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公开(公告)号:US20210230687A1
公开(公告)日:2021-07-29
申请号:US17228477
申请日:2021-04-12
Applicant: ILLUMINA CAMBRIDGE LIMITED
Inventor: Elena Cressina , Antoine Francais , Xiaohai Liu
IPC: C12Q1/6869 , C07H19/06 , C07H21/00 , C07H19/16 , C07H19/20 , C07H19/10 , C07H19/073 , C07H19/14 , C07H21/04 , C12Q1/6809 , C12Q1/6816
Abstract: The present disclosure relates to new nucleotide and oligonucleotide compounds and their use in nucleic acid sequencing applications.
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公开(公告)号:US11059849B2
公开(公告)日:2021-07-13
申请号:US15507853
申请日:2015-09-01
Applicant: DNA Script
Inventor: Thomas Ybert , Sylvain Gariel
Abstract: A modified nucleotide, intended for the synthesis of long chain nucleic acids by enzymatic processes, comprising a “natural” nitrogenous base or a natural nitrogenous base analogue, a ribose or deoxyribose carbohydrate, and at least one phosphate group, characterized in that said nucleotide comprises at least one R group, termed the modifier group, carried by said nitrogenous base or analogue and/or by the oxygen in position 3′ of the ribose or deoxyribose molecule, making it possible to block the polymerization of said nucleotide and/or to allow the interaction of said nucleotide with another molecule, such as a protein, during the nucleic acid synthesis, R comprising at least one functional terminal group.
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公开(公告)号:US20210207192A1
公开(公告)日:2021-07-08
申请号:US17209398
申请日:2021-03-23
Applicant: ABBOTT MOLECULAR INC.
Inventor: Dae Hyun Kim
IPC: C12Q1/6806 , C12N15/10 , C07H19/20 , C07H19/10 , C07H21/04 , C12Q1/6869
Abstract: Provided herein is technology relating to the manipulation and detection of nucleic acids, including but not limited to compositions, methods, and kits related to nucleotides comprising a chemically reactive linking moiety.
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公开(公告)号:US20210196741A1
公开(公告)日:2021-07-01
申请号:US17077267
申请日:2020-10-22
Applicant: GILEAD PHARMASSET LLC
Inventor: Jinfa Du , Dhanapalan Nagarathnam , Michael Joseph Sofia , Peiyuan Wang
IPC: A61K31/7072 , A61K31/706 , A61K31/7064 , A61K31/7076 , C07H19/04 , C07H19/20 , C07H19/06 , C07H19/10 , A61K45/06 , C07H17/02 , C07D417/14
Abstract: Disclosed herein are phosphoramidate prodrugs of nucleoside derivatives for the treatment of viral infections in mammals, which is a compound, its stereoisomer, salt (acid or basic addition salt), hydrate, solvate, or crystalline form thereof, represented by the following structure: Also disclosed are methods of treatment, uses, and processes for preparing each of which utilize the compound represented by formula I.
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公开(公告)号:US20210139525A1
公开(公告)日:2021-05-13
申请号:US16959901
申请日:2019-01-07
Applicant: CERECOR, INC.
Inventor: Stephen B. Thomas , Patrick J. Crutcher , Fabrizio Pertusati , Elisa Pileggi
Abstract: The invention relates to nucleotide prodrugs and pharmaceutical preparations thereof. The invention further relates using the prodrugs of the invention in the treatment of mitochondrial DNA (mtDNA) depletion syndrome (MDS).
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公开(公告)号:US11001602B2
公开(公告)日:2021-05-11
申请号:US16171970
申请日:2018-10-26
Applicant: Roche Diagnostics Operations, Inc.
Inventor: Klaus-Peter Stengele
IPC: C07H19/20 , C07C323/19 , C07C323/32 , C07H19/02 , C07D231/12 , C07D235/28 , C07D207/16 , C07D213/70 , C07C319/14 , C07H1/00 , C07H19/06 , C07H19/10 , C07H19/16 , C07K1/04 , C07K7/08
Abstract: The present disclosure relates to photoactivable protecting groups containing a diarylsulfide chromophore, a method for the synthesis thereof and their use as photoactivable protecting groups using maskless photolithography based array synthesis.
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公开(公告)号:US10982277B2
公开(公告)日:2021-04-20
申请号:US16563443
申请日:2019-09-06
Applicant: Illumina Cambridge Limited
Inventor: Xiaohai Liu , Xiaolin Wu , Geoffrey Paul Smith
IPC: C12Q1/68 , C07H19/073 , C07H19/10 , C07H19/14 , C07H19/173 , C07H19/20 , C12Q1/6869 , C12Q1/6876
Abstract: Some embodiments described herein relate to modified nucleotide and nucleoside molecules with novel 3′-hydroxy protecting groups. Also provided herein are methods to prepare such modified nucleotide and nucleoside molecules and sequencing by synthesis processes using such modified nucleotide and nucleoside molecules.
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公开(公告)号:US10981944B2
公开(公告)日:2021-04-20
申请号:US16273843
申请日:2019-02-12
Applicant: ARCUS BIOSCIENCES, INC.
Inventor: Laurent Pierre Paul Debien , Juan Carlos Jaen , Jaroslaw Kalisiak , Kenneth V. Lawson , Manmohan Reddy Leleti , Erick Allen Lindsey , Dillon Harding Miles , Eric Newcomb , Jay Patrick Powers , Brandon Reid Rosen , Ehesan Ul Sharif
IPC: A01N43/04 , A61K31/70 , C07H19/23 , A61K31/7076 , C07H19/16 , C07H19/20 , C07H19/207 , C07F9/6561 , C07H19/04 , A61K31/706 , A61K45/06 , A61K31/7052 , A61K31/7064 , C07H19/14
Abstract: Compounds that modulate the conversion of AMP to adenosine by 5′-nucleotidase, ecto, and compositions containing the compounds and methods for synthesizing the compounds, are described herein. The use of such compounds and compositions for the treatment and/or prevention of a diverse array of diseases, disorders and conditions, including cancer- and immune-related disorders, that are mediated by 5′-nucleotidase, ecto is also provided.
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公开(公告)号:US20210087219A1
公开(公告)日:2021-03-25
申请号:US17111096
申请日:2020-12-03
Applicant: Alnylam Pharmaceuticals, Inc.
Inventor: Muthiah MANOHARAN , Kallanthottathil G. RAJEEV , Jeremy LACKEY , Jayaprakash K. NAIR
IPC: C07H21/02 , C07H21/00 , C07F9/6512 , C07F9/655 , C07F9/6558 , C07H19/20
Abstract: This invention relates to an oligonucleotide comprising one or more abasic nucleoside monomers of formula IV′: These monomers are useful for modifying of oligonucleotides at one or more positions. This invention also relates to a method of inhibiting the expression of a target gene in a cell. The method comprises contacting the cell with an oligonucleotide having one or more of the above formula (IV′).
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40.
公开(公告)号:US10953030B2
公开(公告)日:2021-03-23
申请号:US16532210
申请日:2019-08-05
Applicant: RIBOSCIENCE LLC
Inventor: Mark Smith , Klaus G. Klumpp
IPC: C07H19/20 , A61K31/7072 , A61K31/7056 , A61K31/4709 , A61K31/4184 , A61K31/4188 , A61K45/06 , A61P1/16 , A61K31/4178 , A61P31/14 , A61K31/683
Abstract: Cytidine nucleoside analogues of Formula I, wherein the variables are as described herein, in combination with uridine nucleoside analogues of Formula II, wherein the variables are as described herein, produce a synergistic effect on the inhibition of HCV polymerase.
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