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(1s,2s,5s)-7-Oxo-6-oxabicyclo[3.2.1]octane-2-carboxylic acid | 851000-67-4

中文名称
——
中文别名
——
英文名称
(1s,2s,5s)-7-Oxo-6-oxabicyclo[3.2.1]octane-2-carboxylic acid
英文别名
——
(1s,2s,5s)-7-Oxo-6-oxabicyclo[3.2.1]octane-2-carboxylic acid化学式
CAS
851000-67-4
化学式
C8H10O4
mdl
——
分子量
170.16
InChiKey
BGLPRPUMBVYBPY-ZLUOBGJFSA-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):
    0.3
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    卡特缩合剂(1s,2s,5s)-7-Oxo-6-oxabicyclo[3.2.1]octane-2-carboxylic acidN-苯基哌嗪N,N-二甲基甲酰胺N,N-二异丙基乙胺 在 silica gel 、 乙酸乙酯 、 hexanes 作用下, 反应 16.08h, 生成 (1s,2s,5s)-2-[(4-Phenylpiperazin-1-yl)carbonyl]-6-oxabicyclo[3.2.1]octan-7-one
    参考文献:
    名称:
    SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES
    摘要:
    本发明提供了I式化合物:其对映异构体,对映体混合物,前药,结晶形式,非晶形式,无定形形式,其溶剂化物,其代谢物和药学上可接受的盐,其中环A取代基团在以下披露中得到充分定义。I式化合物是金属蛋白酶抑制剂,如基质金属蛋白酶和剪切酶的抑制剂,并且在治疗风湿性关节炎,牛皮癣,肿瘤性疾病,过敏和所有需要抑制MMP的疾病中有用。
    公开号:
    US20150025056A1
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文献信息

  • AZA SPIRO ALKANE DERIVATIVES AS INHIBITORS OF METALLOPROTEASES
    申请人:Yao Wenqing
    公开号:US20090124649A1
    公开(公告)日:2009-05-14
    The present invention provides a compound of Formula I or Formula II: enantiomer, diastereomer, prodrug, solvate, metabolite, or pharmaceutically acceptable salt thereof, wherein constituent variables are provided herein. The compounds of Formula I and II are modulators of metalloproteases and are useful in treating diseases associated with metalloprotease activity such as arthritis, cancer, cardiovascular disorders, skin disorders, inflammation and allergic conditions.
    本发明提供了I式或II式的化合物:其对映异构体、顺反异构体、前药、溶剂化物、代谢物或其药学上可接受的盐,其中所述的组分变量已在此处提供。I和II式的化合物是金属蛋白酶的调节剂,并且在治疗与金属蛋白酶活性相关的疾病,例如关节炎、癌症、心血管疾病、皮肤疾病、炎症和过敏症方面很有用。
  • Substituted cyclic hydroxamates as lnhibitors of matrix metalloproteinases
    申请人:Li Yun Long
    公开号:US20080167288A1
    公开(公告)日:2008-07-10
    The present invention provides compounds of the formula: its enantiomers, diastereomers, racemic mixtures thereof, prodrugs, crystalline forms, non-crystalline forms, amorphous forms thereof, solvates thereof, metabolites thereof, and pharmaceutically acceptable salts, wherein the ring A substituent groups are fully defined in the following disclosure. The compounds of formula are inhibitors of metalloproteases such as matrix metalloproteases and sheddases, and are useful in treating diseases such as rheumatoid arthritis, psoriasis, neoplastic diseases, allergies and all those diseases wherein inhibition of MMPs is desirable.
    本发明提供了公式的化合物:其对映异构体、非对映异构体、混合物、前药、晶体形式、非晶体形式、无定形形式、溶剂化物、代谢物和药学上可接受的盐,其中环A的取代基在下面的披露中被完全定义。公式化合物是金属蛋白酶抑制剂,如基质金属蛋白酶和脱落酶,可用于治疗风湿性关节炎、银屑病、肿瘤性疾病、过敏和所有需要抑制MMP的疾病。
  • AZA SPIRO ALKANE DERIVATIVES AS INHIBITORS OF METALLOPROTEASES
    申请人:Yao Wenqing
    公开号:US20110288068A1
    公开(公告)日:2011-11-24
    The present invention provides a compound of Formula I or Formula II: enantiomer, diastereomer, prodrug, solvate, metabolite, or pharmaceutically acceptable salt thereof, wherein constituent variables are provided herein. The compounds of Formula I and II are modulators of metalloproteases and are useful in treating diseases associated with metalloprotease activity such as arthritis, cancer, cardiovascular disorders, skin disorders, inflammation and allergic conditions.
    本发明提供了化合物I或化合物II的化合物:对映体、顺反异构体、前药、溶剂化物、代谢物或其药学上可接受的盐,其中组成变量在此处提供。化合物I和II是金属蛋白酶调节剂,可用于治疗与金属蛋白酶活性相关的疾病,如关节炎、癌症、心血管疾病、皮肤疾病、炎症和过敏症。
  • SUBSTITUTED CYCLIC HYDROXAMATES AS INHIBITORS OF MATRIX METALLOPROTEINASES
    申请人:Li Yun-Long
    公开号:US20110224189A1
    公开(公告)日:2011-09-15
    The present invention provides compounds of the formula: its enantiomers, diastereomers, racemic mixtures thereof, prodrugs, crystalline forms, non-crystalline forms, amorphous forms thereof, solvates thereof, metabolites thereof, and pharmaceutically acceptable salts, wherein the ring A substituent groups are fully defined in the following disclosure. The compounds of formula are inhibitors of metalloproteases such as matrix metalloproteases and sheddases, and are useful in treating diseases such as rheumatoid arthritis, psoriasis, neoplastic diseases, allergies and all those diseases wherein inhibition of MMPs is desirable.
    本发明提供了化合物的公式:其对映异构体,对映体混合物,前药,晶体形式,非晶体形式,无定形形式,其溶剂化物,代谢产物以及药学上可接受的盐,其中环A的取代基在以下披露中完全定义。公式化合物是金属蛋白酶抑制剂,例如基质金属蛋白酶和剪切酶,并且在治疗风湿性关节炎,牛皮癣,肿瘤性疾病,过敏和所有需要抑制MMP的疾病中有用。
  • AZA SPIRO ALKANE DERIVATIVES AS INHIBITORS OF METALLPROTEASES
    申请人:Incyte Holdings Corporation
    公开号:EP3020402A1
    公开(公告)日:2016-05-18
    The present invention provides a compound of Formula I or Formula II: enantiomer, diastereomer, prodrug, solvate, metabolite, or pharmaceutically acceptable salt thereof, wherein constituent variables are provided herein. The compounds of Formula I and II are modulators of metalloproteases and are useful in treating diseases associated with metalloprotease activity such as arthritis, cancer, cardiovascular disorders, skin disorders, inflammation and allergic conditions.
    本发明提供了一种式 I 或式 II 的化合物: 对映体、非对映体、原药、溶媒、代谢物或其药学上可接受的盐,其中组成变量在此提供。式 I 和 II 的化合物是金属蛋白酶的调节剂,可用于治疗与金属蛋白酶活性相关的疾病,如关节炎、癌症、心血管疾病、皮肤疾病、炎症和过敏性疾病。
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