Voozh

cycloartenol synthase activity

inferred from SMILES

part of

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

cycloartenol 24-C-methyltransferase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

👁 Image

Cycloartenol.svg
324 × 171; 18 KB

criterion used

structure representation with unlabelled terminal carbon atoms

0 references

👁 Image

Struktur Cycloartenol.svg
657 × 349; 16 KB

criterion used

structure representation with labelled terminal carbon atoms

0 references

image of molecular model or crystal lattice model

👁 Image

Cycloartenol molecule ball.png
2,000 × 1,115; 429 KB

depicts

ball-and-stick model

0 references

stereoisomer of

(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

2 references

(1S,3R,6S,8S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

2 references

(1S,3R,6S,8S,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

2 references

(1R,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

2 references

(1S,3R,6S,8S,11R,12R,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

1 reference

(1R,3S,6S,8S,11S,12R,15S,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

1 reference

(1S,3R,6S,8S,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

1 reference

(1R,3S,6S,8S,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

1 reference

(1S,3R,6S,8R,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol

1 reference

chemical formula

C₃₀H₅₀O

1 reference

469-38-5 (English)

14 October 2016

CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C

1 reference

469-38-5 (English)

14 October 2016

C[C@H](CCC=C(C)C)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2CC[C@@H]5[C@]3(C4)CC[C@@H](C5(C)C)O)C)C

1 reference

Biosynthesis of sitosterol, cycloartenol, and 24-methylenecycloartanol in tissue cultures of higher plants and of ergosterol in yeast from [1,2-13C2]- and [2-13C2H3]-acetate and [5-13C2H2]MVA

469-38-5 (English)

14 October 2016

2 references

Direct evidence for three 1,2-hydride migrations in the biosynthesis of cycloartenol from [2-13C2H3]acetate in tissue cultures of Physalis peruviana

Morinda citrifolia

1 reference

Antitubercular constituents from the hexane fraction of Morinda citrifolia Linn. (Rubiaceae).

Casearia ilicifolia

1 reference

Some Constituents of Casearia ilicifolia Vent

Digitalis lanata

1 reference

Sterols in Cell Cultures of Digitalis lanata

Euphorbia guyoniana

1 reference

Diterpenoids and triterpenoids from Euphorbia guyoniana

Euphorbia neriifolia

1 reference

Neriifolione, a triterpene from Euphorbia neriifolia

Euphorbia peplus

1 reference

Nonpolar components of the latex of Euphorbia peplus

Euphorbia segetalis

1 reference

A Tetracyclic diterpene and triterpenes from euphorbia segetalis

Nicotiana benthamiana

1 reference

Virus-induced silencing of sterol biosynthetic genes: identification of a Nicotiana tabacum L. obtusifoliol-14alpha-demethylase (CYP51) by genetic manipulation of the sterol biosynthetic pathway in Nicotiana benthamiana L.

Euphorbia tithymaloides

1 reference

Antimalarial and antituberculous poly-O-acylated jatrophane diterpenoids from Pedilanthus tithymaloides

Euphorbia bupleuroides

1 reference

Terpenoids and other constituents from Euphorbia bupleuroides

Aglaia roxburghiana

1 reference

New Cycloartenol Derivatives from Aglaia roxburghiana1

Anastrophyllum donnianum

1 reference

Sphenolobane diterpenoids from the liverwort Anastrophyllum donnianum

Aplysina fistularis

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Artocarpus integer

3 references

4-hydroxyundecyl docosanoate and cycloartenone in Artocarpus integra latex

Triterpenoids from Artocarpus heterophyllus

Triterpenoids from Artocarpus integrifolia Fruits

Avena sativa

1 reference

Biosynthesis of avenacins and phytosterols in roots of Avena sativa cv. Image

Axinella polypoides

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Axinella verrucosa

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Azolla nilotica

1 reference

Chemical constituents of aquatic fern Azolla nilotica

Bryonia dioica

1 reference

Eight Novel Sterols from the Roots of Bryonia dioica JACQ.

Cajanus cajan

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Calendula officinalis

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Camellia japonica

2 references

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects

Camellia sasanqua

1 reference

Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects

Camellia sinensis

1 reference

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Carnegiea gigantea

1 reference

Isolation of 25(27)-dehydrolanost-8-enol from Cereus giganteus and its biosynthetic implications

Carthamus tinctorius

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Baccharoides anthelmintica

1 reference

4α-methylvernosterol and other sterols from Vernonia anthelmintica seeds

Chlamydomonas reinhardtii

1 reference

Dinoflagellates cyclize squalene oxide to lanosterol

Cicer arietinum

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Cimicifuga simplex

1 reference

Cycloarta-16,24-dien-3.BETA.-ol. Revised Structure of Cimicifugenol, a Cycloartane Tritrpenoid.

Clerodendrum splendens

1 reference

24β-ethylsterols, n-alkanes and n-alkanols of Clerodendrum splendens

Cosmos bipinnatus

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Hellenia speciosa

1 reference

Investigation of Costus; V. Triterpenes of Costus speciosus Roots*

Crataegus monogyna

1 reference

Isolation of three triterpenes and several aliphatic alcohols from Crataegus monogyna Jacq.

Crinum latifolium

1 reference

New constituents from Crinum latifolium with inhibitory effects against tube-like formation of human umbilical venous endothelial cells.

Curculigo orchioides

1 reference

Corchioside A, an orcinol glycoside from Curculigo orchioides

Cuscuta campestris

1 reference

Sterols and fatty acids of some non-photosynthetic angiosperms

Dioscorea bartlettii

1 reference

Studies on the Distribution of Phytosterols in Dioscorea Species Tubers

Dioscorea convolvulacea

1 reference

Studies on the Distribution of Phytosterols in Dioscorea Species Tubers

Dioscorea floribunda

1 reference

Studies on the Distribution of Phytosterols in Dioscorea Species Tubers

Dioscorea nelsonii

1 reference

Studies on the Distribution of Phytosterols in Dioscorea Species Tubers

Enteromorpha intestinalis

1 reference

The identification of 28-isofucosterol in the marine green algae Enteromorpha intestinalis and Ulva lactuca

Ephedra equisetina

1 reference

Lipids from leaves ofEphedra equizetina

Euphorbia boetica

1 reference

Triterpenoids from Euphorbia maculata

Euphorbia caducifolia

2 references

3-Epi-cyclolaudenol and known triterpenes from euphorbia caudicifolia

Cyclocaducinol, a cycloartane type triterpene from Euphorbia caducifolia

Euphorbia characias

1 reference

Free triterpenols and sterols produced by in vitro cultures and laticifer cells from Euphorbia characias

Euphorbia cyparissias

1 reference

Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids ofEuphorbia cyparissias

Euphorbia plumerioides

1 reference

Ent-14[S],16β,17-trihydroxyatisan-3-one and further constituents from Euphorbia fidjiana

Euphorbia kansui

1 reference

Inhibitory effect of euphol, a triterpene alcohol from the roots of Euphorbia kansui, on tumour promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skin

Euphorbia lathyris

2 references

A reinvestigation of the biosynthesis of lanosterol in Euphorbia lathyris

Enhancement of Terpenoid Biosynthesis from Mevalonate in a Fraction of the Latex from Euphorbia lathyris

Euphorbia mellifera

1 reference

Triterpenes of Euphorbia polygonifolia

Euphorbia piscatoria

1 reference

Tetra- and Pentacyclic Triterpenes from the Aerial Parts of Euphorbia piscatoria

Euphorbia portulacoides

1 reference

Diterpenes and phloracetophenones from Euphorbia portulacoides

Euphorbia pulcherrima

1 reference

Cytotoxic triterpenoids from the leaves of Euphorbia pulcherrima

Garcinia kola

1 reference

Antimicrobial Activities of the Constituents of Garcinia Kola Seeds

Garcinia mangostana

1 reference

A triterpene from Garcinia mangostana

Gleichenia japonica

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

soybean

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Gossypium hirsutum

2 references

Free and esterified sterols of cotton buds and anthers

Abscission in Cotton Flowers

common sunflower

2 references

Regulation of sterol biosynthesis in sunflower by 24(R,S),25-epiminolanosterol, a novel C-24 methyl transferase inhibitor

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Helianthus debilis

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Hippophae rhamnoides

3 references

Chemical investigation ofHippophaë rhamnoides. II. Main components of the neutral reaction of the saponification products of an extract of the leaves of the sea buckthorn

Phytosterols in Sea Buckthorn ( Hippophaë rhamnoides L.) Berries: Identification and Effects of Different Origins and Harvesting Times

Hippophae rhamnoides L.: chromatographic methods to determine chemical composition, use in traditional medicine and pharmacological effects

Ifloga spicata

1 reference

Chemical constituents of Eria spicata

Ixeris chinensis

1 reference

Composite Constituents: Thirty-Nine Triterpenoids Including Two Novel Compounds from Ixeris chinensis.

Krameria bicolor

2 references

Neolignans, Norneolignans, and Other Components from Krameria sonorae1

Neolignans, nor-neolignans and other compounds from roots of Krameria grayi

Krameria grayi

2 references

Neolignans, Norneolignans, and Other Components from Krameria sonorae1

Neolignans, nor-neolignans and other compounds from roots of Krameria grayi

Krameria sonorae

1 reference

Neolignans, Norneolignans, and Other Components from Krameria sonorae1

Larix gmelinii

1 reference

Neutral compounds of the extractive substances of larix gmelini

Lathyrus sativus

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Lens culinaris

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Lepidagathis cristata

1 reference

An immunosuppressive tryptophan-derived alkaloid from Lepidagathis cristata

Leucilla nuttingi

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Leucosolenia eleanor

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Macrocystis pyrifera

1 reference

Dinoflagellates cyclize squalene oxide to lanosterol

Mangifera indica

4 references

3-oxo-20S,24R-epoxy-dammarane-25ξ,26-diol from Mangifera indica

Sterols, methyl sterols, triterpene alcohols and fatty acids of the kernel fat of different malagasy mango(Mangifera indica) varieties

Triterpenoids from Mangifera indica

Triterpenoids from Mangifera indicafn1fn1Part iii in the series Triterpenoids from Mangifera indica. For part ii see Anjaneyulu et al., 1989.

Maquira coriacea

1 reference

Constituents of the trunk bark of Maquira coriacea.

Mastigophora diclados

1 reference

Chemical constituents of Malagasy liverworts, part II: mastigophoric acid methyl ester of biogenetic interest from Mastigophora diclados (Lepicoleaceae Subf. Mastigophoroideae).

Matricaria matricarioides

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Milleria quinqueflora

1 reference

Millerenolides, sesquiterpene lactones from Milleria quinqueflora

Momordica charantia

1 reference

Triterpene alcohols in the seed oils of Momordica charantia L.

Hypopitys monotropa

1 reference

Sterols and fatty acids of some non-photosynthetic angiosperms

Monotropa uniflora

1 reference

Sterols and fatty acids of some non-photosynthetic angiosperms

Neolitsea aciculata

1 reference

Four 4α-methylsterols and triterpene alcohols from Neolitsea aciculata

Nicotiana tabacum

1 reference

Chemical composition of tobacco seeds (Nicotiana tabacum L.)

Nigella sativa

1 reference

The sterols of Nigella sativa seed oil

Olea europaea

1 reference

Triterpene alcohols and sterols of Spanish olive oil

Oleandra wallichii

1 reference

Fern Constituents : Triterpenoids from Oleandra wallichii

Paeonia emodi

1 reference

Analysis ofPaeonia emodi root oil

Panax ginseng

1 reference

Composition of unsaponifiable lipid from seed oils ofPanax ginseng andP. quiquefolium

American ginseng

1 reference

Composition of unsaponifiable lipid from seed oils ofPanax ginseng andP. quiquefolium

Peridinium foliaceum

1 reference

Dinoflagellates cyclize squalene oxide to lanosterol

Petrosia ficiformis

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Phytolacca americana

1 reference

Characterization of triterpene alcohols of seed oils from some species of theaceae, phytolaccaceae and sapotaceae

Santolina rosmarinifolia

1 reference

Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring

Sapium pachystachys

1 reference

Rigidol, an unusual diterpene from Sapium rigidifolium

Senecio lydenburgensis

1 reference

Cacalol derivatives from Senecio lydenburgensis

Sesamum alatum

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Sesamum angustifolium

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Sesamum indicum

2 references

Final Report on the Safety Assessment of Sesame Oil

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Sesamum radiatum

1 reference

Seed lipids ofSesamum indicum and related wild species in Sudan. The sterols

Solanum aviculare

1 reference

Steroid Production by Callus and Cell Suspension Cultures of Solanum aviculare

Solanum melongena

1 reference

Triterpene alcohols, 4-methylsterols and 4-desmethylsterols of eggplant seed oil: A new phytosterol

Solanum virginianum

1 reference

Steroidal constituents of Solanum xanthocarpum

Streptocaulon juventas

1 reference

A new cardenolide from the roots of Streptocaulon tomentosum

Symphoricarpos albus

1 reference

The occurrence of lanosterol and 24-methylenelanost-8-en-3β-ol in leaves of symphoricarpus albus

common dandelion

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Taraxacum platycarpum

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Tethya aurantia

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Tillandsia recurvata

1 reference

Hydroperoxycycloartanes from Tillandsia recurvata

Tillandsia streptocarpa

1 reference

Evaluation of the antioedematogenic, free radical scavenging and antimicrobial activities of aerial parts of Tillandsiastreptocarpa Baker-Bromeliaceae

Tillandsia usneoides

1 reference

Cycloartane Derivatives fromTillandsia usneoides

Ulva lactuca

1 reference

The identification of 28-isofucosterol in the marine green algae Enteromorpha intestinalis and Ulva lactuca

Vahlia capensis

1 reference

A seco-olean-18-ene triterpene acid from Vahlia capensis

Vigna mungo

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Vitis vinifera

1 reference

The main triterpene compounds of vine leaves and rachises

Woodwardia radicans

1 reference

Triterpenoids from Woodwardia radicans

Xanthosoma robustum

1 reference

Antibacterial hydroperoxysterols from Xanthosoma robustum

Zantedeschia aethiopica

1 reference

Antialgal compounds from zantedeschia aethiopica

Andira parviflora

1 reference

Flavonoids from Amazonian leguminosae

Amberboa ramosa

1 reference

Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship

Capsicum annuum

1 reference

Occurrence of lanosterol and lanostenol in seeds of red pepper (Capsicum annuum)

Cucumis melo

1 reference

Triterpene alcohols in the seeds of two Cucumis species of cucurbitaceae

Cyperus conglomeratus

1 reference

ChemInform Abstract: Two Novel Flavans from Cyperus conglomeratus.

Elaeagnus angustifolia

1 reference

Lipids of the leaves ofElaeagnus angustifolia II. Composition of the neutral lipids

Euphorbia nicaeensis

1 reference

Über Inhaltsstoffe von Euphorbiaceae, 8. Mitt. [1]. Triterpenester und Triterpenalkohole aus Euphorbia biglandulosa Desf. / Constituents of Euphorbiaceae, 8. Comm. [1]. Triterpen Esters and Triterpen Alcohols from Euphorbia biglandulosa Desf.

1 reference

1 reference

Diterpenes from Euphorbia paralias

Euphorbia seguieriana

1 reference

Diterpenes from Euphorbia seguieriana

Euphorbia seguieri

1 reference

Diterpenes from Euphorbia seguieriana

Excoecaria agallocha

1 reference

Constituents of Excoecaria agallocha

Gynura japonica

1 reference

Cerebrosides from the Rhizomes ofGynura Japonica

Herbertus aduncus

1 reference

Herbertane sesquiterpenoids from the liverworts Herbertus aduncus and H. borealis

Heterotheca inuloides

1 reference

Sesquiterpene, Triterpene und Sterine aus Blüten von Heterotheca inuloides (“Mexikanische Arnikablüten”)

Lophozia ventricosa

1 reference

Sesquiterpenoids from the liverwort Lophozia ventricosa

Nelumbo nucifera

1 reference

Selective cholinesterase inhibitory activities of a new monoterpene diglycoside and other constituents from Nelumbo nucifera stamens

Nicotiana debneyi

1 reference

Composition of the leaf surface gum of some Nicotiana species and Nicotiana tabacum cultivars

Nicotiana paniculata

1 reference

Composition of the leaf surface gum of some Nicotiana species and Nicotiana tabacum cultivars

Solidago canadensis

1 reference

New lupane triterpenoids from Solidago canadensis that inhibit the lyase activity of DNA polymerase beta.

Tabernaemontana divaricata

1 reference

New alkaloids from Tabernaemontana divaricata

maize

1 reference

Investigations on the Δ23-, Δ24(28)- and Δ25-Sterols of zea mays

Nicotiana forsteri

1 reference

Composition of the leaf surface gum of some Nicotiana species and Nicotiana tabacum cultivars

Nicotiana fragrans

1 reference

Composition of the leaf surface gum of some Nicotiana species and Nicotiana tabacum cultivars

Oligochaeta divaricata

1 reference

Tyrosinase inhibitory cycloartane type triterpenoids from the methanol extract of the whole plant of Amberboa ramosa Jafri and their structure-activity relationship

Psilotum nudum

1 reference

Sterols and fatty acids of a whisk fernPsilotum nudum

Himatanthus articulatus

1 reference

Chemical Constituents from Himatanthus articulata

Vigna cylindrica

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

Vigna unguiculata

1 reference

A new monodesmosidic triterpenoid saponin from the seeds of Vigna unguiculata subsp. unguiculata

Dendranthema morifolium

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Euphorbia broteri

1 reference

Triterpenes from Euphorbia broteri

Leptadenia hastata

1 reference

Triterpenoids from Leptadenia hastata latex

Solanum aethiopicum

1 reference

Steroidal constituents of Solanum xanthocarpum

Paeonia lactiflora

1 reference

Characterization of fatty acids, triacylglycerols, phytosterols and tocopherols in peony seed oil from five different major areas in China

Beta vulgaris

1 reference

Brassinosteroids and sterols from seeds of Beta vulgaris

Diplopterygium glaucum

1 reference

Triterpene Alcohols and Sterols from the Fern Gleichenia japonica SPR.

Goniophlebium formosanum

1 reference

24S-Chirality of 24-alkylsterols possessing a Δ25-double bond from Polypodium formosanum

Aglaia elaeagnoidea

1 reference

New Cycloartenol Derivatives from Aglaia roxburghiana1

Tethya aurantium

1 reference

Biosynthetic studies of marine lipids. 35. The demonstration of de novo sterol biosynthesis in sponges using radiolabeled isoprenoid precursors

Matricaria discoidea

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Chamomilla suaveolens

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Chrysanthemum morifolium

1 reference

Triterpene alcohols from the flowers of compositae and their anti-inflammatory effects

Actaea simplex

1 reference

Cycloarta-16,24-dien-3.BETA.-ol. Revised Structure of Cimicifugenol, a Cycloartane Tritrpenoid.

Camellia oleifera

1 reference

Triterpene Alcohols from Camellia and Sasanqua Oils and Their Anti-inflammatory Effects

Euphorbia stygiana

1 reference

Triterpenes of Euphorbia polygonifolia

Euphorbia oxyphylla

1 reference

Triterpenes from Euphorbia broteri

Dioscorea hondurensis

1 reference

Studies on the Distribution of Phytosterols in Dioscorea Species Tubers

Pisum sativum

1 reference

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds

tomato

1 reference

Triterpenoids and sterol glucoside from cell cultures of Lycopersicon esculentum

Monticalia firmipes

1 reference

New Sesquiterpenes from Senecio species

Isodon japonicus

1 reference

Biosynthesis of sitosterol, cycloartenol, and 24-methylenecycloartanol in tissue cultures of higher plants and of ergosterol in yeast from [1,2-13C2]- and [2-13C2H3]-acetate and [5-13C2H2]MVA

Rhodomonas salina

1 reference

Dinoflagellates cyclize squalene oxide to lanosterol

Lessertia frutescens

1 reference

Cycloartanol and Sutherlandioside C peracetate from Sutherlandia frutescens and their immune potentiating effects

Ulva intestinalis

1 reference

The identification of 28-isofucosterol in the marine green algae Enteromorpha intestinalis and Ulva lactuca

Monotropa hypopitys

1 reference

Sterols and fatty acids of some non-photosynthetic angiosperms

mass

426.386 dalton

1 reference

InChI=1S/C30H50O/c1-20(2)9-8-10-21(3)22-13-15-28(7)24-12-11-23-26(4,5)25(31)14-16-29(23)19-30(24,29)18-17-27(22,28)6/h9,21-25,31H,8,10-19H2,1-7H3/t21-,22-,23+,24+,25+,27-,28+,29-,30+/m1/s1

469-38-5 (English)

14 October 2016

Cycloartenol

0 references

Identifiers

InChI

1 reference

469-38-5 (English)

14 October 2016

2 references

469-38-5 (English)

14 October 2016

ChEBI release 2020-09-01

CAS Registry Number

469-38-5

2 references

Global Substance Registration System

UNII

YU32VE82N3

cycloartenol (English)

14 October 2016

https://commonchemistry.cas.org/detail?cas_rn=469-38-5

10 April 2021

1 reference

(3beta,9beta)-9,19-Cyclolanost-24-en-3-ol (English)

14 October 2016

2 references

469-38-5 (English)

14 October 2016

imported from Wikimedia project

ChEBI ID

17030

mapping relation type

exact match

2 references

French Wikipedia

International Chemical Identifier

InChI

InChI=1S/C30H50O/c1-20(2)9-8-10-21(3)22-13-15-28(7)24-12-11-23-26(4,5)25(31)14-16-29(23)19-30(24,29)18-17-27(22,28)6/h9,21-25,31H,8,10-19H2,1-7H3/t21-,22-,23+,24+,25+,27-,28+,29-,30+/m1/s1

1 reference

CYCLOARTENOL (English)

14 October 2016

SureChEMBL ID

560780

1 reference

1 reference

1 reference

DSSTOX compound identifier

DTXCID001324322

0 references

NSC number

670193

0 references

Human Metabolome Database ID

HMDB0036591

2 references

reason for deprecated rank

KNApSAcK ID

C00003650

cannot be confirmed by other sources

0 references

UNII

YU32VE82N3

2 references

Global Substance Registration System

UNII

YU32VE82N3

cycloartenol (English)

14 October 2016

Natural Product Atlas ID

NPA031379

2 references

0 references

1 reference