Ayumi Pharmaceutical Corporation

Japan

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        Patent 15
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        United States 9
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2023 4
2022 1
2021 1
2020 2
Before 2020 11
IPC Class
A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis 5
A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID] 5
A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection 5
A61P 11/06 - Antiasthmatics 4
A61P 13/12 - Drugs for disorders of the urinary system of the kidneys 4
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NICE Class
05 - Pharmaceutical, veterinary and sanitary products 4
10 - Medical apparatus and instruments 1
23 - Yarns and threads for textile use 1
Status
Pending 2
Registered / In Force 19

1.

Miscellaneous Design

      
Application Number 1749148
Status Registered
Filing Date 2023-03-24
Registration Date 2023-03-24
Owner AYUMI Pharmaceutical Corporation (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations.

2.

TABLET AND METHOD FOR MANUFACTURING SAME

      
Application Number 18010954
Status Pending
Filing Date 2021-07-02
First Publication Date 2023-08-17
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Yamashita, Miki
  • Takigami, Yusuke

Abstract

The present invention addresses the problem of providing a tablet that contains a high concentration of acetaminophen, satisfies an acetaminophen dissolution rate from the tablet of at least 80% in 15 minutes, and can be manufactured by dry direct compression. The present invention provides a tablet including: acetaminophen that has a median particle diameter in a range from 100 to 350 µm; crystalline cellulose that has a bulk density in a range from 0.10 to 0.23 g/cm3; and at least two types of disintegrants. The at least two types of disintegrants are (a) at least one disintegrant selected from the group consisting of crospovidone, croscarmellose sodium, and sodium starch glycolate, and (b) a disintegrant that is a low-substituted hydroxypropyl cellulose. The acetaminophen content per tablet is at least 86 weight%.

IPC Classes  ?

  • A61K 31/167 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen atom of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
  • A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
  • A61K 47/38 - CelluloseDerivatives thereof
  • A61K 9/20 - Pills, lozenges or tablets

3.

CALONAL

      
Application Number 1728580
Status Registered
Filing Date 2023-03-24
Registration Date 2023-03-24
Owner AYUMI Pharmaceutical Corporation (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations.

4.

Miscellaneous Design

      
Application Number 1728938
Status Registered
Filing Date 2023-03-24
Registration Date 2023-03-24
Owner AYUMI Pharmaceutical Corporation (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations.

5.

TABLET AND METHOD FOR MANUFACTURING SAME

      
Application Number JP2021025101
Publication Number 2022/004871
Status In Force
Filing Date 2021-07-02
Publication Date 2022-01-06
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Yamashita Miki
  • Takigami Yusuke

Abstract

The present invention addresses the problem of providing a tablet that includes a high concentration of acetaminophen, that elutes acetaminophen at a rate of at least 80% in fifteen minutes, and that can be manufactured by dry tableting. The present invention provides a tablet, containing acetaminophen with a median grain diameter in the range 100–350 μm, crystalline cellulose with a bulk density in the range 0.10–0.23 g/cm3, and disintegrants of at least two types, wherein: the disintegrants of at least two types are a disintegrant (a) of at least one type selected from the group consisting of crospovidone, croscarmellose sodium, and sodium starch glycolate, and a disintegrant (b) that is low-substituted hydroxypropylcellulose; and the acetaminophen content per tablet is at least 86% by weight.

IPC Classes  ?

  • A61K 31/167 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen atom of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
  • A61K 9/20 - Pills, lozenges or tablets
  • A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
  • A61K 47/36 - PolysaccharidesDerivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K 47/38 - CelluloseDerivatives thereof
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]

6.

6H-thieno[2,3-e][1,2,4]triazolo[3,4-c][1,2,4]triazepine derivative

      
Application Number 16617201
Grant Number 11186588
Status In Force
Filing Date 2018-05-31
First Publication Date 2021-05-06
Grant Date 2021-11-30
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Aono, Hiroyuki
  • Seki, Iwao
  • Imamura, Miwa
  • Tanaka, Tomomi
  • Shirae, Satoshi
  • Kawashima, Kenji
  • Yamazaki, Yusuke
  • Yamamoto, Minoru

Abstract

The 6H-thieno[2,3-e][1,2,4]triazolo[3,4-c][1,2,4]triazepine derivatives or salts thereof of the present invention have BRD4 inhibitory activity, and thus, they are useful as medicaments, in particular, as prophylaxis and/or therapeutic agents for diseases associated with BRD4.

IPC Classes  ?

  • C07D 495/14 - Ortho-condensed systems
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis

7.

ORALLY DISINTEGRATING TABLET AND MANUFACTURING METHOD THEREFOR

      
Application Number JP2020014429
Publication Number 2020/246120
Status In Force
Filing Date 2020-03-30
Publication Date 2020-12-10
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Takigami Yusuke
  • Yamashita Miki

Abstract

The present invention addresses the problem of providing an orally disintegrating tablet that includes acetaminophen at a high concentration of 75mass% or more, while having a tablet hardness of 50N or more and having a useful quick oral disintegration property. The present invention provides an orally disintegrating tablet including: acetaminophen with a median grain size in the range 80-300μm; a highly moldable crystalline cellulose; and a disintegrant, wherein the acetaminophen content by percent in one tablet is 75mass% or more, the acetaminophen content by quantity in one tablet is 190mg or more, and the orally disintegrating tablet has a tablet hardness of 50N or more.

IPC Classes  ?

  • A61K 9/20 - Pills, lozenges or tablets
  • A61K 47/10 - AlcoholsPhenolsSalts thereof, e.g. glycerolPolyethylene glycols [PEG]PoloxamersPEG/POE alkyl ethers
  • A61K 47/22 - Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
  • A61K 47/26 - Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharidesDerivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
  • A61K 47/32 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers
  • A61K 47/36 - PolysaccharidesDerivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
  • A61K 47/38 - CelluloseDerivatives thereof
  • A61K 47/42 - ProteinsPolypeptidesDegradation products thereofDerivatives thereof, e.g. albumin, gelatin or zein
  • A61K 47/46 - Ingredients of undetermined constitution or reaction products thereof, e.g. skin, bone, milk, cotton fibre, eggshell, oxgall or plant extracts
  • A61K 31/167 - Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen atom of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol

8.

THERAPEUTIC AGENT FOR WOLFRAM SYNDROME

      
Application Number JP2020014194
Publication Number 2020/196873
Status In Force
Filing Date 2020-03-27
Publication Date 2020-10-01
Owner
  • TOKYO MEDICAL UNIVERSITY (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Nakajima Toshihiro
  • Fujita Hidetoshi
  • Kuroda Masahiko
  • Kanekura Kohsuke
  • Hiramoto Masaki
  • Kumagai Katsuyoshi
  • Aono Hiroyuki

Abstract

[Problem] To provide a therapeutic agent for Wolfram syndrome. [Solution] A therapeutic agent for Wolfram syndrome that comprises a calcineurin inhibitor as an active ingredient, wherein the calcineurin inhibitor is cyclosporine, tacrolimus, rapamycin, a pharmaceutically acceptable salt thereof or a pharmaceutically acceptable solvate of the same.

IPC Classes  ?

  • A61K 45/00 - Medicinal preparations containing active ingredients not provided for in groups
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 25/02 - Drugs for disorders of the nervous system for peripheral neuropathies
  • A61K 38/13 - Cyclosporins
  • A61K 31/706 - Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom

9.

6H-THIENO[2,3-E][1,2,4]TRIAZOLO[3,4-C][1,2,4]TRIAZEPINE DERIVATIVE

      
Application Number JP2018021040
Publication Number 2018/221679
Status In Force
Filing Date 2018-05-31
Publication Date 2018-12-06
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Aono Hiroyuki
  • Seki Iwao
  • Imamura Miwa
  • Tanaka Tomomi
  • Shirae Satoshi
  • Kawashima Kenji
  • Yamazaki Yusuke
  • Yamamoto Minoru

Abstract

This 6H-thieno[2,3-e][1,2,4]triazolo[3,4-c][1,2,4]triazepine derivative or a salt thereof has BRD4 inhibitory activity and is therefore useful as a drug, especially as an agent to prevent and/or treat diseases involving BRD4.

IPC Classes  ?

  • C07D 495/14 - Ortho-condensed systems
  • A61K 31/55 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
  • A61P 1/04 - Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
  • A61P 3/00 - Drugs for disorders of the metabolism
  • A61P 3/04 - AnorexiantsAntiobesity agents
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 5/14 - Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 9/12 - Antihypertensives
  • A61P 11/00 - Drugs for disorders of the respiratory system
  • A61P 11/06 - Antiasthmatics
  • A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
  • A61P 15/08 - Drugs for genital or sexual disordersContraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
  • A61P 15/16 - Masculine contraceptives
  • A61P 17/02 - Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
  • A61P 17/06 - Antipsoriatics
  • A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
  • A61P 19/06 - Antigout agents, e.g. antihyperuricemic or uricosuric agents
  • A61P 19/10 - Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
  • A61P 21/00 - Drugs for disorders of the muscular or neuromuscular system
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 25/14 - Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
  • A61P 25/16 - Anti-Parkinson drugs
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
  • A61P 27/02 - Ophthalmic agents
  • A61P 27/06 - Antiglaucoma agents or miotics
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 31/04 - Antibacterial agents
  • A61P 31/12 - Antivirals
  • A61P 31/14 - Antivirals for RNA viruses
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 31/20 - Antivirals for DNA viruses
  • A61P 31/22 - Antivirals for DNA viruses for herpes viruses
  • A61P 35/00 - Antineoplastic agents
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • A61P 37/02 - Immunomodulators
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 37/08 - Antiallergic agents
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups

10.

Inhibition of IL-2 production

      
Application Number 14778925
Grant Number 09650351
Status In Force
Filing Date 2014-03-19
First Publication Date 2016-02-18
Grant Date 2017-05-16
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Nakajima, Toshihiro
  • Aratani, Satoko
  • Nishioka, Kusuki
  • Aono, Hiroyuki

Abstract

IL-2 production can be inhibited by a compound represented by the following formula (I): or a pharmaceutically acceptable salt thereof.

IPC Classes  ?

  • C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
  • A61K 31/428 - Thiazoles condensed with carbocyclic rings

11.

INHIBITION OF PRODUCTION OF IL-2

      
Application Number JP2014057597
Publication Number 2014/148574
Status In Force
Filing Date 2014-03-19
Publication Date 2014-09-25
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Nakajima, Toshihiro
  • Aratani, Satoko
  • Nishioka, Kusuki
  • Aono, Hiroyuki

Abstract

The purpose of the present invention is to find a substance capable of inhibiting the production of IL-2. The production of IL-2 can be inhibited with a compound represented by general formula (I) (wherein R1 to R4 and A are as defined in the description) or a pharmaceutically acceptable salt thereof.

IPC Classes  ?

  • A61K 31/428 - Thiazoles condensed with carbocyclic rings
  • A61P 1/00 - Drugs for disorders of the alimentary tract or the digestive system
  • A61P 11/02 - Nasal agents, e.g. decongestants
  • A61P 11/06 - Antiasthmatics
  • A61P 11/08 - Bronchodilators
  • A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
  • A61P 17/04 - Antipruritics
  • A61P 17/06 - Antipsoriatics
  • A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
  • A61P 21/04 - Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 27/02 - Ophthalmic agents
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 35/00 - Antineoplastic agents
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 37/08 - Antiallergic agents
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2

12.

Method for treating a TRPV1-mediated disease

      
Application Number 13680465
Grant Number 08901155
Status In Force
Filing Date 2012-11-19
First Publication Date 2013-04-11
Grant Date 2014-12-02
Owner
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Oki, Kenji
  • Tsuji, Fumio
  • Setoguchi, Chikako
  • Seki, Iwao
  • Murai, Masaaki
  • Sasano, Minoru

Abstract

A method for treating a TRPV1-mediated disease by administering to a patient a therapeutically effective amount of a compound or a salt thereof having the following formula [I]: 3 are the same or different and represent a hydrogen atom, an unsubstituted lower alkyl group or a lower alkyl group substituted by a monocyclic cycloalkyl group, a polycyclic cycloalkyl group or an aryl group.

IPC Classes  ?

  • A61K 31/44 - Non-condensed pyridinesHydrogenated derivatives thereof
  • C07D 213/36 - Radicals substituted by singly-bound nitrogen atoms
  • A61K 31/4409 - Non-condensed pyridinesHydrogenated derivatives thereof only substituted in position 4, e.g. isoniazid, iproniazid

13.

Method for treating a disease related to the glucocorticoid receptor

      
Application Number 13135790
Grant Number 08440660
Status In Force
Filing Date 2011-07-14
First Publication Date 2011-11-10
Grant Date 2013-05-14
Owner
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Matsuda, Mamoru
  • Nagatsuka, Masato
  • Mori, Toshiyuki
  • Kobayashi, Sachiko
  • Kato, Masatomo
  • Takai, Miwa

Abstract

A method for treating a disease related to the glucocorticoid receptor involving administering a pharmacologically effective amount of a 1,2-hydroquinoline compound.

IPC Classes  ?

  • A61K 31/535 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and at least one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K 31/47 - QuinolinesIsoquinolines

14.

Glucocorticoid receptor agonist comprising 2,2,4-trimethyl-6-phenyl-1,2-dihydroquinoline derivatives having substituted oxy group

      
Application Number 12992237
Grant Number 08426406
Status In Force
Filing Date 2009-05-12
First Publication Date 2011-05-19
Grant Date 2013-04-23
Owner
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Kato, Masatomo
  • Takai, Miwa
  • Matsuyama, Takahiro
  • Kurose, Tatsuji
  • Hagiwara, Yumi
  • Matsuda, Mamoru
  • Mori, Toshiyuki
  • Imoto, Kenji
  • Dota, Atsuyoshi

Abstract

9 or the like represents a lower alkyl group which may have a substituent, a lower alkenyl group, or the like.

IPC Classes  ?

  • A61K 31/5377 - 1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
  • A61K 31/47 - QuinolinesIsoquinolines
  • A61K 31/4709 - Non-condensed quinolines containing further heterocyclic rings
  • A61K 31/506 - PyrimidinesHydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings

15.

1,2-dihydroquinoline derivative having substituted phenylchalcogeno lower alkyl group and ester-introduced phenyl group as substituents

      
Application Number 12312392
Grant Number 08008496
Status In Force
Filing Date 2007-11-14
First Publication Date 2010-03-04
Grant Date 2011-08-30
Owner
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Matsuda, Mamoru
  • Nagatsuka, Masato
  • Mori, Toshiyuki
  • Kobayashi, Sachiko
  • Kato, Masatomo
  • Takai, Miwa

Abstract

The compounds represented in general formula (1) and a salt thereof are useful for glucocorticoid receptor modulator. 8 may be the same or different and represent a hydrogen atom, a lower alkyl group which may have a substituent, an aryl group which may have a substituent, a heterocyclic group which may have a substituent, a lower alkoxy group which may have a substituent and the like; Y represents a lower alkylene group; Z represents a chalcogen atom; and P represents 0, 1, 2 or 3.

IPC Classes  ?

16.

1-2-dihydroquinoline derivative having glucocorticoid receptor binding activity

      
Application Number 11992088
Grant Number 08017775
Status In Force
Filing Date 2006-09-14
First Publication Date 2009-12-31
Grant Date 2011-09-13
Owner
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
  • AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Matsuda, Mamoru
  • Mori, Toshiyuki
  • Kawashima, Kenji
  • Nagatsuka, Masato
  • Kobayashi, Sachiko
  • Yamamoto, Minoru
  • Kato, Masatomo
  • Takai, Miwa
  • Oda, Tomoko

Abstract

9 represents a hydrogen atom or the like.

IPC Classes  ?

17.

RIMATIL

      
Application Number 915496
Status Registered
Filing Date 2006-12-27
Registration Date 2006-12-27
Owner AYUMI Pharmaceutical Corporation (Japan)
NICE Classes  ? 05 - Pharmaceutical, veterinary and sanitary products

Goods & Services

Pharmaceutical preparations; medicines for human purposes; vitamin preparations; medicinal drinks; ointments for pharmaceutical purposes; antibiotics; steroids; radioactive substances for medical purposes; oxygen baths; sterilising preparations; solutions for contact lenses; preparations of microorganisms for medical and veterinary use; antirheumatic agents; antiarthrists agents; veterinary preparations; diagnostic preparations for medical purposes; plasters for medical purposes; disinfectants for hygiene purposes, antiseptics; vermin destroying preparations; fungicides, herbicides; detergents for medical purposes; antiparasitic collars for animals.

18.

ZONE-QUICK

      
Serial Number 74420932
Status Registered
Filing Date 1993-08-03
Registration Date 1996-06-18
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
NICE Classes  ? 10 - Medical apparatus and instruments

Goods & Services

testing threads for medical purpose, particularly for tear volume testing

19.

ZONE-QUICK

      
Application Number 073342600
Status Registered
Filing Date 1993-07-27
Registration Date 1997-06-18
Owner AYUMI Pharmaceutical Corporation (Japan)
NICE Classes  ? 23 - Yarns and threads for textile use

Goods & Services

(1) Test threads for medical purpose, namely for testing the volume of tears in the eyes.

20.

INHIBITION OF IL-2 PRODUCTION

      
Document Number 02907921
Status In Force
Filing Date 2014-03-19
Grant Date 2021-09-07
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Nakajima, Toshihiro
  • Aratani, Satoko
  • Nishioka, Kusuki
  • Aono, Hiroyuki

Abstract

The purpose of the present invention is to find a substance capable of inhibiting the production of IL-2. The production of IL-2 can be inhibited with a compound represented by general formula (I) (wherein R1 to R4 and A are as defined in the description) or a pharmaceutically acceptable salt thereof.

IPC Classes  ?

  • A61K 31/428 - Thiazoles condensed with carbocyclic rings
  • A61P 1/00 - Drugs for disorders of the alimentary tract or the digestive system
  • A61P 11/02 - Nasal agents, e.g. decongestants
  • A61P 11/06 - Antiasthmatics
  • A61P 11/08 - Bronchodilators
  • A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
  • A61P 17/04 - Antipruritics
  • A61P 17/06 - Antipsoriatics
  • A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
  • A61P 21/04 - Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 27/02 - Ophthalmic agents
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 35/00 - Antineoplastic agents
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 37/08 - Antiallergic agents
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2

21.

6H-THIENO[2,3-E][1,2,4]TRIAZOLO[3,4-C][1,2,4]TRIAZEPINE DERIVATIVES

      
Document Number 03064845
Status Pending
Filing Date 2018-05-31
Owner AYUMI PHARMACEUTICAL CORPORATION (Japan)
Inventor
  • Aono, Hiroyuki
  • Seki, Iwao
  • Imamura, Miwa
  • Tanaka, Tomomi
  • Shirae, Satoshi
  • Kawashima, Kenji
  • Yamazaki, Yusuke
  • Yamamoto, Minoru

Abstract

This 6H-thieno[2,3-e][1,2,4]triazolo[3,4-c][1,2,4]triazepine derivative or a salt thereof has BRD4 inhibitory activity and is therefore useful as a drug, especially as an agent to prevent and/or treat diseases involving BRD4.

IPC Classes  ?

  • A61K 31/55 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
  • A61P 1/04 - Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
  • A61P 1/16 - Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
  • A61P 3/00 - Drugs for disorders of the metabolism
  • A61P 3/04 - AnorexiantsAntiobesity agents
  • A61P 3/10 - Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
  • A61P 5/14 - Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
  • A61P 9/00 - Drugs for disorders of the cardiovascular system
  • A61P 9/10 - Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
  • A61P 9/12 - Antihypertensives
  • A61P 11/00 - Drugs for disorders of the respiratory system
  • A61P 11/06 - Antiasthmatics
  • A61P 13/12 - Drugs for disorders of the urinary system of the kidneys
  • A61P 15/08 - Drugs for genital or sexual disordersContraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
  • A61P 15/16 - Masculine contraceptives
  • A61P 17/02 - Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
  • A61P 17/06 - Antipsoriatics
  • A61P 19/02 - Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
  • A61P 19/06 - Antigout agents, e.g. antihyperuricemic or uricosuric agents
  • A61P 19/10 - Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
  • A61P 21/00 - Drugs for disorders of the muscular or neuromuscular system
  • A61P 25/00 - Drugs for disorders of the nervous system
  • A61P 25/14 - Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
  • A61P 25/16 - Anti-Parkinson drugs
  • A61P 25/28 - Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
  • A61P 27/02 - Ophthalmic agents
  • A61P 27/06 - Antiglaucoma agents or miotics
  • A61P 29/00 - Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agentsNon-steroidal antiinflammatory drugs [NSAID]
  • A61P 31/04 - Antibacterial agents
  • A61P 31/12 - Antivirals
  • A61P 31/14 - Antivirals for RNA viruses
  • A61P 31/18 - Antivirals for RNA viruses for HIV
  • A61P 31/20 - Antivirals for DNA viruses
  • A61P 31/22 - Antivirals for DNA viruses for herpes viruses
  • A61P 35/00 - Antineoplastic agents
  • A61P 35/02 - Antineoplastic agents specific for leukemia
  • A61P 37/02 - Immunomodulators
  • A61P 37/06 - Immunosuppressants, e.g. drugs for graft rejection
  • A61P 37/08 - Antiallergic agents
  • A61P 43/00 - Drugs for specific purposes, not provided for in groups
  • C07D 495/14 - Ortho-condensed systems