Chemodex

Lupeol

CHF 81.00
In stock
CDX-L0128-M02525 mgCHF 81.00
CDX-L0128-M100100 mgCHF 244.00
More Information
Product Details
Synonyms β-Viscol; 20(29)-Lupen-3β-ol; 3β-Hydroxy-20(29)-lupene; Clerodol; Fagarasterol; Lupenol; Monogynol B; NSC 90487
Product Type Chemical
Properties
Formula

C30H50O

MW 426.72
CAS 545-47-1
RTECS OK5763000
Source/Host Chemicals Plant
Purity Chemicals ≥97% (HPLC)
Appearance White Powder.
Solubility Soluble in DMSO (1mg/ml), DMF (1mg/ml) or ethanol (1mg/ml). Insoluble in water.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key MQYXUWHLBZFQQO-QGTGJCAVSA-N
Smiles C[C@@]12CC[C@@]3(C)[C@]4(C)CC[C@@]5([H])C(C)(C)[C@@H](O)CC[C@]5(C)[C@@]4([H])CC[C@]3([H])[C@@]1([H])[C@H](C(C)=C)CC2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Lupeol, is a dietary triterpene found in certain fruits, vegetables, and medicinal plants. Lupeol has been shown tohave a broad range of activities, including antioxidant, anti-inflammatory, anticancer, antihyperglycemic, antidyslipidemic, antimutagenic, anti-diabetic, anti-asthma, antiprotozoal, antimicrobial, cardioprotective, hepatoprotective, nephroprotective and neuroprotective properties. It is a multi-target agent targeting proteins such as α-glucosidase, α-amylase, protein tyrosine phosphatase 1B (PTP 1B) and TCA cycle enzymes and targeting pathways such as IL-1 receptor-associated kinase-mediated toll-like receptor 4 (IRAK-TLR4), Bcl-2 family, nuclear factor kappa B (NF-κ), phosphatidylinositol-3-kinase (PI3-K)/Akt and Wnt/β-catenin signaling pathways.

Product References

(1) S. Sunitha, et al.; Fitoterapia 72, 516 (2001) | (2) M.A. Fernandez, et al.; J. Pharm. Pharmacol. 53, 1533 (2001) | (3) Y.J. You, et al.; Phytother. Res. 17, 341 (2003) | (4) M. Saleem, e al.; Oncogene 23, 5203 (2004) | (5) J. Fotie, et al.; J. Nat. Prod. 69, 62 (2006) | (6) M. Saleem, et al.; Clin. Cancer Res. 14, 2119 (2008) | (7) M. Saleem, et al.; Carcinogenesis 30, 808 (2009) | (8) K. Papi Reddy, et al.; Bioorg. Med. Chem. Lett. 19, 4463 (2009) | (9) R.S. Tarapore, et al.; Carcinogenesis 31, 1844 (2010) | (10) H.R. Siddique, et al.; Clin. Cancer Res. 17, 5379 (2011) | (11) H.R. Siddique & M. Saleem; Life Sci. 88, 285 (2011) (Review) | (12) F.S. Tsai, et al.; Adv. Exp. Med. Biol. 929, 145 (2016) (Review) | (13) V.R. Machado, et al.; Nat. Prod. Res. 32, 275 (2018) | (14) A. Malik, et al.; Drug Des. Devel. Ther. 13, 1501 (2019)

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