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(-)-シチシン

Pharmakon1600-01504027

HCID 6708720
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
485-35-8
標準SMILES
O=c1cccc2n1C[C@H]1CNCC2C1
InChIKey
ANJTVLIZGCUXLD-VEDVMXKPSA-N
分子式
C11H14N2O
平均分子量
190.24 g/mol
単同位体質量
190.11061307

概要

LSM-6464 is an alkaloid.

名称と識別子

優先名称
Pharmakon1600-01504027
IUPAC
(9R)-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one
現地名
(-)-シチシン
英語名
CYTISINE
分子式
C11H14N2O
分子量
190.24

名称と別名

Spectrum_001465SpecPlus_000618Spectrum2_000470Spectrum3_001611Spectrum4_001834Spectrum5_000627BSPBio_003241KBioGR_002534KBioSS_001945DivK1c_006714SPECTRUM1504027SPBio_000580
名称をさらに表示
(-)-シチシン(1R,5S)-3,4,5,6-テトラヒドロ-1H-1,5-メタノピリド[1,2-a][1,5]ジアゾシン-8(2H)-オンシチシンシチシン(ラブルニン)シチシニクリンバプチトキシン(1R,5S)-1,2,3,4,5,6-ヘキサヒドロ-1,5-メタノ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オンオイレキシン【アルカロイド】1α,5α-メタノ-1,2,3,4,5,6-ヘキサヒドロ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オンユーレキシンソホリンフルゼ(1R,9S)-7,11-ジアザトリシクロ[7.3.1.02,7]トリデカ-2,4-ジエン-6-オン(1R)-1,2,3,4,5,6-ヘキサヒドロ-1α,5α-メタノ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オン[1R,(-)]-1,2,3,4,5,6-ヘキサヒドロ-1α,5α-メタノ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オンウレキシンシチトンCytisiniclineCytisinSOPHORINE(1R,5S)-1,2,3,4,5,6-Hexahydro-8H-1,5-methanopyrido[1,2-a][1,5]diazocin-8-oneTabaxUlexinULEXINECystisine(-)-CytisineCytisinicline/Cytisin (6039-Sopharma)
CHEBI:95183KBio1_001658KBio2_001945KBio2_004513KBio2_007081KBio3_002461HMS1922B03Pharmakon1600-01504027

データベース識別子

CAS
485-35-8
PubChem CID
6708720
ChEBI
CHEBI:95183

物性

構造計算による物性

XLogP
0.2
極性表面積
32.3 Ų
水素結合供与体数
1
水素結合受容体数
2
回転可能結合数
0
重原子数
14
形式電荷
0
複雑度
332

物理化学的性質

融点
154 · 154-156 °C (lit.)
沸点
218 °C/2 · 218 °C/2 mmHg (lit.)
比旋光度
17 · D17 -120°
比重(密度)
1.0815 · 1.0815 (rough estimate)
屈折率
1.57 · 1.5700 (estimate)
貯蔵温度
2 · Keep in dark place,Sealed in dry,2-8°C
溶解性
439 g/リットル · 439g/リットル
酸解離定数(Pka)
6.11 · 6.11, 13.08(at 25℃)
外見
粉
色
ライトイエロー
水溶解度
439 g/L · 439g/L(16℃)
Merck
14 · 14,2789
InChI
1S/C11H14N2O/c14-11-3-1-2-10-9-4-8(5-12-6-9)7-13(10)11/h1-3,8-9,12H,4-7H2/t8-,9+/m0/s1
InChIKey
ANJTVLIZGCUXLD-DTWKUNHWSA-N
SMILES
O=C1C=CC=C2C3CNCC(C3)CN12
LogP
0.172 · 0.172 (est)
CAS データベース
485 · 485-35-8
NISTの化学物質情報
Cytisine(485-35-8)
EPAの化学物質情報
Cytisine (485-35-8)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

安全データ

wgk
3
tsca
TSCA listed
rtecs
HA4025000
ridadr
UN 2811 6.1/PG 3
毒性
LD50 in mice (mg/kg): 1.73 i.v.; 9.4 i.p.; 101 orally (Barlow, McLeod)
hs_code
29399990
risk_code
25-36/37/38
hazard_code
T
safety_code
26-28-36/37-45
hazard_class
6.1(b)
packing_group
III
Hazard Classifications
Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 Oral
ストレージクラス
6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
有毒物質データの
485-35-8(Hazardous Substances Data)

化学と産業

応用分野 · 5 件

解説C11H14N2O(190.25).シチシンは,マメ科Laburnum anagyroidesなど広く同科の植物に分布するルピンアルカロイド.無色のプリズム晶.融点152~153 ℃.[α]D17"-120°.水,アセトン,メタノール,エタノールに可溶.[CAS 485-35-8]森北出版「化学辞典(第2版)

説明It is an alkaloid that occurs naturally in several plant genera, such as Laburnum and Cytisus of the family Fabaceae. Pi-Zhen-Ye-Huang-Hua (Thermopsis lanceolata R.Br) contains large amount of cytisine, and it is distributed in the northeast, north, and northwest of China. This herb has been traditionally used for treating cough in China and was recorded in “Yue-Wang-Yao-Zhen,”“Jing-ZhuBen-Cao,”“Zhong-Hua-Ben-Cao,” and “Ning-Xia-Zhong-Cao-Yao-Shou-Ce.”

来歴The largest amount of cytisine (about 1–5%) is also found in the seeds of common garden decorative plant Du-Dou (Laburnum anagyroides). In the early twentieth century, cytisine was identified as the toxic component of this plant. The extracts of Laburnum seeds or flowers have been used in traditional medicine for hundreds of years. In the Second World War, the leaves of Laburnum anagyroides were used as a tobacco substitute by soldiers. In 1960s, cytisine was firstly used as a smoking cessation aid in Bulgaria. The pharmacological and clinical studies of cytisine were also conducted in other Eastern European countries such as Poland and Russia. These results were promising. Stoyanov S. and Yanachkova M. studied 70 volunteers with a long experience in smoking. They found that 57% volunteers stopped smoking and 31.4% volunteers decreased cigarettes: reduction of the cigarettes smoked from 20–30 to 3–4 a day. Cytisine was developed and marked as Tabex (Sopharma, Bulgaria), which has been widely distributed in the Eastern Europe .

使用Cytisine occurs in the seeds of Cytisus labur num L. and other Leguminosae.

一般的な説明Cystine ((1R,5S)-1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido[1,2a][1,5]diazocin-8-one) displays classical antidepressant action in various animal models of antidepressant efficacy. Infrared and Raman spectral studies suggest that it has two stable conformers.

調製方法 · 1 件

純化方法Crystallise cytisine from acetone and sublime it in a vacuum. Its solubilities are: 77% (H2O), 7.7% (Me2CO), 28.6% (EtOH), 3.3% (*C6H6), 50% (CHCl3) but it is insoluble in pet ether. The tartrate has m 206-207o [] D +45.9o, the N-tosylate has m 206-207o, and the N-acetate has m 208o. [Bohlmann et al. Angew Chem 67 708 1955, van Tamelen & Baran J Am Chem Soc 77 4944 1955, Isolation: Ing J Chem Soc 2200 1931, Govindachari et al. J Chem Soc 3839 1957, Abs config: Okuda et al. Chem Ind (London) 1751 1961, Beilstein 24 H 134, 24 I 244, 24 II 70, 24 III/IV 321.] TOXIC.

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化合物ノート

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化学的性質

化学的特性Off-White to Tan Crystalline Solid

上流・下流製品情報

下流製品

(1R)-3-(3-ブテニル)-1,2,3,4,5,6-ヘキサヒドロ-1α,5α-メタノ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オン[1R,(-)]-3-ホルミル-1,2,3,4,5,6-ヘキサヒドロ-1α,5α-メタノ-8H-ピリド[1,2-a][1,5]ジアゾシン-8-オン
補足説明 · 1 件

定義ChEBI: An organic heterotricyclic compound that is the toxic principle in Laburnum seeds and is found in many members of the Fabaceae (legume, pea or bean) family. An acetylcholine agonist, it is widely used throughout Eastern Europe as n aid to giving up smoking.