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    • 3. 发明授权
    • Therapeutic substituted β-lactams
    • 治疗性取代的β-内酰胺
    • US07772392B2
    • 2010-08-10
    • US11378925
    • 2006-03-17
    • David W. OldDanny T. DinhRobert M. Burk
    • David W. OldDanny T. DinhRobert M. Burk
    • C07D205/08C07D409/06C07D405/06C07D227/087C07D403/06C07F9/568A61K31/397A61P27/06
    • C07D409/06A61K31/397C07D205/08C07D401/06C07D403/06C07D405/06
    • Compounds comprising or a pharmaceutically acceptable salt or a prodrug thereof; wherein a dashed line indicates the presence or absence of a bond; Y is an organic acid group, or an amide or ester thereof comprising from 1 to 12 carbon atoms; or Y is hydroxymethyl or an ether thereof comprising from 1 to 12 carbon atoms; or Y is a tetrazolyl group; A is —(CH2)6—, cis —CH2CH═CH—(CH2)3—, or —CH2C≡C—(CH2)3—, wherein 1 or 2 carbon atoms may be substituted with S or O; or A is —(CH2)m—Ar—(CH2)o— wherein Ar is interarylene or heterointerarylene, the sum of m and o is from 1 to 4, and wherein one CH2 may be replaced with S or O; J is CHOH, C═O, CH2CHOH, or CH2C═O; and Ar1 is aryl, heteroaryl, CH2-aryl, CH2-heteroaryl, O-aryl, O-heteroaryl, S-aryl, or S-heteroaryl.
    • 包含或其药学上可接受的盐或其前药的化合物; 其中虚线表示存在或不存在键; Y是有机酸基团,或其含有1至12个碳原子的酰胺或酯; 或Y是含有1至12个碳原子的羟甲基或其醚; 或Y为四唑基; A是 - (CH2)6-,顺式-CH2CH = CH-(CH2)3-或-CH2C≡C-(CH2)3-,其中1或2个碳原子可以被S或O取代; 或A是 - (CH 2)m -Ar-(CH 2)o - ,其中Ar是亚芳基或杂亚环烷基,m和o之和为1至4,并且其中一个CH 2可以被S或O取代; J为CHOH,C = O,CH 2 CHOH或CH 2 C = O; 和Ar 1是芳基,杂芳基,CH 2 - 芳基,CH 2 - 杂芳基,O-芳基,O-杂芳基,S-芳基或S-杂芳基。
    • 5. 发明授权
    • Therapeutic beta-lactams
    • 治疗β-内酰胺
    • US08063033B2
    • 2011-11-22
    • US12352903
    • 2009-01-13
    • David W. OldDanny T. DinhRobert M. Burk
    • David W. OldDanny T. DinhRobert M. Burk
    • C07D205/08A61K31/397A61P27/06A61P17/14C07D409/06
    • C07D409/06C07D205/08
    • Compounds comprising or a pharmaceutically acceptable salt or a prodrug thereof, are disclosed, wherein Y is A is —(CH2)6—, cis —CH2CH═CH—(CH2)3—, or —CH2C≡C—(CH2)3—, wherein 1 or 2 carbon atoms may be substituted with S or O; or A is —(CH2)m—Ar—(CH2)o— wherein Ar is substituted or unsubstituted phenyl or monocyclic heteroaryl, the sum of m and o is from 1 to 4, and wherein one CH2 may be replaced with S or O; X is S or O; R is a hydrocarbyl or a hydroxyhydrocarbyl moiety having from 1 to 12 carbon atoms; D is independently a moiety comprising from 1 to 6 non-hydrogen atoms; and n is an integer from 0 to 4. Methods, compositions, and medicaments related thereto are also disclosed.
    • 公开了包含其药学上可接受的盐或其前体药物的化合物,其中Y是A是 - (CH 2)6 - ,顺式-CH 2 CH = CH-(CH 2)3 - 或-CH 2C≡C-(CH 2) 其中1或2个碳原子可被S或O取代; 或A是 - (CH 2)m -Ar-(CH 2)o-,其中Ar是取代或未取代的苯基或单环杂芳基,m和o之和为1至4,并且其中一个CH 2可以被S或O ; X是S或O; R是具有1至12个碳原子的烃基或羟基烃基部分; D独立地为包含1至6个非氢原子的部分; 并且n是0至4的整数。还公开了与之相关的方法,组合物和药物。
    • 6. 发明授权
    • Therapeutic β-lactams
    • 内酰胺治疗
    • US07674786B2
    • 2010-03-09
    • US11569696
    • 2006-05-02
    • David W. OldDanny T. DinhRobert M. Burk
    • David W. OldDanny T. DinhRobert M. Burk
    • C07D205/09A61K31/397A61P27/06
    • C07D205/08
    • Compounds comprising: or a pharmaceutically acceptable salt or a prodrug thereof, are disclosed, wherein Y is a carboxylic acid functional group, sulfonic acid functional group, or phosphonic acid functional group; or an amide or ester thereof comprising from 0 to 12 carbon atoms; or Y is a hydroxymethyl, or tetrazolyl functional group; A is —(CH2)6—, cis —CH2CH═CH—(CH2)3—, or —CH2C≡C—(CH2)3—, wherein 1 or 2 carbon atoms may be substituted with S or O; or A is —(CH2)m—Ar—(CH2)o wherein Ar is substituted or unsubstituted phenyl or monocyclic heteroaryl, the sum of m and o is from 1 to 4, and wherein one CH2 may be replaced by with S or O; R, D, and n are as described. Methods, compositions, and medicaments related thereto are also disclosed.
    • 公开了包含:或其药学上可接受的盐或其前药的化合物,其中Y是羧酸官能团,磺酸官能团或膦酸官能团; 或其包含0至12个碳原子的酰胺或酯; 或Y是羟甲基或四唑基官能团; A是 - (CH2)6-,顺式-CH2CH = CH-(CH2)3-或-CH2C≡C-(CH2)3-,其中1或2个碳原子可以被S或O取代; 或A是 - (CH 2)m -Ar-(CH 2)o,其中Ar是取代或未取代的苯基或单环杂芳基,m和o之和为1至4,并且其中一个CH 2可以被S或O ; R,D和n如上所述。 还公开了与之相关的方法,组合物和药物。