Euphol &#160; ingelesa (Q27106574)

Euphol (ingelesa)

(3S,5S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol ^ingelesa

5 urria 2016

stereoisomer of ^ingelesa

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

(+)-tirucallol ^ingelesa

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

(3S,5R,10S,13S,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol ^ingelesa

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

(3R,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol ^ingelesa

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol ^ingelesa

Erreferentzia bat

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

Lanosterol

Erreferentzia bat

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

(3R,5R,10S,13S,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol ^ingelesa

Erreferentzia bat

based on heuristic ^ingelesa

inferred from InChI ^ingelesa

formula kimikoa

C₃₀H₅₀O

Erreferentzia bat

Euphol (ingelesa)

5 urria 2016

CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C

Erreferentzia bat

Euphol (ingelesa)

5 urria 2016

isomeric SMILES ^ingelesa

C[C@H](CCC=C(C)C)[C@@H]1CC[C@]2([C@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C

Erreferentzia bat

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

Euphol (ingelesa)

5 urria 2016

Erreferentzia bat

Japoniako kamelia

2 erreferentzia

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

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects ^ingelesa

Phytolacca americana

Erreferentzia bat

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

karite

Erreferentzia bat

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

Euphorbia drupifera

Erreferentzia bat

Triterpenoids from leaves of Elaeophorbia drupifera ^ingelesa

Euphorbia abyssinica

Erreferentzia bat

Ingenane and lathyrane diterpenes from the latex of euphorbia acrurensis ^ingelesa

Euphorbia antiquorum

3 erreferentzia

Eupha-7,9(11),24-trien-3beta-ol ("antiquol C") and other triterpenes from Euphorbia antiquorum latex and their inhibitory effects on Epstein-Barr virus activation ^ingelesa

Constituents of the latex of Euphorbia antiquorum ^ingelesa

Constituents of the latex of Euphorbia antiquorum ^ingelesa

Euphorbia kansui

6 erreferentzia

Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus ^ingelesa

Preparative isolation and gas chromatography-mass spectrometry analysis of triterpenoids in kansui radix ^ingelesa

Cytotoxicity and antiviral activity of the compounds from Euphorbia kansui ^ingelesa

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 ^ingelesa

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 ^ingelesa

Cytotoxicity and antiviral activity of the compounds from Euphorbia kansui ^ingelesa

Cajanus cajan

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Camellia sasanqua

2 erreferentzia

Isohelianol: A 3,4-seco-Triterpene Alcohol from Sasanqua Oil ^ingelesa

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects ^ingelesa

garbantzu

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Clusia columnaris

Erreferentzia bat

Flavonoids, benzophenones and a new euphane derivative from Clusia columnaris Engl. ^ingelesa

Clusia multiflora

Erreferentzia bat

Citrans and cyclols from Clusia multiflora☆ ^ingelesa

Euphorbia aleppica

Erreferentzia bat

Pentacyclic diterpene esters from Euphorbia aleppica ^ingelesa

Euphorbia boetica

Erreferentzia bat

Boeticol, a New Tetracyclic Triterpene from Euphorbia boetica ^ingelesa

Euphorbia caducifolia

Erreferentzia bat

Cyclocaducinol, a cycloartane type triterpene from Euphorbia caducifolia ^ingelesa

Tartiku

2 erreferentzia

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

Biosynthesis of Isoprene Units in Euphorbia lathyris Laticifers vs. Other Tissues: MVA and MEP Pathways, Compartmentation and Putative Endophytic Fungi Contribution ^ingelesa

Euphorbia neriifolia

Erreferentzia bat

A new tetracyclic triterpene from the latex of Euphorbia nerifolia ^ingelesa

Euphorbia nicaeensis

Erreferentzia bat

Biologically active compounds from the Euphorbiaceae; Part 1. Triterpenoids of Euphorbia nicaeensis subsp. glareosa ^ingelesa

Euphorbia portulacoides

Erreferentzia bat

Diterpenes and phloracetophenones from Euphorbia portulacoides ^ingelesa

Euphorbia retusa

Erreferentzia bat

Triterpenes and fatty acids from Nepeta aragonensis ^ingelesa

Euphorbia tirucalli

2 erreferentzia

The Effect of Medium Modification and Selected Precursors on Sterol Production by Short-Term Callus Cultures of Euphorbia tirucalli ^ingelesa

On the Active Principles of the Spurge Family (Euphorbiaceae) XI. [1] The Skin Irritant and Tumor Promoting Diterpene Esters of Euphorbia tirucalli L. Originating from South Africa ^ingelesa

Euphorbia trigona

Erreferentzia bat

Triterpenoids from Euphorbia maculata ^ingelesa

Garcinia myrtifolia

Erreferentzia bat

Three prenylated phenolic benzophenones from Garcinia myrtifolia ^ingelesa

Garcinia pseudoguttifera

Erreferentzia bat

Benzophenones of Garcinia pseudoguttifera (Clusiaceae) ^ingelesa

soja

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Aixkol

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Dilista

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Monocyclanthus vignei

Erreferentzia bat

Cycloartanes and other terpenoids and phenylpropanoids from Monocyclanthus vignei ^ingelesa

ilar

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Meloi

Erreferentzia bat

Triterpene alcohols in the seeds of two Cucumis species of cucurbitaceae ^ingelesa

Luzoker

Erreferentzia bat

Triterpene alcohols in the seeds of two Cucumis species of cucurbitaceae ^ingelesa

Euphorbia jolkinii

Erreferentzia bat

Eight New Diterpenoids from the Roots ofEuphorbia nematocypha ^ingelesa

Euphorbia resinifera

Erreferentzia bat

Bioactive triterpene derivatives from latex of two Euphorbia species. ^ingelesa

Euphorbia sapinii

Erreferentzia bat

Terpenoids constituents of Euphorbia sapinii ^ingelesa

Garcinia cymosa

2 erreferentzia

(20R,23E)-Eupha-8,23-diene-3β,25-diol from Tripetalum cymosum ^ingelesa

Friedelin and lanosterol from Garcinia prainiana stimulated glucose uptake and adipocytes differentiation in 3T3-L1 adipocytes ^ingelesa

Dacryodes hopkinsii

Erreferentzia bat

Phytochemistry of Trattinnickia burserifolia, T. rhoifolia, and Dacryodes hopkinsii: chemosystematic implications ^ingelesa

Euphorbia condylocarpa

Erreferentzia bat

Tetracyclic triterpene compounds fromEuphorbia condylocarpa ^ingelesa

Vigna cylindrica

Erreferentzia bat

Triterpene alcohols and 3-oxo steroids of nine Leguminosae seeds ^ingelesa

Euphorbia sulcata

Erreferentzia bat

Triterpenes and fatty acids from Nepeta aragonensis ^ingelesa

Euphorbia broteri

Erreferentzia bat

Triterpenes from Euphorbia broteri ^ingelesa

Garcinia livingstonei

Erreferentzia bat

Non-toxic melanin production inhibitors from Garcinia livingstonei (Clusiaceae). ^ingelesa

Camellia oleifera

2 erreferentzia

Triterpene alcohols from camellia and sasanqua oils and their anti-inflammatory effects ^ingelesa

Isohelianol: A 3,4-seco-Triterpene Alcohol from Sasanqua Oil ^ingelesa

Euphorbia oxyphylla

Erreferentzia bat

InChI=1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h10,21-22,25-26,31H,9,11-19H2,1-8H3/t21-,22+,25+,26+,28-,29+,30-/m1/s1

Triterpenes from Euphorbia broteri ^ingelesa

Identifikatzaileak

InChI

Erreferentzia bat

Euphol (ingelesa)

5 urria 2016

2 erreferentzia

Euphol (ingelesa)

5 urria 2016

ChEBI release 2020-09-01 ^ingelesa

CAS zenbakia

514-47-6

2 erreferentzia

ChEBI ^ingelesa

Euphol (ingelesa)

5 urria 2016

CAS Common Chemistry ^ingelesa

https://commonchemistry.cas.org/detail?cas_rn=514-47-6

9 apirila 2021

URL erreferentzia

ChemSpider-ren identifikatzailea

390292

Erreferentzia bat

ChemSpider-ren identifikatzailea

ChemSpider ^ingelesa

390292

euphol (ingelesa)

5 urria 2016

2 erreferentzia

Euphol (ingelesa)

5 urria 2016

InChIKey ^ingelesa

mapping relation type ^ingelesa

exact match ^ingelesa

2 erreferentzia

ChEBI ^ingelesa

Euphol (ingelesa)

5 urria 2016

InChI=1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h10,21-22,25-26,31H,9,11-19H2,1-8H3/t21-,22+,25+,26+,28-,29+,30-/m1/s1

International Chemical Identifier ^ingelesa

InChI

ChEMBL-en identifikatzailea

CHEMBL465181

Erreferentzia bat

ChEMBL-en identifikatzailea

ChEMBL ^ingelesa

CHEMBL465181

EUPHOL (ingelesa)

5 urria 2016

SureChEMBL ID ^ingelesa

SCHEMBL541497

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

InChIKey ^ingelesa

UniChem compound ID ^ingelesa

525992

Erreferentzia bat

UniChem ^ingelesa

DSSTox substance ID ^ingelesa

DTXSID201318412

Erreferentzia bat

InChIKey ^ingelesa

NSC number ^ingelesa

36571

0 erreferentzia

Human Metabolome Database ID ^ingelesa

HMDB0031438

2 erreferentzia

based on heuristic ^ingelesa

inferred from InChIKey ^ingelesa

InChIKey ^ingelesa

KNApSAcK ID ^ingelesa

C00003745

Erreferentzia bat

ChEBI ^ingelesa

Euphol (ingelesa)

KEGG-ren identifikatzailea

5 urria 2016

Probes And Drugs ID ^ingelesa

PD125778

0 erreferentzia

C08624

Erreferentzia bat

ChEBI ^ingelesa

Euphol (ingelesa)

5 urria 2016

LIPID MAPS ID ^ingelesa

LMPR0106090002

Erreferentzia bat

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

LIPID MAPS ^ingelesa

URL erreferentzia