フルドロキシコルチド

フルドロキシコルチド 化学構造式
1524-88-5
CAS番号.
1524-88-5
化学名:
フルドロキシコルチド
别名:
フルオランドレノロンアセトニド;フルランドレノリド;シナフラン;ハエラン;フルランドレノロンアセトニド;フルドロキシコルチド;6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-(イソプロピリデンビスオキシ)プレグナ-4-エン-3,20-ジオン;リリー33379;フルランドレノロン;6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-(イソプロピリデンジオキシ)プレグナ-4-エン-3,20-ジオン;6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-[(1-メチルエチリデン)ビス(オキシ)]プレグナ-4-エン-3,20-ジオン;ドロコルト;アストニン;アロンドラF;ドレニソン;ドレニゾン;コルドラン;セルマカ;ハルドロンF;フルランデノリド
英語名:
Flurandrenolide
英語别名:
33379;haelan;l33379;cordan;drocort;Sermaka;Astonin;cordran;drenison;alondra-f
CBNumber:
CB8420972
化学式:
C24H33FO6
分子量:
436.51
MOL File:
1524-88-5.mol

フルドロキシコルチド 物理性質

融点 :
247-255°
比旋光度 :
D +140-150° (CHCl3)
沸点 :
578.7±50.0 °C(Predicted)
比重(密度) :
1.0796 (rough estimate)
屈折率 :
1.5980 (estimate)
貯蔵温度 :
-20°C Freezer, Under inert atmosphere
溶解性:
クロロホルム(微量)、酢酸エチル(微量)、メタノール(微量)
外見 :
個体
酸解離定数(Pka):
12.87±0.10(Predicted)
色:
ホワイトからオフホワイト
水溶解度 :
295mg/L(25℃)
EPAの化学物質情報:
Fluradrenolide (1524-88-5)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
WGK Germany  3
RTECS 番号 TU5024800
HSコード  2937220000
有毒物質データの 1524-88-5(Hazardous Substances Data)
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
注意書き
P305+P351+P338 眼に入った場合:水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。

フルドロキシコルチド 価格 もっと(4)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01TRCF598650 フルランデノリド
Flurandrenolide
1524-88-5 2.5mg ¥94200 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCF598650 フルランデノリド
Flurandrenolide
1524-88-5 10mg ¥352200 2024-03-01 購入
Sigma-Aldrich Japan 1284000 United States Pharmacopeia (USP) Reference Standard
Flurandrenolide United States Pharmacopeia (USP) Reference Standard
1524-88-5 100mg ¥55400 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01USP1284000 フルランデノリド
Flurandrenolide
1524-88-5 100mg ¥94200 2024-03-01 購入

フルドロキシコルチド MSDS


Flurandrenolide

フルドロキシコルチド 化学特性,用途語,生産方法

効能

抗炎症薬, 鎮痒薬, グルココルチコイド受容体作動薬

商品名

ドレニゾン (大日本住友製薬)

使用

Flurandrenolide (Cordran, Cordran SP) is a synthetic fluorinated corticosteroid.

適応症

Flurandrenolide (Cordran, Cordran SP) is a synthetic fluorinated corticosteroid.

生物学の機能

Corticosteroids influence all tissues of the body and produce numerous and varying effects in cells. These steroids regulate carbohydrate, lipid, and protein biosynthesis and metabolism (glucocorticoid effects), and they influence water and electrolyte balance (mineralocorticoid effects). Cortisol is the most potent glucocorticoid secreted by the adrenal gland, and aldosterone is the most potent endogenous mineralocorticoid. Both naturally occurring glucocorticoids and related, semisynthetic analogues can be evaluated in terms of their ability to sustain life, to stimulate an increase in blood glucose concentrations and a deposition of liver glycogen, to decrease circulating eosinophils, and to cause thymus involution in adrenalectomized animals. In addition, corticosteroids can affect immune system functions, inflammatory responses, and cell growth. The primary physiologic function of glucocorticoids is to maintain blood glucose levels and, thus, ensure glucose-dependent processes critical to life, particularly brain functions. Cortisol and related steroids accomplish this by stimulating the formation of glucose, by diminishing glucose use by peripheral tissues, and by promoting glycogen synthesis in the liver to increase carbohydrate stores for later release of glucose.

一般的な説明

Flurandrenolide, 6α-fluoro-11β,21-dihydroxy-16α,17-[(1-methylethylidene)bis(oxy)]pregn-4-ene-3,20-dione, although available as a tape product,can stick to and remove damaged skin, so it should beavoided with vesicular or weeping dermatoses.

作用機序

Glucocorticoid action is mediated through the glucocorticoid receptor, which is found primarily in the cytosol of the cell when not bound to glucocorticoids. The GR is stabilized in the cytosol by complexation with phosphorylated proteins, including a 90-kDa protein referred to as a heat shock protein 90. The steroid molecule binds to the GR, resulting in a conformational change of the receptor to dissociate the other proteins and initiate translocation of the steroid–receptor complex into the nucleus. The steroid–nuclear GR complex interacts with particular HRE regions of the cellular DNA, referred to as glucocorticoid-responsive elements and initiates transcription of the DNA sequence to produce mRNA. Finally, the elevated levels of mRNA lead to increased protein synthesis in the endoplasmic reticulum. These proteins then mediate glucocorticoid effects on carbohydrate, lipid, and protein metabolism. An alternative isoform of the GR has been identified. This isoform of the receptor does not bind known glucocorticoids, and its function remains to be determined.

臨床応用

Two major uses of glucocorticoids are in the treatment of rheumatoid diseases and allergic manifestations. Their use in the treatment of severe asthma is well documented, as is the utility of glucocorticoids in sepsis and acute respiratory distress syndrome. They are effective in the treatment of rheumatoid arthritis, acute rheumatic fever, bursitis, spontaneous hypoglycemia in children, gout, rheumatoid carditis, sprue, allergy (including contact dermatitis), and other conditions. The treatment of chronic rheumatic diseases and allergic conditions with glucocorticoids is symptomatic and continuous. Symptoms return after withdrawal of the drug.

副作用

Although side effects and toxicities vary with the drug and, sometimes, with the patient, facial mooning, flushing, sweating, acne, thinning of the scalp hair, abdominal distention, and weight gain are observed with most glucocorticoids. Protein depletion (with osteoporosis and spontaneous fractures), myopathy (with weakness of muscles of the thighs, pelvis, and lower back), and aseptic necrosis of the hip and humerus are other side effects.

フルドロキシコルチド 上流と下流の製品情報

原材料

準備製品


フルドロキシコルチド 生産企業

Global( 94)Suppliers
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InvivoChem
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1524-88-5(フルドロキシコルチド)キーワード:


  • 1524-88-5
  • 20-dione,6-alpha-fluoro-11-beta,16-alpha,17,21-tetrahydroxy-pregn-4-ene-cy
  • 20-dione,6alpha-fluoro-11beta,16alpha,17,21-tetrahydroxy-pregn-4-ene-cycli
  • 33379
  • 6alpha-fluoro-11beta,16alpha,17,21-tetrahydroxyprogesteronecyclic16,17-acetal
  • glucocorticoid
  • haelan
  • haldrone-f
  • l33379
  • pregn-4-ene-3,20-dione,6-fluoro-11,21-dihydroxy-16,17-((1-methylethylidene)bis
  • withacetone
  • 6ALPHA-FLUORO-11BETA,16ALPHA,17,21-TETRAHYDROXYPREGN-4-ENE-3,20-DIONE-16,17-ACETONIDE
  • 4-PREGNEN-6-ALPHA-FLUORO-11-BETA, 16-ALPHA, 17,21-TETROL-3,20-DIONE 16,17-ACETONIDE
  • FLUDROXYCORTIDE
  • FLURANDRENOLIDE
  • 6-alpha-fluoro-11-beta,21-dihydroxy-16-alpha,17-alpha-isopropylidenedioxypregn-4-ene-3,20-dione
  • drenison
  • drocort
  • fluorandrenolone
  • fluorandrenoloneacetonide
  • fluoroandrenoloneacetonide
  • flurandrenolone
  • flurandrenoloneacetonide
  • 6α-Fluoro-11β,21-dihydroxy-16α,17α-(isopropylidenedioxy)pregn-4-ene-3,20-dione
  • 6α-Fluoro-16α-hydroxyhydrocortisone 16,17-acetonide
  • Pregn-4-ene-3,20-dione, 6-fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis(oxy)]-, (6α,11β,16α)-
  • Pregn-4-ene-3,20-dione, 6α-fluoro-11β,16α,17,21-tetrahydroxy-, cyclic 16,17-acetal with acetone (7CI, 8CI)
  • Sermaka
  • FLUORANDRENOLIDE
  • 6α-Fluoro-11β,16α,17,21-tetrahydroxypregn-4-ene-3,20-dione 16,17-acetonide
  • 6a-Fluoro-11b,16a,17,21-tetrahydroxypregn-4-ene-3,20-dione 16,17-acetonide
  • フルオランドレノロンアセトニド
  • フルランドレノリド
  • シナフラン
  • ハエラン
  • フルランドレノロンアセトニド
  • フルドロキシコルチド
  • 6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-(イソプロピリデンビスオキシ)プレグナ-4-エン-3,20-ジオン
  • リリー33379
  • フルランドレノロン
  • 6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-(イソプロピリデンジオキシ)プレグナ-4-エン-3,20-ジオン
  • 6α-フルオロ-11β,21-ジヒドロキシ-16α,17α-[(1-メチルエチリデン)ビス(オキシ)]プレグナ-4-エン-3,20-ジオン
  • ドロコルト
  • アストニン
  • アロンドラF
  • ドレニソン
  • ドレニゾン
  • コルドラン
  • セルマカ
  • ハルドロンF
  • フルランデノリド
  • フルドロキシコルチド (JAN)
  • (1S,2S,4R,8S,9S,11S,12S,13R,19S)-19-フルオロ-11-ヒドロキシ-8-(2-ヒドロキシアセチル)-6,6,9,13-テトラメチル-5,7-ジオキサペンタシクロ[10.8.0.02,9.04,8.013,18]イコサ-17-エン-16-オン
  • グルココルチコイド
  • 皮膚用薬
  • 消炎薬
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