(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート

(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 化学構造式
4720-09-6
CAS番号.
4720-09-6
化学名:
(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート
别名:
アセチルアンドロメドール;(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート;アンドロメドトキシン;グラヤノトキシンI;グラヤノトキシン I
英語名:
ANDROMEDOTOXIN
英語别名:
g-i;asebotoxin;rhodotoxin;rhodotoxine;grayanotoxini;ANDROMEDOTOXIN;GRAYANOTOXIN 1;acetylandromedol;acteylandromedol;acetyllandromedol
CBNumber:
CB4155966
化学式:
C22H36O7
分子量:
412.52
MOL File:
4720-09-6.mol
MSDS File:
SDS

(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 物理性質

融点 :
258-260 to 267-270°
比旋光度 :
D25 -8.8° (c = 2.3 in ethanol)
沸点 :
451.94°C (rough estimate)
比重(密度) :
1.1142 (rough estimate)
屈折率 :
1.5300 (estimate)
酸解離定数(Pka):
13.72±0.70(Predicted)
色:
EtOAc/ペンタンからの結晶

安全性情報

RIDADR  3172
国連危険物分類  6.1(a)
容器等級  I
有毒物質データの 4720-09-6(Hazardous Substances Data)
毒性 LD50 i.p. in mice: 1.31 mg/kg (Hikino, 1976)

(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 化学特性,用途語,生産方法

説明

Fructus Rhododendri (ba li ma) is the dried fruit of Rhododendron molle (Bl.) G. Don (yánɡ zhí zhú), mainly distributed in the Jiangsu, Hubei, and Jiangxi Provinces of China .
“Compendium of Materia Medica” recorded that Rhododendron molle (Bl.) G. Don (yánɡ zhí zhú) can be used to treat waist pain, arm pain, and poisoning. It is effective at lowering blood pressure and slowing the heart rate, but a large dosage can cause death . Rhomotoxin’s formulations include injection and tablet. Side effects include a burning sensation, numbness, dizziness, dry mouth, nausea, vomiting, vertigo, chest tightness, slow heartbeat, and low blood pressure. In addition, pregnant women should use it with caution.

物理的性質

Appearance: white crystalline or powder. Solubility: soluble in water, acetone, and chloroform, almost insoluble in diethyl ether or petroleum ether. Melting point: 265–268 °C. Specific optical rotation: ?50 to ?60°.

来歴

Because rhomotoxin can slow down heart rhythm and blood pressure, Deng Dao ji et al. from the First Affiliated Hospital of Wuhan Medical College researched Fructus Rhododendri in the early 1970s. They extracted the crystallization from fruits and obtained preliminary results by animal testing and clinical application .
Rhomotoxin is a white needle crystal that is extracted from the dried fruit of Rhododendron molle (Bl.) G. Don (yánɡ zhí zhú). Its biological activity is closely related to three-dimensional specificity and hydrophobicity. 5β-hydroxyl, 6β- hydroxyl, and, especially, the 2,3-epoxy groups can affect its biological activity .
Rhomotoxin was acetylated to obtain monoacetate (Japanese Rhododendron II). The melting points of rhomotoxin and Japanese Rhododendron III are identical (284–286 °C). IR and Rf of silica gel thin layer chromatography are identical. Therefore, rhomotoxin is Japanese Rhododendron III .

定義

ChEBI: A tetracyclic diterpenoid that is grayanotoxane in which the pro-R hydrogen at position 14 is substituted by an acetoxy group and in which the 3beta-, 5-, 6beta-, 10-, and 16- positions are su stituted by hydroxy groups.

薬理学

The pharmacological effects of rhomotoxin are mainly displayed in three aspects: (1) analgesic effect: the suspension, infusion, and alcohol made of rhomotoxin fruit have an analgesic effect in mice ; (2) effects on cardiovascular system: the resting heart rate is a bad prognostic indicator of hypertension and other cardiovascular diseases. Rhomotoxin can reduce the resting heart rate; (3) kidney protection: rhomotoxin promotes good blood pressure and a slow heart rate and provides kidney protection. Its mechanism may be related to a reduction in the content of angiotensin II (Ang II), increasing endothelial nitric oxide synthase (eNOS) content, and slowing heart rate .
The plasma concentration of mice decreased rapidly over time following intravenous injection of rhomotoxin; there was no residue after 6 h. Rhomotoxin is rapidly distributed to various organs through the blood circulation and reaches a peak within 5–15 min. The gallbladder (including bile) contained the highest amount, followed by the liver and kidneys. It affects, in order, the gallbladder (including bile), liver, kidney, thyroid, stomach, adrenal gland, heart, lungs, and brain. Rhomotoxin is excreted mainly by the kidney and digestive tract. More prototype drugs are in the urine than in the stool. Rhomotoxin has a stimulating effect on the stomach. A certain amount of rhomotoxin also entered the thyroid and adrenal glands. A very small amount was found in brain tissue, demonstratinge that rhomotoxin does not easily pass through the blood-brain barrier. Plasma dialysis showed that the plasma protein binding rate of rhomotoxin can reach as high as 60% in 30 min .

臨床応用

Rhomotoxin acts as an antihypertensive drug, and it is able to lower the blood pressure in patients with severe hypertension. Its pharmacological effects are related to parasympathetic function. Large-dosage-induced low blood pressure can be restored with ephedrine. Its antihypertensive effect lasts for 0.5–1 h. If blood pressure has not dropped to a satisfactory level, rhomotoxin must not have been added because an excessive drop in blood pressure would lead to shock. Oral administration with aluminum hydroxide can reduce rhomotoxin-induced stomach discomfort. Intramuscular injection can also cause local pain. In addition, procaine reduces its antihypertensive effect. Secondary hypertension and malignant hypertension patients should use it with caution, critical and dying patients should be disabled (including, for example, severe heart failure, cardiomyopathy, atrioventricular block, and severe ventricular arrhythmias).

安全性プロファイル

Poison by subcutaneous,parenteral, intravenous and intraperitoneal routes. Whenheated to decomposition it emits acrid smoke and fumes.

(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 上流と下流の製品情報

原材料

準備製品


(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート 生産企業

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(3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート  スペクトルデータ(IR1、IR2)


4720-09-6((3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート)キーワード:


  • 4720-09-6
  • acetyllandromedol
  • acteylandromedol
  • ANDROMEDOTOXIN
  • (3β,6β,14R)-Grayanotoxane-3,5,6,10,14,16-hexol 14-acetate
  • 6,10,14,16-hexol,14-acetate,(3-beta,6-beta,14r)-grayanotoxane-5
  • 6,10,14,16-hexol,14-acetate,(3beta,6beta,14r)-grayanotoxane-5
  • 9a-methano-9ah-cyclopenta(b)heptalene-2,4,8,11,11a,12(1h)-hexol-dodecahydro
  • acetylandromedol
  • rhodotoxine
  • asebotoxin
  • g-i
  • grayanotoxane-3,5,6,10,14,16-hexol14-acetate
  • grayanotoxini
  • rhodotoxin
  • GRAYANOTOXIN 1
  • 4,8-tetramethyl-,12-acetate(2s,3as,4r,4ar,7r,8r,9as,11r,11ar,12r)-1
  • 4,8-tetramethyl-,12-acetate,(2s,3as,4ar,7r,8r,9as,11r,11ar,12r)--1
  • ANDROMEDOTOXIN USP/EP/BP
  • Grayanotoxane-3,5,6,10,14,16-hexol, 14-acetate, (3β,6β,14R)-
  • アセチルアンドロメドール
  • (3β,6β,14R)-グラヤノトキサン-3,5,6,10,14,16-ヘキサオール14-アセタート
  • アンドロメドトキシン
  • グラヤノトキシンI
  • グラヤノトキシン I
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