퀴닌

그림문자(GHS)

• 그림문자(GHS)

  

• 신호 어

  Warning

• 유해·위험 문구

  H302：삼키면 유해함

  H317：알레르기성 피부 반응을 일으킬 수 있음

• 예방조치문구

  P261：분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.

  P264：취급 후에는 손을 철저히 씻으시오.

  P264：취급 후에는 손을 철저히 씻으시오.

  P280：보호장갑/보호의/보안경/안면보호구를 착용하시오.

  P302+P352：피부에 묻으면 다량의 물로 씻으시오.

  P333+P313：피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.

퀴닌 MSDS

• Quinine

퀴닌 화학적 특성, 용도, 생산

• 물성

  Quinine은 항 말라리아제입니다. Quinine은 DNA 복제를 억제하여 적혈구 형태의 다이아몬드와 말라리아의 분열을 억제합니다. Quinine은 또한 국소 마취와 자극 효과가 있습니다. Quinine은 체온 조절의 중심을 억제 할 수 있고, 높은 복용량을 사용할 때 대뇌 피질의 시각 및 청각 영역의 작용을 억제 할 수 있습니다. Quinine은 불응 기간을 연장시키고 심장 근육의 수축성과 흥분성을 낮 춥니 다. 퀴닌 (Quinine)은 내부 장기의 평활근 세포를 자극하고 리듬 성 수축을 촉진하며 자궁의 색조를 증가시킵니다.

• 개요

  퀴닌(quinine)은 해열·진통·말라리아 예방 등의 효과가 있는 알칼로이드이다.알칼로이드계 화합물의 일종. 기나나무속(Quinine tree)의 나무껍질에서 추출해 낸다. 우리나라에서는 철자 그대로 읽어서 키니네라고도 불렀으며, 말라리아 치료제로 널리 쓰였다.

• 개요

  Quinine, was the first known antimalarial. It is a 4-quinolinemethanol derivative bearing a substituted quinuclidine ring. The use of quinine in Europe began in the seventeenth century, after the Incas of Peru informed the Spanish Jesuits about the antimalarial properties of the bark of an evergreen mountain tree they called quinquina (later called cinchona, after Dona Franciscoa Henriquez de Ribera [1576–1639], Countess of Chinchon and wife of the Peruvian Viceroy).

• 화학적 성질

  Quinine is odorless, but has an intense, bitter taste

• 물리적 성질

  Appearance: white granular or microcrystalline powder. No smell, slightly bitter. Solubility: easily dissolved in ethanol, chloroform, and ethyl. Slightly soluble in water and glycerol. Melting point: 173–175 °C. Specific optical rotation: ?172° (ETOH, C = 1).

• 출처

  Reported present in Cinchona officinalis.

• 역사

  Quinine is a white crystalline alkaloid best known for treating malaria. Quinine is derived from the bark of several species of trees in the genus Cinchona in the Rubiaceae family. Cinchona trees grow on the eastern slopes of the Andes Mountains at elevations of several thousand feet. Because these symptoms were associated with malaria, Cinchona bark powder was recognized as a possible treatment in the 1600s by Jesuit missionaries.
  After decades of work by numerous investigators, quinine was finally isolated in 1820 by Pierre-Joseph Pelletier (1788–1842) and Joseph-Bienaimé Caventou (1795–1877). The name quinine originates from the native word for the Cinchona tree quina quina, which became the Spanish word quino for cinchona. The development of organic synthesis in the middle of the 19th century and the limited supply of quinine stimulated attempts to synthesize it. William Henry Perkins’s (1838–1907) attempt to synthesize quinine in 1856 led to his discovery of mauve, which was a signifi cant discovery in the dye industry (see Indigo).

• 용도

  Because of its relatively constant and well-known fluorescence quantum yield, quinine is also used in photochemistry as a common fluorescence standard. It has been used for imaging of oxygen evolution and oxide formation. Chloride and bromide have been sh

• 제조 방법

  By reaction from cinchona bark (Cinchona officinalis), where it is present at approximately 8%.

• Indications

  Quinine is one of several alkaloids derived from the bark of the cinchona tree. The mechanism by which it exerts its antimalarial activity is not known. It does not bind to DNA at antimalarial dosages. It may poison the parasite’s feeding mechanism, and it has been termed a general protoplasmic poison, since many organisms are affected by it.
  Quinine is rapidly absorbed following oral ingestion, with peak blood levels achieved in 1 to 4 hours. About 70 to 93% of the drug is bound to plasma proteins, depending on the severity of the infection. Quinine is extensively metabolized, with only about 20% of the parent compound eliminated in the urine.
  The primary present-day indication for quinine and its isomer, quinidine, is in the intravenous treatment of severe manifestations and complications of chloroquine- resistant malaria caused by P. falciparum.
  Aside from its use as an antimalarial compound, quinine is used for the prevention and treatment of nocturnal leg muscle cramps, especially those resulting from arthritis, diabetes, thrombophlebitis, arteriosclerosis, and varicose veins.

• 정의

  quinine: A white solid,C₂₀H₂₄N₂O₂·3H₂O, m.p. 57°C. It is apoisonous alkaloid occurring in thebark of the South American cinchonatree, although it is now usually producedsynthetically. It forms saltsand is toxic to the malarial parasite,and so quinine and its salts are used to treat malaria; in small doses itmay be prescribed for colds and influenza.In dilute solutions it has apleasant astringent taste and is addedto some types of tonic water.

• Antimicrobial activity

  Quinine inhibits the erythrocytic stages of human malaria parasites at <1 mg/L, but not the liver stages. It is active against the gametocytes of P. vivax, P. ovale and P. malariae, but not P. falciparum. The dextrarotatory stereoisomer, quinidine, is more active than quinine, but epiquinine (cinchonine) and epiquinidine (cinchonidine) have much lower antimalarial activities.

• 원료

  Resistance is now widespread in South East Asia, where some strains are also resistant to chloroquine, sulfadoxine– pyrimethamine and mefloquine. Cross-resistance with mefloquine has been demonstrated in P. falciparum, but genetic polymorphisms associated with chloroquine resistance are not associated with quinine resistance.

• 일반 설명

  Quinine, a cinchona alkaloid found in the bark of the cinchona tree, is known for its anti-malarial property.

• 위험도

  Skin irritant, ingestion of pure substance adversely affects eyes.

• 건강위험

  The toxicity of quinine is characterized bycinchonism, a term that includes tinnitus,vomiting, diarrhea, fever, and respiratorydepression. Other effects include stimulationof uterine muscle, analgesic effect,and dilation of the pupils. Severe poisoningmay produce neurosensory disorders, causingclouded vision, double vision, buzzing of theears, headache, excitability, and sometimescoma (Ferry and Vigneau 1983). Death fromquinine poisoning is unusual. Massive dosesmay be fatal, however.
  LD50 value, oral (guinea pigs): 1800 mg/kg.

• Pharmaceutical Applications

  A quinolinemethanol from the bark of the Cinchona tree; the laevorotatory stereoisomer of quinidine. Formulated as the sulfate, bisulfate or ethylcarbonate for oral use and as the dihydrochloride for parenteral administration. The salts are highly soluble in water.

• Pharmacokinetics

  Oral absorption: 80–90%
  C_max 600 mg oral: 5 mg/L after 1–3 h
  Plasma half-life: 8.7 h
  Volume of distribution: 1.8 L/kg
  Plasma protein binding: c. 70%
  Quinine is well absorbed by the oral route. Intramuscular administration gives more predictable data than intravenous administration and may be more useful in children. Plasma protein binding rises to 90% in uncomplicated malaria and 92% in cerebral malaria due to high levels of acute-phase proteins. Similarly, the elimination half-life rises to 18.2 h in severe malaria. There is extensive hepatic metabolism to hydroxylated derivatives. Urinary clearance is <20% of total clearance.

• Pharmacology

  In terms of its type of action, quinine is an antimalarial drug similar to chloroquine, although it is inferior in its activity.
  Like chloroquine, quinine binds with plasmodium DNA, thus interfering in the synthesis of nucleic acids and preventing its replication and transcription. Quinine also suppresses a large portion of the enzymatic system and therefore it is characterized as a general protoplasmid toxin. This fact agrees well with the action of quinine on membranes, its local anesthetizing and its cardiodepressive effects.
  Upon oral administration, quinine effectively acts in combination with pyrimethamine, sulfadiazine, and/or tetracycline for treating uncomplicated incidents of chloroquineresistant forms of P. falciparum. Because of the many associated side effects, its use is extremely limited. Currently, the only indication for use is for forms of malaria that are resistant to other synthetic drugs. Synonyms of this drug are bronchopulmin, nicopriv, quinnam, and others.

• Clinical Use

  Falciparum malaria (alone or in combination with tetracycline, doxycycline, clindamycin or pyrimethamine–sulfadoxine)
  Babesiosis (in combination with clindamycin)
  It is particularly used in cerebral malaria if chloroquine resistance is suspected (Ch. 62). It is not recommended for treatment of uncomplicated falciparum malaria.

• 부작용

  Up to 25% of patients experience cardiac dysrhythmia, hypoglycemia, cinchonism (tinnitus, vomiting, diarrhea, headache). Severe effects, including hypotension and hypoglycemia, are of particular importance in children, pregnant women and the severely ill. Rarely, it can induce hemolytic anemia (‘blackwater fever’). Quinine inhibits tryptophan uptake into cells.

• Safety Profile

  Human poison by unspecified route. Experimental poison by subcutaneous, intravenous, intramuscular, and intraperitoneal routes. Moderately toxic experimentally by ingestion. An experimental teratogen. Human systemic effects by ingestion: visual field changes, tinnitus, and nausea or vomiting. Human teratogenic effects by ingestion: developmental abnormahties of the central nervous system, body wall, and musculoskeletal, cardovascular, and hepatoblltary systems. Experimental reproductive effects. Mutation data reported. Can cause temporary loss of vision. Quinine dermatitis is an occupational hazard to barbers particularly, and generally to people who work with quinine tonics, medcaments, or cosmetics. An irritant to mucous membranes. Combustible when exposed to heat or flame. Decomposes on exposure to light. When heated to decomposition it emits toxic fumes of NOx. Used to treat malaria.

• 신진 대사

  Quinine is metabolized in the liver to the 2′-hydroxy derivative, followed by additional hydroxylation on the quinuclidine ring, with the 2,2′-dihydroxy derivative as the major metabolite. This metabolite has low activity and is rapidly excreted. The metabolizing enzyme of quinine is CYP3A4. With the increased use of quinine and its use in combination with other drugs, the potential for drug interactions based on the many known substrates for CYP3A4 is of concern.

• Purification Methods

  Crystallise the quinine from absolute EtOH. It has been used as a chiral catalyst (see previous entry). [Beilstein 23 H 511, 23 I 166, 23 II 416, 23 III/IV 3265, 23/13 V 395.]

• 참고 문헌

  Pelletier, Dumas., Ann. Chim. Phys., 15,291,1337 (1820)
  Hesse., Annalen, 258, 133 (1890)
  Fiihner., Arch. Pharm., 244, 602 (1906)
  Seekles., Rev. Trav. Chim., 42, 72 (1923)
  Kindler., Chem. Ztg., 56, 165 (1932)
  Cohen.,J. Chem. Soc., 999 (1933)
  Velter., Festschrift., 542 (Basle, 1936)
  Woodward, Doering.,J. Amer. Chem. Soc., 67,860 (1945)
  Pharmacology :
  Acton, King., Biochem. J., 15,53 (1921)
  Sterkin, Helfgat., Biochem. Zeit., 207, 8 (1929)
  Wagenaar.,Pharm. Weekbl., 66, 177, 197,250,261 (1929)
  Wagenaar., ibid, 71,316 (1934)
  Monnet., J. Pharm. Chim., 18, 94 (1933)
  Buttle, Henry, Trevan., Biochem. J., 28,426 (1934)
  Seeler, Dusenbery, Malanga.,J. Pharm. Exp. Ther., 78, 159 (1943)
  Marshall., ibid, 85, 299 (1945)

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