Lupeol acetate
Compound with spectra: 11 NMR, and 4 MS (GC)
| SpectraBase Compound ID | 9fF6BbQsLTO |
|---|---|
| InChI | InChI=1S/C32H52O2/c1-20(2)22-12-15-29(6)18-19-31(8)23(27(22)29)10-11-25-30(7)16-14-26(34-21(3)33)28(4,5)24(30)13-17-32(25,31)9/h22-27H,1,10-19H2,2-9H3/t22-,23+,24-,25+,26-,27+,29+,30-,31+,32+/m0/s1 |
| InChIKey | ODSSDTBFHAYYMD-YOJQYFTNSA-N |
| Mol Weight | 468.8 g/mol |
| Molecular Formula | C32H52O2 |
| Exact Mass | 468.396731 g/mol |
| Enantiomer InChIKey | ODSSDTBFHAYYMD-RSOJEYMUSA-N |
| Copyright | Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved. |
|---|---|
| Source of Spectrum | Biologically and Environmentally Important Organic Compounds: GCMS Library |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | Y1-38-880-3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | APC-314-23-2 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | PA-7-239-12(GC_MS) |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- LUPENYL-ACETATE
- LUPEOL-3-ACETATE
- 3-O-ACETYL-LUPEOL
- LUP-20(29)-ENE-3-ACETATE
- 3-BETA-LUP-20-(29)-EN-3-YL-ACETATE
- (1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-yl acetate
- Lupen-20(30)-3Beta-ol acetate
LUP-20(29)-EN-3-YL ACETATE
3b-Acetoxy-lup-20(29)-ene
LUPEPORTLANDOL-ACETATE;3-ALPHA-ACETOXY-19-ALPHA-H-LUP-20(29)-ENE
(1R,3aR,5aR,5bR,9S,11aR)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-yl acetate
Lup-20(29)-en-3-ol, acetate, (3.beta.)-
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl-1-13C)icosahydro-1H-cyclopenta[a]chrysen-9-yl acetate
17-Epilupenyl acetate
17-Epilupenyl acetate
| Title | Journal or Book | Year |
|---|---|---|
| In Vitro Antiprotozoal Activity of Triterpenoid Constituents of Kleinia odora Growing in Saudi Arabia | Molecules | 2013 |
| The Triterpenes 3β-Lup-20(29)-en-3-ol and 3β-Lup-20(29)-en-3-yl Acetate and the Carbohydrate 1,2,3,4,5,6-Hexa-O-acetyl-dulcitol as Photosynthesis Light Reactions Inhibitors | Molecules | 2011 |
| Structural determination of 3β-stearyloxy-urs-12-ene fromMaytenus salicifolia by 1D and 2D NMR and quantitative13C NMR spectroscopy | Magnetic Resonance in Chemistry | 2006 |
| Composite Constituents: Thirty-Nine Triterpenoids Including Two Novel Compounds from Ixeris chinensis. | Chemical and Pharmaceutical Bulletin | 1996 |
| A quinonoid pyranobenzoxanthone and pyranodihydrobenzoxanthone fromArtocarpus communis | Phytochemistry | 1992 |
| Triterpenoids Isolated fromParahancornia amapa | Journal Of The Brazilian Chemical Society | 1991 |
| Triterpenoids of Cnidosculus urens | Phytochemistry | 1985 |
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