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Sinomenine

Sinomenine Structure
CAS No.
115-53-7
Chemical Name:
Sinomenine
Synonyms
CUCOLINE;(4bR,8aS,9S)-4-hydroxy-3,7-dimethoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one;SNM;KUKOLINE;COCULINE;SINOMENIN;SabiaineA;SINOMENINE;SABIANINE A;y-17-methyl-
CBNumber:
CB4399085
Molecular Formula:
C19H23NO4
Molecular Weight:
329.39
MOL File:
115-53-7.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:09

Sinomenine Properties

Melting point 180 °C (dec.)(lit.)
alpha D26 -71° (c = 2.1 in alc)
Boiling point 466.98°C (rough estimate)
Density 1.2012 (rough estimate)
refractive index 1.5000 (estimate)
storage temp. Store at +4°C
solubility Soluble to 65 mg/mL (197.33 mM) in DMSO
pka 9.72±0.40(Predicted)
form Solid
color White to off-white
Merck 13,8620
InChIKey YMEVIMJAUHZFMW-VUIDNZEBSA-N
LogP 1.245 (est)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS08
Signal word  Danger
Hazard statements  H302-H315-H319-H335-H351-H361d-H372
Precautionary statements  P201-P301+P312+P330-P302+P352-P305+P351+P338-P308+P313
Hazard Codes  T,Xn
Risk Statements  45-46-23/24/25-36/37/38-20/21/22-48/20/22-40-22-63
Safety Statements  53-22-26-36/37/39-45-36/37-24/25
RIDADR  1544
WGK Germany  3
RTECS  QD2170000
9
HazardClass  6.1(b)
PackingGroup  III
HS Code  29399990
Toxicity LD50 orally in mice: 580 mg/kg (Fu)

Sinomenine price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 365602 Sinomenine 0.3?mol chloroform of crystallization 115-53-7 100MG ₹4449.08 2022-06-14 Buy
Product number Packaging Price Buy
365602 100MG ₹4449.08 Buy

Sinomenine Chemical Properties,Uses,Production

Description

Isolated by Ohta from Cocculus diversifolius DC., this alkaloid forms colourless crystals from MeOH. It is stated to possess a powerful reflex action and to be aspasm stimulant, finally causing paralysis and death in toxic doses. It is also said to suppress the hypotensive action of dihydroxyphenylethanolethylamine.

Physical properties

Appearance: acicular crystals (crystallized from benzene). Solubility: soluble in ethanol, acetone, chloroform, and dilute alkali; slightly soluble in water, ether, and benzene. Melting point: 219–221?°C. Specific optical rotation:?– 71° (c?=?2.1, ethanol). Its hydrochloride, crystallization (water or ethanol), decomposed at 278?°C.?Its hydroiodide, needle crystal (crystallized from water), decomposed at 272?°C.?Its picrate, which is yellow needle crystal, decomposed at 176?°C.?Sinomenine is sensitive to light and heat to decompose.

History

The chemical structure of sinomenine is composed of four rings, A, B, C, and D, similar to the structure of morphine. Ring A is a benzene ring, and ring B is a half-chair-shaped, six-member ring. The C ring is a twisted-chair-type, sixmember ring that has an a, β-unsaturated ketone structure attached to the B ring. The D ring is a nitrogen-containing, sixmember ring under the B ring. Its structure is shown below; the current structural modification of sinomenine is mainly focused on the A/C active group.
Based on the transformation of the A ring, it was found that the 1-substituted formyl derivative of sinomenine showed the strongest inhibitory effect on the inflammatory response of the mouse ear. The 4-substituted p-chlorobenzoyl-sinomenine has the strongest anti-inflammatory and analgesic activity. The biotransformation and chemical synthesis were also used to prepare the di-sinomenine derivatives linked by carbon and carbon, which was stronger than that of sinomenine and had a strong inhibitory effect on cell inflammatory factors. Sinomenine derivatives of the C ring with a pyrazine ring have a strong inhibitory effect on T, B lymphocyte proliferation reaction, which can be used for the preparation of immunomodulatory drugs. The transformation of C ring carbonyl yielded a series of shift alkali derivatives, with strong anti-inflammatory and analgesic effects. These attempts are important for the development of new drugs.

Uses

weak abortifacient, immunosuppressant, analgesic, antiinflammatory; LD50 (po) 580 mg/kg; (ip) 285 mg/kg(mouse)

Indications

It is mainly used for the treatment of rheumatoid arthritis and other types of rheumatism and arrhythmia in clinical.

Biological Activity

Natural anti-inflammatory morphinan analog. Causes degranulation of mast cells in mammalian tissues to release histamine and suppresses production of proinflammatory cytokines. Also displays antinociceptive activity, possibly through activation of the μ -opioid receptor. Stimulates short-term renewal of human embryonic stem cells (ESCs) in vitro .

Clinical Use

The treatment of rheumatism and rheumatoid arthritis is one of the most important clinical applications of sinomenine. Sinomenine is particularly suitable for the treatment of arrhythmia caused by organic heart disease. Sinomenine is used for the treatment of glomerular disease, which can reduce urinary protein and relieve hematuria symptoms, and the side effects were significantly lower than that of tripterygium glycoside tablets, which are commonly used in clinical practice. In addition, sinomenine can significantly inhibit renal interstitial fibrosis and the production of tissue growth and growth factor TGF-β1. Sinomenine can significantly delay the development of chronic renal failure and effectively treat ankylosing spondylitis.

Purification Methods

Crystallise 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 -78.9o (c 1, EtOH). The picrate has m 159-162o(dec) (from H2O). [Beilstein 21 II 470, 21 III/IV 6670.]

References

Ohta., Ber. ges. Physiol., 33, 352 (1925)
Ohta, Kitasato., Arch. expo Med., 6, 259, 283 (1925)
Raymond-Hamet., Compt. rend. Soc. Biol., 125, 509 (1937)

Sinomenine Preparation Products And Raw materials

Global( 335)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29898 58 Inquiry
SHANDONG ZHI SHANG CHEMICAL CO.LTD +86 18953170293 China 2931 58 Inquiry
Xiamen AmoyChem Co., Ltd +86-592-6051114 +8618959220845 China 6387 58 Inquiry
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CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
Neostar United (Changzhou) Industrial Co., Ltd. +86-519-519-85557386 China 11667 58 Inquiry
Zhengzhou Alfa Chemical Co.,Ltd +8618530059196 China 13127 58 Inquiry
SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
SINOMENINE (9alpha,13alpha,14alpha)-7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-one (9Alpha,13alpha,14alpha)-4-hydroxy-3,7-dimethoxy-17-methyl-7,8-didehydromorphinan-6-one hydrochlo Sinomenine (9alpha,13alpha,14alpha)-7,8-Didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-one Sinomenine 0.3 mol chloroform of crystallization (9alpha,13alpha,14alpha)-4-hydroxy-3,7-dimethoxy-17-methyl-7,8-didehydromorphinan-6-one hydrochloride Sinomenine, >=98% Sinomenine/Sinomenine Hydrochloride COCULINE KUKOLINE Sinomenine std. Sinomenine SINOMENIN SINOMENINE(RG) Sinomenine hydrochorolide Morphinan-6-one,7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methyl-,(9α,13α,14α)- Sinomenine,Coculine,Cucoline,Tuduranine (9a,13a,14a)-7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-one (9α,13α,14α)-7,8-Didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-one SINGLIROXBRUGHROSEFRUITP.E 9α,13α,14α-7,8-Didehydro-4-hydroxy-3,7-dimethoxy-17-methylmorphinan-6-onehydrochloride SNM SinoMenine (Cucoline) (+)-SinoMenine N-oxide SinoMenine (6CI,7CI) 7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methyl-9-alpha,13-alpha,14-alpha-mo 9-alpha,13-alpha,14-alpha-morphinan-6-one,7,8-didehydro-4-hydroxy-3,7-dimethox rphinan-6-one y-17-methyl- SABIANINE A SINOMENIN Sinomenine 115-53-7 SabiaineA Sinomenine I Sinomenine, 98%, from Caulis Sinomenii Sinomenine CRS Sinomenine Standard Sinomenine USP/EP/BP Sinomenine hydrochlo CUCOLINE (4bR,8aS,9S)-4-hydroxy-3,7-dimethoxy-11-methyl-9,10-dihydro-5H-9,4b-(epiminoethano)phenanthren-6(8aH)-one Morphinan-6-one, 7,8-didehydro-4-hydroxy-3,7-dimethoxy-17-methyl-, (9α,13α,14α)- Abametapir Impurity 25 115-53-7 C19H23NO403CHCl3 C19H23NO4 Asymmetric Synthesis Chiral Building Blocks Complex Molecules chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract API Asymmetric Synthesis Chiral Building Blocks Complex Molecules Natural Plant Extract