BERBAMINE Chemical Properties

Melting point:

198.5°C

Boiling point:

655.15°C (rough estimate)

alpha 

D20 +114.6° (c = 1.0 in chloroform)

Density 

1.1648 (rough estimate)

refractive index 

1.5300 (estimate)

storage temp. 

Store at -20°C, protect from light

solubility 

DMSO : 125 mg/mL (205.35 mM; Need ultrasonic)

form 

Powder

pka

pKa (20°): 7.33 in aq methanol

color 

White to yellow

CAS DataBase Reference

478-61-5(CAS DataBase Reference)

BERBAMINE Usage And Synthesis

Description

Berbamine is an alkaloid, separated from Berberidaceae, Menispermaceae, or Ranunculaceae plants. Most of Berberidaceae plants have medicinal value, including their root, root bark, and stem. The plants of Berberis L. and Mahonia Nutt. contain many alkaloids, the most important of which are berberine and a small amount of palmatine, jatrorrhizine, berbamine, oxyacanthine, and so on. These compounds have many biological activities and have been used to replace goldthread and golden cypress. Also they are well succedaneums of berberine in Chinese and Western medicine. Traditional Chinese medicine Oregon grape root has different therapeutic effects for dysentery, enteritis, children pneumonia, and chronic bronchitis. The major treatment diseases of Chinese mahonia are bacillary dysentery, acute gastritis, infectious hepatitis, pneumonia, tuberculosis, bronchitis, sore throat, and so on.

Physical properties

Appearance: odorless and bitter white crystalline, powder, belongs to bisbenzylisoquinoline alkaloid. Melting point: 197–210?°C in petroleum ether. Solubility: easily soluble in dilute hydrochloric acid, sulfuric acid, ethanol, chloroform, and acetone; soluble in ether; slightly soluble in boiling water and petroleum ether; but insoluble in cold water, ammonia, sodium carbonate, and calcium hydroxide solution.

History

Berbamine is an alkaloid mainly from Berberis julianae, Berberis wilsonae, Berberis poiretii, and huanglumu, which belong to Berberidaceae berberis and Mahonia. Nowadays, it mainly comes from chemical synthesis. Berbamine hydrochloride is contained in the 13th volume of the book, Hua xue yao ping di biao sheng guo biao. As early as 1940, the United States scholars had obtained berbamine from Mahonia . Chinese scholars began the research of berbamine extraction and pharmacological activities since the 1980s in the last century .
Although the berbamine study in our country later than the west, the traditional Chinese medicine Berberi’s medicinal records can be traced back to the Tang Dynasty. The book Tang Ben Cao recorded that Oregon grape root could be a therapy for aphtha, kill insects, and remove hot gas in the body. In the Ming Dynasty the book Ben Cao Gang Mu recorded that Oregon grape root could treat metrorrhagia. Now, berbamine is widely used for leukopenia.

Uses

antihypertensive, skeletal muscle relaxant

Definition

ChEBI: Berbamine is a member of isoquinolines and a bisbenzylisoquinoline alkaloid.

Indications

Berbamine is contained in the 13th volume of the book, National Standards for Chemical Drugs.
The current clinical dosage is berbamine hydrochloride tablets. It is used in the prevention and treatment of patients with cancer, which is due to radiotherapy- and chemotherapy-induced neutropenia or due to benzene poisoning, radioactive substances, and drug-induced neutropenia.

Pharmacology

Berbamine can promote hematopoietic function, stimulate myeloid proliferation.
Also berbamine can enhance the content of hematopoietic stem cell and granulocyte-colony stimulating factor (G-CSF), then increase the proliferation and differentiation of bone marrow hematopoietic stem cells and granule progenitor cell, which increase the number of peripheral blood leukocytes. Preclinical and clinical studies showed that berbamine was good for the treatment of leukopenia induced by chemotherapy. Berbamine can inhibit the proliferation of many kinds of tumor cells, such as the human high metastatic breast cancer cells MDA-MB-231, non-small cell lung cancer cells A549, liver cancer cells SMMC772l and HepG2, multiple myeloma cells KM3 and RPMl8226, chronic myeloid leukemia (CML) cells KU812, and imatinib-resistant K562 cells .

Clinical Use

Berbamine is used for the prevention and treatment of cancer patients with neutropenia due to radiotherapy, chemotherapy , benzene poisoning, radioactive substances, and drug.

Enzyme inhibitor

This antihypertensive alkaloid (FW = 608.72 g/mol; CAS 478-61-5; Symbol: BBM) from Berberis lyceum and Mahonia swaseyi is a dihydropyridineclass calcium ion blocker. Berbamine also inhibits KM3 cell growth by inducing G1 arrest as well as apoptosis, by blocking NF-kB signaling through up-regulation of A20, down-regulation of IKKa, p-IkBa, and then inhibition of p65 nuclear translocation, all with a resultant decrease in the expression of the downstream targets of NF- kB. BBM potently suppresses liver cancer cell proliferation and induces cancer cell death by targeting Ca2+/calmodulin-dependent protein kinase II (CAMKII). BBM likewise inhibits in vivo tumorigenicity of liver cancer cells in NOD/SCID mice. These effects are recapitulated by short hairpin RNA-mediated CAMKII knockdown, whereas CAMKII overexpression promotes cancer cell proliferation and increases the resistance of liver cancer cells to BBM. CAMKII was hyperphosphorylated in liver tumors compared with the paired peri-tumor tissues, supporting a role of CAMKII in promoting human liver cancer progression and the clinical potential of BBM in liver cancer therapies.

Purification Methods

Crystallise berbamine from pet ether or *C6H6 (with 1*C6H6 m 129-134o). [Bick Aust J Chem 9 111, 118 1956, Beilstein 27 II 891, 27 III/IV 8732.]

BERBAMINE(478-61-5)Related Product Information

• Berberine hydrochloride
• Berberine
• Berbamine sulphate acid
• Berbamine hydrochloride
• BERBAMINE HCL,BERBAMINE DIHYDROCHLORIDE,BERBAMINE 2HCL
• BERBAMINE
• D-Tetrandrine
• BERBAMINE METHYL ETHER
• L-TETRANDRINE
• E6 BERBAMINE,BERBAMINE E6
• BERBAMINE DIHYDROCHLORIDE(RG)
• BERBERIDIS ROOT P.E./ BERBAMINE HCL
• O-(4-ethoxybutyl)berbamine
• 7-O-ethyl fangchinoline
• AKOS NCG1-0047
• BERBAMINE BENZOLATE
• ZERENEX ZXN000891
• TIMTEC-BB SBB005977