41689-78-5|Lanceolatin A|(E)-8-(3-hydroxy-3-methylbut-1-en-1-yl)-7-methoxy-2-phenyl-4H-chromen-4-one|-范德生物科技公司

Lanceolatin A

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names：
(E)-8-(3-hydroxy-3-methylbut-1-en-1-yl)-7-methoxy-2-phenyl-4H-chromen-4-one
CAS号：
41689-78-5
MDL Number：
MF(分子式)： C21H20O4 MW(分子量)： 336.38
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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询价

中文别名	Lanceolatin A
英文别名	Lanceolatin A;
CAS号	41689-78-5
Inchi	InChI=1S/C21H20O4/c1-21(2,23)12-11-16-18(24-3)10-9-15-17(22)13-19(25-20(15)16)14-7-5-4-6-8-14/h4-13,23H,1-3H3/b12-11+
InchiKey	GWHQUBFEZSVTKH-VAWYXSNFSA-N
分子式 Formula	C21H20O4
分子量 Molecular Weight	336.38
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	Lanceolatin A(CAS:41689-78-5):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	Lanceolatin A exhibits adulticidal activity against Sitophilus oryzae, Rhyzopertha dominica and Tribolium castaneum; from Tephrosia apolline.
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]Shaner NC, Lambert GG, Chammas A, Ni Y, Cranfill PJ, Baird MA, Sell BR, Allen JR, Day RN, Israelsson M, Davidson MW, Wang J. A bright monomeric green fluorescent protein derived from Branchiostoma lanceolatum. Nat Methods. 2013 May;10(5):407-9. doi: 10.1038/nmeth.2413. Epub 2013 Mar 24. PubMed PMID: 23524392; PubMed Central PMCID: PMC3811051.

[2]Pletnev VZ, Pletneva NV, Lukyanov KA, Souslova EA, Fradkov AF, Chudakov DM, Chepurnykh T, Yampolsky IV, Wlodawer A, Dauter Z, Pletnev S. Structure of the red fluorescent protein from a lancelet (Branchiostoma lanceolatum): a novel GYG chromophore covalently bound to a nearby tyrosine. Acta Crystallogr D Biol Crystallogr. 2013 Sep;69(Pt 9):1850-60. doi: 10.1107/S0907444913015424. Epub 2013 Aug 17. PubMed PMID: 23999308; PubMed Central PMCID: PMC3760133.

[3] Castro A, Becerra M, Manso MJ, Anadón R. Neuronal Organization of the Brain in the Adult Amphioxus (Branchiostoma lanceolatum): A Study With Acetylated Tubulin Immunohistochemistry. J Comp Neurol. 2015 Oct 15;523(15):2211-32. doi: 10.1002/cne.23785. Epub 2015 Jun 3. PubMed PMID: 25846052.

[4] Gui X, Wang G, Zhang N, Huang B. New phenylpropanoid and other compounds from Illicium lanceolatum with inhibitory activities against LPS-induced NO production in RAW 264.7 macrophages. Fitoterapia. 2014 Jun;9

[5]51-7. doi: 10.1016/j.fitote.2014.02.015. Epub 2014 Mar 5. PubMed PMID: 24613803.

5: Fobofou SA, Franke K, Porzel A, Brandt W, Wessjohann LA. Tricyclic Acylphloroglucinols from Hypericum lanceolatum and Regioselective Synthesis of Selancins A and B. J Nat Prod. 2016 Apr 22;79(4):743-53. doi: 10.1021/acs.jnatprod.5b00673. Epub 2016 Mar 7. PubMed PMID: 26950610.

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