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公开(公告)号:US3746730A
公开(公告)日:1973-07-17
申请号:US3746730D
申请日:1970-12-17
Applicant: HOFFMANN LA ROCHE
Inventor: MARBET R
IPC: A61K31/59 , C07C51/16 , C07C69/00 , C07C403/00 , C08H17/36
CPC classification number: C07C403/20 , A61K31/59 , C07C51/16 , C07C2601/16 , C07C57/03 , C07C57/26
Abstract: A PROCESS FOR PREPARING POLYENE ACIDS FROM POLYENE ALCOHOLS OR ESTERS THEREOF BY A SINGLE OXIDATION REACTION BY SILVER(1)OXIDE IN THE PRESENCE OF AN ALKALI.
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公开(公告)号:US3317590A
公开(公告)日:1967-05-02
申请号:US32305363
申请日:1963-11-12
Applicant: UNIVERSAL OIL PROD CO
Inventor: LOUIS SCHMERLING
IPC: C07C51/353
CPC classification number: C07C51/353 , C07C57/03 , C07C57/26 , C07C57/04 , C07C57/13
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33.
公开(公告)号:US3251869A
公开(公告)日:1966-05-17
申请号:US24825262
申请日:1962-12-31
Applicant: HERCULES POWDER CO LTD
Inventor: PUTNAM STEARNS T , SPECK RHOADS M , WEISGERBER CYRUS A
CPC classification number: C07C57/02 , C07C57/26 , C08F20/64 , C11D13/00 , Y10S526/911
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公开(公告)号:US3075010A
公开(公告)日:1963-01-22
申请号:US8337361
申请日:1961-01-18
Applicant: UNIVERSAL OIL PROD CO
Inventor: LOUIS SCHMERLING , TOEKELT WALTER G
IPC: C07C51/353 , C07C51/41 , C07C53/126 , C07C57/03 , C07C57/26 , C07C57/30
CPC classification number: C07C57/30 , C07C51/353 , C07C51/41 , C07C53/126 , C07C57/03 , C07C57/26 , Y02P20/582
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公开(公告)号:US2352606A
公开(公告)日:1944-07-04
申请号:US28740839
申请日:1939-07-29
Applicant: KURT ALDER , ERWIN WINDEMUTH
Inventor: KURT ALDER , ERWIN WINDEMUTH
CPC classification number: C07C35/22 , C07C17/30 , C07C29/44 , C07C29/46 , C07C35/28 , C07C41/30 , C07C51/353 , C07C209/60 , C07C253/30 , C07C331/22 , C07C2601/16 , C07C2602/42 , C07C2603/88 , C07C22/02 , C07C211/25 , C07C255/31 , C07C33/14 , C07C33/34 , C07C43/23 , C07C57/26
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公开(公告)号:US20180327343A1
公开(公告)日:2018-11-15
申请号:US15977638
申请日:2018-05-11
Applicant: Samantha E. Shockley , John C. Hethcox , Brian M. Stoltz
Inventor: Samantha E. Shockley , John C. Hethcox , Brian M. Stoltz
IPC: C07C51/08 , C07C57/03 , C07C67/22 , C07C69/52 , C07C231/18 , C07C233/09 , B01J31/12 , B01J31/18
CPC classification number: C07C51/08 , B01J31/12 , B01J31/122 , B01J31/186 , B01J2231/44 , B01J2531/827 , C07B2200/07 , C07C57/03 , C07C67/00 , C07C67/22 , C07C69/52 , C07C201/12 , C07C231/18 , C07C233/09 , C07C253/30 , C07C2601/14 , C07C2601/16 , C07C255/38 , C07C205/57 , C07C57/42 , C07C57/60 , C07C59/48 , C07C57/26 , C07C69/65
Abstract: The present disclosure provides methods for enantioselective synthesis of acyclic α-quaternary carboxylic acid derivatives via iridium-catalyzed allylic alkylation.
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公开(公告)号:US09732056B2
公开(公告)日:2017-08-15
申请号:US14854705
申请日:2015-09-15
Applicant: Givaudan, S.A.
Inventor: Fridtjof Schröder , Urs Mueller , Jurg Daniel Oetiker
IPC: C07C403/20 , C07C69/608 , C07C51/38 , C07C57/26 , C07C67/475 , C07C67/32 , C07D307/92
CPC classification number: C07D307/92 , C07C51/38 , C07C57/26 , C07C67/32 , C07C67/475 , C07C69/608 , C07C403/20 , C07C2601/14 , C07C2601/16 , C07C2602/48
Abstract: Compounds of the formula 1 wherein, R is hydrogen, alkyl or substituted alkyl, aryl or substituted aryl, are useful intermediates in the synthesis of fragrance ingredients such as Ambrox 2
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38.
公开(公告)号:US20170112792A1
公开(公告)日:2017-04-27
申请号:US15126714
申请日:2015-03-19
Applicant: Beth Israel Deaconess Medical Center, Inc.
Inventor: Kun Ping LU , Xiao Zhen ZHOU , Shuo WEI
IPC: A61K31/203 , A61K45/06 , C12Q1/533 , C07C57/26
CPC classification number: A61K31/203 , A61K38/21 , A61K45/06 , C07C57/26 , C12Q1/533 , G01N2333/99 , G01N2500/04 , G01N2800/24 , G01N2800/307 , G01N2800/7028 , G16B35/00 , G16C20/60 , Y02A50/414 , A61K2300/00
Abstract: The invention features all-trans retinoic acid (ATRA)-related compounds capable of associating with Pin1 and methods of identifying the same. The invention also provides methods of treating a condition selected from the group consisting of a proliferative disorder, an autoimmune disease, and an addiction condition characterized by elevated Pin1 marker levels, Pin1 degradation, and/or reduced Pin1 Ser71 phosphorylation in a subject by administering a retinoic acid compound. Additionally, the invention features methods of treating proliferative disorders, autoimmune diseases, and addiction conditions (e.g., diseases, disorders, and conditions characterized by elevated Pin1 marker levels) by administering a retinoic acid compound in combination with another therapeutic compound. The invention also features a co-crystal including Pin1 and a retinoic acid compound. Finally, the invention also provides methods of developing and identifying enhanced Pin1-targeted ATRA-related compounds based on the newly defined unique binding pockets in the Pin1 active site revealed from the co-crystal structure, structure-activity relationship, and structural modeling.
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公开(公告)号:US20160151322A1
公开(公告)日:2016-06-02
申请号:US14982476
申请日:2015-12-29
Applicant: MEIJI SEIKA KAISHA, LTD.
Inventor: Ken Chikauchi , Mizuyo Ida , Takao Abe , Yukiko Hiraiwa , Akihiro Morinaka , Toshiaki Kudo
IPC: A61K31/225 , C07C69/618 , A61K31/235 , C07C69/608 , A61K31/215 , C07D213/55 , A61K31/4406 , C07D295/15 , A61K31/4453 , C07D211/46 , A61K31/445 , C07C69/732 , C07C69/734 , C07C323/54 , C07D295/16 , A61K31/5375 , A61K31/495 , C07C235/84 , A61K31/166 , C07D233/60 , A61K31/4164 , C07D207/12 , A61K31/40 , C07C279/14 , A61K31/24 , C07D309/06 , A61K31/351 , C07C69/60
CPC classification number: A61K31/225 , A61K31/166 , A61K31/194 , A61K31/215 , A61K31/235 , A61K31/24 , A61K31/351 , A61K31/40 , A61K31/407 , A61K31/4164 , A61K31/4406 , A61K31/445 , A61K31/4453 , A61K31/495 , A61K31/5375 , A61K31/546 , A61K45/06 , C07C51/00 , C07C57/13 , C07C57/145 , C07C57/26 , C07C57/42 , C07C57/50 , C07C59/52 , C07C59/64 , C07C59/70 , C07C69/593 , C07C69/60 , C07C69/608 , C07C69/618 , C07C69/732 , C07C69/734 , C07C217/22 , C07C233/65 , C07C235/20 , C07C235/84 , C07C237/22 , C07C279/08 , C07C279/14 , C07C323/54 , C07C2601/08 , C07C2601/14 , C07C2602/08 , C07D207/12 , C07D211/46 , C07D211/60 , C07D213/55 , C07D213/80 , C07D233/60 , C07D295/15 , C07D295/16 , C07D295/192 , C07D309/06 , Y02A50/473 , Y02A50/475 , A61K2300/00
Abstract: A new metallo-β-lactamase inhibitor which acts as a medicament for inhibiting the inactivation of β-lactam antibiotics and recovering anti-bacterial activities is disclosed. The maleic acid derivatives having the general formula (I) have metallo-β-lactamase inhibiting activities. It is possible to recover the anti-bacterial activities of β-lactam antibiotics against metallo-β-lactamase producing bacteria by combining the compound of the general formula (I) with β-lactam antibiotics.
Abstract translation: 公开了一种新的金属 - β-内酰胺酶抑制剂,其用作抑制β-内酰胺抗生素灭活和回收抗细菌活性的药物。 具有通式(I)的马来酸衍生物具有金属 - β-内酰胺酶抑制活性。 通过将通式(I)的化合物与β-内酰胺抗生素结合,可以回收抗β-生物反相抗生素对产生金属 - β-内酰胺酶的细菌的抗菌活性。
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公开(公告)号:US20160096817A1
公开(公告)日:2016-04-07
申请号:US14846016
申请日:2015-09-04
Applicant: Allergan, Inc.
Inventor: Yariv Donde , Jeremiah H. Nguyen , Karen M. Kedzie , Daniel W. Gil , John E. Donello , Wha-Bin Im
IPC: C07D333/56 , C07C57/26 , C07C57/48 , C07C69/738
CPC classification number: C07D333/56 , A61K31/557 , A61K31/5575 , A61K31/559 , C07C57/26 , C07C57/48 , C07C59/90 , C07C69/732 , C07C69/738 , C07D333/62 , C07D409/08
Abstract: Disclosed herein is a method comprising administering a compound to a mammal suffering from an inflammatory bowel disease for the treatment of said disease, said compound having a structure according to Formula I wherein X, Y, B, R2, R3, R4, R5, R6 and n have the meanings found herein.
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