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フィンゴリモド塩酸塩

Fingolimod Hydrochloride

HCID 107969
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
162359-56-0
標準SMILES
CCCCCCCCc1ccc(CCC(N)(CO)CO)cc1.Cl
InChIKey
SWZTYAVBMYWFGS-UHFFFAOYSA-N
分子式
C19H34ClNO2
平均分子量
343.9 g/mol
単同位体質量
343.22780701

概要

Fingolimod hydrochloride is the hydrochloride salt of 2-amino-2-[2-(4-octylphenyl) ethyl]-1,3-propanediol (fingolimod). It has a role as an immunosuppressive agent, a prodrug and a sphingosine-1-phosphate receptor agonist. It contains a fingolimod(1+).

名称と識別子

優先名称
Fingolimod Hydrochloride
IUPAC
2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol;hydrochloride
現地名
フィンゴリモド塩酸塩
英語名
Fingolimod hydrochloride
分子式
C19H34ClNO2
分子量
343.93

名称と別名

Fingolimod hydrochloride162359-56-0Fingolimod HClFTY720GileniaFty 720Fingolimod hydrochloridFTY720 hydrochlorideFingolimod (as hydrochloride)FTY-720 HYDROCHLORIDECHEBI:631122-Amino-2-(2-(4-octylphenyl)ethyl)-1,3-propanediol hydrochloride
名称をさらに表示
フィンゴリモド塩酸塩2-アミノ-2-[2-(4-n-オクチルフェニル)エチル]プロパン-1,3-ジオール塩酸塩フィンゴリモッド塩酸塩フィンゴリモド塩酸塩 (JAN)GilenyaFinFTY720 . HClFingolimod HCFingoliMod FTY120limod hydrochloride
2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol hydrochlorideG926EC510TDTXSID001673641,3-Propanediol, 2-amino-2-(2-(4-octylphenyl)ethyl)-, hydrochloride1,3-Propanediol, 2-amino-2-[2-(4-octylphenyl)ethyl]-, hydrochloride2-amino-2-(2-(4-octylphenyl)ethyl)propane-1,3-diol hydrochloride2-Amino-2-[2-(4-octylphenyl)ethyl]-1,3-propanediol hydrochlorideRefChem:57691

データベース識別子

CAS
162359-56-0
PubChem CID
107969
DTXSID
DTXSID00167364
ChEMBL
CHEMBL544665
ChEBI
CHEBI:63112
UNII
G926EC510T
EC Number
680-631-1

物性

構造計算による物性

極性表面積
66.5 Ų
水素結合供与体数
4
水素結合受容体数
3
回転可能結合数
12
重原子数
23
形式電荷
0
複雑度
258

実験および物理化学的性質

Human Drugs · 2 件

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

物理化学的性質

融点
102 · 102-107°C
貯蔵温度
-20 °C · -20°C
溶解性
10 mg/mL、透明 · 水:可溶10mg/mL、透明
外見
粉
色
白からベージュ
由来生物
synthetic
水溶解度
10 mg/mL, · water: 10mg/mL, clear
Merck
14 · 14,4083
安定性
-20 °C · -20°C の DMSO またはエタノール溶液で最大 3 か月間保存できます。
InChI
InChI=1S/C19H33NO2.ClH/c1-2-3-4-5-6-7-8-17-9-11-18(12-10-17)13-14-19(20,15-21)16-22;/h9-12,21-22H,2-8,13-16,20H2,1H3;1H
InChIKey
SWZTYAVBMYWFGS-UHFFFAOYSA-N
SMILES
C1(C=CC(CCCCCCCC)=CC=1)CCC(N)(CO)CO.Cl
CAS データベース
162359 · 162359-56-0(CAS DataBase Reference)

化学的性質

化学的特性White Solid

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。

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 0.9% (1 of 109) of reports.

Warning

H315 (83.5%): Causes skin irritation [Warning Skin corrosion/irritation]

P203, P260, P261, P263, P264, P264+P265, P270, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P318, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 109 reports by companies from 13 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Hazard Classes and CategoriesSkin Irrit. 2 (83.5%)

毒性情報

Drug Induced Liver Injury · 6 件

Drug Induced Liver Injury Rank (DILIrank 2.0)

Fingolimod hydrochloride

vMost-DILI-concern

8

Warnings & precautions

DOI:10.1016/j.drudis.2016.02.015

安全データ

wgk
3
rtecs
TY3130000
毒性
LD50 orally in rats: 300-600 mg/kg (Troncoso)
hs_code
29221990
risk_code
36/37/38-52/53
hazard_code
Xi
safety_code
26-61
Hazard Classifications
STOT RE 2
ストレージクラス
11 - Combustible Solids

化学と産業

薬理情報

FDA Pharmacological Classification · 4 件

FINGOLIMOD HCL

Sphingosine 1-Phosphate Receptor Modulators [MoA]; Sphingosine 1-phosphate Receptor Modulator [EPC]

FINGOLIMOD HYDROCHLORIDE

Sphingosine 1-phosphate Receptor Modulator [EPC]; Sphingosine 1-Phosphate Receptor Modulators [MoA]

MeSH Pharmacological Classification · 2 件

Agents that affect the function of G-protein coupled SPHINGOSINE 1-PHOSPHATE RECEPTORS. Their binding to the receptors blocks lymphocyte migration and are often used as IMMUNOSUPPRESSANTS.

Agents that suppress immune function by one of several mechanisms of action. Classical cytotoxic immunosuppressants act by inhibiting DNA synthesis. Others may act through activation of T-CELLS or by inhibiting the activation of HELPER CELLS. While immunosuppression has been brought about in the past primarily to prevent rejection of transplanted organs, new applications involving mediation of the effects of INTERLEUKINS and other CYTOKINES are emerging.

応用分野 · 3 件

用途スフィンゴシンのアナログで す。体内でりん酸化され、スフィンゴシン 1- りん酸 1 受容体のアゴニストとして働きま す。自己反応性リンパ球の中枢神経系への浸 潤を妨げ、免疫抑制作用を示します。

説明Approved by the U.S. FDA in September 2010, fingolimod (also referred to as FTY720) is the first approved oral therapy for the relapsing-remitting form ofmultiple sclerosis (RRMS). Because of fingolimod’s structural resemblance to sphingosine, a metabolite of sphingolipids that constitutes the cell membrane of all eukaryotic cells, it was hypothesized that fingolimod may be affecting sphingolipid metabolism in cells. A series of elegant in vitro and in vivo studies confirmed that fingolimod is converted to (S)-fingolimod phosphate primarily by sphingosine kinase- 2 and that (S)-fingolimod phosphate mediates multiple biological processes by binding to novel GPCR’s referred to as sphingosine-1-phosphate (S1P) receptors. S1P receptors are divided into five subtypes, S1P1–5, which have varying tissue and cellular distribution. S1P1–3 receptors are ubiquitously expressed in the immune, cardiovascular, and central nervous systems, S1P4 is restricted to the hematopoietic system, and S1P5 is mostly localized in the white matter of CNS. S1P1–3 receptors play important roles in endothelial barrier function, maintaining vascular tone, regulating heart rate and allowing for lymphocyte egress fromsecondary lymphoid organs. The functional role of S1P4 is unknown,while the S1P5 receptor is thought to be involved in natural killer cell trafficking and oligodendrocyte function.

使用Fingolimod Hydrochloride is a derivative of ISP-1 (myriocin), a fungal metabolite of the Chinese herb Iscaria sinclarii as well as a structural analogue of Sphingosine. Fingolimod is a novel immune modulator that prolongs allograft transplant survival in numerous models by inhibiting lymphocyte emigration from lymphoid organs. Fingolimod is reported to be phosphorylated by sphingosine kinase to FTY720-P, which has been shown to potently stimulate GTPgS binding activity in S1P-transfected CHO cells (EC50 = 210 pM, 4.9 nM, 4.3 nM, and 1 nM for S1P1, S1P3, S1P4 and S1P5, respectively).

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補足説明

定義ChEBI: The hydrochloride salt of 2-amino-2-[2-(4-octylphenyl) ethyl]-1,3-propanediol (fingolimod).

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化合物ノート

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