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disodium;selenite

中文名称
——
中文别名
——
英文名称
disodium;selenite
英文别名
——
disodium;selenite化学式
CAS
——
化学式
Na2O3Se
mdl
——
分子量
172.95
InChiKey
BVTBRVFYZUCAKH-UHFFFAOYSA-L
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

计算性质

  • 辛醇/水分配系数(LogP):
    -8.87
  • 重原子数:
    6
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.2
  • 氢给体数:
    0
  • 氢受体数:
    3

ADMET

代谢
大部分膳食硒以硒代甲硫氨酸(硒的主要膳食形式)或硒代半胱氨酸的形式存在,这两种形式都能很好地被吸收。其他形式的硒包括硒酸盐和亚硒酸盐,它们不是膳食的主要成分,但常用于强化食品和膳食补充剂中。人体内存在两种储备硒池。第一种是硒代甲硫氨酸,它除了具有甲硫氨酸的生理功能外,没有已知的独立生理功能。第二个储备池是存在于肝脏谷胱甘肽过氧化物酶中的硒。摄入的亚硒酸盐、硒酸盐和硒代半胱氨酸都直接代谢为硒化物,即硒的还原形式。硒代甲硫氨酸也可以代谢为硒化物。/亚硒酸盐/
Most dietary selenium is in the form of selenomethionine (the major dietary form of selenium) or selenocysteine, both of which are well absorbed. Other forms of selenium include selenate and selenite, which are not major dietary constituents, but are commonly used in fortified foods and dietary supplements. Two pools of reserve selenium are present in the body. The first is as selenomethionine, which is not known to have a physiological function separate from that of methionine. The second reserve pool is the selenium found in liver glutathione peroxidase. Ingested selenite, selenate, and selenocysteine are all metabolized directly to selenide, the reduced form of selenium. Selenomethionine can also be metabolized to selenide. /Selenite/
来源:Hazardous Substances Data Bank (HSDB)
代谢
在饮水中添加亚硒酸钠(Na2SeO3)14天后,小鼠呼出的气体中形成了二甲基硒化物和二甲二硒化物。呼出似乎是一种硒排出的次要形式。
The addition of sodium selenite (Na2SeO3) to the drinking water of mice for 14 days resulted in the formation of dimethylselenide and also dimethyldiselenide in the breath. Exhalation seems to be a minor form of selenium elimination.
来源:Hazardous Substances Data Bank (HSDB)
代谢
使用富集稳定同位素作为示踪剂的HPLC-ICP MS方法对静脉注射到大鼠体内的亚硒酸盐和硒化物进行了分类。在剂量关系实验中,将含有82(Se)富集的亚硒酸盐或硒化物静脉注射到8周龄的雄性Wistar大鼠中(每组三只大鼠),亚硒酸盐组的单次剂量为10、25、50、100和200微克/千克体重,硒化物组的单次剂量为2、5、10、25和50微克/千克体重。1小时或24小时后处死动物,测定肝脏、肾脏、血清以及膀胱内残留尿液或24小时尿液中硒-82的浓度和分布。在时间过程实验中,分别以50和10微克/千克的剂量注射含有82(Se)富集的亚硒酸盐和硒化物,并在5、15、30、60和180分钟后处死动物。结果表明,亚硒酸盐被肝脏直接吸收的效率大约是硒化物的一半,后者在红细胞中代谢成硒化物后被肝脏吸收。尽管亚硒酸盐和硒化物在血液中的代谢方式不同,且只有一部分亚硒酸盐直接排入尿液中,但被肝脏吸收的硒-82的代谢方式在亚硒酸盐和硒化物之间是不可区分的。来自硒化物而非亚硒酸盐的硒-82被认为在血液中发生氧化还原反应。这些结果表明,尽管静脉注射亚硒酸盐被机体利用的效率较低,但它在肝脏内的利用方式与硒化物相似,且更为安全。/硒化物/
Selenate and selenite injected intravenously into rats were speciated by the HPLC-ICP MS method with use of an enriched stable isotope as the tracer. In dose-relation experiments, 82(Se)-enriched selenate or selenite was injected intravenously into male Wistar rats of 8 weeks of age (three rats/group) at single doses of 10, 25, 50, 100 and 200 ug/kg body weight for the selenate group, and 2, 5, 10, 25 and 50 ug/kg body weight for the selenite group. The animals were sacrificed 1 or 24 hr later, and the concentrations and distributions of selenium-82 in the liver, kidneys, serum, and urine remaining in the bladder or 24-hr urine were determined. In time-course experiments, (82)Se-enriched selenate and selenite were injected at doses of 50 and 10 ug/kg body weight, respectively, and the animals were sacrificed 5, 15, 30, 60 and 180 min later. It was suggested that selenate is directly taken up by the liver with an efficiency of approximately 1/2 compared with selenite, the latter being taken up by the liver after being metabolized to selenide in red blood cells. Although selenate and selenite were metabolized differently in the bloodstream, and also a part of only selenate was excreted directly into the urine, the selenium-82 taken up by the liver was shown to be metabolized in a manner indistinguishable between selenate and selenite. Selenium-82 of selenite origin but not of selenate origin was suggested to undergo redox reaction in the bloodstream. These results suggest that although parenteral selenate is utilized less efficiently by the body, it is utilized in the liver in a similar manner to selenite much more safely. /Selenite/
来源:Hazardous Substances Data Bank (HSDB)
代谢
用于研究体内硒的代谢途径的亚硒酸盐和硒酸盐,使用富集了(82)Se的...。确定了在器官和体液中(82)Se的浓度以及其成分的分布,这取决于给大鼠静脉注射(82)Se-亚硒酸盐和硒酸盐后的剂量和时间。亚硒酸盐在几分钟内被红细胞摄取,被谷胱甘肽还原为硒化物,然后运输到血浆中,选择性地与白蛋白结合并转移到肝脏。与亚硒酸盐相反,完整的硒酸盐要么直接被肝脏摄取,要么排入尿液中。在肝脏中检测到来自亚硒酸盐的(82)Se和来自硒酸盐的(82)Se,它们以两种硒峰材料A和B的形式存在。前者在体内和体外被甲基化为后者。后者与主要的尿液代谢物相同,被鉴定为Se-甲基-N-乙酰-硒己糖胺(硒糖)。硒的特定化学物种代谢途径通过硒化物作为无机和有机硒源的假定共同中间体以及作为硒蛋白合成利用和硒排泄甲基化之间的检查点代谢物来解释。/亚硒酸盐/
Metabolic pathways for Se in the body were studied for selenite and selenate, with the use of enriched (82)Se ... . The concentrations of (82)Se in organs and body fluids and the distributions of their constituents depending on the dose and time after the intravenous administration of (82)Se-selenite and -selenate to rats were determined. Selenite was taken up by red blood cells within several minutes, reduced to selenide by glutathione, and then transported to the plasma, bound selectively to albumin and transferred to the liver. Contrary to selenite, intact selenate was either taken up directly by the liver or excreted into the urine. The (82)Se of selenite origin and that of selenate origin were detected in the forms of the two Se peak materials in the liver, A and B. The former one was methylated to the latter in vivo and in vitro. The latter one was identical with the major urinary metabolite and it was identified as Se-methyl-N-acetyl-selenohexosamine (selenosugar). The chemical species-specific metabolic pathway for Se was explained by the metabolic regulation through selenide as the assumed common intermediate for the inorganic and organic Se sources and as the checkpoint metabolite between utilization for the selenoprotein synthesis and methylation for the excretion of Se. /Selenite/
来源:Hazardous Substances Data Bank (HSDB)
代谢
硒可以通过吸入和摄入被吸收,而一些硒化合物也可能通过皮肤吸收。一旦进入人体,硒主要分布到肝脏和肾脏。硒是一种必需的微量元素,是谷胱甘肽过氧化物酶、碘甲状腺原氨酸5'-脱碘酶和硫氧还蛋白还原酶的组成部分。有机硒首先代谢为无机硒。无机硒逐步还原为中间体氢硒化物,然后转化为硒磷酸和硒半胱氨酸tRNA被纳入硒蛋白,或者转化为硒化物的甲基化代谢物后排入尿液中。元素硒在排泄前也会被甲基化。硒主要通过尿液和粪便排出,但某些硒化合物也可能通过呼吸排出。(L619)
Selenium may be absorbed through inhalation and ingestion, while some selenium compounds may also be absorbed dermally. Once in the body, selenium is distributed mainly to the liver and kidney. Selenium is an essential micronutrient and is a component of glutathione peroxidase, iodothyronine 5'-deiodinases, and thioredoxin reductase. Organic selenium is first metabolized into inorganic selenium. Inorganic selenium is reduced stepwise to the intermediate hydrogen selenide, which is either incorporated into selenoproteins after being transformed to selenophosphate and selenocysteinyl tRNA or excreted into the urine after being transformed into methylated metabolites of selenide. Elemental selenium is also methylated before excretion. Selenium is primarily eliminated in the urine and feces, but certain selenium compounds may also be exhaled. (L619)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 毒性总结
硒可以轻易地替代生物分子中的硫,并在许多生化反应中替代硫,特别是在硒的浓度高而硫的浓度低时。通过影响线粒体和微粒体的电子传递,使细胞呼吸中氧化反应所需的巯基酶失活,这可能是急性硒中毒的一个因素。硒代甲硫氨酸(一种常见的有机硒化合物)似乎也可以随机地替代蛋白质合成中的甲硫氨酸。这种替代可能会影响蛋白质的结构和功能性,例如,通过改变二硫键。无机形式的硒似乎通过氧化还原催化与组织巯基反应,导致形成活性氧种,并通过氧化应激造成损害。(L619)
Selenium readily substitutes for sulfur in biomolecules and in many biochemical reactions, especially when the concentration of selenium is high and the concentration of sulfur is low. Inactivation of the sulfhydryl enzymes necessary for oxidative reactions in cellular respiration, through effects on mitochondrial and microsomal electron transport, might contribute to acute selenium toxicity. Selenomethionine (a common organic selenium compound) also appears to randomly substitute for methionine in protein synthesis. This substitution may affect the structure and functionability of the protein, for example, by altering disulfide bridges. Inorganic forms of selenium appear to react with tissue thiols by redox catalysis, resulting in formation of reactive oxygen species and causing damage by oxidative stress. (L619)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 致癌物分类
3, 其对人类致癌性无法分类。
3, not classifiable as to its carcinogenicity to humans. (L135)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 健康影响
长期口服高浓度硒化合物可能会产生一种叫做硒中毒的疾病。硒中毒的主要症状包括脱发、指甲变脆和神经系统异常(例如四肢麻木和其他奇怪的感觉)。动物研究显示,硒还可能影响精子生产和女性生殖周期。
Chronic oral exposure to high concentrations of selenium compounds can produce a disease called selenosis. The major signs of selenosis are hair loss, nail brittleness, and neurological abnormalities (such as numbness and other odd sensations in the extremities). Animal studies have shown that selenium may also affect sperm production and the female reproductive cycle. (L619)
来源:Toxin and Toxin Target Database (T3DB)
毒理性
  • 暴露途径
该物质可以通过吸入其气溶胶和通过摄入被身体吸收。
The substance can be absorbed into the body by inhalation of its aerosol and by ingestion.
来源:ILO-WHO International Chemical Safety Cards (ICSCs)
毒理性
  • 暴露途径
口服(L619);吸入(L619);皮肤给药(L619)
Oral (L619) ; inhalation (L619) ; dermal (L619)
来源:Toxin and Toxin Target Database (T3DB)
吸收、分配和排泄
通过喂食单一稳定硒同位素(82Se-亚硒酸盐)来耗尽大鼠体内的内生自然丰度硒,然后同时给予(76)Se-亚硒酸盐和(77)Se-硒代甲硫氨酸(77Se-SeMet)。生物样本通过HPLC-ICPMS进行定量和形态分析。追踪并检查了标记的(76)Se和(77)Se的代谢物与内生硒的相互作用,而没有受到相应内生自然丰度同位素的干扰。在完全相同的生物学和分析条件下比较了两种营养硒化合物在器官之间和器官内的分布和代谢差异:(1)除了胰腺外,亚硒酸盐在器官和体液中的分布效率高于SeMet。(2)SeMet以完整形式被器官摄取。(3)来自SeMet的硒在胰腺中有选择性地分布,并且大部分与完整SeMet一起与蛋白质结合。(4)在肝脏中检测到硒糖A和B,但没有检测到三甲基硒onium(TMSe)。(5)在肾脏中检测到硒糖B和TMSe。
... Rats were depleted of endogenous natural abundance selenium by feeding a single selenium stable isotope ((82)Se-selenite) and then administered (76)Se-selenite and (77)Se-selenomethionine ((77)Se-SeMet)simultaneously. Biological samples were subjected to quantification and speciation analysis by HPLC-ICPMS. Metabolites of the labeled (76)Se and (77)Se and interaction with endogenous selenium were traced and examined without interference from the corresponding endogenous natural abundance isotopes. Differences in the distribution and metabolism among organs and between the two nutritional selenocompounds were compared under exactly identical biological and analytical conditions: (1) selenite was distributed more efficiently than SeMet in organs and body fluids except the pancreas. (2) SeMet was taken up by organs in its intact form. (3) Selenium of SeMet origin was distributed selectively in the pancreas and mostly bound to a protein together with intact SeMet. (4) Selenosugars A and B but not trimethylselenonium (TMSe) were detected in the liver. (5) Selenosugar B and TMSe were detected in the kidneys.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
通过腹膜内注射的方式给老鼠注入了含有硒的钠盐(75)Se亚硒酸钠(5 mg/kg),结果发现亚硒酸形式的硒在前叶垂体中积聚。最大硒含量在2小时后观察到,此时前叶垂体的硒含量为2.9 mg/g湿重。未经处理的鼠垂体中的硒含量为0.48 mg/g湿重。
Rats were injected intraperitoneally with (75)Se sodium selenite (5 mg/kg), and it was concluded that selenium in the form of selenite accumulated in the anterior pituitary gland. The maximum selenium content was observed after 2 hours, at which time the anterior pituitary gland contained 2.9 mg/g wet weight. The selenium contact in pituitary glands from untreated rats was 0.48 mg/g wet weight.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
在充足补充饮食(1.0毫克/千克)的情况下,67%的亚硒酸盐示踪剂量通过尿液排出,而在缺乏状态下,同一剂量的仅有6%被排出。
With an adequate supplementation of the diet (1.0 mg/kg), 67% of a tracer dose of selenite was excreted in the urine, whereas in a state of deficiency only 6% of the same dose was excreted. /Selenite/
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
亚硒酸盐的示踪剂量在红细胞中积累,转移到血浆蛋白,然后到肝脏。尽管可能存在其他转运蛋白,不同器官可能对硒源有不同的偏好,但硒蛋白P似乎参与了将硒从肝脏运输到其他组织的运输过程。/亚硒酸盐/
A tracer dose of selenite accumulated in red blood cells, translocated to plasma proteins, and then to the liver. Selenoprotein P seems to be involved in the transport of Se from the liver to other tissues, even though other transporters may exist and different organs may have different preferences for selenium sources. /Selenite/
来源:Hazardous Substances Data Bank (HSDB)

反应信息

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文献信息

  • Peptide analog type-B CCK receptor ligands
    申请人:Abbott Laboratories
    公开号:US05340802A1
    公开(公告)日:1994-08-23
    Peptide analog type-B CCK receptor ligands or pharmaceutically-acceptable salts thereof, which are useful for treating central nervous system disorders, substance abuse, gastrointestinal disorders, endocrine disorders, eating-related disorders and for the treatment of shock, respiratory and cardiocirculatory insufficiencies.
    肽类模拟物B型CCK受体配体或其药学上可接受的盐,可用于治疗中枢神经系统疾病、物质滥用、胃肠道疾病、内分泌失调、进食相关障碍以及休克、呼吸和心血管功能不足的治疗。
  • XARADA, TAKEHSI
    作者:XARADA, TAKEHSI
    DOI:——
    日期:——
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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