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リコリン

Lycorine

HCID 72378
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基本情報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
476-28-8
標準SMILES
O[C@H]1[C@H]2c3cc4c(cc3CN3CCC(=C[C@@H]1O)[C@H]23)OCO4
InChIKey
XGVJWXAYKUHDOO-DANNLKNASA-N
分子式
C16H17NO4
平均分子量
287.315 g/mol
単同位体質量
287.11575802

名称と識別子

優先名称
Lycorine
IUPAC
(1S,2S,12bS,12cS)-2,4,5,7,12b,12c-Hexahydro-1H,10H-[1,3]dioxolo[4,5-j]pyrrolo[3,2,1-de]phenanthridine-1,2-diol
現地名
リコリン
英語名
LYCORINE
分子式
C16H17NO4
分子量
287.31

名称と別名

リコリン(1S)-2,4,5,7,12bβ,12cα-ヘキサヒドロ-1H-[1,3]ジオキソロ[4,5-j]ピロロ[3,2,1-de]フェナントリジン-1α,2β-ジオール2,4,5,7,12bβ,12cα-ヘキサヒドロ-1H-[1,3]ジオキソロ[4,5-j]ピロロ[3,2,1-de]フェナントリジン-1α,2β-ジオール(-)-リコリン3,12-ジデヒドロ-9,10-[メチレンビス(オキシ)]ガランタン-1α,2β-ジオール3,12-ジデヒドロ-9,10-メチレンジオキシガランタン-1α,2β-ジオール(1S,17S,18S,19S)-5,7-ジオキサ-12-アザペンタシクロ[10.6.1.02,10.04,8.015,19]ノナデカ-2,4(8),9,15-テトラエン-17,18-ジオール(1S,2S,12bS,12cS)-2,4,5,7,12b,12c-ヘキサヒドロ-1H-[1,3]ジオキソロ[4,5-j]ピロロ[3,2,1-de]フェナントリジン-1,2-ジオール4,5-エタノ-8,9-(メチレンジオキシ)-1,2,4aα,5,6,10bβ-ヘキサヒドロフェナントリジン-1α,2β-ジオールamaryllineLYCORINLYCORINE
名称をさらに表示
LicorineAmarylineBelamarinenarcissineNSC 401360NSC 683873galanthidine

データベース識別子

CAS
476-28-8
PubChem CID
72378
DTXSID
DTXSID60197208
ChEMBL
CHEMBL400092
ChEBI
CHEBI:6601
UNII
I9Q105R5BU
EC Number
207-503-6
Nikkaji
J5.973K

物性

物理化学的性質

融点
253 · 253-255℃ (dec.)
比旋光度
16 · D16 -129° (c = 0.16 in 98% alc)
沸点
429.61 °C · 429.61°C (rough estimate)
比重(密度)
1.53 · 1.53
屈折率
1.55 · 1.5500 (estimate)
貯蔵温度
2 · 2-8°C
溶解性
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
外見
粉
酸解離定数(Pka)
13.55 · 13.55±0.40(Predicted)
色
White to off-white
InChI
InChI=1S/C16H17NO4/c18-11-3-8-1-2-17-6-9-4-12-13(21-7-20-12)5-10(9)14(15(8)17)16(11)19/h3-5,11,14-16,18-19H,1-2,6-7H2/t11-,14-,15,16+/m0/s1
InChIKey
XGVJWXAYKUHDOO-KDMZPGMDSA-N
SMILES
[C@H]1(O)[C@]2([H])C3N(CCC3=C[C@@H]1O)CC1C2=CC2OCOC=2C=1

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
ridadr
UN 2811 6.1/PG 3
risk_code
25
hazard_code
T
safety_code
45

化学と産業

応用分野 · 4 件

解説リコリンはいヒガンバナの主アルカロイド.各種ヒガンバナ科植物中に広く分布する."分解点276 ℃.[α]D "-120°(エタノール).エタノール,石油エーテル,クロロホルムに可溶.アメーバ赤痢に有効であるといわれており,細胞分裂に対してはコルヒチン様の細胞分裂促進作用をもつ.毒性がやや強い.LD50 41 mg/kg(イヌ,静注).[CAS 476-28-8]森北出版「化学辞典(第2版)

説明Lycoris radiate, a traditional Chinese medicine (TCM), is the bulb of the amaryllidaceous Lycoris radiata herb. It has been applied for clinical purposes for centuries. It is firstly recorded in Tujing Bencao and mainly used for the pyogenic infections. According to A Supplement to Compendium of Materia Medica, lycoris radiate may be used for treating acute throat trouble, phlegm node, baihuodan, and pulmonary abscess.There are about 20 Lycoris species in the world, which are widely distributed in China and Japan. Lycoris radiate is an amazing horticultural plant with a graceful shape and a bright color. In TCM, it is acrid in taste and neutral in nature, with functions of detoxication, easy expectoration, and diuresis and emesis promotion. According to the modern medicine, lycoris radiate is considered to be in favor of the central nervous system and cardiovascular system.The main active ingredients extracted from the lycoris herbs are about 40 alkaloids with various contents. Pharmacological tests indicate that galanthamine, lycorine, lycoramine, lycorenine, and crinine are the major effective medicinal ingredients. Lycorine may be used to treat amebic dysentery and against cancer. Moreover, galanthamine, dihydrogalanthamine, and lycoramine may be used to treat infantile paralysis and restore nerve functions and against traumatic paraplegia, etc. Lycoris radiate is famous because galanthamine has been approved by FDA as an anti-Alzheimer disease drug. Lycoris radiate is the only natural source for galanthamine with extremely low content (

来歴In 1895, Morishima successfully extracted lycorine from the bulb of Lycoris radiata. However, its structure was unidentified until in 1935. In 1959, its stereochemical structure was dissected by monocrystal.The solvent extraction method, chromatographic separation, and resin absorption are commonly used for lycorine extraction. However, lycorine obtained from these techniques is not pure enough and often mixed with other alkaloids. The great differences in the efficacies of different alkaloids prevent such blending from being directly used. Furthermore, the separation and purification process so required has an adverse effect on and limits the development and utilization of the medicinal value of lycorine.

使用Lycorine is an analgesic, more so than aspirin, and a hypotensive, as are caranine and galanthine . The analgesic activity exhibited by the Amaryllidaceae alkaloids is attributed to their resemblance to the morphine and codeine skeletons. Lycorine also has antiarrhythmic action, and lycorine hydrochloride is a strong broncholytic. In fact, lycorine shows a relaxant effect on an isolated epinephrine-precontracted pulmonary artery and increases contractility and the rate of an isolated perfused heart. These effects are mediated by stimulation of b-adrenergic receptors.Lycorine also has a strong inhibitory effect on parasite (Encephalitozoon intestinalis) development and antifungal activity against Candida albicans. Additionally, lycorine has antifeedant, antimalarial, emetic, anti-inflammatory, antiplatelet , as well as antifertility activities. Galanthine, in turn, shows mild in vitro activity against Tripanosoma brucei rhodesiense and Plasmodium falciparum.

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化合物ノート

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このページの内容基本情報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
調製方法 · 1 件

純化方法It crystallises as orange crystals from MeOH (m 281-283o), CHCl3/EtOH (m 272-274o), pyridine or from EtOH (m 277o, dec). It has been distilled under high vacuum. The hydrochloride has m 288o (from MeOH/HCl), and the picrate has m 196-197o(from EtOH), [Cook et al. J Chem Soc 4176 1954, Martin & Tu J Org Chem 46 3763 1981, Beilstein 27 II 547, 27 III/IV 6463.]

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補足説明 · 1 件

定義ChEBI: An indolizidine alkaloid that is 3,12-didehydrogalanthan substituted by hydroxy groups at positions and 2 and a methylenedioxy group across positions 9 and 10. Isolated from Crinum asiaticum, it has been shown to exhibit antimalarial activit .