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2,3,5-Trimethyl-6-(6-carboxyhexyl)-1,4-benzochinon | 58185-97-0

中文名称
——
中文别名
——
英文名称
2,3,5-Trimethyl-6-(6-carboxyhexyl)-1,4-benzochinon
英文别名
7-(2,4,5-Trimethyl-3,6-dioxocyclohexa-1,4-dien-1-yl)heptanoic acid
2,3,5-Trimethyl-6-(6-carboxyhexyl)-1,4-benzochinon化学式
CAS
58185-97-0
化学式
C16H22O4
mdl
——
分子量
278.348
InChiKey
HPJSNEGBSHYMAH-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

物化性质

  • 熔点:
    71-72 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
  • 沸点:
    427.1±24.0 °C(Predicted)
  • 密度:
    1.101±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    20
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    71.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Quinones. 4. Novel eicosanoid antagonists: synthesis and pharmacological evaluation
    作者:Mitsuru Shiraishi、Kaneyoshi Kato、Shinji Terao、Yasuko Ashida、Zenichi Terashita、Go Kito
    DOI:10.1021/jm00129a030
    日期:1989.9
    A new series of omega-phenyl-omega-quinonylalkanoic acids and related compounds was synthesized. The compounds were tested for their inhibitory effects on U-44069-induced contraction of the rabbit aorta. (+/- )-7-(3,5,6-Trimethyl-1,4-benzoquinon-2-yl)-7-phenylheptanoic acid (4d) (AA-2414) with pA2 value of 8.28 was one of the most potent compounds. Compound 4d inhibited U-46619-induced contraction of the guinea pig lung (pA2 = 8.29) and U-44069-induced aggregation of the guinea pig platelet (IC50 = 3.5 x 10(-7) M). Compound 4d displaced the binding of [3H]U-46619 to guinea pig platelets (IC50 = 7.4 x 10(-9) M). Compound 4d also showed very potent inhibitory effects with an MED of 0.3 mg/kg (po) on U-46619-, LTD4-, PAF-, or IgG1-induced bronchoconstriction in guinea pigs. The enantiomers of 4d were prepared. The R-(+) isomer 8a was active in both in vitro and in vivo tests, but the S-(-) isomer 8b was much less active. We concluded that the antiasthmatic effects of 4d were based mainly on the TXA2 receptor antagonistic action. In addition, compound 4d showed potent inhibitory effects on PGD2-, PGF2 alpha-, and 11-epi-PGF2 alpha-induced contraction of the guinea pig tracheal strips. The diverse inhibitory effects might be expressed in terms of eicosanoid-antagonistic activity.
  • OKAMOTO, KAYOKO;WATANABE, MASAZUMI;KAWADA, MITSURU;GOTO, GIICHI;ASHIDA, Y+, CHEM. AND PHARM. BULL., 1982, 30, N 8, 2797-2819
    作者:OKAMOTO, KAYOKO、WATANABE, MASAZUMI、KAWADA, MITSURU、GOTO, GIICHI、ASHIDA, Y+
    DOI:——
    日期:——
  • FR2269333
    申请人:——
    公开号:——
    公开(公告)日:——
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