Comparison

Aminoglutethimide European Partner

Item no. HY-B0237-10mM
Manufacturer MedChem Express
CASRN 125-84-8
Amount 10 mM/1 mL
Quantity options 100 mg 10 mM/1 mL 500 mg
Category
Type Inhibitors
Specific against other
Purity 98.79
Citations [1]Fassnacht, M., et al., Aminoglutethimide suppresses adrenocorticotropin receptor expression in the NCI-h295 adrenocortical tumor cell line. J Endocrinol, 1998. 159(1): p. 35-42.|[2]Neves, M.A., et al., An efficient steroid pharmacophore-based strategy to identify new aromatase inhibitors. Eur J Med Chem, 2009. 44(10): p. 4121-7.|[3]Bastida, C.M., et al., Aminoglutethimide, a steroidogenesis inhibitor, abolishes hormonal induction of ornithine decarboxylase in steroidogenic tissues: evidence for its role as cAMP-dependent protein kinase inhibitor. Biochem Biophys Res Commun, 2001. 281(1): p. 244-8.
Smiles O=C(C(CC)(C1=CC=C(N)C=C1)CC2)NC2=O
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias DL-Aminoglutethimide
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Targets
Cytochrome P450
Shipping Temperature
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Molecular Weight
232.28
Product Description
Aminoglutethimide is an aromatase inhibitor with IC50 of 10 μM.
Target: Aromatase
Aminoglutethimide inhibits ACTH receptor (ACTH-R) mRNA expression in ovine adrenocortical cells in a time-dependent fashion. Aminoglutethimide significantly suppresses steroid secretion and the baseline ACTH-R mRNA expression in a dose-dependent fashion (300 μM AG, 5±1%; 30 μM AG, 64±1%; 3 μM AG, 108±19% compared with control cells, 100±11%) by affecting the gene expression or by decreasing transcript accumulation via an effect on RNA stability, in the human NCI-h295 adrenocortical carcinoma cell line, which expresses functional ACTH receptors and produces steroids of the glucocorticoid, mineralocorticoid and androgen pathway [1, 2].
Aminoglutethimide (150 mg/kg) abolishes the induction of ornithine decarboxylase (ODC) and almost depletes the gonads and plasma of progesterone or testosterone elicited by human chorionic gonadotropin (hCG) in the ovary of adult female mice and the testis of immature male mice, which is related to an inhibition of cAMP-dependent protein kinase (IC50 287 μM) rather than blockade of the steroidogenic pathway [3].
Manufacturer - Research Area
Endocrinology
Solubility
DMSO : 50 mg/mL (ultrasonic)
Manufacturer - Pathway
Metabolic Enzyme/Protease
Clinical information
Launched
Isoform
Aromatase/CYP19A1

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 10 mM/1 mL
Available: In stock
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