CN108635351A - The medicinal usage of berberine sulphate - Google Patents

The medicinal usage of berberine sulphate Download PDF

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Publication number
CN108635351A
CN108635351A CN201810352364.4A CN201810352364A CN108635351A CN 108635351 A CN108635351 A CN 108635351A CN 201810352364 A CN201810352364 A CN 201810352364A CN 108635351 A CN108635351 A CN 108635351A
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CN
China
Prior art keywords
dpp
berberine sulphate
medicinal usage
sulphate
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201810352364.4A
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Chinese (zh)
Inventor
不公告发明人
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai Hua Zi Biological Technology Co Ltd
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Shanghai Hua Zi Biological Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shanghai Hua Zi Biological Technology Co Ltd filed Critical Shanghai Hua Zi Biological Technology Co Ltd
Priority to CN201810352364.4A priority Critical patent/CN108635351A/en
Publication of CN108635351A publication Critical patent/CN108635351A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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
    • A61K31/4375Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

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  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The title of the present invention is the medicinal usage of berberine sulphate.Affiliated technical field is medical science.The technical problems to be solved by the invention are to be related to berberine sulphate or its pharmaceutically acceptable solvate and its purposes as therapeutic agent especially as inhibitors of dipeptidyl IV.The main points of the technical solution of the technical problems to be solved by the invention are test of the compound to DPP IV enzyme inhibition activities.

Description

The medicinal usage of berberine sulphate
Technical field
The present invention relates to pharmaceutical technology fields, specifically, the present invention relates to compound berberine sulphates to be used as two peptidyls The medicinal usage of 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 refers to, including DPP4, DP4, DAP-IV, FAP β, adenosine deaminase complex protein 2, adenosine deaminase binding protein (ADAbp), bis- peptidyls of Dipeptidylaminopeptidase IV, Xaa-Pro--aminopeptidase, Gly-Pro naphthalenes 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, leukocyte antigen CD26, glycylprolyl Dipeptidylaminopeptidase, two peptidyl-peptide hydrolases, glycylprolyl aminopeptidase, two peptidyls- Aminopeptidase IV, DPPIV/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, is removed from the amino terminal (ends N-) 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 can inhibit dipeptidyl peptidase-IV (DipeptidylpeptidaseIV, DPP-IV) active chemical combination Object and/or pharmaceutically acceptable solvate, this kind of compound can be used for treating diabetes, as diabetes B, hyperglycemia, Metabolic syndrome, hyperinsulinemia, obesity, angiocardiopathy and abnormal such as atherosclerosis, cranial vascular disease, maincenter god Include schizophrenia, anxiety disorder, Bipolar depression, depression, insomnia, cognitive disorder, stomach and intestine through systemic disease or exception Disease and exception, cancer, inflammation and inflammatory disease, respiratory disease and exception, skeletal muscle is abnormal, osteoporosis, climacteric 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 is the results show that inhibit DPP8/9 that can cause such as anaemia, alopecia, decrease of platelet and splenomegaly Equal toxic reactions [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 exploitation for the selective depressant selected are of great significance [Bhumika DP, ManJunath DG.Recent 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, there is still a need for the strong selective DPP-IV inhibitors of structure novel, activity to meet clinical treatment for this field Demand.
Invention content
DPP IV (Dipeptidyl peptidase IV, DPP-IV, CD26, EC 3.4.14.5) is a kind of 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 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 proximal end Pipe, prostate, the differentiation surface epithelial cell of corpus luteum and leukocyte sub-type such as lymphocyte and Expression of Macrophages.It is deposited in serum In the soluble protein form of DPP-IV, structure and function is identical as embrane-associated protein form but lacks hydrophobic transmembrane structure Domain.
Inhibit DPP-IV that can become diabetes B and fat attractive therapy.Although DPP-IV inhibitor energy It is effectively improved the sugar tolerance of diabetes B patient, but the half-life period of many inhibitor is shorter, or is more toxic.Therefore, it is necessary to open Hair has more the DPP-IV of advantage in pharmaceutical activity, stability, selectivity, toxicity, pharmacokinetics or medicine at least one aspect of characteristic Inhibitor is treated for diabetes B.Therefore, the present invention provides a kind of novel DPP-IV inhibitors.
Specific implementation mode
Test example below is for illustrating the present invention.
Compound berberine sulphate (CAS used in the present invention:It is 316-41-6) obtained by mm Suppliers.
Biological assessment
Test example 1
The compounds of this invention tests DPP-IV enzyme inhibition activities:
Instrument:
Microplate reader, Envision (PerkinElmer, USA)
Material:
People source DPP-IV is obtained to be expressed in insect cell using baculovirus expression system.Substrate, Ala-Pro- AMC。
Process:
DPP-IV can the ultraviolet excitation production of the la-Pro-AMC generations of specific for hydrolysis substrate A product AMC, AMC through 355nm The transmitting light of raw 460nm, fluorescent value linear change at 460nm wavelength, is calculated DPP4 activity in dynamic cooling water of units of measurement time. Experiment uses MERK-0431 compounds as a contrast.
Sample is dissolved with DMSO, Cord blood, DMSO in final system concentration control do not influence to detect it is active Within the scope of.
It is 17.57 that compound MERK-0431, which is IC50 [nM] to the inhibiting effect of DPP-IV,.
Compound berberine sulphate is 92.2% to the inhibiting effect of DPP-IV in a concentration of 20 μ g/mL.
Conclusion:Compound berberine sulphate in the present invention has good inhibiting effect 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 cannot limit this hair It is bright.

Claims (2)

1. application of the compound berberine sulphate in preparing DPP IV (DPP-IV) inhibitor medicaments.
2. compound berberine sulphate is not more than 92.2% in a concentration of 20 μ g/mL to the inhibiting effect of DPP-IV.
CN201810352364.4A 2018-04-19 2018-04-19 The medicinal usage of berberine sulphate Pending CN108635351A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810352364.4A CN108635351A (en) 2018-04-19 2018-04-19 The medicinal usage of berberine sulphate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810352364.4A CN108635351A (en) 2018-04-19 2018-04-19 The medicinal usage of berberine sulphate

Publications (1)

Publication Number Publication Date
CN108635351A true CN108635351A (en) 2018-10-12

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810352364.4A Pending CN108635351A (en) 2018-04-19 2018-04-19 The medicinal usage of berberine sulphate

Country Status (1)

Country Link
CN (1) CN108635351A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1481796A (en) * 2003-06-13 2004-03-17 吴开敏 Medication for adiposity
CN1494902A (en) * 2002-04-23 2004-05-12 吴开敏 Application of high-solubility berberine in preparation of medicine.

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1494902A (en) * 2002-04-23 2004-05-12 吴开敏 Application of high-solubility berberine in preparation of medicine.
CN1481796A (en) * 2003-06-13 2004-03-17 吴开敏 Medication for adiposity

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Application publication date: 20181012

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