1721-69-3|Betulin diacetate|Lup-20(29)-ene-3,28-diol, diacetate, (3beta)-|-范德生物科技公司

Betulin diacetate

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names：
Lup-20(29)-ene-3,28-diol, diacetate, (3beta)-
CAS号：
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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中文别名	Betulin diacetate
英文别名	Betulin diacetate
CAS号	1721-69-3
SMILES	CC1(C)[C@@H](OC(C)=O)CC[C@]2(C)[C@@]3([H])CC[C@]4([H])[C@@]5([H])[C@H](C(C)=C)CC[C@@](COC(C)=O)5CC[C@](C)4[C@@](C)3CC[C@@]12[H]
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
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Betulin diacetate(CAS:1721-69-3):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Betulin diacetate is a bioactive chemical.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[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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