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2-(3,5-dichloro-pyridin-4-yl)-1-(2-furan-2-yl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-ethanone | 1072077-71-4

中文名称
——
中文别名
——
英文名称
2-(3,5-dichloro-pyridin-4-yl)-1-(2-furan-2-yl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-ethanone
英文别名
2-(3,5-Dichloropyridin-4-yl)-1-[2-(furan-2-yl)-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl]ethanone
2-(3,5-dichloro-pyridin-4-yl)-1-(2-furan-2-yl-8-methoxy-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-ethanone化学式
CAS
1072077-71-4
化学式
C18H12Cl2N4O3
mdl
——
分子量
403.224
InChiKey
WOWDDTFMTILECG-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):
    3.3
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    82.5
  • 氢给体数:
    0
  • 氢受体数:
    6

文献信息

  • TRIAZOLOPYRIDINES AS PHOSPHODIESTERASE INHIBITORS FOR TREATMENT OF DERMAL DISEASES
    申请人:Felding Jakob
    公开号:US20100113442A1
    公开(公告)日:2010-05-06
    The present invention relates to a compound according to formula (I), wherein X and Y are either C and N or N and C; Z is CH 2 , CH 2 —CH 2 , CH 2 —NH, or NH; R 1 is halogen, or R 1 is alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, cycloalkyl, alkoxycarbonyl, aryl, all of which are optionally substituted; R 2 is hydrogen, or R 2 is alkyl, cycloalkyl, alkoxy, heterocycloalkyl, aryl, heteroaryl, alkoxycarbonyl, aminocarbonyl, amino, all of which are optionally substituted; A is aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl or heterocycloalkenyl, all of which are optionally substituted; and pharmaceutically acceptable salts, hydrates, or solvates hereof. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating diseases, e.g. dermal diseases, with said compounds, and to the use of said compounds in the manufacture of medicaments, in particular for the treatment of dermal diseases.
    本发明涉及一种化合物,其化学式为(I),其中X和Y分别为C和N或N和C;Z为CH2, - , -NH或NH;R1为卤素,或R1为烷基,烯基,炔基,卤代烷基,烷氧基,环烷基,烷氧羰基,芳基,所有这些均可选择性地被取代;R2为氢,或R2为烷基,环烷基,烷氧基,杂环烷基,芳基,杂芳基,烷氧羰基,基羰基,基,所有这些均可选择性地被取代;A为芳基,环烷基,环烯基,杂芳基,杂环烷基或杂环烯基,所有这些均可选择性地被取代;以及其药学上可接受的盐,合物或溶剂化物。本发明进一步涉及所述化合物在治疗中的应用,包括含有该化合物的制药组合物,使用该化合物治疗疾病的方法,例如皮肤疾病,并且涉及使用该化合物制造药物,特别是用于治疗皮肤疾病。
  • US8829190B2
    申请人:——
    公开号:US8829190B2
    公开(公告)日:2014-09-09
  • [EN] TRIAZOLOPYRIDINES AS PHOSPHODIESTERASE INHIBITORS FOR TREATMENT OF DERMAL DISEASES<br/>[FR] TRIAZOLOPYRIDINES COMME INHIBITEURS DE PHOSPHODIESTÉRASES POUR LE TRAITEMENT DE MALADIES DERMIQUES
    申请人:LEO PHARMA AS
    公开号:WO2008125111A1
    公开(公告)日:2008-10-23
    [EN] The present invention relates to a compound according to formula (I), wherein X and Y are either C and N or N and C; Z is CH2, CH2-CH2, CH2-NH, or NH; R1 is halogen, or R1 is alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, cycloalkyl, alkoxycarbonyl, aryl, all of which are optionally substituted; R2 is hydrogen, or R2 is alkyl, cycloalkyl, alkoxy, heterocycloalkyl, aryl, heteroaryl, alkoxycarbonyl, aminocarbonyl, amino, all of which are optionally substituted; A is aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocycloalkyl or heterocycloalkenyl, all of which are optionally substituted; and pharmaceutically acceptable salts, hydrates, or solvates hereof. The invention further relates to said compounds for use in therapy, to pharmaceutical compositions comprising said compounds, to methods of treating diseases, e.g. dermal diseases, with said compounds, and to the use of said compounds in the manufacture of medicaments, in particular for the treatment of dermal diseases.
    [FR] La présente invention porte sur un composé représenté par la formule (I), dans laquelle X et Y représentent soit C et N, soit N et C ; Z représente CH2, CH2-CH2, CH2-NHou NH ; R1 représente halogène ou R1 représente alkyle, alcényle, alcynyle, haloalkyle, alcoxy, cycloalkyle, alcoxycarbonyle, aryle, tous étant facultativement substitués ; R2 représente hydrogène ou R2 représente alkyle, cycloalkyle, alcoxy, hétérocycloalkyle, aryle, hétéroaryle, alcoxycarbonyle, aminocarbonyle, amino, tous étant facultativement substitués ; A représente aryle, cycloalkyle, cycloalcényle, hétéroaryle, hétérocycloalkyle ou hétérocycloalcényle, tous étant facultativement substitués. L'invention porte aussi sur les sels pharmaceutiquement acceptables, hydrates ou solvates de ce composé. L'invention porte en outre sur lesdits composés pour une utilisation en thérapie, sur des compositions pharmaceutiques comprenant lesdits composés, sur des procédés de traitement de maladies, par exemple des maladies dermiques, par lesdits composés, et sur l'utilisation desdits composés dans la fabrication de médicaments, en particulier pour le traitement de maladies dermiques.
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同类化合物

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