Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Berbamine derivative and application of salt thereof

A technology of berbamine and its derivatives, applied in the application field of compounds and their derivatives, to achieve strong anti-leukemia and solid tumor activity, and light toxic effects

Inactive Publication Date: 2008-10-01
HANGZHOU BENSHENG PHARMA
View PDF0 Cites 33 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

So far, there have been no reports or patents that other berbamine derivatives and their salts except 4ethoxybutyl berbamine can antagonize the transcription of BCR / ABL fusion gene and the activity of nuclear transcription factor NF-κB. 4 Berbamine derivatives other than ethoxybutyl berbamine and their salts are used in the preparation of hematological malignancies such as leukemia, multiple myeloma, lymphoma, and solid tumors such as liver cancer, lung cancer, breast cancer, and prostate cancer , Osteosarcoma and other drug application research and patent reports

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Berbamine derivative and application of salt thereof
  • Berbamine derivative and application of salt thereof
  • Berbamine derivative and application of salt thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Example 1: Comparison of newly synthesized berbamine derivative 4-chlorobenzoyl berbamine with known berbamine derivative 4ethoxybutyl berbamine and berbamine anti-human leukemia activity

[0046] (1) Experimental materials

[0047] Cell line: human K562 leukemia cell line was purchased from Shanghai Cell Bank, Chinese Academy of Sciences.

[0048] Reagents: The standard berbamine was purchased from China National Institute of Pharmaceutical and Biological Products, and the berbamine derivatives 4-chlorobenzoyl berbamine and 4-ethoxybutyl berbamine were synthesized by ourselves.

[0049] Instruments: cell incubator, microplate reader

[0050] (2) Experimental method

[0051] Take 8,000 well-grown leukemia cells and inoculate them into wells of a 96-well cell culture plate. The culture medium is 1640 cell culture medium containing 10% fetal bovine serum. Drugs of different concentrations were added, mixed evenly, and placed in a carbon dioxide (5% CO2) cell incubator...

Embodiment 2

[0054] Embodiment 2: Comparison of anti-human leukemia activity of newly synthesized berbamine derivative 4-chlorobenzoyl berbamine and its hydrochloride-hydrochloride 4-chlorobenzoyl berbamine

[0055] (1) Experimental materials

[0056] Cell line: human K562 leukemia cell line was purchased from Shanghai Cell Bank, Chinese Academy of Sciences.

[0057] Reagent: berbamine derivative 4-chlorobenzoyl berbamine and its hydrochloride - 4-chlorobenzoyl berbamine hydrochloride is synthesized by ourselves.

[0058] Instruments: cell incubator, microplate reader

[0059] (2) Experimental method

[0060] Take 8,000 well-grown leukemia cells and inoculate them into wells of a 96-well cell culture plate. The culture medium is 1640 cell culture medium containing 10% fetal bovine serum. Drugs of different concentrations were added, mixed evenly, and placed in a carbon dioxide (5% CO2) cell incubator at 37° C. for 48 hours. The concentration of viable cells was then determined by the ...

Embodiment 3

[0063] Embodiment 3: newly synthesized berbamine derivatives 3,4,5-trimethoxybenzoyl berbamine, 4-methoxybenzoyl berbamine and 2-methylbenzoyl berbamine anti Human leukemia activity assay

[0064] (1) Experimental materials

[0065] Cell line: human K562 leukemia cell line was purchased from Shanghai Cell Bank, Chinese Academy of Sciences.

[0066] Reagents: 3,4,5-trimethoxybenzoyl berbamine, 4-methoxybenzoyl berbamine and 2-methylbenzoyl berbamine were synthesized by ourselves.

[0067] Instruments: cell incubator, microplate reader

[0068] (2) Experimental method

[0069] Take 8,000 well-grown leukemia cells and inoculate them into wells of a 96-well cell culture plate. The culture medium is 1640 cell culture medium containing 10% fetal bovine serum. After cultivating at 37° C. in a carbon dioxide (5% CO 2 ) cell incubator for 24 hours, add different concentrations of medicines, mix well, and continue to put in a carbon dioxide (5% CO 2 ) cell incubator at 37° C. to cu...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides an application of a type of berbamine derivatives and salts thereof in the preparation of drugs for the treatment of tumors, which is mainly applied in the preparation of the drugs for the prevention and treatment of nuclear transcription factor NF-kBp65 activity-related diseases and BCR / ABL transcription activity-related diseases. The drugs are combined and prepared by the compounds of the invention and one or more pharmaceutically acceptable excipients. The preparation forms comprise solid preparations, semi-solid preparations or liquid preparations. The type of berbamine derivatives and the salts thereof provided by the invention have broader and stronger anti-leukemia and anti-solid-tumor activity, the tumors proved to be sensitive are leukemia, multiple myeloma, liver cancer, osteosarcoma and breast cancer; the toxicity and the side effects are lighter. An in vitro cell culture system and animal experiments confirm that the berbamine derivatives and the salts thereof have no significant toxicity or side effects to the growth of normal human hematopoietic cells and experimental animals under the anti-tumor dosage, which are superior to the commonly used chemotherapy drugs.

Description

technical field [0001] The present invention relates to the application of compounds and derivatives thereof, and mainly relates to the application of berbamine derivatives and salts thereof. Background technique [0002] The BCR / ABL fusion gene is an oncogene formed by the fusion of the ABL gene on chromosome 9 and the BCR gene on chromosome 22 of hematopoietic cells, which is found in more than 95% of chronic myeloid leukemia and 20-30% of acute lymphoblastic leukemia [Lancet 2007;370:342-50]. A large amount of research data has confirmed that: the tyrosine protein kinase expressed by the BCR / ABL fusion gene is one of the main factors leading to the malignant proliferation of leukemia cells. According to this pathogenesis, Druker et al. found in 1996 that: tyrosine protein kinase inhibitor imatinib (imatinib) can effectively treat BCR / ABL fusion gene-positive leukemia, including chronic myeloid leukemia and acute lymphoblastic leukemia [N Engl J Med. 2001, 344: 1038-1042...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): A61K31/4375A61P35/00
Inventor 徐荣臻于晓方俞永平谢进文古莹张旭照干小仙
Owner HANGZHOU BENSHENG PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products