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丽春花碱 | 2718-25-4

中文名称
丽春花碱
中文别名
麗春花定鹼
英文名称
(+/-)Rhoeadin
英文别名
rac-2,3;10,11-bis-methanediyldioxy-8β-methoxy-16-methyl-rheadane;Rhoeadine;(1R,14R,24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene
丽春花碱化学式
CAS
2718-25-4
化学式
C21H21NO6
mdl
MFCD00075892
分子量
383.401
InChiKey
XRBIHOLQAKITPP-SBHAEUEKSA-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:
    222°C
  • 比旋光度:
    D23 +235° (c = 1.01 in chloroform); D22 +174° (c = 0.69 in pyridine)
  • 沸点:
    510.32°C (rough estimate)
  • 密度:
    1.3202 (rough estimate)
  • LogP:
    3.920 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    28
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.428
  • 拓扑面积:
    58.6
  • 氢给体数:
    0
  • 氢受体数:
    7

SDS

SDS:5c7c4e23d08cdcfc333c519ebe21524e
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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
    —— rhoeagenine 5574-77-6 C20H19NO6 369.374

反应信息

  • 作为反应物:
    描述:
    盐酸丽春花碱 生成 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    �ber Rhoeadin und Rhoeagenin
    摘要:
    DOI:
    10.1007/bf01518844
  • 作为产物:
    描述:
    5-(7-methyl-8,9-dihydro-7H-[1,3]dioxolo[4',5':4,5]benzo[1,2-d]azepin-6-yl)-benzo[1,3]dioxole-4-carboxylic acid; sodium salt 生成 丽春花碱
    参考文献:
    名称:
    生物碱类rhoeadine的全合成。初步沟通。
    摘要:
    AbstractDie Umwandlung des Phtalidisochinolins (–)‐Bicucullin (1) in das Benzazepinalkaloid (+)‐Rhoeadin (8) und in sein unnatürliches Isomeres werden beschrieben.
    DOI:
    10.1002/hlca.19710540736
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文献信息

  • Compounds and compositions for treating infection
    申请人:Chepkwony Paul Kiprono
    公开号:US20090069277A1
    公开(公告)日:2009-03-12
    Compounds from 14 Kenyan plants, including from the root of Dovyalis abyssinica and Clutia robusta have been characterized and isolated, and their uses are disclosed.
    来自14种肯尼亚植物的化合物,包括 Dovyalis abyssinica 和 Clutia robusta 的根部已经被鉴定和分离,它们的用途也被公开了。
  • COMPOUNDS AND COMPOSITIONS FOR TREATING INFECTION
    申请人:Chepkwony Paul Kiprono
    公开号:US20120190734A1
    公开(公告)日:2012-07-26
    Compounds from 14 Kenyan plants, including from the root of Dovyalis abyssinica and Clutia robusta have been characterized and isolated, and their uses are disclosed.
    来自14种肯尼亚植物的化合物已经被鉴定和分离,包括来自阿比西尼亚多维亚利斯和强健小簇花的根部,它们的用途已经被披露。
  • UTILIZATION OF PHOSPHOKETOLASE FOR PRODUCTION OF AROMATIC AMINO ACID DERIVED PRODUCTS
    申请人:Danmarks Tekniske Universitet
    公开号:EP3656857A1
    公开(公告)日:2020-05-27
    The invention provides a genetically modified microorganism for production of aromatic amino acid derivatives; where the microorganism is capable of expressing enhanced levels of DAHP synthase and chorismate mutase, and further comprises transgenes encoding polypeptides having enzymatic activity of phosphoketolase and phosphate acetyltransferase. The invention further provides a method for producing aromatic amino acid derivatives using the genetically modified microorganism of the invention; as well as the use of the genetically modified microorganism for aromatic amino acid derivatives production.
    本发明提供了一种用于生产芳香族氨基酸衍生物的转基因微生物;其中该微生物能够表达更高水平的DAHP合成酶和氯氨酸突变酶,并进一步包含编码具有磷酸酮酶和磷酸乙酰转移酶酶活性的多肽的转基因。本发明进一步提供了一种利用本发明的转基因微生物生产芳香族氨基酸衍生物的方法;以及利用转基因微生物生产芳香族氨基酸衍生物的方法。
  • Benzylisoquinoline alkaloid (BIA) precursor producing microbes, and methods of making and using the same
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US10752903B2
    公开(公告)日:2020-08-25
    Methods and engineered yeast cells for generating a benzylisoquinoline alkaloid product are provided herein. A method comprises providing engineered yeast cells and a feedstock to a reactor. In the reactor, the engineered yeast cells are subjected to fermentation by incubating the engineered yeast cells for a time period to produce a solution comprising the BIA product and cellular material. The solution comprises not more than one class of molecule selected from the group of protoberberine, morphinan, isopavine, aporphine, and benzylisoquinoline. Additionally, at least one separation unit is used to separate the BIA product from the cellular material to provide the product stream comprising the BIA product.
    本文提供了生成苄基异喹啉生物碱产品的方法和工程酵母细胞。一种方法包括向反应器提供工程酵母菌细胞和原料。在反应器中,通过培养工程酵母菌细胞一段时间,使工程酵母菌细胞进行发酵,以产生一种包含苄基异喹啉生物碱产品和细胞材料的溶液。该溶液包含不多于一种选自原小檗碱、吗啡烷、异小檗碱、卟吩和苄基异喹啉组的分子。此外,至少一个分离装置用于将 BIA 产物从细胞材料中分离出来,以提供包含 BIA 产物的产品流。
  • Nemeckova,A.; Santavy,F., Collection of Czechoslovak Chemical Communications, 1965, vol. 30, p. 912 - 914
    作者:Nemeckova,A.、Santavy,F.
    DOI:——
    日期:——
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同类化合物

高山罂粟精宁 高山罂粟宁 乙基丽春花宁 丽春花碱 N-Methylporphyroxin (+)-Isorhoeagenin (24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene rhoeagenine N-Methyl-14-O-demethyl-epiporphyroxin 10,11-methanediyldioxy-2,8β-dimethoxy-16-methyl-(6α)-rheadan-3-ol epialpinine cis-Alpinigenin (4bS,10bR)-2,3,7,8-Tetramethoxy-6-oxo-6,10b,12,13-tetrahydro-4bH-5-oxa-11-aza-benzo[3,4]cyclohepta[1,2-a]naphthalene-11-carbaldehyde Alpinigenine Rhoeadin O-Methyl-porphyroxin Glaudin glaucamine natuerliches (+)-Papaverrubin E (1R,14R,24R)-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaen-24-ol (1R,11S)-11,17-dimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaen-16-ol (1R)-11,17-dimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaen-16-ol (1R,11S)-11,16,17-trimethoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene (1R)-17-methoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene-11,16-diol (14R,24S)-24-methoxy-13-methyl-5,7,19,21,25-pentaoxa-13-azahexacyclo[12.11.0.02,10.04,8.015,23.018,22]pentacosa-2,4(8),9,15(23),16,18(22)-hexaene (1R,11S)-11,16,17-trimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene Glaucamin 8-acetoxy-2,3,10,11-tetramethoxy-16-methyl-rheadane Porphyroxin Glaucamine Papaverrubin E Rhoeagenin Rhoeadin Dubirhein 11-Ethoxy-16,17-dimethoxy-22-methyl-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene 16,18,19-Trimethoxy-13-methyl-5,7,22-trioxa-13-azapentacyclo[12.8.0.02,10.04,8.015,20]docosa-2,4(8),9,15(20),16,18-hexaen-21-ol N-Methylporphyroxine Alpinin 17-Methoxy-6,8,12-trioxa-22-azapentacyclo[11.9.0.02,10.05,9.014,19]docosa-2(10),3,5(9),14,16,18-hexaene-11,16-diol Alkaloid RC Papaverrubin G Papaverrubin B Alpinigenin 18,19-Dimethoxy-13-methyl-5,7,22-trioxa-13-azapentacyclo[12.8.0.02,10.04,8.015,20]docosa-2,4(8),9,15(20),16,18-hexaen-21-ol N-Methyl-14-O-demethylepiporphyroxine