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    • 35. 发明申请
    • METHOD FOR REDUCING MERCAPTANS IN HYDROCARBONS
    • 减少碳氢化合物的方法
    • WO2012057935A3
    • 2012-06-14
    • PCT/US2011052155
    • 2011-09-19
    • CHEVRON USA INCHE ZUNQINGZHOU ZHENLI LIN
    • HE ZUNQINGZHOU ZHENLI LIN
    • C10G27/02C10G27/06C10G31/08C10G33/00C10L1/04
    • C10G27/02C10G27/06C10G33/00C10G2300/1033C10G2300/202C10G2400/08
    • A method for reducing mercaptan concentration in a liquid hydrocarbon, comprising: contacting a mercaptan-rich liquid hydrocarbon having a first concentration of mercaptan sulfur with a composition comprising an oxidizing agent and water wherein the molar ratio of the oxidizing agent to mercaptan sulfur in the mercaptan-rich liquid hydrocarbon is from 3:1 to 10:1; and separating the water from the liquid hydrocarbon to yield a mercaptan-depleted liquid hydrocarbon having a second concentration of mercaptan sulfur, the second concentration being less than the first concentration; wherein a major amount of mercaptan compounds in the mercaptan-rich liquid hydrocarbon are converted to at least one sulfur oxoacid or salt thereof, having the formula: [RSOx]nY wherein R is a hydrocarbyl group; x is an integer from 1 to 3; n is 1 or 2; and Y is hydrogen, an alkaline metal, or alkaline earth metal.
    • 一种用于降低液体烃中硫醇浓度的方法,包括:使具有第一浓度的硫醇硫的富硫醇液体烃与包含氧化剂和水的组合物接触,其中硫醇中的氧化剂与硫醇的摩尔比 富液体烃为3:1至10:1; 并从液态烃中分离出水,得到具有第二浓度的硫醇硫的硫醇贫乏液体烃,第二浓度小于第一浓度; 其中所述富硫醇溶液中的主要量的硫醇化合物被转化成至少一种具有下式的硫代酸或其盐:其中R是烃基的[RSO x] n Y; x是1至3的整数; n为1或2; Y是氢,碱金属或碱土金属。
    • 38. 发明申请
    • 4-AMINOTHIAZOLE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF CYCLIN-DEPENDENT KINASES
    • 4-氨基噻唑衍生物,它们的制备及其作为依赖于细胞周期蛋白依赖性激酶的抑制剂的用途
    • WO9921845A2
    • 1999-05-06
    • PCT/US9822809
    • 1998-10-27
    • AGOURON PHARMACHONG WESLEY K MCHU SHAO SONGDUVADIE ROHIT RLI LINXIAO WEIYANG YI
    • CHONG WESLEY K MCHU SHAO SONGDUVADIE ROHIT RLI LINXIAO WEIYANG YI
    • C07D277/20A61K31/426A61K31/427A61K31/4439A61K31/454A61K31/496A61K31/551A61P35/00A61P43/00C07D213/00C07D235/00C07D277/42C07D277/56C07D333/00C07D417/06C07D417/12C07D417/14C07D521/00A61K31/425A61K31/44A61K31/47A61K31/50
    • C07D231/12C07D233/56C07D249/08C07D277/42C07D417/06C07D417/12C07D417/14
    • This invention is directed to aminothiazole compounds of formula (I) wherein R is a substituted or unsubstituted group selected from: C1-6-alkyl; C1-6-alkenyl; C1-6-alkynyl; C1-6-alkoxyl; C1-6-alcohol; carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, cycloalkyl; carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, aryl; carbonyl; ether; (C1-6-alkyl)-carbonyl; (C1-6-alkyl)-aryl; (C1-6-alkyl)-cycloalkyl; (C1-6-alkyl)-(C1-6-alkoxyl); aryl-(C1-6-alkoxyl); thioether; thiol; and sulfonyl; wherein when R is substituted, each substituent independently is a halogen; haloalkyl; C1-6-alkyl; C1-6-alkenyl; C1-6-alkynyl; hydroxyl; C1-6-alkoxyl; amino; nitro; thiol; thioether; imine; cyano; amido; phosphonato; phosphine; carboxyl; thiocarbonyl; sulfonyl; sulfonamide; ketone; aldehyde; ester; oxygen; carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, cycloalkyl; or carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, aryl; and R is a carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, ring structure having a substituent at the position adjacent to the point of attachment, which ring structure is optionally further substituted, where each substituent of R independently is a halogen; haloalkyl; C1-6-alkyl; C1-6-alkenyl; C1-6-alkynyl; hydroxyl; C1-6-alkoxyl; amino; nitro; thiol; thioether; imine; cyano; amido; phosphonato; phosphine; carboxyl; thiocarbonyl; sulfonyl; sulfonamide; ketone; aldehyde; ester; oxygen; carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, cycloalkyl; or carbocyclic or heterocyclic, monocyclic or fused or non-fused polycyclic, aryl; or a pharmaceutically acceptable salt of a compound of formula (I), or a prodrug or pharmaceutically active metabolite of a compound of formula (I) or pharmaceutically acceptable salt thereof, for inhibiting cyclin-dependent kinases (CDKs), such as CDK1, CDK2, CDK4, and CDK6. The invention is also directed to the therapeutic or prophylactic use of pharmaceutical compositions containing such compounds and to methods of treating malignancies and other disorders by administering effective amounts of such compounds.
    • 本发明涉及式(I)的氨基噻唑化合物,其中R 1是取代或未取代的选自以下的基团:C 1-6 - 烷基; C 1-6 - 链烯基; C 1-6 - 炔基; C 1-6 - 烷氧基取代; C 1-6 - 醇; 碳环或杂环,单环或稠合或非稠合多环,环烷基; 碳环或杂环,单环或稠合或非稠合多环,芳基; 羰; 醚; (C 1-6 - 烷基)羰基; (C 1-6 - 烷基) - 芳基; (C 1-6 - 烷基) - 环烷基; (C 1-6 - 烷基) - (C 1-6 - 烷氧基); 芳基 - (C 1-6 - 烷氧基); 硫醚; 巯基; 和磺酰基; 其中当R 1被取代时,每个取代基独立地为卤素; 卤代; C 1-6 - 烷基; C 1-6 - 链烯基; C 1-6 - 炔基; 羟; C 1-6 - 烷氧基取代; 氨基; 硝基; 巯基; 硫醚; 亚胺; 氰基; 酰胺基; 膦酸; 膦; 羧基; 硫代羰基; 磺酰基; 磺胺; 酮; 醛; 酯; 氧; 碳环或杂环,单环或稠合或非稠合多环,环烷基; 或碳环或杂环,单环或稠合或非稠合的多环芳基; 并且R 2是碳环或杂环的单环或稠合或非稠合的多环环结构,其在与连接点相邻的位置上具有取代基,该环结构任选进一步被取代,其中R 2的每个取代基 >独立地为卤素; 卤代; C 1-6 - 烷基; C 1-6 - 链烯基; C 1-6 - 炔基; 羟; C 1-6 - 烷氧基取代; 氨基; 硝基; 巯基; 硫醚; 亚胺; 氰基; 酰胺基; 膦酸; 膦; 羧基; 硫代羰基; 磺酰基; 磺胺; 酮; 醛; 酯; 氧; 碳环或杂环,单环或稠合或非稠合多环,环烷基; 或碳环或杂环,单环或稠合或非稠合的多环芳基; 或式(I)化合物的药学上可接受的盐,或式(I)化合物或其药学上可接受的盐的前药或药学活性代谢物用于抑制细胞周期蛋白依赖性激酶(CDK)如CDK1,CDK2 ,CDK4和CDK6。 本发明还涉及含有这些化合物的药物组合物的治疗或预防用途以及通过施用有效量的这些化合物治疗恶性肿瘤和其他病症的方法。
    • 39. 发明申请
    • CONTROL CIRCUIT FOR CONTROLLING THE MAXIMUM OUTPUT CURRENT OF POWER CONVERTER AND METHOD THEREOF
    • 用于控制功率转换器的最大输出电流的控制电路及其方法
    • US20130063986A1
    • 2013-03-14
    • US13611091
    • 2012-09-12
    • TA-YUNG YANGLI LINYUE-HONG TANGJUNG-SHENG CHEN
    • TA-YUNG YANGLI LINYUE-HONG TANGJUNG-SHENG CHEN
    • H02M3/335
    • H02M3/33507H02M2001/0003
    • A control circuit of the power converter according to the present invention comprises a feedback circuit, an output circuit and an adaptive clamping circuit. The feedback circuit generates a feedback signal in accordance with an output of the power converter. The output circuit generates a switching signal in accordance with the feedback signal for regulating the output of the power converter. The adaptive clamping circuit limits the level of the feedback signal under a first level for a first load condition. The feedback circuit determines a slew rate of the feedback signal for increasing the level of the feedback signal from the first level to a second level. The adaptive clamping circuit is disabled and the level of the feedback signal can be increased to the second level for a second load condition.
    • 根据本发明的功率转换器的控制电路包括反馈电路,输出电路和自适应钳位电路。 反馈电路根据功率转换器的输出产生反馈信号。 输出电路根据用于调节功率转换器的输出的反馈信号产生开关信号。 自适应钳位电路在第一负载条件下将反馈信号的电平限制在第一电平。 反馈电路确定用于将反馈信号的电平从第一电平增加到第二电平的反馈信号的转换速率。 自适应钳位电路被禁用,并且反馈信号的电平可以在第二负载条件下增加到第二电平。
    • 40. 发明申请
    • METHOD AND APPARATUS FOR A LED DRIVER WITH HIGH POWER FACTOR
    • 用于具有高功率因数的LED驱动器的方法和装置
    • US20120081039A1
    • 2012-04-05
    • US13073095
    • 2011-03-28
    • TA-YUNG YANGLI LINCHIH-HSIEN HSIEHCHUH-CHING LICHI-YIN LOKUO-HSIEM HUANG
    • TA-YUNG YANGLI LINCHIH-HSIEN HSIEHCHUH-CHING LICHI-YIN LOKUO-HSIEM HUANG
    • H05B37/02
    • H05B33/0815
    • A control circuit of a LED driver according to the present invention comprises an output circuit, an input circuit and an input-voltage detection circuit. The output circuit generates a switching signal to produce an output current for driving at least one LED in response to a feedback signal. The switching signal is coupled to switch a transformer. The input circuit samples an input signal for generating the feedback signal. The input signal is correlated to the output current of the LED driver. The input-voltage detection circuit generates an input-voltage signal in response to an input voltage of the LED driver. The input circuit will not sample the input signal when the input-voltage signal is lower than a threshold. The control circuit can eliminate the need of the input capacitor for improving the reliability of the LED driver.
    • 根据本发明的LED驱动器的控制电路包括输出电路,输入电路和输入电压检测电路。 输出电路产生开关信号以产生用于响应于反馈信号驱动至少一个LED的输出电流。 开关信号被耦合以切换变压器。 输入电路对输入信号进行采样以产生反馈信号。 输入信号与LED驱动器的输出电流相关。 输入电压检测电路根据LED驱动器的输入电压产生输入电压信号。 当输入电压信号低于阈值时,输入电路不会对输入信号进行采样。 控制电路可以消除输入电容器的需要,提高LED驱动器的可靠性。