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5-({5-[N-(6-carboxynaphthyl)carbamoyl]-3-[(4-methylphenyl)carbonylamino]-phenyl}carbonylamino)naphthalene-2-carboxylic acid | 325981-25-7

中文名称
——
中文别名
——
英文名称
5-({5-[N-(6-carboxynaphthyl)carbamoyl]-3-[(4-methylphenyl)carbonylamino]-phenyl}carbonylamino)naphthalene-2-carboxylic acid
英文别名
5-[[3-[(6-Carboxynaphthalen-1-yl)carbamoyl]-5-[(4-methylbenzoyl)amino]benzoyl]amino]naphthalene-2-carboxylic acid
5-({5-[N-(6-carboxynaphthyl)carbamoyl]-3-[(4-methylphenyl)carbonylamino]-phenyl}carbonylamino)naphthalene-2-carboxylic acid化学式
CAS
325981-25-7
化学式
C38H27N3O7
mdl
——
分子量
637.648
InChiKey
TVUAPQULUTYIQO-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):
    6.3
  • 重原子数:
    48
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.03
  • 拓扑面积:
    162
  • 氢给体数:
    5
  • 氢受体数:
    7

文献信息

  • NAPHTHYLSULFONIC ACIDS AND RELATED COMPOUNDS AS GLUCOSE UPTAKE AGONISTS
    申请人:TELIK, INC.
    公开号:EP1200396A1
    公开(公告)日:2002-05-02
  • US6653321B1
    申请人:——
    公开号:US6653321B1
    公开(公告)日:2003-11-25
  • [EN] NOVEL NAPHTHYLSULFONIC ACIDS AND RELATED COMPOUNDS AS GLUCOSE UPTAKE AGONISTS<br/>[FR] NOUVEAUX ACIDES NAPHTYLSULFONIQUES ET COMPOSES APPARENTES UTILISES COMME AGONISTES DE CAPTAGE DU GLUCOSE
    申请人:TELIK INC
    公开号:WO2001012591A1
    公开(公告)日:2001-02-22
    Methods for treating conditions associated with hyperglycemia, especially Type II diabetes, with novel naphthylsulfonic acids and related compounds are provided. Compounds of formula (1) where: R?1 and R2¿ are, independently, hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, R3 is a substituent on the B ring; and is -SO¿2OR?6, -C(O)OR6, -SO2NR62-C(O)NR62 or tetrazolyl; the linker -WY- between the naphthyl and phenyl intersects the A ring of the naphthyl and is, independently, -C(O)NR?7-, -NR7¿C(O)-, -C(O)O-, -OC(O)-, -CH=CH-, -NR7CH2-, -CH2NR?7-, -NR7C(O)NR7- -NR7¿C(O)O-, -OC(O)NR?7-, -NR7SO¿2O-, -OSO2NR7-, -OC(O)O-, -SO¿2?NR?7-, -NR7SO¿2-, -OSO2-, or -SO2O-; each R?6 and R7¿ is, independently, hydrogen or lower alkyl; optionally in the form of single stereoisomers or mixtures of stereoisomers, or the pharmaceutically acceptable salts thereof; are useful in methods of stimulating the kinase activity of the insulin receptor, enhancing the activation of the insulin receptor by insulin, and stimulating the uptake of glucose into cells. A variety of antidiabetic compounds and pharmaceutical compositions comprising the antidiabetic compounds are also disclosed.
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