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Adeninnicotinat | 2574-36-9

中文名称
——
中文别名
——
英文名称
Adeninnicotinat
英文别名
7H-purin-6-amine;pyridine-3-carboxylic acid
Adeninnicotinat化学式
CAS
2574-36-9
化学式
C5H5N5*C6H5NO2
mdl
——
分子量
258.239
InChiKey
XVTDSQJAFPHQGF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.71
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    131
  • 氢给体数:
    3
  • 氢受体数:
    7

文献信息

  • [EN] PYRIDINYL DERIVATIVES AS INHIBITORS OF ENZYME NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE<br/>[FR] DÉRIVÉS DE PYRIDINYLE UTILISÉS EN TANT QU'INHIBITEURS DE L'ENZYME NICOTINAMIDE PHOSPHORIBOSYLTRANSFÉRASE
    申请人:TOPOTARGET AS
    公开号:WO2010142735A1
    公开(公告)日:2010-12-16
    The present application discloses a compound of the formula (I) wherein Q is optionally substituted pyridyl; p is 0-6; Y is formulae (i), (ii) and (iii) where X is =O, =S and =N-CN, r is 1-12, R is -Z-A, Z is a single bond, -S(=O)2-, >P=O, >C=O, -C(=O)NH-, and -C(=S)NH-; and A is hydrogen, C1-12-alkyl, C3-12-cycloalkyl, - [CH2CH2O]1-10-(C1-6-alkyl), C1-12-alkenyl, aryl, heterocyclyl, and heteroaryl; B is a single bond, -NRN-, -S(=O)2- and -O-; wherein RN is selected from hydrogen, C1-12-alkyl, C3-12-cycloalkyl, -[CH2CH2O]1-10-(C1-6-alkyl), C1-12-alkenyl, aryl, heterocyclyl, and heteroaryl; s is 0-6; and Cy is aryl, cycloalkyl, heterocyclyl, and heteroaryl. The compounds are usefuld for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT).
    本申请公开了一种化合物,其化学式为(I),其中Q是可选择取代的吡啶基;p为0-6;Y是式(i)、(ii)和(iii),其中X为=O、=S和=N-CN,r为1-12,R为-Z-A,Z为单键,-S(=O)2-,>P=O,>C=O,-C(=O)NH-和-C(=S)NH-;A为氢、C1-12-烷基、C3-12-环烷基、-[CH2CH2O]1-10-(C1-6-烷基)、C1-12-烯基、芳基、杂环烷基和杂芳基;B为单键,-NRN-,-S(=O)2-和-O-;其中RN从氢、C1-12-烷基、C3-12-环烷基、-[CH2CH2O]1-10-(C1-6-烷基)、C1-12-烯基、芳基、杂环烷基和杂芳基中选择;s为0-6;Cy为芳基、环烷基、杂环烷基和杂芳基。这些化合物可用作治疗由烟酰胺磷酸核糖转移酶(NAMPRT)平升高引起的疾病或症状的药物。
  • [EN] SQUARIC ACID DERIVATIVES AS INHIBITORS OF THE NICOTINAMIDE<br/>[FR] DÉRIVÉS DE L'ACIDE SQUARIQUE UTILISÉS COMME INHIBITEURS DU NICOTINAMIDE
    申请人:TOPOTARGET AS
    公开号:WO2009156421A1
    公开(公告)日:2009-12-30
    The present application discloses novel squaric acid derivatives of the formula A: from -C(=O)-, -S(=O)2-, -C(=S)- and -P(=O)(R5)-; B: -, -O-, -NR6- and -C(=O)-NR6-; D : -, -O-, -CR7R8- and -NR9; m=0-12; n = 0-12; m+n = 1-20; p=0-2; R1 : heteroaryl, aryl; R2 : H, C1-12-alkyl, C3-12-cycloalkyl, -[CH2CH2O]1-10-(C1-6-alkyl),C1-12-alkenyl, aryl, heterocyclyl, heteroaryl; R3 : C1-12-alkyl, C3-12-cycloalkyl, -[CH2CH2O]1-10-(C1-6-alkyl), C1-12-alkenyl, aryl, heterocyclyl, heteroaryl; or R2 and R3 : N-containing heterocyclic/heteroaromatic ring; R4 and R4* : H, C1-12-alkyl, C1-12-alkenyl; and pharmaceutically acceptable salts and prodrugs thereof, and their use in the treatment of diseases/conditions caused by an elevated level of NAMPRT (inflammatory and tissue repair disorders, particularly rheumatoid arthritis, inflammatory bowel disease, asthma and CPOD, osteoarthritis, osteoporosis and fibrotic diseases; dermatosis; autoimmune diseases including systemic lupus erythematosis, multiple sclerosis, psoriatic arthritis, ankylosing spondylitis, tissue and organ rejection, Alzheimer's disease, stroke, atherosclerosis, restenosis, diabetes, glomerulonephritis, cancer, cachexia, inflammation associated with infection and viral infections, adult respiratory distress syndrome, ataxia telengiectasia).
    本申请公开了公式A的新颖方酸生物:来自-C(=O)-,-S(=O)2-,-C(=S)-和-P(=O)(R5)-;B:-,-O-,-NR6-和-C(=O)-NR6-;D:-,-O-,-CR7R8-和-NR9;m=0-12;n=0-12;m+n=1-20;p=0-2;R1:杂环烷基,芳基;R2:H,C1-12-烷基,C3-12-环烷基,-[CH2CH2O]1-10-(C1-6-烷基),C1-12-烯基,芳基,杂环烷基,杂环芳基;R3:C1-12-烷基,C3-12-环烷基,-[CH2CH2O]1-10-(C1-6-烷基),C1-12-烯基,芳基,杂环烷基,杂环芳基;或R2和R3:含氮杂环/杂芳环;R4和R4*:H,C1-12-烷基,C1-12-烯基;以及其药学上可接受的盐和前药,以及它们在治疗由NAMPRT平升高引起的疾病/症状中的用途(炎症和组织修复紊乱,特别是类风湿关节炎,炎症性肠病,哮喘和CPOD,骨关节炎,骨质疏松症和纤维化疾病;皮肤病;自身免疫疾病,包括系统性红斑狼疮,多发性硬化,屑病性关节炎,强直性脊柱炎,组织和器官排斥,阿尔茨海默病,中风,动脉粥样硬化,再狭窄,糖尿病,肾小球肾炎,癌症,虚弱,与感染和病毒感染相关的炎症,成人呼吸窘迫综合征,遗传性毛细血管扩张症)。
  • [EN] NOVEL CYANOGUANIDINES<br/>[FR] NOUVELLES CYANOGUANIDINES
    申请人:TOPOTARGET AS
    公开号:WO2009086835A1
    公开(公告)日:2009-07-16
    This application discloses novel cyanoguanidines of the formula (I) wherein A is selected from -C(=O)-, -S(=O)2-, -C(=S)-, and -P(=O)(R5)-, wherein R5 is selected from C1-6-alkyl, C1-6-alkoxy, and hydroxy; B is selected from a single bond, -O-, -NR6- and -C(=O)-NR6-, wherein R6 is selected from hydrogen, optionally substituted C1-12-alkyl, optionally substituted C1-12-alkenyl, optionally substituted aryl, optionally substituted heterocyclyl, and optionally substituted heteroaryl; and m is an integer of 0-12 and n is an integer of 0-12, wherein the sum m+n is 1-20; and R1 is selected from optionally substituted heteroaryl; and pharmaceutically acceptable salts thereof, and prodrugs thereof. The compounds are usefuld for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT).
    该申请公开了一种新型啶化合物,其化学式为(I),其中A从-C(=O)-,-S(=O)2-,-C(=S)-和-P(=O)(R5)-中选择,其中R5选择自C1-6-烷基,C1-6-烷氧基和羟基;B从单键,-O-,-NR6-和-C(=O)-NR6-中选择,其中R6选择自氢,可选择地取代的C1-12-烷基,可选择地取代的C1-12-烯基,可选择地取代的芳基,可选择地取代的杂环烷基和可选择地取代的杂环芳基;m为0-12的整数,n为0-12的整数,其中m+n之和为1-20;R1选择自可选择地取代的杂环芳基;以及其药学上可接受的盐和前药。这些化合物可用作治疗由烟酰胺磷酸核糖转移酶(NAMPRT)平升高引起的疾病或病况的药物。
  • [EN] SIRT1 ACTIVATING COMPOUNDS<br/>[FR] COMPOSÉS D'ACTIVATION DE SIRT1
    申请人:HARVARD COLLEGE
    公开号:WO2020081654A1
    公开(公告)日:2020-04-23
    Provided herein are methods and compositions for preventing or treating aging, or an aging-related disorder, a disorder associated with inflammation, or for modulating an immune response in a subject in need thereof. In some embodiments, the methods comprise administering to the subject an effective amount of a compound of Formulas I-XIII.
    本文提供了用于预防或治疗衰老、衰老相关疾病、与炎症相关的疾病或调节需要者免疫反应的方法和组合物。在某些实施例中,这些方法包括向受试者施用化合物I-XIII的有效量。
  • [EN] PYRIDINYL DERIVATIVES COMPRISING A CYANOGUANIDINE OR SQUARIC ACID MOIETY<br/>[FR] DÉRIVÉS DE PYRIDINYLE COMPRENANT UN GROUPEMENT CYANOGUANIDINE OU ACIDE SQUARIQUE
    申请人:TOPOTARGET AS
    公开号:WO2011121055A1
    公开(公告)日:2011-10-06
    The present application discloses compounds of the formula (I) wherein X = opt.subst. pyrid-3-yl or pyrid-4-yl; Q = opt.subst. Ci-6 alkylene or a single bond; Y is formula (i) wherein D is = N-CN, or formula (ii) B = is opt.subst. C1-6 alkylene; A = (formula) Z = -J-V, wherein J = -C(=0)-, -C(=O)-O, -S(=O)2-, -P(=O)(OR4)-, -C(=O)-NR4- and -C(=S)-NR4-, and V = opt.subst. C1-12-alkyl, opt.subst. C3-12-cycloalkyl, -[CH2CH2O]1-10-( opt.subst. C1-6-alkyl), opt.subst. C1-12- alkenyl, opt.subst. aryl, opt.subst. heterocyclyl, or opt.subst. heteroaryl; q = 0-2, and r = 0- 2; and pharmaceutically acceptable salts thereof, and prodrugs thereof. The application also discloses the compound for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT), e.g. inflammatory and tissue repair disorders; dermatosis; autoimmune diseases, Alzheimer's disease, stroke, athersclerosis, restenosis, diabetes, glomerulonephritis, cancer, cachexia, inflammation associated with infection and certain viral infections, including Acquired Immune Deficiency Syndrome (AIDS), adult respiratory distress syndrome, ataxia telengiectasia.
    本申请公开了以下式(I)的化合物,其中X = opt.subst.吡啶-3-基或吡啶-4-基; Q = opt.subst. Ci-6烷基或单键; Y是式(i),其中D = N-CN,或式(ii)中的B = opt.subst. C1-6烷基; A = (式) Z = -J-V,其中J = -C(=0)-,-C(=O)-O,-S(=O)2-,-P(=O)(OR4)-,-C(=O)-NR4-和-C(=S)-NR4-,V = opt.subst. C1-12-烷基,opt.subst. C3-12-环烷基,-[CH2CH2O]1-10-(opt.subst. C1-6-烷基),opt.subst. C1-12-烯基,opt.subst. 芳基,opt.subst. 杂环烷基,或opt.subst. 杂环芳基; q = 0-2,r = 0-2; 及其药学上可接受的盐和前药。该申请还公开了该化合物用作治疗由烟酰胺磷酸核糖转移酶(NAMPRT)平升高引起的疾病或病症的药物,例如炎症和组织修复紊乱; 皮肤病; 自身免疫疾病,阿尔茨海默病,中风,动脉粥样硬化,再狭窄,糖尿病,肾小球肾炎,癌症,虚弱症,与感染和某些病毒感染相关的炎症,包括获得性免疫缺陷综合症(AIDS),成人呼吸窘迫综合征,遗传性毛细血管扩张。
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