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Anastrozole

SIGMA/A2736 - ≥98% (HPLC)

Synonym: 2;2"-[5-(1H-1;2;4-Triazol-1-ylmethyl)-1; 3-Phenylene]bis(2-methyl-propiononitrile; Arimidex; ICI-D1033; ZD1033; a,a,a′,a′-Tetramethyl-5-(1H-1,2,4-triazol-1-ylmethyl)-1,3-benzenediacetonitrile

CAS Number: 120511-73-1
Empirical Formula (Hill Notation): C17H19N5
Molecular Weight: 293.37
Linear Formula: C17H19N5
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-A2736-10MG 10 mg
$106.00
1/EA
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45-A2736-50MG 50 mg
$419.00
1/EA
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assay ≥98% (HPLC)
form solid
InChI 1S/C17H19N5/c1-16(2,9-18)14-5-13(8-22-12-20-11-21-22)6-15(7-14)17(3,4)10-19/h5-7,11-12H,8H2,1-4H3
InChI key YBBLVLTVTVSKRW-UHFFFAOYSA-N
originator AstraZeneca
Quality Level 100 
solubility DMSO: 40 mg/mL
storage temp. room temp
Application: Anastrozole (aromatase inhibitor) has been used:
• as a positive control in DNA fragmentation (ladder) assay
• to investigate its effects along with extra virgin olive oil and its major fatty acid component (omega-9 OA) in estrogen receptor positive mammary adenocarcinoma cells
• to study its effects on viability, cell proliferation and apoptosis in Glioblastoma multiforme model in vivo

Biochem/physiol Actions: Anastrozole, which contains a triazole functional group, reversibly binds to the cytochrome P-450 component of aromatase. Binding interferes with the catalytic properties of aromatase, which results in inhibition of estrogen synthesis.
Biochem/physiol Actions: The aromatase enzyme converts adrenal androgens to estrogen; this enzymatic activity is the primary source of estrogen production in postmenopausal women. One treatment for estrogen receptor-positive breast cancer in postmenopausal women is through inhibition of aromatase. Anastrozole is a nonsteroidal, benzyl-triazole derivative that inhibits aromatase through competitive inhibition and is used to treat estrogen receptor-positive breast cancer. This compound is considered a third-generation, Type II aromatase inhibitor because it is more selective and less effective (if at all) on other steroidal hormones than first and second generation inhibitors.
Features and Benefits: This compound is featured on the Nuclear Receptors (Steroids)  page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
Features and Benefits: This compound was developed by AstraZeneca . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
Packaging: 10, 50 mg in glass bottle
Purity ≥98% (HPLC)
Storage Temp. room temp
UNSPSC 51111800

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