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benzyloxycarbonyl-L-valyl-N-[(1S)-1-[[5-(3-methylbenzyl)-1,3,4-oxadiazole-2-yl]carbonyl]-2-methylpropyl]-L-prolinamide | 208840-22-6

中文名称
——
中文别名
——
英文名称
benzyloxycarbonyl-L-valyl-N-[(1S)-1-[[5-(3-methylbenzyl)-1,3,4-oxadiazole-2-yl]carbonyl]-2-methylpropyl]-L-prolinamide
英文别名
L-Prolinamide, N-((phenylmethoxy)carbonyl)-L-valyl-N-((1S)-2-methyl-1-((5-((3-methylphenyl)methyl)-1,3,4-oxadiazol-2-yl)carbonyl)propyl)-;benzyl N-[(2S)-3-methyl-1-[(2S)-2-[[(2S)-3-methyl-1-[5-[(3-methylphenyl)methyl]-1,3,4-oxadiazol-2-yl]-1-oxobutan-2-yl]carbamoyl]pyrrolidin-1-yl]-1-oxobutan-2-yl]carbamate
benzyloxycarbonyl-L-valyl-N-[(1S)-1-[[5-(3-methylbenzyl)-1,3,4-oxadiazole-2-yl]carbonyl]-2-methylpropyl]-L-prolinamide化学式
CAS
208840-22-6
化学式
C33H41N5O6
mdl
——
分子量
603.718
InChiKey
FPGAGACTKJTPFT-MYKRZTLLSA-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):
    5.5
  • 重原子数:
    44
  • 可旋转键数:
    13
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    144
  • 氢给体数:
    2
  • 氢受体数:
    8

SDS

SDS:20ab8fb6ba7a41944bccd26fc6df2577
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文献信息

  • Remedies for inflammatory bowel diseases
    申请人:——
    公开号:US20030212115A1
    公开(公告)日:2003-11-13
    Prophylactic and/or therapeutic drugs against ulcerative colitis, which include five-member heterocyclic compounds represented by the formula (I) or these nontoxic salts as active principle, 1 (wherein Z represents the group containing &agr;-aminocarbonyl group, R 1 represents (1) substituted alkyl, alkenyl or alkynyl groups, (2) OH, (3) amino, (4) alkylamino, (5) dialkylamino, etc., X and Y represent oxygen atom, sulfur atom or substituted nitrogen atom.)
    预防和/或治疗溃疡性结肠炎的药物,包括由式(I)表示的五元杂环化合物或这些无毒盐作为活性成分,其中Z代表含有α-氨基羰基的基团,R1代表(1)取代烷基、烯基或炔基基团,(2) OH,(3) 氨基,(4) 烷基氨基,(5) 二烷基氨基等,X和Y代表氧原子、硫原子或取代的氮原子。
  • Airway mucus secretion inhibitors
    申请人:——
    公开号:US20030216324A1
    公开(公告)日:2003-11-20
    Prophylactic and/or therapeutic drugs against diseases with the augmentative airway mucus secretion, which include five-member heterocyclic compounds represented by the formula (I) or these nontoxic salts as active principle, 1 (wherein Z represents the group containing &agr;-aminocarbonyl group, R 1 represents (1) substituted alkyl, alkenyl or alkynyl groups, (2)OH, (3)amino, (4)alkylamino, (5)dialkylamino, etc., X and Y represent oxygen atom, sulfur atom or substituted nitrogen atom.)
    预防和/或治疗增多的气道粘液分泌疾病的药物,包括由式(I)所代表的五元杂环化合物或这些无毒盐作为活性原理,其中Z代表含有α-氨基羰基的基团,R1代表(1)取代烷基、烯基或炔基基团,(2) OH,(3) 氨基,(4) 烷基氨基,(5) 二烷基氨基等,X和Y代表氧原子、硫原子或取代的氮原子。
  • Tri-peptide Inhibitors of Serine Elastases
    申请人:Cheronis John C.
    公开号:US20090156509A1
    公开(公告)日:2009-06-18
    The present invention provides compounds of formula (I): where X is R 1 —(CR 3 R 4 ) n OC(O)—; R 1 —(CR 3 R 4 ) n C(O)—; R 1 —C(O)NH(CR 3 R 4 ) n OC(O)—; R 1 —C(O)NH(CR 3 R 4 ) n C(O)—; R 1 —C(O)(CR 3 R 4 ) n OC(O)—; or R 1 —C(O)(CR 3 R 4 ) n C(O)—; where R 1 is optionally substituted C 5-10 aryl or heteroaryl; OH or NH 2 ; where R 3 and R 4 are independently H or methyl; and n is 0 to 6; and Y is —CF 3 or one of: where R 2 is C 1-8 alkyl optionally substituted with halo or —OH; —(CR 6 R 7 ) p —C 5-6 aryl optionally substituted with halo, —OH, C 1-8 alkyl, C 1-8 haloalkyl, —(CH 2 ) m C(O)NH 2 or —(CH 2 ) m OCH 3 ; where R 6 and R 7 are independently H or methyl; m is 0 to 4, and p is 0 or 1 or a pharmaceutically acceptable salt, ester, metabolite or prodrug thereof
    本发明提供了式(I)的化合物:其中X为R1—(CR3R4)nOC(O)—; R1—(CR3R4)nC(O)—; R1—C(O)NH(CR3R4)nOC(O)—; R1—C(O)NH(CR3R4)nC(O)—; R1—C(O)(CR3R4)nOC(O)—; 或R1—C(O)(CR3R4)nC(O)—;其中R1为可选择的取代C5-10芳基或杂环芳基; OH或NH2;其中R3和R4独立地为H或甲基; n为0到6;以及Y为—CF3或下列之一:其中R2为C1-8烷基,可选择地取代卤或—OH; —(CR6R7)p—C5-6芳基,可选择地取代卤,—OH,C1-8烷基,C1-8卤代烷基,—(CH2)mC(O)NH2或—(CH2)mOCH3;其中R6和R7独立地为H或甲基; m为0到4,p为0或1或其药学上可接受的盐,酯,代谢物或前药。
  • REMEDIES FOR INFLAMMATORY BOWEL DISEASES
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1323420A1
    公开(公告)日:2003-07-02
    Prophylactic and/or therapeutic drugs against ulcerative colitis, which include five-member heterocyclic compounds represented by the formula (I) or these nontoxic salts as active principle, (wherein Z represents the group containing α-aminocarbonyl group, R1 represents (1) substituted alkyl, alkenyl or alkynyl groups, (2)OH, (3)amino, (4)alkylamino, (5)dialkylamino, etc., X and Y represent oxygen atom, sulfur atom or substituted nitrogen atom.)
    溃疡性结肠炎的预防和/或治疗药物,其活性成分包括由式(I)代表的五元杂环化合物或这些无毒盐、 (其中 Z 代表含有α-氨基羰基的基团,R1 代表(1)取代的烷基、烯基或炔基,(2)OH,(3)氨基,(4)烷基氨基,(5)二烷基氨基等,X 和 Y 代表氧原子、硫原子或取代的氮原子)。
  • AIRWAY MUCUS SECRETION INHIBITORS
    申请人:ONO PHARMACEUTICAL CO., LTD.
    公开号:EP1323419A1
    公开(公告)日:2003-07-02
    Prophylactic and/or therapeutic drugs against diseases with the augmentative airway mucus secretion, which include five-member heterocyclic compounds represented by the formula (I) or these nontoxic salts as active principle, (wherein Z represents the group containing α-aminocarbonyl group, R1 represents (1) substituted alkyl, alkenyl or alkynyl groups, (2)OH, (3)amino, (4)alkylamino, (5)dialkylamino, etc., X and Y represent oxygen atom, sulfur atom or substituted nitrogen atom.)
    预防和/或治疗气道粘液分泌增多性疾病的药物,其活性成分包括由式(I)代表的五元杂环化合物或这些无毒盐、 (其中 Z 代表含有α-氨基羰基的基团,R1 代表(1) 取代的烷基、烯基或炔基,(2)OH,(3)氨基,(4)烷基氨基,(5)二烷基氨基等,X 和 Y 代表氧原子、硫原子或取代的氮原子)。
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