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Merck
CN

SMB00084

Hypaphorine

≥95% (LC/MS-ELSD)

别名:

Hypaforin, Lenticin

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关于此项目

经验公式(希尔记法):
C14H18N2O2
分子量:
246.30
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352205
MDL number:
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assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

C[N+](C)(C)C(Cc1c[nH]c2ccccc12)C([O-])=O

InChI

1S/C14H18N2O2/c1-16(2,3)13(14(17)18)8-10-9-15-12-7-5-4-6-11(10)12/h4-7,9,13,15H,8H2,1-3H3

InChI key

AOHCBEAZXHZMOR-UHFFFAOYSA-N

General description

Hypaphorine is a natural product derived from a plant source. It is an indolic compound, initially isolated from Pisolithus tinctorius, an ectomycorrhizal fungus. This compound is made up of tryptophan and three methyl groups. It is recently identified as one of the components of human milk. Hypaphorinecan also be sourced from marine organisms.

Biochem/physiol Actions

Hypaphorine is known to reduce glucose levels in rat models. Along with this, it possesses anti-inflammatory and certain neurological functions.
Hypaphorine has demostrated sleep promoting properties by increasing non-rapid eye movement sleep duration for the first hour after it is administered in mice.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Hypaphorine attenuates lipopolysaccharide-induced endothelial inflammation via regulation of TLR4 and PPAR-g dependent on PI3K/Akt/mTOR signal pathway
Sun H, et al.
International Journal of Molecular Sciences, 18(4), 844-844 (2017)
Hypaphorine, an indole alkaloid from Erythrina velutina, induced sleep on normal mice
Ozawa M, et al.
Bioorganic & Medicinal Chemistry Letters, 18(14) (2008)
Competitive antagonism between IAA and indole alkaloid hypaphorine must contribute to regulate ontogenesis
Jambois A, et al.
Physiologia Plantarum, 123(2) (2005)



全球贸易项目编号

货号GTIN
SMB00084-1MG04061826168288