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MedKoo Cat#: 528021 | Name: Lupeol benzoate

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Lupeol benzoate is a bioactive chemical.

Chemical Structure

Lupeol benzoate
Lupeol benzoate
CAS#1617-69-2

Theoretical Analysis

MedKoo Cat#: 528021

Name: Lupeol benzoate

CAS#: 1617-69-2

Chemical Formula: C37H54O2

Exact Mass: 530.4124

Molecular Weight: 530.84

Elemental Analysis: C, 83.72; H, 10.25; O, 6.03

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Synonym
Lupeol benzoate
IUPAC/Chemical Name
Lup-20(29)-en-3-ol, benzoate, (3beta)-
InChi Key
GGGPJWXHMZSCEW-WEZIXBNWSA-N
InChi Code
InChI=1S/C37H54O2/c1-24(2)26-16-19-34(5)22-23-36(7)27(31(26)34)14-15-29-35(6)20-18-30(39-32(38)25-12-10-9-11-13-25)33(3,4)28(35)17-21-37(29,36)8/h9-13,26-31H,1,14-23H2,2-8H3/t26-,27+,28-,29+,30-,31+,34+,35-,36+,37+/m0/s1
SMILES Code
CC1(C)[C@@H](OC(C2=CC=CC=C2)=O)CC[C@]3(C)[C@@]4([H])CC[C@]5([H])[C@@]6([H])[C@H](C(C)=C)CC[C@@](C)6CC[C@](C)5[C@@](C)4CC[C@@]13[H]
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 530.84 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
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Epub 2012 Sep 15. PubMed PMID: 22986293. 11: Azizuddin, Khan AM, Choudhary MI. Tyrosinase inhibitory potential of natural products isolated from various medicinal plants. Nat Prod Res. 2011 Apr;25(7):750-3. doi: 10.1080/14786419.2010.513684. PubMed PMID: 21462074. 12: Cuca Suarez LE, Pattarroyo ME, Lozano JM, Delle Monache F. Biological activity of secondary metabolites from Peltostigma guatemalense. Nat Prod Res. 2009;23(4):370-4. doi: 10.1080/14786410802228439. PubMed PMID: 19296377. 13: Gao XH, Xie N, Feng F. [Studies on chemical constituents of Salacia prinoides]. Zhong Yao Cai. 2008 Sep;31(9):1348-51. Chinese. PubMed PMID: 19180955. 14: Srinivasan GV, Ranjith C, Vijayan KK. Identification of chemical compounds from the leaves of Leea indica. Acta Pharm. 2008 Jun;58(2):207-14. doi: 10.2478/v10007-008-0002-7. PubMed PMID: 18515230. 15: Hovaneissian M, Archier P, Mathe C, Culioli G, Vieillescazes C. Analytical investigation of styrax and benzoin balsams by HPLC- PAD-fluorimetry and GC-MS. Phytochem Anal. 2008 Jul-Aug;19(4):301-10. PubMed PMID: 17994534. 16: Shang XY, Li S, Wang YH, Wang SJ, Yang YC, Shi JG. [Chemical constitutents of Bauhinia aurea]. Zhongguo Zhong Yao Za Zhi. 2006 Dec;31(23):1953-5. Chinese. PubMed PMID: 17348187. 17: Kouam SF, Ngadjui BT, Krohn K, Wafo P, Ajaz A, Choudhary MI. Prenylated anthronoid antioxidants from the stem bark of Harungana madagascariensis. Phytochemistry. 2005 May;66(10):1174-9. PubMed PMID: 15924922. 18: Sultana S, Saleem M, Sharma S, Khan N. Lupeol, a triterpene, prevents free radical mediated macromolecular damage and alleviates benzoyl peroxide induced biochemical alterations in murine skin. Indian J Exp Biol. 2003 Aug;41(8):827-31. PubMed PMID: 15248479. 19: Zhang Q, Tan W, Chen K. [Studies on the chemical constituents of Ampelopsis humulifolia var. heterophylla (Thunb.) K. Koch]. Zhong Yao Cai. 2003 Sep;26(9):636-7. Chinese. PubMed PMID: 14692319. 20: Saleem M, Alam A, Arifin S, Shah MS, Ahmed B, Sultana S. Lupeol, a triterpene, inhibits early responses of tumor promotion induced by benzoyl peroxide in murine skin. Pharmacol Res. 2001 Feb;43(2):127-34. PubMed PMID: 11243713.