SINOMENINE HYDROCHLORIDE

SINOMENINE HYDROCHLORIDE Basic information
Product Name:SINOMENINE HYDROCHLORIDE
Synonyms:hydroxy-dimethoxy-methyl-BLAH-azatetracyclo[BLAH]hexadeca-BLAH,BLAH,BLAH,BLAH-tetraenone;Sinomenine Hydrocloride;Cucoline hydrochloride;(9a,13a,14a)-4-Hydroxy-3,7-dimethoxy-17-methyl-7,8-didehydromorphinan-6-one hydrochloride;SINOMENINE HYDROCHLORIDE;SINOMENINE HCL;(9α,13α,14α)- 7,8-Didehydro-4- hydroxy-3,7-diMet;7,8-Didehydro-4-hydroxy-3,7-diMethoxy-17-Methyl- 9α,13α,14α-Morphinan-6-one Hydrochloride
CAS:6080-33-7
MF:C19H24ClNO4
MW:365.85
EINECS:
Product Categories:Alkaloids;Inhibitors;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;APIs;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;chemical reagent
Mol File:6080-33-7.mol
SINOMENINE HYDROCHLORIDE Structure
SINOMENINE HYDROCHLORIDE Chemical Properties
Melting point 231.0 to 235.0 °C
storage temp. Inert atmosphere,2-8°C
solubility H2O: soluble20mg/mL, clear
form powder
color white to beige
optical activity[α]/D -70 to -90°, c = 1 in H2O
Water Solubility Soluble to 100 mM in water
Safety Information
Safety Statements 24/25
WGK Germany 3
RTECS QD2163000
HS Code 29334900
MSDS Information
SINOMENINE HYDROCHLORIDE Usage And Synthesis
DescriptionSinomenine is a natural plant alkaloid commonly used to alleviate inflammation associated with rheumatoid arthritis. It activates histamine release, reduces joint stiffness and pain, and alters cytokine generation without producing gastrointestinal adverse events. Sinomenine also impairs signaling through NF-κB, resulting in immunosuppression as well as reduced inflammation and pain. It enhances the bioavailability of some compounds, at least in part through an inhibition of drug export by transporters like P-glycoprotein.
Chemical PropertiesWhite Solid
UsesSinomenine is an optical isomer of Methoxythebainone. Sinomenine was extracted from root of Sinomenium acutum. Sinomenine has anti-inflammatory and analgesic effect.
Purification MethodsCrystallise the salt from water (1g/1.5mL) or EtOH. The free base [115-53-7] M 329.4, has m 161o (from EtOH) (and again at 182o) after crystallisation from *C6H6, and [] D 20 -78.9o (c 1, EtOH). The picrate has m 159-162o(dec) (from H2O). [Beilstein 21 II 470, 21 III/IV 6670.]
SINOMENINE HYDROCHLORIDE Preparation Products And Raw materials
CUCURBITACIN IIA Coptisine chloride JATRORRHIZINE HCL(RG) Oxyresveratrol Ligustrazine Hydrochloride SANGUINARINE Berberine hydrochloride 4-Guanidinobutyl 4-hydroxy-3,5-diMethoxybenzoate hydrochloride STACHYDRINE HYDROCHLORIDE Betaine hydrochloride SECO-ISOLARICIRESINOL DIGLUCOSIDE Lycorine hydrochloride Corydaline Arbutin TETRAHYDROPALMATINE HYDROCHLORIDE Ursolic acid Palmatine chloride Cucurbitacin IIb

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