CN107252425A - The medicinal usage of Dehydrocorydaline - Google Patents
The medicinal usage of Dehydrocorydaline Download PDFInfo
- Publication number
- CN107252425A CN107252425A CN201710563291.9A CN201710563291A CN107252425A CN 107252425 A CN107252425 A CN 107252425A CN 201710563291 A CN201710563291 A CN 201710563291A CN 107252425 A CN107252425 A CN 107252425A
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- CN
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- Prior art keywords
- dpp
- dehydrocorydaline
- compound
- medicinal usage
- technical
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
The title of the present invention is the medicinal usage of Dehydrocorydaline.Affiliated technical field is medical science.The technical problems to be solved by the invention are to be related to Dehydrocorydaline or its pharmaceutically acceptable solvate and its as purposes of the therapeutic agent especially as inhibitors of dipeptidyl IV.The main points of the technical scheme of the technical problems to be solved by the invention are the test to DPP IV enzyme inhibition activities to the compound.
Description
Technical field
The present invention relates to pharmaceutical technology field, specifically, it is used as dipeptides the present invention relates to compound Dehydrocorydaline
The medicinal usage of base peptase IV (DPP-IV) inhibitor.
Background technology
DPP IV (IUBMB enzyme nomenclature EC.3.4.14.5) is a kind of II types memebrane protein, in the literature with a variety of
Title is referred to, including DPP4, DP4, DAP-IV, FAP β, ADCP 2, ABP
(ADAbp), bis- peptidyls of Dipeptidylaminopeptidase IV, Xaa-Pro--aminopeptidase, Gly-Pro naphthyls amidase, rear proline
(postproline) Dipeptidylaminopeptidase IV, lymphocyte antigen CD26, glycoprotein GP110, DPP IV, sweet ammonia
Acyl Prolyl iminopeptidase, glycyl Prolyl iminopeptidase, X- prolyl pipeptidyl bases aminopeptidase, pepX, HLA
CD26, glycylprolyl Dipeptidylaminopeptidase, two peptidyl-peptide hydrolases, glycylprolyl aminopeptidase, two peptidyls-
Aminopeptidase IV, DPP IV/CD26, aminoacyl-prolyl pipeptidyl base aminopeptidase, T cell triggering molecule Tp103, X-
PDAP.DPP IV is referred to herein as " DPP-IV ".
DPP-IV is a kind of non-classical serine aminopeptidase, and it is removed from the amino terminal (N- ends) of peptide and protein
Remove Xaa-Pro dipeptides.Some naturally occurring peptides are also it has been reported that the DPP-IV dependences of X-Gly or X-Ser type dipeptides are slow
Release.
The present invention relates to the change that can suppress dipeptidyl peptidase-IV (Dipeptidyl peptidase IV, DPP-IV) activity
Compound and/or pharmaceutically acceptable solvate, this kind of compound can be used for treatment diabetes, such as diabetes B, high blood
Sugar, metabolic syndrome, hyperinsulinemia, obesity, angiocardiopathy and abnormal such as atherosclerosis, cranial vascular disease, in
Pivot nervous system disease is abnormal including schizophrenia, anxiety disorder, Bipolar depression, depression, insomnia, cognitive disorder,
Gastrointestinal disease and exception, cancer, inflammation and inflammatory disease, respiratory disease and exception, skeletal muscle are abnormal, osteoporosis, more
Term symptom or exception, periodontal disease such as gingivitis, and various immunoregulatory disorders.
DPP-IV belongs to serine peptide enzyme family, belong to together the family also have DPP2, DPP8, DPP9, FAP and
POP etc..Animal model experiment result shows that such as anaemia, alopecia, decrease of platelet and splenomegaly can be caused by suppressing DPP8/9
Deng toxic reaction [Lankas GR, Leiting B, et al.Dipeptidyl peptidase IV inhibition for
the treatment of type2diabetes:potential importance of selectivity over
dipeptidyl peptidases8and9.Diabetes,2005,54:2988-2994].Therefore, for the single targets of DPP-IV
The design and significant [Bhumika DP, the ManJunath DG.Recent of exploitation for the selective depressant selected
approaches to medicinal chemistry and therapeutic potential of dipeptidyl
peptidase-4(DPP-4)inhibitors.European Journal of Medicinal Chemistry,2014,74:
574-605], this is also the difficult point and key point of new selective DPP-IV inhibitor research and development.
Therefore, this area still needs the strong selective DPP-IV inhibitors of structure novelty, activity to meet clinical treatment
Demand.
The content of the invention
DPP IV (Dipeptidyl peptidase IV, DPP-IV, CD26, EC 3.4.14.5) is a class energy
The serine protease of specific for hydrolysis polypeptide or protein N-terminal Xaa-Pro or Xaa-Ala dipeptides.DPP-IV is atypia
Serine protease, the Ser-Asp-His catalytic triads in its C-terminal region are different from typical serine protease, are backward
Arrangement.DPP-IV is II type integral membrane proteins, is distributed widely in mammal and respectively organizes.DPP-IV is small in intestines, liver, kidney near-end
Pipe, prostate, the differentiation surface epithelial cell of corpus luteum and leukocyte sub-type such as lymphocyte and Expression of Macrophages.Deposited in serum
In DPP-IV soluble protein form, its 26S Proteasome Structure and Function is identical with embrane-associated protein form but lacks hydrophobic transmembrane structure
Domain.
Diabetes B and fat attractive therapy can be turned into by suppressing DPP-IV.Although DPP-IV inhibitor energy
The sugar tolerance of diabetes B patient is effectively improved, but the half-life period of many inhibitor is shorter, or toxicity is larger.Accordingly, it would be desirable to open
Send out in pharmaceutical activity, stability, selectivity, toxicity, pharmacokinetics or medicine for characteristic more DPP-IV of advantage in terms of at least one
Inhibitor is treated for diabetes B.Therefore, the invention provides a class novel DPP-IV inhibitors.
Embodiment
Following test example is for illustrating the present invention.
Compound Dehydrocorydaline (CAS used in the present invention:30045-16-0) obtained by mm Suppliers.Biology is commented
Valency
Test example 1
The compounds of this invention is tested DPP-IV enzyme inhibition activities：
Instrument:
ELIASA, Envision (PerkinElmer, USA)
Material:
People source DPP-IV, is obtained to be expressed using baculovirus expression system in insect cell.
Substrate, Ala-Pro-AMC.
Process:
DPP-IV can the ultraviolet excitation production of specific for hydrolysis substrate A la-Pro-AMC generations product AMC, AMC through 355nm
Fluorescent value linear change at 460nm wavelength in raw 460nm transmitting light, dynamic cooling water of units of measurement time, calculating obtains DPP4 activity.
Experiment is used as control compound using MERK-0431.
Sample DMSO dissolves, Cord blood, and concentration controls of the DMSO in final system is not influenceing detection activity
Within the scope of.
Compound MERK-0431 is that IC50 [nM] is 17.57 to DPP-IV inhibitory action.
Compound Dehydrocorydaline is 63.8% to DPP-IV inhibitory action when concentration is 20 μ g/mL.
Conclusion：Compound Dehydrocorydaline in the present invention has certain inhibitory action to DPP-IV enzymes.
The present invention can be summarized with others without prejudice to the concrete form of the spirit or essential characteristics of the present invention.Therefore, nothing
By from the point of view of which point, the embodiment above of the invention can only all be considered the description of the invention and can not limit this hair
It is bright.
Claims (1)
1. application of the compound Dehydrocorydaline in DPP IV (DPP-IV) inhibitor medicaments are prepared.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710563291.9A CN107252425A (en) | 2017-07-12 | 2017-07-12 | The medicinal usage of Dehydrocorydaline |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710563291.9A CN107252425A (en) | 2017-07-12 | 2017-07-12 | The medicinal usage of Dehydrocorydaline |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN107252425A true CN107252425A (en) | 2017-10-17 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201710563291.9A Pending CN107252425A (en) | 2017-07-12 | 2017-07-12 | The medicinal usage of Dehydrocorydaline |
Country Status (1)
| Country | Link |
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| CN (1) | CN107252425A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113143922A (en) * | 2021-05-07 | 2021-07-23 | 广州医科大学 | Application of DHC in preparation of atherosclerosis treatment preparation |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014144130A2 (en) * | 2013-03-15 | 2014-09-18 | Als Mountain Llc | Pharmaceutical composition comprising an ampk activator and a serotonergic agent and methods of use thereof |
-
2017
- 2017-07-12 CN CN201710563291.9A patent/CN107252425A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014144130A2 (en) * | 2013-03-15 | 2014-09-18 | Als Mountain Llc | Pharmaceutical composition comprising an ampk activator and a serotonergic agent and methods of use thereof |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113143922A (en) * | 2021-05-07 | 2021-07-23 | 广州医科大学 | Application of DHC in preparation of atherosclerosis treatment preparation |
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| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
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| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20171017 |
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| WD01 | Invention patent application deemed withdrawn after publication |