54815-36-0

Basic information

• Product Name: jujubogenin
• Synonyms: jujubogenin;(23R)-16β,23:16,30-Diepoxy-5α-dammar-24-ene-3β,20-diol;(23R)-16β,23:16,30-Diepoxydammar-24-ene-3β,20-diol
• CAS NO: 54815-36-0
• Molecular Formula: C₃₀H₄₈O₄
• Molecular Weight: 472.69972
• Mol File: 54815-36-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 576.3±50.0 °C(Predicted)
• Appearance: /
• Density: 1.14±0.1 g/cm3(Predicted)
• PKA: 14.66±0.70(Predicted)
• CAS DataBase Reference: jujubogenin(CAS DataBase Reference)
• NIST Chemistry Reference: jujubogenin(54815-36-0)
• EPA Substance Registry System: jujubogenin(54815-36-0)

Safety Data

• Hazardous Substances Data: 54815-36-0(Hazardous Substances Data)

Upstream product

• 55466-05-2 jujuboside B (Compound I) 
• 55466-05-2 Zizyphus saponin III 

Downstream Products

• 769950-30-3 (2E)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enoic acid 3,4,5-trimethoxyphenyl ester 
• 769949-95-3 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-N-(2,4,5-trichlorophenyl)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxamide 
• 769950-29-0 (2E)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enoic acid 4-nitrophenyl ester 
• 769949-76-0 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxylic acid 3,4,5-trimethoxyphenyl ester 
• 769950-31-4 (2E)-N-(4-chlorophenyl)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enamide 
• 769950-27-8 (2E)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enoic acid 4-chlorophenyl ester 
• 769949-91-9 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-N-(1,1'-[biphenyl]-4-yl)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxamide 
• 769950-28-9 (2E)-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enoic acid 4-methoxyphenyl ester 
• 769949-80-6 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carbothioic acid S-(2,6-dichlorophenyl) ester 
• 769949-88-4 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-N-(3,4-dichlorophenyl)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxamide 
• 769949-66-8 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxylic acid 2,4-dichlorophenyl ester 
• 769949-75-9 (1'S,2'S,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthrene]-2'-carboxylic acid (1,1'-biphenyl)-4-yl ester 
• 769949-60-2 (2E)-N-phenyl-2-methyl-3-[(1'S,2'R,4'aR,4'bR,7'S,8'aR,10'aR)-tetradecahydro-4'b,8',8',10'a-tetramethyl-7'-[(methylsulfonyl)oxy]-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]prop-2-enamide 
• 769950-35-8 (2E)-3-[(1'S,2'R,4'aR,4'bS,,8'aS,10'aR)-3',4,4'4'a,4'b,5,5',8',8'a,9'10',10'a-dodecahydro-4'b8',8',10'a-tetramethyl-5-oxospiro[furan-3(2H),1'(2'H)-phenanthren]-2'-yl]-2-methylprop-2-enoic acid 3,4,5-trimethoxyphenyl ester 

Relevant articles and documents

Dammarane-type saponins from Ziziphus jujube

Two new dammarane-type saponins jujubosides D and E, together with three known compounds, were isolated from the seeds of Ziziphus jujube. Their structures were elucidated on the basis of chemical and spectroscopic evidence. Compounds 1-5 showed lipoxygenase-inhibiting activity.