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(S)-4-((2-methoxyethyl)(4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl)amino)-2-(quinazolin-4-ylamino)butanoic acid | 2376257-44-0

中文名称
——
中文别名
——
英文名称
(S)-4-((2-methoxyethyl)(4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl)amino)-2-(quinazolin-4-ylamino)butanoic acid
英文别名
Bexotegrast;(2S)-4-[2-methoxyethyl-[4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl]amino]-2-(quinazolin-4-ylamino)butanoic acid
(S)-4-((2-methoxyethyl)(4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl)amino)-2-(quinazolin-4-ylamino)butanoic acid化学式
CAS
2376257-44-0
化学式
C27H36N6O3
mdl
——
分子量
492.621
InChiKey
CWOFQJBATWQSHL-DEOSSOPVSA-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

物化性质

  • 沸点:
    769.7±60.0 °C(Predicted)
  • 密度:
    1.27±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    36
  • 可旋转键数:
    14
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    113
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    (S)-4-((2-methoxyethyl)(4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl)amino)-2-(quinazolin-4-ylamino)butanoic acid磷酸 作用下, 以 甲醇异丙醇 为溶剂, 生成 (S)-4-((2-methoxyethyl)(4-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)butyl)amino)-2-(quinazolin-4-ylamino)butanoic acid phosphate
    参考文献:
    名称:
    [EN] INTEGRIN INHIBITOR AND USES THEREOF
    [FR] INHIBITEUR D'INTÉGRINE ET SES UTILISATIONS
    摘要:
    Provided herein are integrin inhibitors, compositions thereof, and methods of their uses. Crystalline forms of salts of the inhibitors are also described, along with methods of preparing the crystalline forms. X-ray powder diffraction data, thermogravimetric analysis, and differential scanning calorimetry data are provided for the crystalline forms. The integrin inhibitors are useful for treatment of, inter alia, fibrotic diseases.
    公开号:
    WO2022109598A1
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文献信息

  • AMINO ACID COMPOUNDS AND METHODS OF USE
    申请人:Pliant Therapeutics, Inc.
    公开号:US20190276449A1
    公开(公告)日:2019-09-12
    The invention relates to compounds of formula (A) and formula (I): or a salt thereof, wherein R 1 , R 2 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , q and p are as described herein. Compounds of formula (A), formula (I), and pharmaceutical compositions thereof are αvβ6 integrin inhibitors that are useful for treating fibrosis such as idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP).
    该发明涉及以下化合物的公式(A)和公式(I):或其盐,其中R1、R2、R10、R11、R12、R13、R14、R15、R16、q和p如本文所述。公式(A)、公式(I)的化合物及其药物组合物是αvβ6整合素抑制剂,可用于治疗纤维化疾病,如特发性肺纤维化(IPF)和非特异性间质性肺炎(NSIP)。
  • [EN] DOSAGE FORMS AND REGIMENS FOR AMINO ACID COMPOUNDS<br/>[FR] FORMES POSOLOGIQUES ET SCHÉMAS DE TRAITEMENT POUR DES COMPOSÉS D'ACIDES AMINÉS
    申请人:PLIANT THERAPEUTICS INC
    公开号:WO2020210404A1
    公开(公告)日:2020-10-15
    The invention relates to dosage forms for daily administration of compounds of formula (A) and formula (I): or a salt thereof, wherein R1, R2, R10, R11, R12, R13, R14, R15, R16, q and p are as described herein. Compounds of formula (A), formula (I), and pharmaceutical compositions thereof are ανβ6 integrin inhibitors that are useful for treating fibrosis such as idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP),
    该发明涉及用于每日给药的化合物(A)和化合物(I)的剂型:或其盐,其中R1、R2、R10、R11、R12、R13、R14、R15、R16、q和p如本文所述。化合物(A)、化合物(I)及其药物组成物是ανβ6整合素抑制剂,可用于治疗纤维化疾病,如特发性肺纤维化(IPF)和非特异性间质性肺炎(NSIP)。
  • [EN] TREATMENT OF RESPIRATORY DISEASES WITH AMINO ACID COMPOUNDS<br/>[FR] TRAITEMENT DE MALADIES RESPIRATOIRES AVEC DES COMPOSÉS ACIDES AMINÉS
    申请人:PLIANT THERAPEUTICS INC
    公开号:WO2021225912A1
    公开(公告)日:2021-11-11
    The invention relates to methods of therapy using compounds of formula (I) and formula (II): or a salt thereof, wherein R1, R2, R10, R11, R12, R13, R14, R15, R16, q and p are as described herein. Compounds of formula (II) and pharmaceutical compositions thereof are integrin inhibitors that are useful in therapy for a condition, for example, caused by or associated with an infectious agent, shock, pancreatitis, or trauma. The condition can include one or more of pulmonary fibrosis associated with rheumatoid arthritis or progressive familial intrahepatic cholestasis (PFIC).
    该发明涉及使用化合物的疗法方法的公式(I)和公式(II):或其盐,其中R1、R2、R10、R11、R12、R13、R14、R15、R16、q和p如此处所述。公式(II)的化合物及其药物组成物是整合素抑制剂,可用于治疗某种疾病,例如由感染性因子、休克、胰腺炎或创伤引起或相关的疾病。该疾病可能包括与类风湿性关节炎或进行性家族性肝内胆汁淤积症(PFIC)相关的肺纤维化。
  • Amino acid compounds and methods of use
    申请人:Pliant Therapeutics, Inc.
    公开号:US10793564B2
    公开(公告)日:2020-10-06
    The invention relates to compounds of formula (A) and formula (I): or a salt thereof, wherein R1, R2, R10, R11, R12, R13, R14, R15, R16, q and p are as described herein. Compounds of formula (A), formula (I), and pharmaceutical compositions thereof are αvβ6 integrin inhibitors that are useful for treating fibrosis such as idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP).
    本发明涉及式(A)和式(I)化合物: 或其盐,其中 R1、R2、R10、R11、R12、R13、R14、R15、R16、q 和 p 如本文所述。式(A)、式(I)化合物及其药物组合物是αvβ6整合素抑制剂,可用于治疗纤维化,如特发性肺纤维化(IPF)和非特异性间质性肺炎(NSIP)。
  • Dosage forms and regimens for amino acid compounds
    申请人:Pliant Therapeutics, Inc.
    公开号:US11419869B2
    公开(公告)日:2022-08-23
    The invention relates to dosage forms for daily administration of compounds of formula (A) and formula (I): or a salt thereof, wherein R1, R2, R10, R11, R12, R13, R14, R15, R16, q and p are as described herein. Compounds of formula (A), formula (I), and pharmaceutical compositions thereof are αvβ6 integrin inhibitors that are useful for treating fibrosis such as idiopathic pulmonary fibrosis (IPF) and nonspecific interstitial pneumonia (NSIP).
    本发明涉及每日服用式(A)和式(I)化合物的剂型: 或其盐,其中 R1、R2、R10、R11、R12、R13、R14、R15、R16、q 和 p 如本文所述。式(A)、式(I)化合物及其药物组合物是αvβ6整合素抑制剂,可用于治疗纤维化,如特发性肺纤维化(IPF)和非特异性间质性肺炎(NSIP)。
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