morus australis and Broussonetia papyrifera
Betula platyphylla var. japonica
1 reference
stated in
Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica.
Hypericum elatum
1 reference
stated in
Root-bark constituents ofHypericum elatum andH. androsaemum
Rhododendron metternichii
1 reference
stated in
[Studies on the constituents of Rhododendron metternichii Sieb. et Zucc. var. hondoense Nakai (author's transl)]
Pongamia pinnata var. pinnata
1 reference
stated in
Constituents of the stem bark of Pongamia pinnata with the potential to induce quinone reductase
Rosmarinus officinalis
1 reference
stated in
New Triterpenoids from Salvia nicolsoniana
Mesua ferrea
1 reference
stated in
Pyranoxanthones from
Diospyros ferrea
1 reference
stated in
Coumaroyl triterpene lactone, phenolic and naphthalene glycoside from stem bark of Diospyros angustifolia
Stemodia maritima
1 reference
stated in
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Monascus purpureus
1 reference
stated in
Secondary metabolites from the red mould rice of Monascus purpureus BCRC 38113.
Diospyros japonica
1 reference
stated in
Naphthoquinone Derivatives from the Ebenaceae. III. Shinanolone from Diospyros japonica SIEB.
Bolboschoenus fluviatilis
1 reference
stated in
The constituents of Scirpus fluviatilis(Torr). A. Gray. I. The structures of two new hydroxystilbene dimers, scirpusin A and B.
Diospyros lotus
1 reference
stated in
Naphthoquinone Derivatives from the Ebenaceae. II. Isodiospyrin, Bisisodiospyrin, and Mamegakinone from Diospyros lotus L. and D. morrisiana HANCE
Diospyros kaki
1 reference
stated in
Naphthoquinone Derivatives from the Ebenaceae. IV. Naphthoquinone Derivatives from Diospyros kaki THUNB. and D. kaki THUNB. var. sylvestris MAKINO
Morus alba
2 references
stated in
Inhibitory effects of constituents from Morus alba var. multicaulis on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.
stated in
Four analogues of artocarpin and cyclotocarpin from morus alba
Peganum nigellastrum
1 reference
stated in
Alkaloids and phenylpropanoids from Peganum nigellastrum
Prunus dulcis
1 reference
stated in
Antioxidant constituents of almond [Prunus dulcis (Mill.) D.A. Webb] hulls
Cussonia bancoensis
1 reference
stated in
In vivo anti-nociceptive and anti-inflammatory effect of the two triterpenes, ursolic acid and 23-hydroxyursolic acid, from Cussonia bancoensis
Garcinia celebica
2 references
stated in
Phenolic compounds from the fruit of Garcinia dulcis.
stated in
Cytotoxic prenylated xanthones from the young fruit of Garcinia mangostana
Paeonia × suffruticosa
1 reference
stated in
Palbinone and triterpenes from Moutan Cortex (Paeonia suffruticosa, Paeoniaceae) stimulate glucose uptake and glycogen synthesis via activation of AMPK in insulin-resistant human HepG2 Cells
Prunus avium
1 reference
stated in
Antioxidant constituents of almond [Prunus dulcis (Mill.) D.A. Webb] hulls
Dracocephalum komarovii
1 reference
stated in
Trypanocidal constituents of Dracocephalum komarovi
Solanum aviculare
1 reference
stated in
Occurrence of betulinic acid in different callus cultures of Solanum aviculare
Identifiers
InChI
InChI=1S/C30H48O3/c1-18(2)19-10-15-30(25(32)33)17-16-28(6)20(24(19)30)8-9-22-27(5)13-12-23(31)26(3,4)21(27)11-14-29(22,28)7/h19-24,31H,1,8-17H2,2-7H3,(H,32,33)
0 references
InChIKey
QGJZLNKBHJESQX-UHFFFAOYSA-N
0 references
PubChem CID
2371
1 reference
stated in
PubChem
retrieved
26 December 2021
inferred from
InChIKey
UniChem compound ID
27241914
1 reference
stated in
UniChem
Human Metabolome Database ID
HMDB0245862
1 reference
based on heuristic
inferred from InChIKey
Probes And Drugs ID
PD011651
0 references
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