プロピオン酸フルチカゾン

Fluticasone Propionate

HCID 444036CAS 80474-14-2

基本情報

標準SMILES
CCC(=O)O[C@]1(C(=O)SCF)[C@H](C)C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
InChIKey
WMWTYOKRWGGJOA-CENSZEJFSA-N
分子式
C25H31F3O5S
平均分子量
500.6 g/mol
単同位体質量
500.18442975

概要

Fluticasone Propionate can cause developmental toxicity according to state or federal government labeling requirements.

名称と識別子

優先名称
Fluticasone Propionate
IUPAC
[(6S,8S,9R,10S,11S,13S,14S,16R,17R)-6,9-difluoro-17-(fluoromethylsulfanylcarbonyl)-11-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-yl] propanoate
現地名
プロピオン酸フルチカゾン
英語名
Fluticasone propionate
分子式
C25H31F3O5S
分子量
500.57

名称と別名

FLUTICASONE PROPIONATE80474-14-2FloventCutivateFlixotideFlonaseFlovent HFAFlovent DiskusFlovent Diskus 50Flovent Diskus 100Flovent Diskus 250Xhance
名称をさらに表示
プロピオン酸フルチカゾンフルチカゾンプロピオン酸エステルフルチカゾンプロピオン酸エステル (JAN)フルチカゾンプロピオナートフルチカソンプロピオナート6α,9-ジフルオロ-11β-ヒドロキシ-16α-メチル-3-オキソ-17-(1-オキソプロポキシ)アンドロスタ-1,4-ジエン-17β-カルボチオ酸S-(フルオロメチル)プロチカゾンスカイロンフルチカノーズ6α,9-ジフルオロ-16α-メチル-11β-ヒドロキシ-17-(プロパノイルオキシ)-3-オキソアンドロスタ-1,4-ジエン-17β-カルボチオ酸S-(フルオロメチル)フルナーゼ(1R,2R,3aS,3bS,5S,9aS,9bR,10S,11aS)-5,9b-ジフルオロ-1-{[(フルオロメチル)スルファニル]カルボニル}-10-ヒドロキシ-2,9a,11a-トリメチル-7-オキソ-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-シクロペンタ[a]フェナントレン-1-イル プロパノアート6α,9-ジフルオロ-11β-ヒドロキシ-17-(プロピオニルオキシ)-16α-メチル-3-オキソアンドロスタ-1,4-ジエン-17β-カルボチオ酸S-(フルオロメチル)フロラーズ6α,9-ジフルオロ-11β-ヒドロキシ-16α-メチル-3-オキソ-17α-(プロピオニルオキシ)アンドロスタ-1,4-ジエン-17β-カルボチオ酸S-フルオロメチルファビ6α,9-ジフルオロ-11β-ヒドロキシ-16α-メチル-3-オキソ-17-(プロパノイルオキシ)アンドロスタ-1,4-ジエン-17β-カルボチオ酸S-(フルオロメチル)キリガミールミリカレットフルタイドFluticasone propionate for impurity C identification CRSFluticasone propionate for impurity C identificationZoflutflutideFLUNASEFLIXONASE
CCI-18781ArmonAir RespiClickCCI 18781DTXSID8045511Fluticasone-17-propionateO2GMZ0LF5Wcci18781Flonase Allergy Relief

データベース識別子

CAS
80474-14-2
PubChem CID
444036
DTXSID
DTXSID8045511
ChEMBL
CHEMBL1473
ChEBI
CHEBI:31441
UNII
O2GMZ0LF5W
EC Number
617-082-4
Nikkaji
J457.058H

物性

構造計算による物性

XLogP
4
極性表面積
106 Ų
水素結合供与体数
1
水素結合受容体数
9
回転可能結合数
6
重原子数
34

実験および物理化学的性質

Drugs · 2 件

Pharmaceuticals -> Dermatologicals -> Corticosteroids, dermatological preparations

Pharmaceuticals -> Listed in ZINC15

SolubilityInsoluble
Human Drugs · 3 件

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Pharmaceuticals

Endocrine DisruptorsPotential endocrine disrupting compound
Melting Point261-273 °C
Physical DescriptionSolid

物理化学的性質

融点
275 °C · 275 °C
比旋光度
30 ° · D +30° (c = 0.35)
沸点
568.3 · 568.3±50.0 °C(Predicted)
比重(密度)
1.32 · 1.32±0.1 g/cm3(Predicted)
屈折率
31 ° · 31 ° (C=1, Dioxane)
貯蔵温度
Store at RT
化学的性質 · 1 件

化学的特性Fluticasone propionate is a white to off-white powder with a molecular weight of 500.6, and 17 the empirical formula is C25H31F3O5S. It is practically insoluble in water, freely soluble in 18 dimethyl sulfoxide and dimethylformamide, and slightly soluble in methanol and 95% ethanol.

安全と法規制

GHS分類

GHS Classification · 5 件

This chemical does not meet GHS hazard criteria for 10% (2 of 20) of reports.

Danger

H302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]

P203, P233, P260, P261, P264, P270, P271, P272, P273, P280, P284, P301+P317, P302+P352, P304+P340, P318, P319, P321, P330, P333+P317, P342+P316, P362+P364, P391, P403, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 20 reports by companies from 17 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

危険有害性情報

Regulatory Information · 2 件

Hazard Traits - Developmental Toxicity

Fluticasone propionate: Does not have an individual approval but may be used under an appropriate group standard

Hazard Classes and CategoriesAcute Tox. 4 (20%)

安全データ

wgk
2
rtecs
BV7980000
毒性
LD50 oral in rat: > 2gm/kg
hs_code
29372900
safety_code
22-24/25
Hazard Classifications
Repr. 2STOT RE 2

化学と産業

薬理情報

Protein BindingFluticasone propionate is 99% protein bound in serum. Topical fluticasone propionate is only 91% protein bound in serum however.
PharmacodynamicsSystemically, fluticasone propionate activates glucocorticoid receptors, and inhibits lung eosinophilia in rats. Fluticasone propionate as a topical formulation is also associated with vasoconstriction in the skin.
Mechanism of ActionFluticasone propionate works through an unknown mechanism to affect the action of various cell types and mediators of inflammation. Fluticasone propionate activates glucocorticoid receptors and inhibits lung eosinophilia in rats.
Biological Half-Life7.8 hours for intravenous fluticasone propionate. A study of 24 healthy Caucasian males shows a half life of 14.0 hours following intravenous administration and 10.8 hours following inhalation.
Metabolism/MetabolitesFluticasone propionate is cleared from hepatic metabolism by cytochrome P450 3A4. Fluticasone propionate is hydrolysed at the FIVE-S-fluoromethyl carbothioate group, forming an inactive metabolite.
FDA Pharmacological Classification · 6 件

FLUTICASONE PROPIONATE

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

ALLERGY RELIEF NASAL

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

FLUTICASONE PROPIONATE NASAL

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

用途と製造

Use ClassificationPharmaceuticals
応用分野 · 3 件

用途吸入ステロイド薬気道の炎症を抑制し,喘息症状を改善する

使用Fluticasone Propionate is a derivative of Flumethasone, a glucocorticoid that has antiallergic, anti-asthmatic, and anti-inflammatory properties. It is used in the treatment of seasonal rhinitis and asthma. Compared to beclomethasone dipropionate, fluticasone propionate is reported to have a comparable side effect profile, but twice the activity in the treatment of asthma.

一般的な説明Fluticasone Propionate is the propionate salt form of fluticasone, a synthetic trifluorinated glucocorticoid receptor agonist with antiallergic, antiinflammatory and antipruritic effects. Binding and activation of the glucocorticoid receptor results in the activation of lipocortin that in turn inhibits cytosolic phospholipase A2, which triggers cascade of reactions involved in synthesis of inflammatory mediators, such as prostaglandins and leukotrienes. Secondly, mitogen-activated protein kinase (MAPK) phosphatase 1 is induced, thereby leads to dephosphorylation and inactivation of Jun N-terminal kinase directly inhibiting c-Jun mediated transcription. Finally, transcriptional activity of nuclear factor (NF)-kappa-B is blocked, thereby inhibits the transcription of cyclooxygenase 2, which is essential for prostaglandin production.

調製方法 · 1 件

製造方法Fluticasone propionate, synthesized by Glaxo Wellcome and launched in 1993, is a trifluorinated glucocorticosteroid. It shows good topical antiinflammatory activity and is commonly used as a safe and effective inhaled treatment for asthma and allergic rhinitis.Fluticasone propionate can be synthesized from 9 by using BrCH2F,2a ClCH2F,5a or S-(monofluoromethyl) diarylsulfonium tetrafluoroborate 5f,g directly. Using BrCH2F can get an ideal yield; however, BrCH2F is costly and will destroy to the ozone layer. In addition, 9 reacted with BrCH2Cl or Br2CH2 and then by an anion exchange with AgF,2c,5e KF, or tetrabutylammonium fluoride5b to afford 1 in a low yield.Improved Synthesis of Fluticasone Propionate

サプライヤー50 社

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
广州佳途科技股份有限公司81960175 18933936954 · [email protected]
補足説明 · 1 件

定義ChEBI: Fluticasone propionate is a trifluorinated corticosteroid that consists of 6alpha,9-difluoro-11beta,17alpha-dihydroxy-17beta-{[(fluoromethyl)sulfanyl]carbonyl}-16-methyl-3-oxoandrosta-1,4-diene bearing a propionyl substituent at position 17; has anti-inflammatory, anti-asthmatic and anti-allergic activity. It has a role as an anti-allergic agent, an anti-asthmatic drug, an anti-inflammatory drug, a dermatologic drug, a bronchodilator agent and an adrenergic agent. It is a corticosteroid, a steroid ester, an 11beta-hydroxy steroid, a propanoate ester, a fluorinated steroid, a thioester and a 3-oxo-Delta(1),Delta(4)-steroid. It derives from a fluticasone. It derives from a hydride of an androstane.

関連反応

4 件

関連ノート

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