469-39-6

Usage

Uses

Used in Pharmaceutical Industry:
Cycloleucalenol is used as a precursor molecule for the synthesis of other biologically active compounds. Its role in the biosynthesis pathway of triterpenes makes it a valuable component in the development of new pharmaceuticals.
Used in Research and Development:
Cycloleucalenol is used as a subject of study in scientific research to explore its potential applications and properties. Further investigation is necessary to fully understand its capabilities and how it can be harnessed for various uses.
Used in Antibacterial Applications:
Although not commonly utilized in its pure form, cycloleucalenol is used for its antibacterial properties. Its potential in this area is currently being explored, and it may contribute to the development of new antibacterial agents in the future.

InChI:InChI=1/C30H50O/c1-19(2)20(3)8-9-21(4)23-12-14-28(7)26-11-10-24-22(5)25(31)13-15-29(24)18-30(26,29)17-16-27(23,28)6/h19,21-26,31H,3,8-18H2,1-2,4-7H3/t21-,22+,23-,24+,25+,26+,27-,28+,29-,30+/m1/s1

Upstream product

• 78330-42-4 Acetic acid (3S,4S,9S,10R,13R,14S,17R)-17-((R)-4-acetyl-1,5-dimethyl-hexyl)-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 78330-45-7 Methanesulfonic acid (R)-2-isopropyl-5-[(3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexyl ester 
• 78342-57-1 Acetic acid (3S,4S,10R,13R,14S,17R)-17-((R)-4-isopropyl-1,5-dimethyl-hex-5-enyl)-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 98263-86-6 (R)-2-Isopropyl-5-[(3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexanoic acid methyl ester 
• 98263-83-3 Acetic acid (3S,4S,10R,13R,14S,17R)-17-((R)-5,6-dihydroxy-4-isopropyl-1,5-dimethyl-hexyl)-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 78330-42-4 Acetic acid (3S,4S,10R,13R,14S,17R)-17-((R)-4-acetyl-1,5-dimethyl-hexyl)-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 78330-44-6 (R)-5-((3S,4S,10R,13R,14S,17R)-3-Hydroxy-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl)-2-isopropyl-hexanoic acid methyl ester 
• 98263-85-5 (R)-5-((3S,4S,10R,13R,14S,17R)-3-Hydroxy-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl)-2-isopropyl-hexanoic acid 
• 78342-58-2 (R)-2-Isopropyl-5-[(3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexan-1-ol 
• 78342-57-1 cyclohomonervilol acetate 
• 78330-44-6 (R)-5-((3S,4S,9S,10R,13R,14S,17R)-3-Hydroxy-4,13,14-trimethyl-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl)-2-isopropyl-hexanoic acid methyl ester 
• 78342-58-2 (R)-2-Isopropyl-5-[(3S,4S,9S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexan-1-ol 
• 78330-51-5 cyclohomonervilol 
• 78330-45-7 Methanesulfonic acid (R)-2-isopropyl-5-[(3S,4S,9S,10R,13R,14S,17R)-4,13,14-trimethyl-3-(tetrahydro-pyran-2-yloxy)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-17-yl]-hexyl ester 

Downstream Products

• 1449-09-8 24-methylenecycloartanol 
• 4657-58-3 cycloartanol 
• 16910-32-0 obtusifoliol 
• 34443-88-4 24-methylenecycloartan-3β-ol 
• 98263-87-7 Benzoic acid (3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-17-((1R,4R)-1,4,5-trimethyl-hexyl)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 98263-87-7 Benzoic acid (3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-17-((1R,4S)-1,4,5-trimethyl-hexyl)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 78330-50-4 cyclonervilol 
• 98263-87-7 Benzoic acid (3S,4S,10R,13R,14S,17R)-4,13,14-trimethyl-17-((R)-1,4,5-trimethyl-hexyl)-tetradecahydro-cyclopropa[9,10]cyclopenta[a]phenanthren-3-yl ester 
• 10376-42-8 cycloeucalenol acetate 
• 1255-12-5 cycloeucalenone 
• 124513-78-6 3β-benzoyloxy-24-methylene-9β,19-cyclo-31-nor-lanostane 
• 119272-03-6 phthalic acid mono-(24-methylene-9β,19-cyclo-31-nor-lanostan-3β-yl ester) 

Relevant academic research and scientific papers

Cycloartane triterpenes from the fruit peel of Musa sapientum

Five novel cycloartane-type triterpenes were isolated from the nonsaponifiable lipids obtained from the methanol extract of the fruit peel of Musa sapientum L. (banana). Their structures were determined to be 3- epicycloeucalenol, 3-epicyclomusalenol, 24-methylenepollinastanone, 28- norcyclomusalenone and 24-oxo-29-norcycloartanone by spectroscopic and chemical methods.

Biotransformation of cycloartane-type triterpenes by the fungus Glomerella fusarioides

Biotransformation of three cycloartane-type triterpenes, cycloartenol (1), 24-methylenecycloartanol (2), and cycloartenone (3), by the fungus Glomerella fusarioides was studied. Compound 1 was converted to 3, cycloart-25-ene-3β, 24-diol (4), and cycloartane-3β,24,25-triol (5). Compound 2 was metabolized to cycloeucalenol (6) and two new compounds, 24-methylcycloartane-3β,24, 241-triol (7) and 241-methoxy-24-methylcycloartane- 3β,24-diol (8). Compound 3 was converted into two new metabolites, 4α,4β,14α-trimethyl-9β,19-cyclopregnane-3,20-dione (9) and 25-hydroxy-24-methoxycycloartan-3-one (14), and four known compounds, viz., cycloartane-3,24-dione (10), 24-hydroxycycloart-25-en-3-one (11), (23E)-25-hydroxycycloart-23-en-3-one (12), and 24,25-dihydroxycycloartan-3-one (13). The structures of four new metabolites, 7, 8, 9, and 14, were established by spectroscopic methods.