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公开(公告)号:US20170218001A1
公开(公告)日:2017-08-03
申请号:US15313049
申请日:2015-05-22
Applicant: University College Cork , Katholieke Universiteit Leuven
Inventor: Anita MAGUIRE , Alan Ford , Jan BALZARINI , Wim DEHAEN
IPC: C07F9/6561 , C07F9/6558 , C07F9/6512
CPC classification number: C07F9/65616 , C07F9/6512 , C07F9/65583
Abstract: The present invention relates to a compound of formula (I), or a pharmaceutically acceptable salt or prodrug thereof, and their use in medicine particular as anti-viral agents; wherein: X is selected from O and NR11; Y is selected from O, S and NR12; A is selected from —(CR1R2)n-, —(CR9R10)—, —(CR9R10)—(CR1R2)n-, —(CR1R3)—(CR2R4)—(CR1R2)n-, —CR3═CR4—(CR1R2)n- and —C≡C—(CR1R2)n-; R1 and R2 are independently selected from H, alkyl, hydroxyl, hydroxymethyl and halogen; R3 and R4 are independently selected from H and alkyl, or R3 and R4 together with the carbon atoms to which they are attached form a mono or bicyclic ring system selected from cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl and heteroaryl; R5 is selected from H, P(═O)(OH)2 and P(═O)(OH)—O—P(═O)(OH)2; R6 is selected from H and alkyl; R7 and R8 are independently selected from H, alkyl, halogen and hydroxymethyl R9 and R19 together with the carbon atoms to which they are attached form a mono or bicyclic ring system selected from cycloalkyl, cycloalkenyl, heterocycloalkyl and heterocycloalkenyl; R11 is selected from H and alkyl; R12 is selected from H and alkyl; m is 0, 1, 2 or 3; n is 1, 2 or 3; p is 0 or 1; q is 0, 1, 2 or 3; r is 0, 1, 2, 3, 4 or 5; s is 0 or 1; Base is a natural or non-natural nucleobase, and wherein each alkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl and heteroaryl may be optionally substituted as described herein.
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公开(公告)号:US20240293391A1
公开(公告)日:2024-09-05
申请号:US18567504
申请日:2022-06-24
Applicant: Katholieke Universiteit Leuven
Inventor: Wim DEHAEN , Steven DE JONGHE , Dominique SCHOLS , Tom VAN LOY
IPC: A61K31/4725 , A61K31/47 , A61K31/4709 , A61P31/18 , C07D215/06 , C07D401/12
CPC classification number: A61K31/4725 , A61K31/47 , A61K31/4709 , A61P31/18 , C07D215/06 , C07D401/12
Abstract: The invention relates to isoquinoline and pyridine based CXCR4 antagonists and their use in the treatment and prevention of viral infections such as HIV.
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