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Flurandrenolide

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
MDL Number:
MFCD00079290
MOL File:
1524-88-5.mol
Last updated:2024-03-26 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)
FDA UNII 8EUL29XUQT
NCI Dictionary of Cancer Terms glucocorticoid
ATC code D07AC07
EPA Substance Registry System Fluradrenolide (1524-88-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
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 price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 1284000 Flurandrenolide United States Pharmacopeia (USP) Reference Standard 1524-88-5 100mg $436 2024-03-01 Buy
Cayman Chemical 20933 Flurandrenolide ≥98% 1524-88-5 1mg $25 2024-03-01 Buy
Cayman Chemical 20933 Flurandrenolide ≥98% 1524-88-5 5mg $94 2024-03-01 Buy
Cayman Chemical 20933 Flurandrenolide ≥98% 1524-88-5 10mg $175 2024-03-01 Buy
Cayman Chemical 20933 Flurandrenolide ≥98% 1524-88-5 25mg $406 2024-03-01 Buy
Product number Packaging Price Buy
1284000 100mg $436 Buy
20933 1mg $25 Buy
20933 5mg $94 Buy
20933 10mg $175 Buy
20933 25mg $406 Buy

Flurandrenolide Chemical Properties,Uses,Production

Originator

Haelan ,Lilly ,UK ,1962

Uses

antiinflammatory; Glucocorticoid; antipsoriatic.

Uses

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

Definition

ChEBI: Flurandrenolide is a 21-hydroxy steroid.

Indications

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

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

Global( 94)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 8095 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23556 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9271 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29067 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
Henan Alfa Chemical Co., Ltd
+8618339805032 alfa4@alfachem.cn China 12755 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58

View Lastest Price from Flurandrenolide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
	Flurandrenolide pictures 2024-03-26 Flurandrenolide
1524-88-5
US $30.00-0.80 / kg 1kg 99% g,kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Flurandrenolide USP/EP/BP pictures 2021-06-05 Flurandrenolide USP/EP/BP
1524-88-5
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Flurandrenolide pictures 2020-02-01 Flurandrenolide
1524-88-5
US $1.00 / KG 1KG Min98% HPLC g/kg/ton Career Henan Chemical Co
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