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2-Butenoic acid, 2-methyl-, 7-[[2,3-dihydroxy-2-(1-methoxyethyl)-3-methyl-1-oxobutoxy]methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl ester, [1S-[1alpha(Z),7(2S*,3R*),7aalpha]]- | 303-34-4

中文名称
——
中文别名
——
英文名称
2-Butenoic acid, 2-methyl-, 7-[[2,3-dihydroxy-2-(1-methoxyethyl)-3-methyl-1-oxobutoxy]methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl ester, [1S-[1alpha(Z),7(2S*,3R*),7aalpha]]-
英文别名
[7-[(Z)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-methoxyethyl)-3-methylbutanoate
2-Butenoic acid, 2-methyl-, 7-[[2,3-dihydroxy-2-(1-methoxyethyl)-3-methyl-1-oxobutoxy]methyl]-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-yl ester, [1S-[1alpha(Z),7(2S*,3R*),7aalpha]]-化学式
CAS
303-34-4
化学式
C21H33NO7
mdl
——
分子量
411.5
InChiKey
QHOZSLCIKHUPSU-QPEQYQDCSA-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:
    96.5-97.0℃
  • 比旋光度:
    D -4° (10% alc)
  • 沸点:
    531.2°C (rough estimate)
  • 密度:
    1.21±0.1 g/cm3 (20 ºC 760 Torr)
  • LogP:
    1.280
  • 物理描述:
    Lasiocarpine appears as colorless plates or beige crystalline solid. (NTP, 1992)
  • 颜色/状态:
    COLORLESS PLATES
  • 溶解度:
    less than 0.1 mg/mL at 68° F (NTP, 1992)
  • 稳定性/保质期:
    DECOMP SLOWLY ON STANDING IN AIR @ ROOM TEMP
  • 旋光度:
    SPECIFIC OPTICAL ROTATION: -3.0 DEG @ 16 °C/D (IN ETHANOL)
  • 分解:
    When heated to decomposition it emits toxic fumes of /nitrogen oxides/.

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    29
  • 可旋转键数:
    10
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    106
  • 氢给体数:
    2
  • 氢受体数:
    8

ADMET

代谢
对LASIOCARPINE的研究已经证实了混合功能氧化酶系统的大鼠肝微粒体部分形成了吡咯代谢物。去氢毛茛碱已被分离和鉴定为LASIOCARPINE的微粒体氧化的产物。
STUDIES WITH LASIOCARPINE HAVE CONFIRMED THE FORMATION OF PYRROLIC METABOLITES BY THE MIXED-FUNCTION OXIDASE SYSTEM OF THE MICROSOMAL FRACTION OF RAT LIVER. DEHYDROHELIOTRIDINE HAS BEEN ISOLATED & IDENTIFIED AS A PRODUCT OF MICROSOMAL OXIDATION OF LASIOCARPINE.
来源:Hazardous Substances Data Bank (HSDB)
代谢
在尿液中...注射后16小时获得...对大鼠...未改变的毛果芸香碱(剂量的1-1.5%),海葵啶(1.5-3%),海葵啶N-氧化物(6%)和具有欧普因和7-天使海葵啶(预期部分水解产物)色谱性质的碱基痕迹。...24小时尿液样本中的代谢物...给药毛果芸香碱的8.5%。
IN URINE ... OBTAINED 16 HR AFTER INJECTION ... TO RATS ... UNCHANGED LASIOCARPINE (1-1.5% OF DOSE), HELIOTRIDINE (1.5-3%), HELIOTRIDINE N-OXIDE (6%) & TRACES OF BASES WITH CHROMATOGRAPHIC PROPERTIES OF EUROPINE & 7-ANGELYHELIOTRIDINE (EXPECTED PRODUCTS OF PARTIAL HYDROLYSIS). ... METABOLITES IN 24-HR URINE SAMPLE ... 8.5% OF ADMIN LASIOCARPINE.
来源:Hazardous Substances Data Bank (HSDB)
代谢
人类胚胎肝脏切片将吡咯里西啶生物碱LASIOCARPINE转化为吡咯,这通过正艾尔利希显色反应得到指示,而肺组织则没有。
HUMAN EMBRYONIC LIVER SLICES CONVERTED THE PYRROLIZIDINE ALKALOID LASIOCARPINE INTO PYRROLES, AS INDICATED BY A POS EHRLICH COLOR REACTION, WHEREAS LUNG TISSUE DID NOT.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 致癌性证据
致癌性分类:1)人类证据:不可用;2)动物证据:充分。对人类致癌风险的总体评估为2B组:该物质可能对人类致癌。/来自表格/
Classification of carcinogenicity: 1) evidence in humans: not available; 2) evidence in animals: sufficient. Overall summary evaluation of carcinogenic risk to humans is Group 2B: The agent is possibly carcinogenic to humans. /From table/
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 致癌物分类
国际癌症研究机构致癌物:鹰靛蓝
IARC Carcinogenic Agent:Lasiocarpine
来源:International Agency for Research on Cancer (IARC)
毒理性
  • 致癌物分类
国际癌症研究机构(IARC)致癌物分类:2B组:可能对人类致癌
IARC Carcinogenic Classes:Group 2B: Possibly carcinogenic to humans
来源:International Agency for Research on Cancer (IARC)
毒理性
  • 致癌物分类
国际癌症研究机构专著:第10卷:(1976年)一些天然存在的物质
IARC Monographs:Volume 10: (1976) Some Naturally Occurring Substances
来源:International Agency for Research on Cancer (IARC)
毒理性
  • 相互作用
LASIOCARPINE (7.8毫克/千克,IP每周两次,持续4周,然后每周一次,持续18周)并未阻止AFROTOXIN B1(饮食中2 PPM)引发肝癌,但改变了病理模式,即在同时接受AFROTOXIN和LASIOCARPINE的大鼠中,肝癌与坏死后肝硬化有关,而在单独接受AFROTOXIN的大鼠中,则没有这种关系。
LASIOCARPINE (7.8 MG/KG, IP TWICE WEEKLY FOR 4 WK, THEN ONCE A WK FOR 18 WK) DID NOT PREVENT INITIATION OF LIVER TUMORS BY AFLATOXIN B1 (2 PPM IN DIET), BUT ALTERED THE PATHOGENIC PATTERN IN THAT, IN RATS RECEIVING AFLATOXIN & LASIOCARPINE, THE LIVER TUMORS WERE ASSOC WITH POSTNECROTIC CIRRHOSIS, WHEREAS IN RATS DEVELOPING LIVER TUMORS WITH AFLATOXIN ALONE THEY WERE NOT.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
LASROCARPINE(随机标记,44%在氨基醇中)通过静脉给药给大鼠(总剂量为5毫克),4小时后标记分布如下:胴体,6.4%;肠道,8.6%;睾丸,0.1%;肺,0.05%;肾脏,0.26%;心脏,0.05%;脾,0.01%;大脑,0.03%;尿液,27.2%;肝脏,2.8%,呼出的二氧化碳,9.3% 肝部分馏得到1.73%在三氯乙酸提取物中,0.6%在蛋白质中,0.48%在脂质中,0.005%在核酸中。
LASROCARPINE (RANDOMLY LABELLED, 44% IN THE AMINO ALCOHOL) WAS ADMIN IP TO RATS (TOTAL DOSE, 5 MG) DISTRIBUTION OF LABEL AFTER 4 HR WAS AS FOLLOWS: CARCASS, 6.4%; INTESTINES, 8.6%; TESTES, 0.1%; LUNG, 0.05%; KIDNEY, 0.26%; HEART, 0.05%; SPLEEN, 0.01%; BRAIN, 0.03%; URINE, 27.2%; LIVER, 2.8%, EXPIRED CO2, 9.3% FRACTIONATION OF LIVER RESULTED IN 1.73% IN A TRICHLOROACETIC ACID EXTRACT, 0.6% IN PROTEIN, 0.48% IN LIPID & 0.005% IN NUCLEIC ACIDS.
来源:Hazardous Substances Data Bank (HSDB)

安全信息

  • 危险等级:
    6.1(b)
  • 危险类别:
    6.1(b)
  • 包装等级:
    III