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    • 2. 发明授权
    • Vitamin D analogues
    • 维生素D类似物
    • US06310226B1
    • 2001-10-30
    • US09297387
    • 1999-04-30
    • Martin John CalverleyHenrik Pedersen
    • Martin John CalverleyHenrik Pedersen
    • A61K31593
    • C07C401/00
    • The present invention relates to compounds of formula (I) in which formula X is hydrogen or hydroxy; R1 and R2 which may be the same or different, stand for hydrogen or C1-C5 hydrocarbyl; or R1 and R2, taken together with the carbon atom bearing the group X, can form a C3C8 carbocyclic ring; Q is methylene, ethylene, tri- or tetra-methylene and may optionally be substituted with an oxy group, —OR3, in which R3 is hydrogen, methyl or ethyl; Y is either a single bond or C1-C2 hydrocarbylene; and one or more carbons with in R1, R2, and/or Y may optionally be substituted with one or more fluorine atoms, or with a hydroxyl group. The compounds show anti-inflammatory and immunomodulating effects as well as strong activity in inducing differentiation and inhibiting undesirable proliferation of certain cells.
    • 本发明涉及式(I)化合物,其中式X为氢或羟基; R 1和R 2可以相同或不同,代表氢或C 1 -C 5烃基; 或者R 1和R 2与带有基团X的碳原子一起可以形成C 3 C 8碳环; Q是亚甲基,亚乙基,三 - 或四亚甲基并且可以任选地被氧基取代,-OR 3,其中R 3是氢,甲基或乙基; Y是单键或C1-C2亚烃基; 并且在R1,R2和/或Y中具有一个或多个碳可以任选地被一个或多个氟原子或羟基取代。 这些化合物显示出抗炎和免疫调节作用,以及在诱导分化和抑制某些细胞的不期望的增殖方面具有很强的活性。
    • 8. 发明授权
    • Fungal lypolytic and amylase enzyme composition and methods using the same
    • 真菌溶血酶和淀粉酶组成及使用方法
    • US08012732B2
    • 2011-09-06
    • US12552572
    • 2009-09-02
    • Janne BrunstedtJørn Dalgaard MikkelsenHenrik PedersenJørn Borch Søe
    • Janne BrunstedtJørn Dalgaard MikkelsenHenrik PedersenJørn Borch Søe
    • C12P1/00C12N9/00C12N9/20C12N1/20C12N15/00C07H21/04
    • A21D8/042A23C19/0328A23D7/02A23K20/189A23K50/75A23L7/107A23L7/109A23L7/111A23L27/60A23L29/06C11B3/003C12N9/18C12P7/62C12P19/44C12Y301/01
    • A fungal wild-type lipolytic enzyme having a higher ratio of activity on polar lipids compared with triglycerides, wherein the enzyme preferably has a phospholipid:triglyceride activity ratio of at least 4. Preferably, the lipolytic enzyme according to the present invention has a glycolipid:triglyceride hydrolyzing activity ratio of at least 1.5. In one embodiment, the fungal lipolytic enzyme according to the present invention comprises an amino acid sequence as shown in SEQ ID NO: 1 or SEQ ID No. 2 or SEQ ID No. 4 or SEQ ID No. 6 or an amino acid sequence which has at least 90% identity thereto. The present invention further encompasses a nucleic acid encoding a fungal lipolytic enzyme, which nucleic acid is selected from the group consisting of: (a) a nucleic acid comprising a nucleotide shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7; (b) a nucleic acid which is related to the nucleotide sequence of SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7 by the degeneration of the genetic code; and (c) nucleic acid comprising a nucleotide sequence which has at least 90% identity with the nucleotide sequence shown in SEQ ID No. 3, SEQ ID No. 5 or SEQ ID No. 7.
    • 与甘油三酯相比,极性脂质活性比例更高的真菌野生型脂肪分解酶,其中所述酶优选具有至少为4的磷脂:甘油三酯活性比。优选地,根据本发明的脂肪分解酶具有糖脂: 甘油三酯水解活性比至少为1.5。 在一个实施方案中,根据本发明的真菌脂肪分解酶包含如SEQ ID NO:1或SEQ ID No.2或SEQ ID No.4或SEQ ID No.6所示的氨基酸序列或氨基酸序列, 与其具有至少90%的同一性。 本发明还包括编码真菌脂肪分解酶的核酸,该核酸选自:(a)包含SEQ ID No.3,SEQ ID No.5或SEQ ID No.5所示核苷酸的核酸 第7号 (b)通过遗传密码的退化与SEQ ID No.3,SEQ ID No.5或SEQ ID No.7的核苷酸序列有关的核酸; 和(c)核酸,其包含与SEQ ID No.3,SEQ ID No.5或SEQ ID No.7所示的核苷酸序列具有至少90%同一性的核苷酸序列。