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    • 1. 发明授权
    • Truncated keratinocyte growth factor (KGF) having increased biological activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US06677301B1
    • 2004-01-13
    • US09573068
    • 2000-05-16
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • C07K1448
    • C07K14/50A61K38/00A61K47/6415A61K47/642
    • The present invention relates to a keratinocyte growth factor fragment, KGFdes1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratinocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues. C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R- (SEQ ID NO: 2) of the KGF163 N-terminus. The present invention also relates to a DNA molecule encoding KGFdes1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGFdes1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGFdes1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGFdes1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子KGF163的氨基酸序列的一部分组成的角质形成细胞生长因子片段KGFdes1-23或其类似物。 与成熟的重组角质形成细胞生长因子rKGF相比,该片段显示出促有丝分裂活性的至少2倍的增加,但是缺少包含前23个氨基酸残基的序列。 C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R-(SEQ ID NO:2)。 本发明还涉及编码KGFdes1-23的DNA分子,表达载体和含有DNA分子的转化宿主,以及通过培养转化的宿主生产KGFdes1-23的方法。 本发明还涉及KGFdes1-23与毒素分子的结合物及其用于治疗表皮的过度增殖性疾病的用途。 此外,本发明涉及含有KGFdes1-23和药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。
    • 2. 发明申请
    • Truncated keratinocyte growth factor (KGF) having increased biological activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US20090093400A1
    • 2009-04-09
    • US11811560
    • 2007-06-11
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • A61K38/18C07K14/475C07K16/22C07H21/00C12N1/21C12P21/02
    • C07K14/50A61K38/00A61K47/6415A61K47/642
    • The present invention relates to a keratinocyte growth factor fragment, KGFdes1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratinocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues; C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R- (SEQ ID NO: 2) of the KGF163 N-terminus. The present invention also relates to a DNA molecule encoding KGFdes1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGFdes1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGFdes1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGFdes1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子KGF163的氨基酸序列的一部分组成的角质形成细胞生长因子片段KGFdes1-23或其类似物。 与成熟的重组角质形成细胞生长因子rKGF相比,该片段表现出促有丝分裂活性的至少2倍的增加,但缺少包含前23个氨基酸残基的序列; C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R-(SEQ ID NO:2)。 本发明还涉及编码KGFdes1-23的DNA分子,表达载体和含有DNA分子的转化宿主,以及通过培养转化的宿主生产KGFdes1-23的方法。 本发明还涉及KGFdes1-23与毒素分子的结合物及其用于治疗表皮的过度增殖性疾病的用途。 此外,本发明涉及含有KGFdes1-23和药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。
    • 3. 发明授权
    • Truncated keratinocyte growth factor (KGF) having increased biological activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US07247452B2
    • 2007-07-24
    • US10998425
    • 2004-11-29
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • C12N15/19C12N1/21C12N5/10C12N15/66C07K14/475
    • C07K14/50A61K38/00A61K47/6415A61K47/642
    • The present invention relates to a keratinocyte growth factor fragment, KGFdes1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratinocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues, C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R- (SEQ ID NO: 2) of the KGF163 N-terminus. The present invention also relates to a DNA molecule encoding KGFdes1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGFdes1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGFdes1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGFdes1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子的一部分氨基酸序列组成的角质形成细胞生长因子片段,KGF 或其类似物,KGF 163 。 与成熟的重组角质形成细胞生长因子rKGF相比,该片段显示出促有丝分裂活性的至少2倍的增加,但是缺少包含前23个氨基酸残基的序列CNDMTPEQMATNVNCSSPERH-TR-(SEQ ID NO:2) KGF 163 N末端。 本发明还涉及编码KGF Sub1-23的DNA分子,表达载体和含有该DNA分子的转化宿主,以及生产KGF 通过培养转化的宿主。 本发明进一步涉及一种KGF Sub1.33和毒素分子的缀合物及其用于治疗表皮过度增殖性疾病的用途。 此外,本发明涉及含有KGF和其药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。
    • 4. 发明授权
    • Truncated keratinocyte growth factor (KGF) having increased biological activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US07084119B2
    • 2006-08-01
    • US10700653
    • 2003-11-04
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • A61K38/18C07K14/475
    • C07K14/50A61K38/00A61K47/6415A61K47/642
    • The present invention relates to a keratinocyte growth factor fragment, KGFdes1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratinocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues; C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R- (SEQ ID NO: 2) of the KGF163 N-terminus. The present invention also relates to a DNA molecule encoding KGFdes1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGFdes1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGFdes1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGFdes1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子的一部分氨基酸序列组成的角质形成细胞生长因子片段KGF 或其类似物,KGF 163 。 与成熟的重组角质形成细胞生长因子rKGF相比,该片段表现出促有丝分裂活性的至少2倍的增加,但缺少包含前23个氨基酸残基的序列; C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R-(SEQ ID NO:2)。 本发明还涉及编码KGF Sub1-23的DNA分子,表达载体和含有该DNA分子的转化宿主,以及生产KGF 通过培养转化的宿主。 本发明进一步涉及一种KGF Sub1.33和毒素分子的缀合物及其用于治疗表皮过度增殖性疾病的用途。 此外,本发明涉及含有KGF和其药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。
    • 5. 发明授权
    • Truncated keratinocyte growth factor (KGF) having increased biological
activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US6074848A
    • 2000-06-13
    • US74950
    • 1998-05-08
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • C12N15/09A61K38/00A61K38/18A61K38/22A61K47/48A61P35/00A61P43/00C07H21/04C07K14/47C07K14/50C12N1/15C12N1/19C12N1/21C12N5/10C12N15/12C12N15/19C12P21/02C12R1/19C12R1/91C12N15/66
    • C07K14/50A61K47/48261A61K47/48269A61K38/00
    • The present invention relates to keratinocyte growth factor fragment, KGF.sub.des1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF.sub.163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratonocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues, C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R-(SEQ ID NO: 2) of the KGF.sub.163 N-terminus. The present invention also relates to a DNA molecule encoding KGF.sub.des1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGF.sub.des1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGF.sub.des1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGF.sub.des1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子KGF163的一部分氨基酸序列组成的角质形成细胞生长因子片段KGFdes1-23或其类似物。 与成熟的重组角质细胞生长因子rKGF相比,该片段显示出促有丝分裂活性的至少2倍的增加,但是缺少包含前23个氨基酸残基的序列CNDMTPEQMATNVNCSSPERH-TR-(SEQ ID NO:2) KGF163 N末端。 本发明还涉及编码KGFdes1-23的DNA分子,表达载体和含有DNA分子的转化宿主,以及通过培养转化的宿主生产KGFdes1-23的方法。 本发明还涉及KGFdes1-23与毒素分子的结合物及其用于治疗表皮的过度增殖性疾病的用途。 此外,本发明涉及含有KGFdes1-23和药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。
    • 9. 发明授权
    • Truncated keratinocyte growth factor (KGF) having increased biological
activity
    • 截短的角质形成细胞生长因子(KGF)具有增加的生物活性
    • US5677278A
    • 1997-10-14
    • US410941
    • 1995-03-27
    • Denis J. GospodarowiczFrank R. Masiarz
    • Denis J. GospodarowiczFrank R. Masiarz
    • C12N15/09A61K38/00A61K38/18A61K38/22A61K47/48A61P35/00A61P43/00C07H21/04C07K14/47C07K14/50C12N1/15C12N1/19C12N1/21C12N5/10C12N15/12C12N15/19C12P21/02C12R1/19C12R1/91C07K14/475
    • C07K14/50A61K47/48261A61K47/48269A61K38/00
    • The present invention relates to a keratinocyte growth factor fragment, KGF.sub.des1-23, or an analog thereof that is composed of a portion of an amino acid sequence of mature, full length keratinocyte growth factor, KGF.sub.163. The fragment exhibits at least a 2-fold increase in mitogenic activity as compared to a mature, recombinant keratinocyte growth factor, rKGF, but lacks a sequence comprising the first 23 amino acid residues, C-N-D-M-T-P-E-Q-M-A-T-N-V-N-C-S-S-P-E-R-H-T-R- (SEQ ID NO: 2) of the KGF.sub.163 N-terminus. The present invention also relates to a DNA molecule encoding KGF.sub.des1-23, an expression vector and a transformed host containing the DNA molecule, and a method of producing KGF.sub.des1-23 by culturing the transformed host. The present invention further relates to a conjugate of KGF.sub.des1-23 and a toxin molecule, and the use thereof for treatment of hyperproliferative disease of the epidermis. Moreover, the present invention relates to a therapeutic composition containing KGF.sub.des1-23 and a pharmaceutically acceptable carrier and the use thereof for wound healing purposes.
    • 本发明涉及由成熟的全长角质形成细胞生长因子KGF163的氨基酸序列的一部分组成的角质形成细胞生长因子片段KGFdes1-23或其类似物。 与成熟的重组角质形成细胞生长因子rKGF相比,该片段显示出促有丝分裂活性的至少2倍的增加,但缺少包含前23个氨基酸残基CNDMTPEQMATNVNCSSPERH-TR-(SEQ ID NO:2)的序列 KGF163 N末端。 本发明还涉及编码KGFdes1-23的DNA分子,表达载体和含有DNA分子的转化宿主,以及通过培养转化的宿主生产KGFdes1-23的方法。 本发明还涉及KGFdes1-23与毒素分子的结合物及其用于治疗表皮的过度增殖性疾病的用途。 此外,本发明涉及含有KGFdes1-23和药学上可接受的载体的治疗组合物及其用于伤口愈合目的的用途。