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Flutamide

Catalog No. T0489   CAS 13311-84-7
Synonyms: SCH 13521

Flutamide (SCH 13521) is an antiandrogen with about the same potency as cyproterone in rodent and canine species.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Flutamide Chemical Structure
Flutamide, CAS 13311-84-7
Pack Size Availability Price/USD Quantity
200 mg In stock $ 30.00
500 mg In stock $ 46.00
1 g In stock $ 48.00
5 g Inquiry $ 92.00
1 mL * 10 mM (in DMSO) In stock $ 51.00
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Purity: 99.92%
Purity: 99.6%
Purity: 99.41%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Flutamide (SCH 13521) is an antiandrogen with about the same potency as cyproterone in rodent and canine species.
Targets&IC50 Androgen receptor:55 nM(Ki)
In vitro Flutamide significantly reduced the prostate weight in rats from 319 mg to 245 mg. Co-administration of Flutamide with a luteinizing hormone-releasing hormone (LHRH) agonist compounded side effects, further decreasing prostate weight to 101 mg and markedly diminishing prostatic ornithine decarboxylase (ODC) activity.
In vivo The concurrent use of Flutamide and leuprorelin can be employed in the treatment of prostate cancer. The active metabolite of Flutamide, Flutamide-OH, binds directly to the androgen receptors in the anterior pituitary of rats (Ki=55 nM). Flutamide does not affect the proliferation of androgen-sensitive clones in the Shionogi SC-115 mouse mammary carcinoma cells when cultured, displaying only antiandrogenic effects without any androgenic activity.
Kinase Assay Androgen Receptor Assay: Aliquots of 100 μl cytosol are incubated at 0-4°C for 18 h with 100 μl of the indicated saturating concentration of [3H]T in the presence or absence of increasing concentrations of nonlabeled T, DHT, flutamide (FLU) or flutamide-OH (FLU-OH). At the end of the incubation, free and bound T are separated by the addition of 200 μl dextran-coated charcoal (1 % charcoal, 0.1% dextran T-70, 0.1% gelatin, 1.5 mM EDTA and 50 mM Tris (pH 7.4)) for 15 min before centrifugation at 2300 × g for another 15 min at 0-4°C. Aliquots (350 μl) of the supernatant are transferred to scintillation vials with 10 ml of an aqueous counting solution before counting in a Beckman LS 330 counter.
Cell Research Effect of flutamide on the growth of an androgen-sensitive clone (SEM-l) of mouse mammary carcinoma Shionogi cells in culture. The cells are incubated up to 40 days in medium (MEM + 2% dextran-coated charcoal extracted fetal calf serum) containing the compounds at a concentration of 1 μM. Media are changed every second day.(Only for Reference)
Synonyms SCH 13521
Molecular Weight 276.21
Formula C11H11F3N2O3
CAS No. 13311-84-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 51 mg/mL (184.6 mM)

Ethanol: 51 mg/mL (184.6 mM)

TargetMolReferences and Literature

1. Simard J, et al. Mol Cell Endocrinol, 1986, 44(3), 261-270. 2. Luthy IA, et al. J Steroid Biochem, 1988, 31(5), 845-852. 3. Crawford ED, et al. N Engl J Med, 1989, 321(7), 419-424. 4. Marchetti B, et al. J Steroid Biochem, 1988, 29(6), 691-698.

TargetMolCitations

1. Yang R, Wang X, Wang J, et al. Insights into the sex-dependent reproductive toxicity of 2-ethylhexyl diphenyl phosphate on zebrafish (Danio rerio). Environment International. 2022, 158: 106928.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library Anti-Cancer Clinical Compound Library Drug Repurposing Compound Library Anti-Cancer Approved Drug Library Anti-Cancer Drug Library Drug-Fragment Library Drug-induced Liver Injury (DILI) Compound Library Bioactive Compound Library FDA-Approved Drug Library Anti-Cancer Compound Library

Related Products

Related compounds with same targets
Apalutamide ACP-105 2,2,5,7,8-Pentamethyl-6-Chromanol Clascoterone LGD-2226 RU 58841 ARD-1676 Androgen receptor degrader-1

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Keywords

Flutamide 13311-84-7 Endocrinology/Hormones Androgen Receptor Inhibitor SCH-13521 SCH 13521 inhibit SCH13521 inhibitor

 

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