24-METHYL-CYCLOARTENOL

Structure

2D structure of 24-METHYL-CYCLOARTENOL
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 9547213

Names and identifiers

Name

24-METHYL-CYCLOARTENOL

Also reported as

24-METHYLENE-CYCLOARTANOL

IUPAC name

(2aR,3R,5aS,7aR,9S,11aR,12aS)-2a,5a,8,8-tetramethyl-3-((R)-6-methyl-5-methyleneheptan-2-yl)tetradecahydro-1H,12H-cyclopenta[a]cyclopropa[e]phenanthren-9-ol

SMILES

C[C@H](CCC(=C)C(C)C)[C@H]1CC[C@@]2([C@@]1(CC[C@]34C2CC[C@@H]5[C@]3(C4)CC[C@@H](C5(C)C)O)C)C

General information

Molecular formula

C31H52O

Molecular weight

440.76 g/mol

Monoisotopic mass

440.4018 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
No

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Cyperus esculentus L. tuber -
Yan, M.H., Guan, Z.X. (1983). Studies on fatty acids and unsaponifiable constituents of oil from tubers of Cyperus esculentus L. Chih Wu Hsueh Pao, 25(3), 254-263
Euphorbia cyparissias L. - -
Hemmers, H., Gulz, P.G., Marner, F.J. (1989). Tetra- and pentacyclic triterpenoids from epicuticular wax of Euphorbia cyparissias L., Euphorbiaceae. Z Naturforsch Ser C, 44(7/8), 563-567 doi:10.1515/znc-1989-7-804
Euphorbia cyparissias L. - -
Oksuz, S., Gil, R.R., Chai, H.B., Pezzuto, J.M., Cordell, G.A., Ulubelen, A. (1994). Biologically active compounds from the Euphorbiaceae; 2. two triterpenoids of Euphorbia cyparissias. Planta Med, 60(6), 594-596 doi:10.1055/s-2006-959586
Euphorbia cyparissias L. - -
Starratt, A.N. (1966). Triterpenoid constituents of Euphorbia cyparissias. Phytochemistry, 5, 1341-1344 doi:10.1016/s0031-9422(00)86134-8
Euphorbia cyparissias L. exudate -
Ponsinet, G., Ourisson, G. (1967). In vitro biosynthesis of triterpenes in Euphorbia latex. Phytochemistry, 6, 1235-1243
Euphorbia helioscopia L. subsp. helioscopia exudate -
Ponsinet, G., Ourisson, G. (1967). In vitro biosynthesis of triterpenes in Euphorbia latex. Phytochemistry, 6, 1235-1243
Euphorbia peplus L. - -
Ferreira, M.J.U., Lobo, A.M., Wyler, H. (1993). Triterpenoids and steroids from Euphorbia peplus. Fitoterapia, 64(1), 85-87
Euphorbia peplus L. aerial parts -
Baisted, D.J., Gardner, R.L., Mcreynolds, L.A. (1968). Phytosterol biosynthesis from lanosterol in Euphorbia peplus. Phytochemistry, 7, 945-949 doi:10.1016/s0031-9422(00)82179-2
Euphorbia peplus L. exudate -
Giner, J.L., Berkowitz, J.D., Andersson, T. (2000). Nonpolar components of the latex of Euphorbia peplus. J Nat Prod, 63(2), 267-269 doi:10.1021/np990081g
Juglans regia L. seed 4 ppm
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
Ononis natrix L. subsp. natrix - -
Sanfeliciano, A., Barrero, A.F., Medarde, M., Migueldelcorral, J.M., Calle, M.V. (1983). An isocoumarin and other phenolic components of Ononis natrix. Phytochemistry, 22(9), 2031-2033 doi:10.1016/0031-9422(83)80038-7
Prunus persica (L.) Batsch seed -
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
Sambucus ebulus L. seed -
Chiarlo, B., Ambrosetti, P., Bolla, A. (1979). The constituents of the drupes of Sambucus ebulus. ii. fatty acids, sterol, aliphatic and triterpenic alcohols. Chromatographia, 12, 494-495 doi:10.1007/bf02302997
Sambucus nigra L. flower -
List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.