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Evoxine - CAS 522-11-2

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Category
ADCs
Product Name
Evoxine
Catalog Number
522-11-2
CAS Number
522-11-2
Description
Evoxine (haploperine) is a furoquinoline alkaloid with hypnotic and sedative effects. It is found naturally in a variety of Australian and African plants including Evodia xanthoxyloides and Teclea gerrardii..
Molecular Weight
347.36
Molecular Formula
C18H21NO6
COA
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MSDS
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Structure
CAS 522-11-2 Evoxine
Specification
Purity
98 % (TLC).
Melting Point
154-155 °C.
Appearance
Solid powder
Application
ADCs Cytotoxin
Storage
Store at +4 °C, in dark place.
Solubility
methanol, ethanol; not in water.
Reference Reading
1.Terpenoids from Diplophyllum taxifolium with quinone reductase-inducing activity.
Wang X1, Zhang JZ1, Zhou JC1, Shen T1, Lou HX2. Fitoterapia. 2016 Mar;109:1-7. doi: 10.1016/j.fitote.2015.11.023. Epub 2015 Nov 30.
Two new ent-prenylaromadendrane-type diterpenoids, diplotaxifols A (1) and B (2), a new ent-eudesmol, ent-eudesma-4(15),11(13)-dien-6α,12-diol (3), eight new eudesmanolides enantiomers (4-11) of the corresponding compounds from higher plants along with four known ent-eudesmanolides (12-15) were isolated from the 95% EtOH extract of Chinese liverwort Diplophyllum taxifolium. Their structures were elucidated on the basis of MS, NMR and IR spectral data, and confirmed by single-crystal X-ray diffraction analysis. The quinone reductase-inducing activity of the compounds was evaluated.
2.A new sesquiterpenoid from Polyalthia petelotii.
Yang C1, Peng W1, Yang B1, Zhang J1, Chen Y1. Nat Prod Res. 2015 Dec 15:1-6. [Epub ahead of print]
A new sesquiterpenoid (‒)-ethyl dihydrophaseate (1) was isolated from the stems and leaves of Polyalthia petelotii, together with two clerodane diterpenoids, 16α-hydroxycleroda-3,13(14)Z-dien-15,16-olide (2), 15-hydroxy-cis-ent-cleroda-3,13(E)-diene (3), a eudesmane sesquiterpenoid, eudesm-4(15)-ene-7α,11-diol (4), an aromatic aldehyde, vanillin (5), a bisisoquinolines alkaloid, spinosine (6) and an aporphine alkaloid, (‒)-oliveroline-β-N-oxide (7). Their structures were established by extensive spectroscopic analysis, including 2D-NMR techniques. Compounds 3, 4 and 6 were isolated from the genus Polyalthia for the first time and the others obtained originally from P. petelotii. The isolates were assessed for their cytotoxicity against five human tumour lines (HL-60, SMMC-7721, A-549, MCF-7 and SW-480), and the result showed that only 2 displayed weak inhibitory activity.
3.Litsea Species as Potential Antiviral Plant Sources.
Guan Y1,2, Wang D1,2, Tan GT3, Van Hung N4, Cuong NM5, Pezzuto JM3, Fong HH6, Soejarto DD6,7, Zhang H1,2. Am J Chin Med. 2016 Apr;44(2):275-90. doi: 10.1142/S0192415X16500166.
Litsea verticillata Hance (Lauraceae), a Chinese medicine used to treat swelling caused by injury or by snake bites, was the first plant identified by our National Institutes of Health (NIH)-funded International Cooperative Biodiversity Group (ICBG) project to exhibit anti-HIV activities. From this plant, we discovered a class of 8 novel litseane compounds, prototypic sesquiterpenes, all of which demonstrated anti-HIV activities. In subsequent studies, 26 additional compounds of different structural types were identified. During our continuing investigation of this plant species, we identified two new litseanes, litseaverticillols L and M, and a new sesquiterpene butenolide, litseasesquibutenolide. Litseaverticillols L and M were found to inhibit HIV-1 replication, with an IC[Formula: see text] value of 49.6[Formula: see text][Formula: see text]M. To further determine the antiviral properties of this plant, several relatively abundant isolates, including a litseane compound, two eudesmane sesquiterpenes and three lignans, were evaluated against an additional 21 viral targets.
4.Sesquiterpenoids from the roots of Vladimiria muliensis.
Chen JJ1, Bai W1, Gobu FR1, Wu CH1, Zeng J1, Sun M1, Gao K1. J Asian Nat Prod Res. 2015 Dec;17(12):1188-95. doi: 10.1080/10286020.2015.1119130. Epub 2015 Dec 16.
An unusual aromadendrane-type sesquiterpenoid with a rare hemiketal-containing 10/3 ring system, named vladimuliecin C (1), and one new eudesmane-type sesquiterpenoid, named vladimuliecin D (4), together with four known sesquiterpenoids, were isolated from the roots of Vladimiria muliensis. The structures of these compounds were elucidated by analysis of spectroscopic data. The absolute configuration of 1 was assigned by X-ray diffraction analysis. A possible biosynthetic process for the formation of 1 is proposed. Compound 1 showed moderate cytotoxicity against three human tumor cell lines.
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