Palmatine

Palmatine Struktur
3486-67-7
CAS-Nr.
3486-67-7
Englisch Name:
Palmatine
Synonyma:
palmatin;berbericinine;o,o-dimethyldemethyleneberberine;7,8,13,13a-tetrahydro-2,3,9,10-tetramethoxyberbinium;7,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-berbiniu;g)quinolizinium,5,6-dihydro-2,3,9,10-tetramethoxy-dibenzo(;2,3,9,10-TETRAMETHOXY-5,6-DIHYDRO-ISOQUINO[3,2-A]ISOQUINOLINYLIUM;matine;Palatine;Burasaine
CBNumber:
CB6781763
Summenformel:
C21H22NO4+
Molgewicht:
352.4
MOL-Datei:
3486-67-7.mol

Palmatine Eigenschaften

Schmelzpunkt:
205°C
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Löslichkeit
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Aggregatzustand
Powder
Farbe
Yellow
LogP
-1.120 (est)
CAS Datenbank
3486-67-7(CAS DataBase Reference)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Toxizität mouse,LD50,subcutaneous,135mg/kg (135mg/kg),Russian Pharmacology and Toxicology Vol. 31, Pg. 129, 1968.
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.

Palmatine Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This quaternary alkaloid occurs frequently in the Rhoeadales, being found in Cop tis japonica Mak. (Ranunculaceae); Berberis heteropoda Schrenk; B. vulgaris L. (Berberidaceae); Coscinium blumeatum Miers; Fibrauria chloroleuca Miers;Jatrorrhiza palmata (Lam.) Miers. (Menispermaceae); and Phellodendron amurense Rupr. (Rutcaeae). The base is usually obtained as the iodide dihydrate forming orange-yellow needles from H20, m.p. 241°C (dec.). Other salts that have been prepared include the chloride, green-yellow needles from H20, m.p. 205°C (dec.); nitrate, yellow needles, from H20, m.p. 239°C (dec.); perchlorate, m.p. 262°C (dec.); sulphate, m.p. 250°C; platinichloride, m.p. 236°C and the thiocyanate, m.p. 210°C (dec.). The alkaloid resembles berberine in yielding addition compounds with CHCl3 and Me2CO. On catalytic hydrogenation it gives tetrahydropalmatine, while on oxidation with alkaline KMn04 it furnishes corydaldine and hemipinic acid.

Physikalische Eigenschaften

Appearance: yellow needle crystal, odorless, taste very bitter. Solubility: freely solu ble in hot water, sparingly soluble in water, slightly soluble in ethanol and chloroform, and almost insoluble in ether. Melting point: 205 °C. Relative density: 1.2 g/cm3 .

History

In the middle of the last century, Garrison health team of China and Honghe state hospital interviewed to explore the medicinal use of Huangteng in the screen edge of ethnic minority areas firstly and found its detoxification and anti-inflammatory effect of antibacterial. Then, it was promoted to be used in Yunnan province after the initial clinical validation.
Palmatine on the market is mostly natural, which is mainly obtained from the extraction of dry rattan of Huangteng, one plant of Menispermaceae. The palmatine is abundant in the dry rattan of Huangteng with more than 2% palmatine chloride . It is an important part of technological research to obtain natural palmatine with high quality and high purity
Honghe state in Yunnan province isolated and extracted palmatine from Huangteng firstly and then produced needle, tablets, ointment and topical solution, and other dosage forms for the treatment of various suppurative infections. It is now believed that the optimum conditions for the extraction of palmatine should be acid water decocting, firstly extracted from the rattan of Huangteng and then adjusted to pH 9-10, and NaCl salting out, which is obtained by precipitation purifica tion step by step, while ultrasonic can be used as an auxiliary means of extraction.
The growth period of Huangteng is very long so that the extraction of natural palmatine cannot meet the market demand. Therefore, in order to alleviate the con tradiction of resources, researchers began to explore the method of chemical synthe sis of palmatine and its active derivatives in place of natural palmatine. At present, the improved synthetic method using berberine as raw material is the one with high yield, the total yield of which is 54%, and the purity of palmatine is 99%

Indications

Palmatine is included in the Pharmacopoeia of the People’s Republic of China (2015). As an antibacterial drug, palmatine is used to treat upper respiratory tract infections, tonsillitis, enteritis, dysentery, urinary tract infections, surgical and gynecological bacterial infections such as inflammation, and so on. Locally, it can treat conjunctivitis when dropping eyes and Candida albicans infection when used in vaginal topically

Pharmakologie

Palmatine is a detoxification agent with a variety of pharmacological effects.
Broad-spectrum antimicrobial antiviral effect: It can inhibit the activity of West Nile virus NS2B-NS3 protein, the Asian influenza A virus, dengue virus, and yellow fever virus. Also, it has an inhibitory effect on a variety of Gram-positive and Gram-negative bacteria, especially on fungi. Palmatine inhibits the proliferation of the Cordyceps epidermis and other 12 kinds of fungi to different degrees and has a good effect on shallow or deep infection caused by Candida albicans.
Enhance the ability of leukocyte phagocytosis: 0.3 mL/100 g, once/day, a total of 10 days of intraperitoneal injection can enhance the macrophage phagocytosis func tion. Palmatine has a different degree of prophylactic or therapeutic effect on rat adjuvant arthritis when orally administered with suspension prepared by 0.5% car boxymethylcellulose for 9 days on dose of 0.5 mg/100 g. Palmatine can partially counter allergy caused by trichosanthin, and its anti-inflammatory effects may be related to the immune mechanism. Studies have shown that palmatine can improve cellular immunity, humoral immunity, and non-specific immune function
Insect resistance: Palmatine has a significant anti-Trichomonas vaginalis activity in vitro; the anti-vaginal trichomonas activity is equivalent to metronidazole, with seven different concentrations (20, 10, 5, 2.5, 1.25, 0.625, and 0.3125 μg/mL) and different times (2–48 h).
Cardiovascular system: Palmatine can protect myocardial infarction, having a slight excitement on the frog heart and antiarrhythmic effect. It can also lower blood pressure when injecting intravenously anesthetized rabbits.
In addition, the palmatine also showed an inhibition of central nervous function. However, the mechanism of pharmacological mechanism of brassinone is still not clear and need further studies

Clinical Use

Palmatine has an effect of detoxification; therefore, it is used mainly for gynecologi cal inflammation, such as acute and chronic pelvic inflammatory disease, acute and chronic annex inflammation, cervical erosion, endometritis, mycoplasma vaginitis, puerperal infection, bacillary dysentery, enteritis, urinary tract infection, surgical infection, conjunctivitis, respiratory tract infections, and so on.
At present, palmatine has achieved some curative effect in combination therapy, but the small amount of adverse reactions of palmatine preparations in clinical treat ment cannot be ignored, such as allergic reactions and symptoms of catarr

Einzelnachweise

Feist, Sandstede., Arch. Pharm., 256, 1 (1918)
Spath, Quietensky., Ber., 58,2267 (1925)
Haworth, Koepfli, Perkin., J. Chem. Soc., 548 (1927)
Feist, Awe, Etzrodt., Chem. Zentr., I, 2374 (1935)
Spath, Meinhard., Ber., 75,400 (1942)

Palmatine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Palmatine Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 312)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21695 55
Shanghai Zheyan Biotech Co., Ltd.
18017610038
zheyansh@163.com CHINA 3620 58
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Zhejiang ZETian Fine Chemicals Co. LTD
18957127338
stella@zetchem.com China 2141 58
Chengdu GLP biotechnology Co Ltd
028-87075086 13350802083
scglp@glp-china.com CHINA 1824 58
Chengdu Biopurify Phytochemicals Ltd.
+8618080483897
sales@biopurify.com China 3424 58
Nanjing Dolon Biotechnology Co.,Ltd.
18905173768
sales@dolonchem.com CHINA 2972 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Shaanxi Pioneer Biotech Co., Ltd .
+8613259417953
sales@pioneerbiotech.com China 3000 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58

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  • 3486-67-7
  • C21H22O4N
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  • API
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
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  • Natural Plant Extract
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