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gamma-Cyclodextrin hydrate | 91464-90-3

中文名称
——
中文别名
——
英文名称
gamma-Cyclodextrin hydrate
英文别名
(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55R,56R)-5,10,15,20,25,30,35,40-octakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39-hexadecaoxanonacyclo[36.2.2.23,6.28,11.213,16.218,21.223,26.228,31.233,36]hexapentacontane-41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56-hexadecol;hydrate
gamma-Cyclodextrin hydrate化学式
CAS
91464-90-3
化学式
C48H82O41
mdl
——
分子量
1315.1
InChiKey
SPKUKQHKKVTYOE-SMTXKKGASA-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:
    267 °C (dec.)(lit.)
  • 物理描述:
    DryPowder
  • 稳定性/保质期:
    遵照规定使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    -18.23
  • 重原子数:
    89
  • 可旋转键数:
    8
  • 环数:
    30.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    634
  • 氢给体数:
    25
  • 氢受体数:
    41

安全信息

  • TSCA:
    Yes
  • 安全说明:
    S24/25
  • WGK Germany:
    3
  • 海关编码:
    35051000
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335

文献信息

  • NEW PHARMACEUTICAL COMPOSITIONS OF MELOXICAM WITH IMPROVED SOLUBILITY AND BIOAVAILABILITY
    申请人:Hexal AG
    公开号:EP1007049A1
    公开(公告)日:2000-06-14
  • ASSOCIATIONS OF XANTHOGENATES AND CYCLODEXTRINS, AND THEIR USE
    申请人:Amtmann Eberhard
    公开号:US20100240606A1
    公开(公告)日:2010-09-23
    The invention is related to association products of xanthates and cyclodextrins, pharmaceutical formulations made therefrom, and medicaments containing these formulations for treating Alzheimer's, viral, tumor, cardiovascular, and autoimmune diseases such as rheumatism, multiple sclerosis, alopecia areata, lupus erythematosus, stroke, lung edema, or for use as radio-protectors. The association products contain a xanthate of general formula I whereby R 1 represents a possibly substituted aryl or alkyl residue and R 2 represents a metal atom, a possibly substituted alkyl, alkoxy, amino or ammonium group or halogen, and a cyclodextrin, whereby the cyclodextrin can be either a substituted or non-substituted alpha-, beta- or gamma-cyclodextrin. Furthermore, the invention is related to the use of the association products for chemical syntheses.
  • US6284269B1
    申请人:——
    公开号:US6284269B1
    公开(公告)日:2001-09-04
  • US8435966B2
    申请人:——
    公开号:US8435966B2
    公开(公告)日:2013-05-07
  • [EN] NEW PHARMACEUTICAL COMPOSITIONS OF MELOXICAM WITH IMPROVED SOLUBILITY AND BIOAVAILABILITY<br/>[FR] NOUVELLES COMPOSITIONS PHARMACEUTIQUES DE MELOXICAM PRESENTANT UNE SOLUBILITE ET UNE BIODISPONIBILITE AMELIOREES
    申请人:HEXAL AG
    公开号:WO1999009988A1
    公开(公告)日:1999-03-04
    (EN) Pharmaceutical compositions containing enolic carboxamide type antiinflammatory agent meloxicam that exhibit improved wettability, aqueous solubility, dissolution behaviour over a broad range of pH, and that are prepared by crystal structure modification of the drug through dry or wet mechanical homogenization with two further components - one of them is selected from a group of oligo - and dissolution improving, or alkalizing agent. The application of the formulations according to the present invention results in an improved biovailability and effectiveness of meloxicam.(FR) Compositions pharmaceutiques contenant un agent anti-inflammatoire de type carboxamide énolique, désigné meloxicam, présentant des caractéristiques améliorées de mouillabilité, de solubilité aqueuse, de comportement à la dissolution sur une plage importante de pH et dont la préparation consiste à modifier la structure cristalline du médicament par homogénéisation mécanique sèche ou humide avec deux constituants supplémentaires, dont l'un est sélectionné dans un groupe oligo améliorant la dissolution ou consiste en un agent d'alcalinisation. Ces formulations permettent d'améliorer la biodisponibilité et l'efficacité de meloxicam.
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