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| 99664-42-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
99664-42-3
化学式
C36H34N2O10
mdl
——
分子量
654.673
InChiKey
RUOUTOWRFSOLNO-TVLXLKRTSA-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:
    911.0±65.0 °C(Predicted)
  • 密度:
    1.370±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

反应信息

  • 作为产物:
    描述:
    顺式-曲尼司特 为溶剂, 生成
    参考文献:
    名称:
    Utsuki, Tadanobu; Hirayama, Fumitoshi; Uekama, Kaneto, journal of the chemical society-perkin transactions 2, 1993, # 1, p. 109 - 114
    摘要:
    DOI:
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文献信息

  • Effect of UV-Absorbing Agents on Photodegradation of Tranilast in Oily Gels.
    作者:Naohide HORI、Makiko FUJII、Kazuhiko IKEGAMI、Den-ichi MOMOSE、Noriyasu SAITO、Mitsuo MATSUMOTO
    DOI:10.1248/cpb.47.1713
    日期:——
    Tranilast (TL) oily gels containing UV-absorbing agents (UV absorber) were prepared, and the effect of the agents against photodegradation of TL was investigated. When 0.1% TL oily gel without UV absorber was exposed to light, TL was photochemically decomposed to the extent of 74.1% of its initial content at the end of the first hour. Although there were differences in the preventive effect on photodegradation of TL depending on the UV absorbers employed, 2-(2-benzotriazolyl)-p-cresol (BTPC) was the most effective absorber. The addition of UV absorbers to the oily gel did not affect the release of TL from the gel, the skin permeation, or the skin concentration of TL following topical application. UV absorbers added to TL oily gel penetrated into skin; however, their concentration in skin was similar to that following application of commercial sunscreen. These results suggest that the addition of UV absorbers to the oily gel of TL may be useful in preventing photodegradation of TL in the gel.
  • Hyaluronidase-inhibitory and anti-allergic activities of the photo-irradiated products of tranilast.
    作者:HISAO KAKEGAWA、NAOKI MITSUO、HITOSHI MATSUMOTO、TOSHIO SATOH、MASAAKI AKAGI、KENJI TASAKA
    DOI:10.1248/cpb.33.3738
    日期:——
    We found that N-(trans-3, 4-dimethoxycinnamoyl) anthranilic acid (tranilast) is readily transformed by photo-irradiation to N-(cis-3, 4-dimethoxycinnamoyl) anthranilic acid (cis-isomer) and a cyclobutane derivative (dimer). Of these photo-irradiated products of tranilast, the cis-isomer was found to inhibit hyaluronidase more effectively than tranilast. From these results, it wsa expected that the cis-isomer might have more effective anti-allergic activity than tranilast ; indeed, the cis-isomer was found to show more effective prevention than tranilast of (1) histamine release from sensitized rat peritoneal mast cells induced by antigen (egg white albumin), (2) histamine release from rat peritoneal mast cells induced by concanavalin A and calcium ionophore A-23187, and (3) the 48 h homologous passive cutaneous anaphylaxis (PCA) in rats.
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同类化合物

二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2S,3R,4S)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2R,3S,4R)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 r-1,t-2-二甲基-t-3,c-3,4-二苯基环丁烷 r-1,t-2,c-3-三苯基-c-4-氰基环丁烷 3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-甲氧基-4-(2,2,3,3-四甲基环丙基)苯 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 (1R,2S,3S,4R)-3,4-二(苯基)环丁烷-1,2-二甲酸二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基]酯 4,9-bis(2-methoxyphenyl)-3a,4,9,9a-tetrahydro-1H-4,9-epoxybenzo[f]isoindole-1,3(2H)-dione (2S,3R)-1-(Hydroxy-phenyl-methyl)-2,3-diphenyl-4-[1-phenyl-meth-(E)-ylidene]-cyclobutanol 2,3,5,6-Tetraphenyl-1,4-cyclohexandion (1S,2S,3S,4S)-3,4-Bis-[2-(di-p-tolyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester endo-1,2-dicarbomethoxy-5,5-dimethyl-exo-3,4-diphenylbicyclo<2.1.0>pentane 2-Methylen-3,4-dihydroxy-trans-5,6-diphenylbicyclo<3.1.0>hexan 1,1,4,4-Tetramethyl-2,3b,5,6b-tetraphenyl-1,3a,3b,4,6a,6b-hexahydro-1,4-digerma-cyclobutadicyclopentene 6-Ethyl-2,6-diphenyl-bicyclo[3.1.0]hexane (1S,2S,4R,5R)-1,2,4,5-Tetraphenyl-tricyclo[3.1.0.02,4]hexane (4R,5S)-4-(3,4-dimethoxyphenyl)-5-nitro-5-(4-nitrobenzyl)tetrahydro-2H-pyran-2-one (1R,2R,3S,4S)-ethyl 1-acetyl-4-hydroxy-3-nitro-2,4-diphenylcyclopentanecarboxylate 3,4-bis-(4-hydroxy-3-methoxy-phenyl)-cyclobutane-1,2-dicarboxylic acid 1r,2c-diacetyl-3t,4t-diphenyl-cyclobutane 3,7-Diphenyl-tetracyclo<3.3.0.02,8.03,7>octan 3,3-Dimethyl-1-phenyl-tricyclo[4.1.0.02,7]heptane (3S,4R)-ethyl 1,2,3,4-tetrahydro-1-methyl-2-oxo-4-p-tolylpyridine-3-carboxylate (2R,3R)-2,3-diphenylcyclopropane-1,1-dimethanol methyl 1-formyloxy-9,9-bis(4-methoxyphenyl)pentacyclo<4.3.0.02,5.03,8.04,7>nonane-4-carboxylate (3-Cyanomethyl-2,4-diphenyl-cyclobutyl)-acetonitrile γ-Truxinsaeure (1R,6S)-1,7-Diphenyl-bicyclo[4.1.0]heptane 4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid 2,5,6-trimethyl-3,4-diphenyl-cyclohex-3-enecarboxylic acid 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.13,17.18,12.04,7.013,16.019,22>tetracosa-1,3(23),8,10,12(24),17-hexaen (3S,4R)-3,4-diphenyltetracyclo[11.5.0.02,5.06,12]octadeca-1,5,7,10,12,14,17-heptaene (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Ethyl 4-(7-phenyl-7-bicyclo[2.2.1]heptanyl)benzoate 5-Methyl-5,6-diphenylcyclohexa-1,3-diene 4,4',4'',4'''-cyclobutane-1,2,3,4-tetrayl-tetrakis-benzamidine (1R,2R,3S,4S)-3,4-Diphenyl-cyclobutane-1,2-dicarboxylic acid bis-dimethylamide 3,4,12,13-Tetraphenylpentacyclo<13.3.1.16,10.02,5.011,14>eicosa-1(19),6,8,10(20),15,17-hexaen 1'-[(tert-butoxy)carbonyl]-4,10-dimethyl-14,33-dinitrospiro(2,12-dioxa-18,22,25,29-tetraazahexacyclo-[29.2.2.23,6.28,11.213,16.222,25]tritetraconta-3,5,8,10,13,15,31,33,34,38,40,42-dodecaene-7,4'-piperidine)-17,30-dione 4,4'-Dibrom-β-truxinsaeure-dimethylester 1ξ-bromo-2r,3c-bis-bromomethyl-1ξ,4t-diphenyl-cyclobutane (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Methyl-[3,4,4-triphenyl-thietan-(2Z)-ylidene]-amine