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经验公式(希尔记法):
C32H44O16
化学文摘社编号:
分子量:
684.68
UNSPSC Code:
12352205
NACRES:
NA.25
MDL number:
SMILES string
O1[C@@H]([C@H]([C@H](C1)Cc4cc(c(cc4)O[C@@H]5O[C@@H]([C@H]([C@@H]([C@H]5O)O)O)CO)OC)CO)c2cc(c(cc2)O[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO)OC
InChI
1S/C32H44O16/c1-42-20-8-14(3-5-18(20)45-31-28(40)26(38)24(36)22(11-34)47-31)7-16-13-44-30(17(16)10-33)15-4-6-19(21(9-15)43-2)46-32-29(41)27(39)25(37)23(12-35)48-32/h3-6,8-9,16-17,22-41H,7,10-13H2,1-2H3/t16-,17-,22+,23+,24+,25+,26-,27-,28+,29+,30+,31+,32+/
InChI key
PBLWZMSRSJTRHJ-NCIRKIHRSA-N
biological source
plant
assay
≥90% (LC/MS-ELSD)
form
solid
mol wt
684.68
solubility
water: slightly soluble
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Clemastanin B, a furanoid lignan, is commonly produced by Clematis stans, Radix Isatidis, Plocama calabrica, Sedum sarmentosum, and Brassica rapa plants. Existing research indicates that this secondary metabolite, derived from plant source, exhibits various biological properties, including antiviral, antiinflammatory, and antioxidant activities.
Application
It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.
Biochem/physiol Actions
Clemastanin B has antioxidant and anti-inflammatory activities, it exerts its anti-influenza activity by inhibiting the virus multiplication, prophylaxsis and blocking the virus attachment.
Features and Benefits
- High quality compound suitable for multiple research applications
- Compatible with HPLC and mass spectrometry techniques
Other Notes
For additional information on our range of Biochemicals, please complete this form.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Ping Xiao et al.
Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan, 36(3), 369-376 (2016-07-30)
To study the antiviral activities of clemastanin B (CB), epigoitrin, phenylpropanoids portion (PEP) and the mixture of phenylpropanoids, alkaloids and organic acid fractions (PEP+ALK+OA) from Banlangen (Radix Isatidis). The experiment consisted of four parts: therapeutic action, prophylaxsis action, inhibition of
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