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S-15183a | 686345-39-1

中文名称
——
中文别名
——
英文名称
S-15183a
英文别名
(+/)-S-15183a;(3-heptyl-7-methyl-6,8-dioxoisochromen-7-yl) octanoate
S-15183a化学式
CAS
686345-39-1
化学式
C25H36O5
mdl
——
分子量
416.558
InChiKey
YMXPNDJGGNEMOH-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

  • 沸点:
    546.7±50.0 °C(Predicted)
  • 密度:
    1.08±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.7
  • 重原子数:
    30
  • 可旋转键数:
    14
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    69.7
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    S-15183a 在 palladium on activated charcoal 氢气 作用下, 以 甲醇 为溶剂, 20.0 ℃ 、101.32 kPa 条件下, 反应 3.0h, 以60%的产率得到3-Heptyl-7-methyl-isochroman-6,8-diol
    参考文献:
    名称:
    S-15183a and b, New Sphingosine Kinase Inhibitors, Produced by a Fungus.
    摘要:
    在筛选鞘氨醇激酶抑制剂的过程中,我们在真菌Zopfiella inermis SANK 15183的培养液中发现两种活性化合物。通过光谱分析,我们确定这两种化合物(分别命名为S-15183a和b)的结构为新氮杂菲酮类代谢产物。S-15183a和b分别以2.5和1.6μM的IC50值抑制大鼠肝脏中的鞘氨醇激酶。S-15183a还能抑制完整血小板中的内源性SPH激酶活性。
    DOI:
    10.7164/antibiotics.54.415
  • 作为产物:
    描述:
    1-壬炔4-二甲氨基吡啶 、 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodide 、 gold(lll) acetate 、 四丁基碘化铵三乙胺N,N-二异丙基乙胺三氟乙酸2-碘酰基苯甲酸 作用下, 以 四氢呋喃二氯甲烷1,2-二氯乙烷 为溶剂, 反应 0.02h, 生成 S-15183a
    参考文献:
    名称:
    利用邻炔基苯甲醛的环异构化合成氮杂苯酮和相关分子。
    摘要:
    DOI:
    10.1002/anie.200353037
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文献信息

  • Methods, compositions and compound assays for inhibiting amyloid-beta protein production
    申请人:Merchiers Gerard Pascal
    公开号:US20050277612A1
    公开(公告)日:2005-12-15
    A method for identifying compounds that inhibit amyloid-beta precursor protein processing in cells, comprising contacting a test compound with a SPHK polypeptide, or fragment thereof, and measuring a compound-SPHK property related to the production of amyloid-beta peptide. Cellular assays of the method measure indicators including phosphorylated kinase substrate and/or amyloid beta peptide levels. Therapeutic methods, and pharmaceutical compositions including effective amyloid-beta precursor processing-inhibiting amounts of SPHK expression inhibitors, are useful for treating conditions involving cognitive impairment such as Alzheimer's Disease.
    一种鉴定抑制细胞中淀粉样β前体蛋白加工的化合物的方法,包括将测试化合物与 SPHK 多肽或其片段接触,并测量与淀粉样β肽的产生有关的化合物-SPHK 特性。该方法的细胞测定指标包括磷酸化激酶底物和/或淀粉样 beta 肽平。治疗方法和药物组合物包括有效的淀粉样β前体加工抑制量的SPHK表达抑制剂,可用于治疗涉及认知障碍的疾病,如阿尔茨海默病。
  • JPH10182627A
    申请人:——
    公开号:JPH10182627A
    公开(公告)日:1998-07-07
  • [EN] METHODS, COMPOSITIONS AND COMPOUND ASSAYS FOR INHIBITING AMYLOID-BETA PROTEIN PRODUCTION<br/>[FR] METHODES, COMPOSITIONS ET DOSAGES DESTINES A L'INHIBITION DE LA PRODUCTION DE PROTEINES BETA-AMYLOIDES
    申请人:GALAPAGOS GENOMICS NV
    公开号:WO2005103692A2
    公开(公告)日:2005-11-03
    A method for identifying compounds that inhibit amyloid-beta precursor protein processing in cells, comprising contacting a test compound with a SPHK polypeptide, or fragment thereof, and measuring a compound-SPHK property related to the production of amyloid-beta peptide. Cellular assays of the method measure indicators including phosphorylated kinase substrate and/or amyloid beta peptide levels. Therapeutic methods, and pharmaceutical compositions including effective amyloid-beta precursor processing-inhibiting amounts of SPHK expression inhibitors, are useful for treating conditions involving cognitive impairment such as Alzheimer’s Disease.
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同类化合物

萘啶霉素 苯酚,4-(4-吗啉基磺酰)- 焦曲二醇 核丛青霉素 异色酮VI [(7R)-7-甲基-6,8-二氧代-3-[(E)-丙-1-烯基]异苯并吡喃-7-基]2,4-二羟基-6-甲基苯甲酸酯 (E,E,E)-(-)-7-(乙酰氧基)-3-(1,3,5-庚三烯基)-7-甲基-6H-2-苯并吡喃-6,8(7H)-二酮 (7S,8S)-5-氯-3-[(1E,3E)-3,5-二甲基庚-1,3-二烯基]-7,8-二羟基-7-甲基-8H-异苯并吡喃-6-酮 (7R,8R)-5-氯-3-[(1E,3E,5S)-3,5-二甲基庚-1,3-二烯-1-基]-7,8-二羟基-7-甲基-7,8-二氢-6H-异色烯-6-酮 Acetic acid 2-((11S,13S,16S,17R)-11,17-dihydroxy-13,16-dimethyl-3-oxo-10,11,12,13,14,15,16,17-octahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxo-ethyl ester (+/-)-5-Chlorrotioramin Acetic acid 3-((1E,3E,5E)-hepta-1,3,5-trienyl)-7-methyl-6,8-dioxo-2,6,7,8-tetrahydro-isoquinolin-7-yl ester Acetic acid 6-acetoxy-7-methyl-8-oxo-3-((E)-propenyl)-3,4,5,6,7,8-hexahydro-1H-isochromen-7-yl ester 3-((1E,3E,5E)-Hepta-1,3,5-trienyl)-7-hydroxy-2,7-dimethyl-2H-isoquinoline-6,8-dione Deacetylwortmin Acetic acid 3-((1E,3E,5E)-hepta-1,3,5-trienyl)-2,7-dimethyl-6,8-dioxo-2,6,7,8-tetrahydro-isoquinolin-7-yl ester 7,8-Dihydro-7,8-dihydroxy-3,5,7-trimethyl-2-benzopyran-6-on (7R,8S)-7,8-Dihydroxy-3,7-dimethyl-5-((E)-3-oxo-but-1-enyl)-7,8-dihydro-isochromen-6-one 5-bromo-3-(3-methoxyphenyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl acetate (7R,8S)-5-Bromo-7,8-dihydroxy-3,7-dimethyl-7,8-dihydro-isochromen-6-one 3-(3-chlorophenyl)-7-hydroxy-7-methyl-6H-isochromene-6,8(7H)-dione t-Butyl-6-dimethyl-2,2-carbethoxy-5-dihydro-2,3-pyron-4 ethyl 2-[3-[(1E,3E,5S)-3,5-dimethylhepta-1,3-dienyl]-7-hydroxy-7-methyl-6-oxoisochromen-8-ylidene]acetate [(7S)-3-(3-acetyloxypropyl)-5-chloro-7-methyl-6,8-dioxoisochromen-7-yl] butanoate [5-Bromo-3-(4-methoxyphenyl)-7-methyl-6,8-dioxoisochromen-7-yl] 3-phenylpropanoate 5-cyano-2-methyl-4-oxo-5-(3-oxo-butyl)-4,5-dihydro-pyrrole-3-carboxylic acid ethyl ester 1-O-methyl 4-O-[7-methyl-3-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]-6,8-dioxoisochromen-7-yl] butanedioate Lunatsaeure-A-methylester (2S,4S)-2,4-Dimethyl-hexanoic acid (R)-3-((E)-2-methoxycarbonyl-vinyl)-7-methyl-6,8-dioxo-2,6,7,8-tetrahydro-isoquinolin-7-yl ester (2S,4S)-2,4-Dimethyl-hexanoic acid (R)-3-(2-methoxycarbonyl-ethyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl ester [3-((R)-7-Hydroxy-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-3-yl)-propyl]-carbamic acid tert-butyl ester ethyl 2-[5-bromo-3-[(1E,3E,5S)-3,5-dimethylhepta-1,3-dienyl]-7-hydroxy-7-methyl-6-oxoisochromen-8-ylidene]acetate (E)-3-((7R,8R)-7,8-Dihydroxy-7-methyl-6-oxo-7,8-dihydro-6H-isochromen-3-yl)-acrylic acid methyl ester (R)-5-chloro-3-((S,1E,3E)-3,5-dimethylhepta-1,3-dien-1-yl)-7-methyl-6,8-dioxo-2-phenyl-2,6,7,8-tetrahydroisoquinolin-7-yl acetate cazisochromene methyl 2-[(1R,3R)-7-bromo-1-hydroxy-1-methyl-5,8-dioxo-3,4-dihydroisochromen-3-yl]acetate (7R,8S,7′R,8′S)-5-[(7′,8′-dihydroxy-3′,7′-dimethyl-6′-oxo-7′,8′-dihydro-6′H-isochromen-5′-yl)methyl]-7,8-dihydroxy-3,7-dimethyl-7,8-dihydro-6H-isochromen-6-one (5-Bromo-7-methyl-6,8-dioxo-3-phenylisochromen-7-yl) acetate Bis-boc-Mitorubrinic acid t-butyl ester methyl 4-(5-bromo-7-hydroxy-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-3-yl)butanoate (Z)-2-((2-(4-bromo-3-methyl-5-oxofuran-2(5H)-ylidene)ethoxy)methyl)-5-oxo-5,6-dihydro-2H-pyran-2-yl acetate 3-<(1E)-1,3-dimethylpent-1-enyl>-8,9-dihydro-7-methoxy-9-oxo-8-(2-oxopropyl)-1H-naphtho<2,3-c>pyran-8,10-diyl diacetate Dothideomynone C 5-bromo-3-(4-methoxy-4-oxobutyl)-7-methyl-6,8-dioxo-7,8-dihydro-6H-isochromen-7-yl cyclopentanecarboxylate (R)-7-acetoxy-2-amino-5-chloro-3-((S)-3,5-dimethyl-hepta-1,3t-dien-t-yl)-7-methyl-2H-isoquinoline-6,8-dione