ChemicalBook > CAS DataBase List > Flurandrenolide

Flurandrenolide

Product Name
Flurandrenolide
CAS No.
1524-88-5
Chemical Name
Flurandrenolide
Synonyms
33379;cordan;haelan;l33379;drocort;Sermaka;Astonin;cordran;drenison;alondra-f
CBNumber
CB8420972
Molecular Formula
C24H33FO6
Formula Weight
436.51
MOL File
1524-88-5.mol
More
Less

Flurandrenolide Property

Melting point:
247-255°
alpha 
D +140-150° (CHCl3)
Boiling point:
578.7±50.0 °C(Predicted)
Density 
1.0796 (rough estimate)
refractive index 
1.5980 (estimate)
storage temp. 
-20°C Freezer, Under inert atmosphere
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
pka
12.87±0.10(Predicted)
form 
Solid
color 
White to Off-White
Water Solubility 
295mg/L(25 ºC)
EPA Substance Registry System
Fluradrenolide (1524-88-5)
More
Less

Safety

WGK Germany 
3
RTECS 
TU5024800
HS Code 
2937220000
Hazardous Substances Data
1524-88-5(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

Precautionary statements

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
1284000
Product name
Flurandrenolide
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
100mg
Price
$436
Updated
2024/03/01
Cayman Chemical
Product number
20933
Product name
Flurandrenolide
Purity
≥98%
Packaging
1mg
Price
$25
Updated
2024/03/01
Cayman Chemical
Product number
20933
Product name
Flurandrenolide
Purity
≥98%
Packaging
5mg
Price
$94
Updated
2024/03/01
Cayman Chemical
Product number
20933
Product name
Flurandrenolide
Purity
≥98%
Packaging
10mg
Price
$175
Updated
2024/03/01
Cayman Chemical
Product number
20933
Product name
Flurandrenolide
Purity
≥98%
Packaging
25mg
Price
$406
Updated
2024/03/01
More
Less

Flurandrenolide Chemical Properties,Usage,Production

Originator

Haelan ,Lilly ,UK ,1962

Uses

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

Uses

antiinflammatory; Glucocorticoid; antipsoriatic.

Indications

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

Definition

ChEBI: Flurandrenolide is a 21-hydroxy steroid.

brand name

Cordran (Oclassen); Cordran (Watson).

Therapeutic Function

Glucocorticoid, Antiinflammatory

Biological Functions

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.

General Description

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.

Mechanism of action

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.

Clinical Use

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.

Side effects

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.

Flurandrenolide Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Flurandrenolide Suppliers

ecochem international chemical broker
Tel
--
Fax
--
Email
export@ecochem.dk
Country
Europe
ProdList
6371
Advantage
66
kemikalieimport
Tel
--
Fax
--
Email
Sales@kemikalieimport.dk
Country
Europe
ProdList
6685
Advantage
47
More
Less

View Lastest Price from Flurandrenolide manufacturers

Henan Fengda Chemical Co., Ltd
Product
Flurandrenolide 1524-88-5
Price
US $30.00-0.80/kg
Min. Order
1kg
Purity
99%
Supply Ability
g,kg-tons, free sample is available
Release date
2024-03-26
Career Henan Chemical Co
Product
Flurandrenolide 1524-88-5
Price
US $1.00/KG
Min. Order
1KG
Purity
Min98% HPLC
Supply Ability
g/kg/ton
Release date
2020-01-29

1524-88-5, FlurandrenolideRelated Search:


  • 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
  • Pregn-4-ene-3,20-dione, 6-fluoro-11,21-dihydroxy-16,17-((1-methylethylidene)bis(oxy))-, (6alpha,11beta,16alpha)-
  • Astonin
  • Flurandrenolide,6α-Fluoro-11β,16α,17,21-tetrahydroxypregn-4-ene-3,20-dione 16,17-acetonide
  • Flurandrenolide (100 mg)
  • (6α,11β,16α)-6-Fluoro-11,21-dihydroxy-16,17-[(1-Methylethylidene)bis(oxy)]pregn-4-ene-3,20-dione
  • Fluadrenolone
  • (2S,6aR,6bS,7S,8aS,8bS,11aR,12aS,12bS)-2-fluoro-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a,10,10-tetraMethyl-5,6,6a,6b,7,8,8a,8b,11a,12,12a,12b-dodecahydro-1H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4(2H)-one
  • Fludroxycortide Solution, 100ppm
  • Pregn-4-ene-3,20-dione,6-fluoro-11,21-dihydroxy-16,17-[(1-Methylethylidene)bis(oxy)]-, (6a,11b,16a)-
  • 6alpha-fluoro-16alpha-hydroxyhydrocortisone16,17-acetonide
  • acetonideof6alpha-fluoro-16alpha-hydroxyhydrocortisone
  • alondra-f
  • c16,17-acetalwithacetone
  • clic16,17-acetalwithacetone
  • cordan
  • cordran
  • (6alpha,11beta,16alpha)-(oxy))
  • 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
  • Flunisolide Impurity 1
  • 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
  • Flurandrenolide USP/EP/BP
  • Flurandrenolide (1.0mg/ml in DMSO)
  • Flurandrenolide (1284000)
  • Riboflavin Impurity 16
  • 4-PREGNEN-6α-FLUORO-11β, 16α, 17, 21-TETROL-3, 20-DIONE 16, 17-ACETONIDE
  • Flurandrenolide (Fludroxycortide
  • C13807000 Flurandrenolide
  • 1524-88-5
  • C24H33FO6
  • CORDRAN