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(3R,4S,5S,6R,9R,11R,12R,13S,14R)-6-(((2S,4S,6R)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecane-2,10-dione | 1379596-15-2

中文名称
——
中文别名
——
英文名称
(3R,4S,5S,6R,9R,11R,12R,13S,14R)-6-(((2S,4S,6R)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecane-2,10-dione
英文别名
2'-deoxyerythromycin A;(3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-[(2S,4S,6R)-4-(dimethylamino)-6-methyloxan-2-yl]oxy-14-ethyl-7,12,13-trihydroxy-4-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-oxacyclotetradecane-2,10-dione
(3R,4S,5S,6R,9R,11R,12R,13S,14R)-6-(((2S,4S,6R)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-3,5,7,9,11,13-hexamethyl-1-oxacyclotetradecane-2,10-dione化学式
CAS
1379596-15-2
化学式
C37H67NO12
mdl
——
分子量
717.938
InChiKey
QUFJXCFMWOURKH-MKRHZNTKSA-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:
    788.4±60.0 °C(Predicted)
  • 密度:
    1.17±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    50
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.95
  • 拓扑面积:
    174
  • 氢给体数:
    4
  • 氢受体数:
    13

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

点击查看最新优质反应信息

文献信息

  • Synthesis and antibacterial activity of desosamine-modified macrolide derivatives
    作者:Nicolas LeTourneau、Pavan Vimal、Dorota Klepacki、Alexander Mankin、Artem Melman
    DOI:10.1016/j.bmcl.2012.05.110
    日期:2012.7
    Structural factors behind erm macrolide resistance were studied through synthesis of new macrolide derivates possessing truncated desosamine sugar moieties and subsequent determination of their antibacterial activity. Synthesized compounds with 2'-deoxy and 3'-desmethyl desosamine rings demonstrated decreased antibacterial activity on the native Staphylococcus aureus strain and were inactive against constitutively resistance S. aureus. The obtained results indicate that steric repulsion between the dimethylated A2058 and desosamine ring cannot be considered as a primary reason for erm-resistance. (C) 2012 Published by Elsevier Ltd.
  • An Approach to the Site-Selective Deoxygenation of Hydroxy Groups Based on Catalytic Phosphoramidite Transfer
    作者:Peter A. Jordan、Scott J. Miller
    DOI:10.1002/anie.201109033
    日期:2012.3.19
    Selective: The deoxygenation of simple and complex natural products employing a readily synthesized phosphoramidite and tetrazole catalysts can be executed as a two‐step process, without the need to isolate intermediate deoxygenation precursors. Furthermore, a peptide‐based tetrazole catalyst controls the site selectivity of deoxyerythromycin synthesis (see scheme), thus overcoming the notorious challenges
    选择性:使用易于合成的亚磷酰胺和四唑催化剂对简单和复杂的天然产物进行脱氧可以作为两步过程进行,无需分离中间脱氧前体。此外,基于肽的四唑催化剂控制脱氧红霉素合成的位点选择性(参见方案),从而克服了未受保护的红霉素 A 的臭名昭著的挑战。
  • [EN] MACROLIDE COMPOUND AND ITS USE OF TREATMENT CHRONIC RESPIRATORY DISEASE<br/>[FR] COMPOSÉ MACROLIDE ET SON UTILISATION POUR LE TRAITEMENT D'UNE MALADIE RESPIRATOIRE CHRONIQUE
    申请人:BEIJING CONTINENT PHARMACEUTICALS CO LTD
    公开号:WO2021138847A1
    公开(公告)日:2021-07-15
    Provided herein is macrolide compound and its use of treatment chronic respiratory disease. Specifically, it provides the compounds of formula (I) or pharmaceutically acceptable salts, stereoisomers and application thereof. The compounds are useful for treating chronic respiratory disease.
    本文提供了大环内酯类化合物及其用于治疗慢性呼吸道疾病的用途。具体而言,提供了式(I)的化合物或其药学上可接受的盐、立体异构体及其应用。这些化合物可用于治疗慢性呼吸道疾病。
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