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Betulin diacetate

NMR下載 COA and HPLC MSDS下載
names：
Lup-20(29)-ene-3,28-diol, diacetate, (3beta)-
CAS號：
1721-69-3
MDL Number：
MF(分子式)： C34H54O4 MW(分子量)： 526.802
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文別名	Betulin diacetate
英文別名	Betulin diacetate
CAS號	1721-69-3
Inchi	InChI=1S/C34H54O4/c1-21(2)24-12-17-34(20-37-22(3)35)19-18-32(8)25(29(24)34)10-11-27-31(7)15-14-28(38-23(4)36)30(5,6)26(31)13-16-33(27,32)9/h24-29H,1,10-20H2,2-9H3/t24-,25+,26-,27+,28-,29+,31-,32+,33+,34+/m0/s1
InchiKey	MIROITGPMGDCGI-MQXQNARFSA-N
分子式 Formula	C34H54O4
分子量 Molecular Weight	526.802
溶解度Solubility
性狀	Solid powder
儲藏條件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

產(chǎn)品說明	Betulin diacetate(CAS:1721-69-3):僅限應(yīng)用于工業(yè)或者科學(xué)研究過程中非醫(yī)療目的，不應(yīng)用于人類或動物的臨床診斷以及治過程療，該產(chǎn)品非藥用，非食用。
Introduction	Betulin diacetate is a bioactive chemical.
Application1
Application2
Application3

警示圖
危險性	Warning
危險性警示
安全聲明
安全防護
備注

[1]Mikhailenko MA, Shakhtshneider TP, Eltsov IV, Kozlov AS, Kuznetsova SA, Karacharov АА, Boldyrev VV. Supramolecular architecture of betulin diacetate complexes with arabinogalactan from Larix sibirica. Carbohydr Polym. 2016 Mar 15;138:1-7. doi: 10.1016/j.carbpol.2015.11.047. Epub 2015 Nov 2[1]PubMed PMID: 26794731.

[2]Shakhtshneider TP, Kuznetsova SA, Zamay AS, Zamay TN, Spivak EA, Mikhailenko MA, Malyar YN, Kuznetsov BN, Chesnokov NV, Boldyrev VV. New composites of betulin esters with arabinogalactan as highly potent anti-cancer agents. Nat Prod Res. 2016 Jun;30(12):1382-7. doi: 10.1080/14786419.2015.1060591. Epub 2015 Jul 13. PubMed PMID: 26165861.

[3] Alakurtti S, Heiska T, Kiriazis A, Sacerdoti-Sierra N, Jaffe CL, Yli-Kauhaluoma J. Synthesis and anti-leishmanial activity of heterocyclic betulin derivatives. Bioorg Med Chem. 2010 Feb 15;18(4):1573-82. doi: 10.1016/j.bmc.2010.01.003. Epub 2010 Jan 7. PubMed PMID: 20116263.

[4] Rybina AV, Shepelevich IS, Talipov RF, Galin FZ, Spirikhin LV. [Transformation of betulin diacetate by the Prins reaction]. Bioorg Khim. 2008 Jul-Aug;34(4):536-9. Russian. PubMed PMID: 18695727.

[5] Symon AV, Veselova NN, Kaplun AP, Vlasenkova NK, Fedorova GA, Liutik AI, Gerasimova GK, Shvrts VI. [Synthesis and antitumor activity of cyclopropane derivatives of betulinic and betulonic acids]. Bioorg Khim. 2005 May-Jun;31(3):320-5. Russian. PubMed PMID: 16004391.

6: Yuan XH, Li BG, Zhang XY, Qi HY, Zhou M, Zhang GL. Two diterpenes and three diterpene glucosides from Phlogacanthus curviflorus. J Nat Prod. 2005 Jan;68(1):86-9. PubMed PMID: 15679324.7: Tanaka R, Kinouchi Y, Wada S, Tokuda H. Potential anti-tumor promoting activity of lupane-type triterpenoids from the stem bark of Glochidion zeylanicum and Phyllanthus flexuosus. Planta Med. 2004 Dec;70(12):1234-6. PubMed PMID: 15643564.8: Madureira AM, Ferreira MJ, Gyémánt N, Ugocsai K, Ascenso JR, Abreu PM, Hohmann J, Molnár J. Rearranged jatrophane-type diterpenes from euphorbia species. Evaluation of their effects on the reversal of multidrug resistance. Planta Med. 2004 Jan;70(1):45-9. PubMed PMID: 14765292.9: Akihisa T, Ogihara J, Kato J, Yasukawa K, Ukiya M, Yamanouchi S, Oishi K. Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase. Lipids. 2001 May;36(5):507-12. PubMed PMID: 11432464.

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