ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
化工社オープンプロジェクト:[email protected]AIアクセス:llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.7.8
  1. ホーム
  2. /化合物

チオニンクロリド

3-Imino-3H-phenothiazin-7-amine-hydrogen chloride (1:1)

HCID 65043
ノート反応
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
部分構造検索類似構造を探す

基本情報

CAS
581-64-6
標準SMILES
Nc1ccc2nc3ccc(=[NH2+])cc-3sc2c1.[Cl-]
InChIKey
ANRHNWWPFJCPAZ-UHFFFAOYSA-M
分子式
C12H10ClN3S
平均分子量
263.75 g/mol
単同位体質量
263.0283962

概要

Thionine is an organic chloride salt composed of 3,7-diaminophenothiazin-5-ium and chloride ions in a 1:1 ratio. A strongly metachromatic dye, useful for the staining of acid mucopolysaccharides. It is also a common nuclear stain and can be used for the demonstration of Nissl substance in nerve cells of the CNS. It has a role as a fluorochrome and a histological dye. It contains a thionine cation.

名称と識別子

優先名称
3-Imino-3H-phenothiazin-7-amine-hydrogen chloride (1:1)
IUPAC
(7-aminophenothiazin-3-ylidene)azanium chloride
現地名
チオニンクロリド
英語名
Thionine
分子式
C12H10ClN3S
分子量
263.74

名称と別名

3-Imino-3H-phenothiazin-7-amine-hydrogen chloride (1:1)DTXSID60936593RefChem:1068034DTXCID001365198635-76-7ThionineThionin581-64-6Lauth's VioletKatalysin3,7-Diaminophenothiazin-5-ium chlorideThionin chloride
名称をさらに表示
チオニンクロリド3,7-ジアミノフェノチアジン-5-イウム·クロリドチオニンラウツバイオレットトロンビン ヒトThioniFIBRINOGENASElauthschesviolettapprox.90%dyecontentThionin hydrochlorideCOAGULATION FACTOR FLA
Lauthsches violett3,7-Diaminophenazathionium chlorideC.I. 52000Thionine ChlorideVTT2SAT5H0NSC-95913,7-diamino-5lambda4-phenothiazin-5-ylium chlorideNSC-56342

データベース識別子

CAS
581-64-6
PubChem CID
65043
DTXSID
DTXSID90883445
ChEMBL

物性

構造計算による物性

極性表面積
89.3 Ų
水素結合供与体数
2
水素結合受容体数
4
回転可能結合数
0
重原子数
17
形式電荷
0
複雑度
388

物理化学的性質

貯蔵温度
20 °C · −20°C
溶解性
2 O: · H2O: 1 mL/バイアル 透明からわずかに濁った、無色の溶液
外見
粉
色
白い
Merck
9346 · 9346
Specific Activity
2 · ≥2,000units/mg protein
CAS データベース
581 · 581-64-6(CAS DataBase Reference)
EPAの化学物質情報
Thionin (581-64-6)

化学的性質

化学的特性dark green to black powder or crystals

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。

毒性情報

Health EffectsThionins are cytotoxic to animal cells. (L1249)
Exposure RoutesInjestion or dermal contact. (L1817)
Toxicity SummaryThionins are thought to attack the cell membrane and render it permeable. This results in the inhibition of sugar uptake and allows potassium and phosphate ions, proteins, and nucleotides to leak from cells. (L1249)
Signs and SymptomsThionins are cytotoxic to animal cells. (L1249)
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

安全データ

wgk
2
tsca
TSCA listed
rtecs
XO8950000
risk_code
36/37/38-42
hazard_code
Xn,B
safety_code
22-24-26-36/37
ストレージクラス
10 - Combustible liquids

化学と産業

薬理情報

Metabolism/Metabolites · 1 件

Free toxin may be removed by opsonization via the reticuloendothelial system (primarily the liver and kidneys) or it may be degraded through cellular internalization via the lysosomes. Lysosomes are membrane-enclosed organelles that contain an array of digestive enzymes, including several proteases.

用途と製造

UsesThionins are small plant proteins that are toxic to animal cells. They are mainly found in seeds where they may act as a defence against consumption by animals. (L1249)
応用分野 · 3 件

説明Thrombin is the last enzyme in the clotting cascade functioning to cleave fibrinogen to fibrin and potentiates the procoagulation process by activating factors V, VIII, XI, and XIII. Conversely, thrombin aids the anticoagulant process by activating protein C. Activated protein C inhibits activated factors V and VIII ultimately down-regulating further thrombin production. Thrombin is often used as a potent platelet activator in vitro. Platelet responses to thrombin are mediated through protease-activated receptors (PARs). Thrombin-mediated signaling regulates a diverse range of metabolic processes including activation of phospholipases in platelets, endothelial cells, and cardiac myocytes.

使用Thrombin is used for site specific cleavage of recombinant fusion proteins containing an accessible thrombin recognition site for removal of affinity tags. Thrombin has been used in a study to assess in vitro hemostatic properties of French lyophilized plasma.

一般的な説明Thrombin is the final coagulation protease in regard to hemostasis, promoting both procoagulant and anticoagulant effects. Thrombin is also known as coagulation factor IIa. It is a serine endopeptidase that hydrolyzes peptide and ester bonds specifically at the carboxylic side of arginine. This enzyme converts fibrinogen to fibrin.

調製方法

関連反応

0 件
反応記録を作成

現在のフィルター条件では反応記録がありません。

化合物ノート

読み込み中…

このページの内容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
CHEMBL593252
ChEBI
CHEBI:52295
UNII
VTT2SAT5H0

製造方法The first thiazine dye, named after its dis coverer, was Lauth's Violet, which was obtained in 1876 by joint oxidation of 1,4-phenylenediamine and hydrogen sulfide with iron(III) chloride.

上流・下流製品情報

下流製品

photochromic polythioazine
補足説明 · 1 件

定義ChEBI: An organic chloride salt composed of 3,7-diaminophenothiazin-5-ium and chloride ions in a 1:1 ratio. A strongly metachromatic dye, useful for the staining of acid mucopolysaccharides. It is also a common nuclear stain and can be used for the demonstration f Nissl substance in nerve cells of the CNS.