KR950701345A - 엘라스타제 저해활성을 갖는 신규 펩티드 및 그의 제조방법 - Google Patents
엘라스타제 저해활성을 갖는 신규 펩티드 및 그의 제조방법Info
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- KR950701345A KR950701345A KR1019940703771A KR19940703771A KR950701345A KR 950701345 A KR950701345 A KR 950701345A KR 1019940703771 A KR1019940703771 A KR 1019940703771A KR 19940703771 A KR19940703771 A KR 19940703771A KR 950701345 A KR950701345 A KR 950701345A
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- gly
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- leu
- cys
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/81—Protease inhibitors
- C07K14/8107—Endopeptidase (E.C. 3.4.21-99) inhibitors
- C07K14/811—Serine protease (E.C. 3.4.21) inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Abstract
Description
Claims (26)
- 하기 아미노산 배역;Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Glu-Leu-Leu상기 배열에서, Xl1은 Arg 또는 Glu이고, X15는 Ile, Leu 또는 Val이고, X18은 Ile 또는 Phe 이고, X46은 Tyr은 Tyr 또는 Gln이다.로 구성되는 아미노산을 포함함을 특징으로 하는 엘라스타제 저해 활성을 갖는 펩티드.
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-IIe-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Gly-Cys-Gly-Asn-Gly-Ans-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-Leu-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Tyr-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-Val-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Gly-Cys-Gln-Gly-Asp-Glu-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Pro-Cys-Val-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-Gin-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-Val-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Pro-Cys-Val-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Ans-Lys-Phe-Gin-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Prp-Cys-IIe-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Ans-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-IIe-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Cys-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-Gln-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Prp-Cys-IIe-Ala-Phe-IIe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Ans-Lys-Phe-Gln-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Prp-Cys-Ile-Ala-Phe-Phe-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Cys-Gly-Gln-Gly-Asp-Gly-Ans-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제1항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 펩티드 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-Xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Cys-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu상기 배열에서, Xl1은 Arg 또는 Glu이고, X15는 Ile, Leu 또는 Val이고, X18은 Ile 또는 Phe 이고, X46은 Tyr은 Tyr 또는 Gln이다.을 코드하는 유전자.
- 하기 아미노산 배열 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-Xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 하기 아미노산 배열:Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-Xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu상기 배열에서, Xl1은 Arg 또는 Glu이고, X15는 Ile, Leu 또는 Val이고, X18은 Ile 또는 Phe 이고, X46은 Tyr은 Tyr 또는 Gln이다.을 코드하는 유전자를 포함하는 플라스미드를 보유하는 숙주 미생물:
- 제14항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 숙주 미생물 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Pro-Cys-IIe-Ala-Phe-Ile-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Asp-Glu-Val-Pro-Gly-Asp-Glu-Glu-Leu-Leu
- 제15항에 있어서, 전기 숙주 미생물이 에시리히아 콜리 JM109-pCD17I15G3(FERM BP-4556)임을 특징으로 하는 숙주 미생물.
- 제14항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 숙주 미생물.Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Pro-Cys-Ile-Ala-Phe-Ile-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Tyr-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Asp-Glu-Val-Pro-Gly-Asp-Glu-Glu-Leu-Leu
- 제17항에 있어서, 전기 숙주 미생물이 에시리히아 콜리 콜리 JM109-pCD17V15G3Q46(FERM BP-4557)임을 특징으로 하는 숙주 미생물.
- 제14항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 배열임을 특징으로 하는 숙주 미생물.Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Pro-Cys-Ile-Ala-Phe-Ile-Gln-Leu-Trp-Ala-Phe-AsP-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Gln-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제19항에 있어서, 전기 숙주 미생물이 에시리히아 콜리 JM109-pCD17I15G3(FERM BP-4560)임을 특징으로 하는 숙주 미생물.
- 제14항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 숙주 미생물 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Arg-Gly-Pro-Cys-Ile-Ala-Phe-Ile-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Gln-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu
- 제21항에 있어서, 전기 숙주 미생물이 에시리히아 콜리 JM109-pCD17I15G3(FERM BP-4558)임을 특징으로 하는 숙주 미생물.
- 제14항에 있어서, 전기 아미노산 배열이 하기의 배열임을 특징으로 하는 숙주 미생물 :Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Glu-Gly-Pro-Cys-Ile-Ala-Phe-Ile-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Pro-Tyr-Gly-Gly-Cys-Gln-Gly-Asn-Gly-Asn-Lys-Phe-Gln-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Glu-Leu-Leu
- 제23항에 있어서, 전기 숙주 미생물이 에시리히아 콜리 JM109-pCD17I15G3(FERM BP-4556)임을 특징으로 하는 숙주 미생물.
- 하기 아미노산 배열;Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-Xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Cys-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Asp-Glu-Glu-Glu-Leu-Leu상기 배열에서, Xl1은 Arg 또는 Glu이고, X15는 Ile, Leu 또는 Val이고, X18은 Ile 또는 Phe 이고, X46은 Tyr은 Tyr 또는 Gln이다.을 코드하는 유전자를 포함하는 플라스미드를 보유하는 숙주 미생물에서 생성되는 엘라스타제 저해활성을 갖는 펩티드 생성물.
- 하기 아미노산 배열;Thr-Val-Gly-Ala-Cys-Asn-Leu-Pro-Val-Ile-Xll-Gly-Prp-Cys-Xl5-Ala-Phe-X18-Gln-Leu-Trp-Ala-Phe-Asp-Ala-Val-Lys-Gly-Lys-Cys-Val-Leu-Phe-Prp-Tyr-Gly-Cys-Gly-Gln-Gly-Asn-Gly-Ans-Lys-Phe-X46-Ser-Glu-Lys-Glu-Cys-Arg-Glu-Tyr-Cys-Gly-Val-Pro-Gly-Asp-Glu-Asp-Glu-Glu-Leu-Leu상기 배열에서, Xl1은 Arg 또는 Glu이고, X15는 Ile, Leu 또는 Val이고, X18은 Ile 또는 Phe 이고, X46은 Tyr은 Tyr 또는 Gln이다.을 코드하는 유전자를 포함하는 플라스미드를 보유하는 숙주 미생물에서 생성되는 엘라스타제 저해활성을 갖는 펩티드 생성물의 제조방법으로서, (a)전기한 숙주 미생물을 증식 배지에서 배양하고, (b) 전기 공정(a)에서 배양된 전기한 숙주 미생물의 균체를 원심분리하여 침전물을 회수한 후, (c) 전기 공정(b)에서 회수된 균체에서 엘라스타제 저해활성을 갖는 펩티드 생성물을 추출 · 회수하는 공정을 포함함을 특징으로 하는 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1993-31758 | 1993-02-22 | ||
JP5031758A JP2769083B2 (ja) | 1993-02-22 | 1993-02-22 | エラスターゼ阻害活性を有する新規ペプチドおよびその製造方法 |
PCT/JP1994/000284 WO1994019371A1 (fr) | 1993-02-22 | 1994-02-21 | Nouveau peptide presentant une activite inhibitrice de l'elastase et son procede de production |
Publications (2)
Publication Number | Publication Date |
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KR950701345A true KR950701345A (ko) | 1995-03-23 |
KR100213662B1 KR100213662B1 (ko) | 1999-08-02 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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KR1019940703771A KR100213662B1 (ko) | 1993-02-22 | 1994-02-21 | 엘라스타제 저해활성을 갖는 신규 펩티드 및 그의 제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US5541288A (ko) |
EP (1) | EP0643075A4 (ko) |
JP (1) | JP2769083B2 (ko) |
KR (1) | KR100213662B1 (ko) |
AU (1) | AU676019B2 (ko) |
CA (1) | CA2134240C (ko) |
WO (1) | WO1994019371A1 (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7078383B2 (en) * | 1988-09-02 | 2006-07-18 | Dyax Corp. | ITI-D1 Kunitz domain mutants as HNE inhibitors |
US5663143A (en) * | 1988-09-02 | 1997-09-02 | Dyax Corp. | Engineered human-derived kunitz domains that inhibit human neutrophil elastase |
US20060134087A1 (en) * | 1988-09-02 | 2006-06-22 | Dyax Corp. | ITI-D1 Kunitz domain mutants as hNE inhibitors |
US5650394A (en) * | 1993-11-04 | 1997-07-22 | Adeza Biomedical | Use of urinastatin-like compounds to prevent premature delivery |
JP3469584B2 (ja) * | 1996-03-11 | 2003-11-25 | バイエル コーポレイション | ヒト ビクニン |
CA2356404C (en) * | 1998-12-22 | 2010-03-30 | Bayer Aktiengesellschaft | Method for accelerating the rate of mucociliary clearance |
US20070140979A1 (en) * | 1998-12-22 | 2007-06-21 | Bayer Aktiengesellschaft | Method for accelerating the rate of mucociliary clearance |
US6989369B2 (en) | 2003-02-07 | 2006-01-24 | Dyax Corp. | Kunitz domain peptides |
SG10201708400QA (en) | 2014-02-24 | 2017-11-29 | Takeda Gmbh | Uti fusion proteins |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2066033T3 (es) * | 1989-05-13 | 1995-03-01 | Bayer Ag | Inhibidores de las proteinasas, procedimiento para su preparacion y composiciones farmaceuticas que los contienen. |
CA2055425A1 (en) * | 1990-11-13 | 1992-05-14 | Hideaki Morishita | Polypeptide, dna fragment encoding the same and process for producing the same, and enzyme inhibition process, drug composition and methods of treating using the same |
DE69233108T2 (de) * | 1991-03-01 | 2004-04-29 | Dyax Corp., Cambridge | Hemmstoffe für menschliche neutrophile elastase und menschliches kathepsin g |
CA2082226A1 (en) * | 1991-11-08 | 1993-05-09 | Hideaki Morishita | Polypeptide, dna fragment encoding the same, drug composition containing the same and process for producing the same |
-
1993
- 1993-02-22 JP JP5031758A patent/JP2769083B2/ja not_active Expired - Fee Related
-
1994
- 1994-02-21 AU AU61151/94A patent/AU676019B2/en not_active Ceased
- 1994-02-21 KR KR1019940703771A patent/KR100213662B1/ko not_active IP Right Cessation
- 1994-02-21 EP EP94907668A patent/EP0643075A4/en not_active Withdrawn
- 1994-02-21 US US08/325,243 patent/US5541288A/en not_active Expired - Fee Related
- 1994-02-21 CA CA002134240A patent/CA2134240C/en not_active Expired - Fee Related
- 1994-02-21 WO PCT/JP1994/000284 patent/WO1994019371A1/ja not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO1994019371A1 (fr) | 1994-09-01 |
EP0643075A4 (en) | 1997-02-26 |
US5541288A (en) | 1996-07-30 |
AU676019B2 (en) | 1997-02-27 |
CA2134240C (en) | 2000-08-01 |
JPH06247998A (ja) | 1994-09-06 |
CA2134240A1 (en) | 1994-08-23 |
JP2769083B2 (ja) | 1998-06-25 |
EP0643075A1 (en) | 1995-03-15 |
AU6115194A (en) | 1994-09-14 |
KR100213662B1 (ko) | 1999-08-02 |
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