Isonicotinic acid derivative and its preparation method and use

A derivative, isonicotinic acid technology, applied in the field of isonicotinic acid amide derivatives and their preparation, isonicotinic acid derivatives, isonicotinic acid ester derivatives, can solve the problem of affecting physiological functions, cancer cell proliferation and recurrence, Injury to normal cells and other problems, to achieve a broad-spectrum anti-cancer effect

Active Publication Date: 2021-07-23
XIAMEN INST OF RARE EARTH MATERIALS
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Treatment with surgery sometimes fails to eradicate cancer cells, allowing cancer cells to spread and recur
In addition, surgical treatment may lead to irreversible serious consequences, such as cervical cancer and bladder cancer surgery may lead to infertility and sexual dysfunction, etc.; radiation therapy for cancer will damage normal cells; therefore drug treatment is a better choice
However, due to the continuous emergence of multidrug resistance, the treatment of cancer is difficult
In addition: the current clinically used anticancer drugs still cannot achieve a satisfactory level of specificity. When a patient undergoes chemotherapy, normal cells in the body are often also poisoned, which seriously affects the normal physiological functions and is associated with has many side effects

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
  • Isonicotinic acid derivative and its preparation method and use
  • Isonicotinic acid derivative and its preparation method and use
  • Isonicotinic acid derivative and its preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0079] Synthesis of embodiment 1 intermediate 3-substituted phenyl-5-hydroxymethyl-isoxazole (II-1) or intermediate 3-substituted phenyl-5-aminomethyl-isoxazole (II-2) :

[0080] Using substituted benzaldehyde as raw material, it is prepared by synthesis of oxime, 1,3-dipolar cycloaddition reaction, methylsulfonyl esterification reaction, azidation and reduction reaction (R 2 and n as defined above), see the following process for details:

[0081]

[0082] The specific synthetic process of intermediate 3-substituted phenyl-5-hydroxymethyl-isoxazole (II-1) or intermediate 3-substituted phenyl-5-aminomethyl-isoxazole (II-2) is detailed See the three applications of the applicant with publication numbers CN103360382A, CN103664991A and CN103601762A, the full texts of which are incorporated herein by reference.

Embodiment 2

[0083] Synthesis of isonicotinic acid lipid derivatives shown in embodiment 2 formula (I)

[0084] Wherein the reaction of isonicotinic acid and 3-phenyl-5-hydroxymethyl-isoxazole is exemplified:

[0085] Synthesis of [(3-phenyl-isoxazol-5-yl)-methyl]-pyridine-3-carboxylate (YP-77)

[0086]

[0087] Add 0.123g (1mmol) of nicotinic acid and 0.206g (1mmol) of DCC into a 50mL round bottom flask, add 10mL of dry THF, stir and react in an ice bath for 30min, and dissolve 0.175g (1mmol) of 5-hydroxymethyl-3- Phenyl-isoxazole and 0.122 g (1 mmol) of DMAP in 10 mL THF were slowly added dropwise to the reaction system, stirred in an ice bath for 30 min, and then naturally rose to room temperature for reaction. After the TLC detection reaction was completed, the reaction solution was concentrated in vacuo, and the residue was directly separated by column (V (石油醚) :V (乙酸乙酯) =5:1~2:1) to obtain the target compound [(3-phenyl-isoxazol-5-yl)-methyl]-pyridine-3-carboxylate (YP-77).

...

Embodiment 3

[0103] Embodiment 3 biological activity test

[0104] MTT method was used to test the activity of the specific compound against colorectal cancer cell line HCT-116, human lung cancer cell line A549 and breast cancer cell line MCF-7. The specific test process is as follows:

[0105] (1) Spread the lung cancer cell line A549 in a 96-well plate, add 100 μL of culture medium, and wait for the cells to grow to 90%, add 1 μL of drugs into the wells, and detect 8 different concentrations of each drug (respectively, the initial concentration of the drug Concentration, 50μM, 5μM, 500nM, 50nM, 5nM, 500pM, 50pM), for each drug concentration, do 3 replicate wells in parallel, after culturing for 18h, add 20μL of the prepared 5mg / mL MTT solution to each well for 4 hours Afterwards, the medium was aspirated, and 150 μL of DMSO was added to each well, and the optical density (OD) value of the compound to be tested was measured at a wavelength of 595 nm. The negative control is DMSO. The i...

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 belongs to the field of medicinal chemistry, and relates to a class of isonicotinic acid derivatives with novel structures, a preparation method and application thereof. The present invention mainly relates to isonicotinic acid derivatives represented by formula (I), stereoisomers, racemates, tautomers, or pharmaceutically acceptable salts thereof, and preparation methods thereof and in the preparation of anticancer Uses in medicine. In formula (I): Z is selected from O, S, NR 3 , where R 3 for hydrogen or C 1 ~C 6 the alkyl group; R 1 from C 1 ~C 6 Alkyl, C 1 ~C 6 Alkoxy, halo C 1 ~C 6 Alkyl, aryl, aryloxy, heteroaryl, heteroaryloxy, heterocyclyl, heterocyclyloxy, halogen; R 2 selected from halogen, cyano, nitro, C 1 ~C 6 Alkyl, C 1 ~C 6 Alkoxy or halo C 1 ~C 6 Alkyl; m is an integer of 0-4; n is an integer of 0-5; with the proviso that Z is selected from NR 3 , when m is 0 and n is 1, R 2 Not halogen.

Description

technical field [0001] The invention belongs to the field of medicinal chemistry and relates to a class of isonicotinic acid derivatives with novel structures, in particular to isonicotinic acid ester derivatives and isonicotinic acid amide derivatives containing isoxazole heterocycles and their preparation methods and applications. Background technique [0002] Most cancers are found in the middle to advanced stages, and the overall response to treatment is poor. Cancer has posed a huge threat to human existence. [0003] Treatment methods for cancer include surgery, radiation therapy, and chemotherapy. Treatment with surgery sometimes fails to eradicate cancer cells, allowing the cancer to spread and recur. In addition, surgical treatment may lead to irreversible serious consequences, such as cervical cancer and bladder cancer surgery may lead to infertility and sexual dysfunction, etc.; radiation therapy for cancer will damage normal cells; therefore drug treatment is a...

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 Patents(China)
IPC IPC(8): C07D413/12A61K31/4439A61P35/00
Inventor 雍建平卢灿忠
Owner XIAMEN INST OF RARE EARTH MATERIALS
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap