betulonic aldehyde

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Products Intro: Product Name:betulonic aldehyde
CAS:4439-98-9
Purity:97%HPLC Package:1KG
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Products Intro: Product Name:lup-28-al-20(29)-en-3-one
CAS:4439-98-9
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Products Intro: Product Name:Betulonaldehyde
CAS:4439-98-9
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
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Products Intro: Product Name:Betulonaldehyde
CAS:4439-98-9
Purity:>98% Package:10mg;25mg;50mg
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Products Intro: Product Name:Betulonaldehyde
CAS:4439-98-9
Purity:95% Package:10mg;50mg;100mg
betulonic aldehyde Basic information
Product Name:betulonic aldehyde
Synonyms:betulonic aldehyde;Betulonic aldehyde, 97%, Semi-Synthetic;Betulonaldehyde;lup-28-al-20(29)-en-3-one;Lup-20(29)-en-28-al, 3-oxo-;(1R,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-9-oxoicosahydro-3aH-cyclopenta[a]chrysene-3a-carbaldehyde
CAS:4439-98-9
MF:C30H46O2
MW:438.68
EINECS:
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Mol File:4439-98-9.mol
betulonic aldehyde Structure
betulonic aldehyde Chemical Properties
Melting point 165-166 °C
Boiling point 511.7±33.0 °C(Predicted)
density 1.037±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility DMF: 10 mg/ml
form A crystalline solid
Safety Information
MSDS Information
betulonic aldehyde Usage And Synthesis
Biological ActivityBetulonaldehyde is a pentacyclic triterpenoid and derivative of the cholesterol biosynthesis inhibitor betulin that has been found in Betula.1 It is active against P. falciparum (IC50 = 3.36 μg/ml) and cytotoxic to NCI H187 lung cancer cells and non-cancerous Vero cells (IC50s = 19.23 and 17.09 μg/ml, respectively).2 Topical application of betulonaldehyde (1 mg/ear) reduces ear edema induced by phorbol 12-myristate 13-acetate in mice.3 It has also been used a precursor in the semisynthesis of C-2 and C-28 betulonic aldehyde derivatives.1
References1.Ayers, S., Benkovics, T., Marshall, J., et al.Autoxidation products of betulonaldehydeJ. Nat. Prod.79(10)2758-2761(2016) 2.Wisetsai, A., Schevenels, F.T., and Lekphrom, R.Chemical constituents and their biological activities from the roots of diospyros filipendulaNat. Prod. Res.1-5(2019) 3.Yasukawa, K., Yu, S., Yamanouchi, S., et al.Some lupane-type triterpenes inhibit tumor promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skinPhytomedicine1(4)309-313(1995)
betulonic aldehyde Preparation Products And Raw materials
Raw materialsBetulonicacid-->Betulin-->Betulinic acid
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