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Flurandrenolide

Flurandrenolide Structure
CAS No.
1524-88-5
Chemical Name:
Flurandrenolide
Synonyms
33379;haelan;l33379;cordan;drocort;Sermaka;Astonin;cordran;drenison;alondra-f
CBNumber:
CB8420972
Molecular Formula:
C24H33FO6
Molecular Weight:
436.51
MOL File:
1524-88-5.mol
Modify Date:
2024/3/26 17:16:27

Flurandrenolide Properties

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)
form Solid
pka 12.87±0.10(Predicted)
color White to Off-White
Water Solubility 295mg/L(25 ºC)
EPA Substance Registry System Fluradrenolide (1524-88-5)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
WGK Germany  3
RTECS  TU5024800
HS Code  2937220000
NFPA 704
0
2 0

Flurandrenolide Chemical Properties,Uses,Production

Uses

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

Indications

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

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

Global( 96)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20366 58 Inquiry
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AFINE CHEMICALS LIMITED +86-0571-85134551 China 15395 58 Inquiry
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 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)) Flunisolide Impurity 1 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 1524-88-5 C24H33FO6 CORDRAN Intermediates & Fine Chemicals