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(1S,14S,18R,20S,23S,28S,34R)-28-[(2R)-2,3-dihydroxy-2-methylpropyl]-18-hydroxy-34-[(1S)-1-hydroxyethyl]-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo[12.11.11.03,11.04,9.016,20]hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptone

中文名称
——
中文别名
——
英文名称
(1S,14S,18R,20S,23S,28S,34R)-28-[(2R)-2,3-dihydroxy-2-methylpropyl]-18-hydroxy-34-[(1S)-1-hydroxyethyl]-23,31-dimethyl-12-thia-10,16,22,25,27,30,33,36-octazapentacyclo[12.11.11.03,11.04,9.016,20]hexatriaconta-3(11),4,6,8-tetraene-15,21,24,26,29,32,35-heptone
英文别名
——
CAS
——
化学式
C35H48N8O11S
mdl
——
分子量
788.9
InChiKey
KPKZJLCSROULON-RCGKFKHASA-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

计算性质

  • 辛醇/水分配系数(LogP):
    -1.7
  • 重原子数:
    55
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    317
  • 氢给体数:
    11
  • 氢受体数:
    12

ADMET

代谢
各种观察表明,绿色蘑菇毒蝇伞的一种有毒成分毒蝇碱本身并不具有毒性,但会在肝脏中进行生物激活。使用3H-去甲基毒蝇碱,一种毒蝇碱的有毒衍生物,得出结论...3H-去甲基毒蝇碱,以及很可能毒蝇碱本身,在大鼠和小鼠的肝脏中未经代谢。在处理过的动物的尿液中发现的次要排泄产物是被3H标记的衍生物的自降解化合物。
VARIOUS OBSERVATIONS SUGGESTED THAT PHALLOIDINE, A POISONOUS CONSTITUENT OF THE GREEN MUSHROOM, AMANITA PHALLOIDES, WOULD NOT BE TOXIC PER SE, BUT WOULD UNDERGO BIOACTIVATION IN THE LIVER. USING (3)H-DEMETHYLPHALLOIN, A TOXIC DERIVATIVE OF PHALLOIDINE, /IT WAS CONCLUDED/...THAT (3)H-DEMETHYLPHALLOIN, AND MOST PROBABLY ALSO PHALLOIDINE, ARE UNMETABOLIZED IN THE LIVERS OF RATS AND MICE. A SECONDARY EXCRETORY PRODUCT IN THE URINE OF TREATED ANIMALS WAS FOUND TO BE AN AUTODEGRADATION COMPOUND OF THE (3)H-LABELED DERIVATIVE.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 相互作用
使用利福平预处理(100或300毫克/千克,口服)可以保护小鼠免受鬼笔菌素(3毫克/千克,腹膜内注射)的毒性影响,这反映在死亡率下降上。
PRETREATMENT WITH RIFAMPICIN (100 OR 300 MG/KG, ORAL) PROTECTED MICE AGAINST THE TOXICITY OF PHALLOIDIN (3 MG/KG, IP) AS REFLECTED BY THE DECREASE IN THE MORTALITY RATE.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 相互作用
在实验鼠中,由鬼笔鹅膏素诱导的急性肝出血性坏死可以通过使用从飞蓟中提取的植物化合物水飞蓟宾进行治疗而得到预防。预先使用单剂量的水飞蓟宾可以完全消除毒素引起的形态学变化,并显著降低血清酶的活性。
IN MICE, THE ACUTE HEMORRHAGIC NECROSIS OF THE LIVER INDUCED BY PHALLOIDIN WAS PREVENTED BY TREATMENT WITH SILYBIN, A PLANT COMPOUND ISOLATED FROM SILYBUM MARIANUM. PRETREATMENT WITH A SINGLE DOSE OF SILYBIN COMPLETELY ABOLISHED THE MORPHOLOGIC CHANGES INDUCED BY THE TOXIN, AND SIGNIFICANTLY DECREASED THE ACTIVITIES OF SERUM ENZYMES.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
实验性体外血液灌流,使用活性炭和Amberlite XAD-4离子交换树脂,比血液透析更能增加(14)C标记的鬼笔鹅膏素肝素化的牛血血浆中的消除。
EXPERIMENTAL IN VITRO HEMOPERFUSION WITH ACTIVATED CHARCOAL AND AMBERLITE XAD-4 ION EXCHANGE RESIN INCREASED THE ELIMINATION OF (14)C-LABELED PHALLOIDIN FROM HEPARINIZED CATTLE BLOOD PLASMA MORE THAN HEMODIALYSIS.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
由于鬼笔毒素中毒导致的小鼠死亡率,在使用螺内酯单独治疗后降低了30-45%,或者在联合使用二氢链霉素呋喃唑酮和酵母治疗后也降低了30-45%。
THE MORTALITY RATE IN MICE DUE TO POISONING BY PHALLOIDIN WAS DECREASED BY 30-45% AFTER TREATMENT WITH SPIRONOLACTONE ALONE OR AFTER COMBINED TREATMENT WITH DIHYDROSTREPTOMYCIN, NIFUROXAZIDE, AND YEAST.
来源:Hazardous Substances Data Bank (HSDB)
毒理性
  • 解毒与急救
显然,二苯并噻吩,像其他稳定化合物一样,通过非特异性地稳定细胞质膜来发挥其保护作用,可能是通过释放自由基。
APPARENTLY DIBENZOTHIOLINE, LIKE OTHER STABILIZING COMPOUNDS, EXERTS ITS PROTECTIVE ACTION BY A NONSPECIFIC STABILIZATION OF THE CELL PLASMA MEMBRANE, PROBABLY BY RELEASE OF THIO RADICALS.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
在成年和新生(17-19天大)大鼠中,活体和体外实验比较了肝细胞对秋水仙碱的摄取、结合和消除。在两个年龄组中,肝脏中毒素的浓度与毒性之间没有关系。尽管新生大鼠对秋水仙碱的耐受性显著高于成年大鼠,但新生大鼠肝脏中毒素的浓度更高,消除速度显著慢于成年大鼠。秋水仙碱在肝脏中的非常紧密的结合和高浓度通过一个非常低的解离常数来解释。
THE UPTAKE, BINDING AND ELIMINATION OF PHALLOIDIN BY LIVER WAS COMPARED IN ADULT AND BABY (17-19 DAYS OLD) RATS IN VIVO AND IN VITRO. IN BOTH GROUPS, THERE WAS NO RELATION BETWEEN THE CONCENTRATION OF THE POISON IN THE LIVER AND THE TOXICITY. ALTHOUGH BABY RATS SHOWED A SIGNIFICANTLY HIGHER TOLERANCE AGAINST PHALLOIDIN THAN THE ADULT ANIMALS, THE CONCENTRATION OF THE POISON IN THE LIVER OF BABY RATS WAS HIGHER, AND THE ELIMINATION WAS SIGNIFICANTLY SLOWER THAN IN ADULT RATS. THE VERY TIGHT BINDING AND CONCENTRATION OF PHALLOIDIN IN THE LIVER WAS EXPLAINED BY AN EXTREMELY LOW DISSOCIATION CONSTANT.
来源:Hazardous Substances Data Bank (HSDB)
吸收、分配和排泄
aMAnita phalloides 提取物给药后,大鼠尿液中在第一天检测到PHALLOIN和GAMMA-AMANITIN,第二天检测到PHALLOIDIN。
PHALLOIN AND GAMMA-AMANITIN WERE DETECTED WITHIN THE FIRST DAY AND PHALLOIDIN WITHIN THE SECOND DAY IN THE URINE OF RATS AFTER ADMINISTRATION OF AMANITA PHALLOIDES EXTRACTS.
来源:Hazardous Substances Data Bank (HSDB)

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-N,3,3-三甲基-N-(苯甲基)丁酰胺 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素(1-6) 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸