Chemodex

Anastrozole

As low as CHF 84.00
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CDX-A0802-M500500 mgCHF 84.00
CDX-A0802-G0011 gCHF 135.00
 

Specifications / Handling

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Product Details
Synonyms Anastrol; ICI-D 1033; ZD 1033; α,α,α',α'-Tetramethyl-5-(1H-1,2,4-triazol-1-ylmethyl)-1,3-benzenediacetonitrile
Product Type Chemical
Properties
Formula C17H19N5
MW 293.37
CAS 120511-73-1
RTECS CZ1465000
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance White crystalline powder.
Solubility Soluble in DMF (10 mg/ml), DMSO (10 mg/ml), ethanol (20 mg/ml), methanol or chloroform.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key YBBLVLTVTVSKRW-UHFFFAOYSA-N
Smiles CC(C)(C#N)C1=CC(CN2C=NC=N2)=CC(C(C)(C)C#N)=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
Product Specification Sheet
Datasheet Download PDF Download PDF

Scientific Background Information

Product Description

Anastrozole is a highly potent, non-steroidal aromatase inhibitor that selectively inhibits the aromatase enzyme (CYP19A1) responsible for converting androgens to estrogens. With an IC50 in the low nanomolar range (typically ~15 nM), it effectively suppresses estrogen synthesis, making it a key compound in hormone-related cancer research. It is selective for aromatase/CYP19A1 over the cytochrome P450 (CYP) isoforms CYP1A2, CYP2A6, CYP2C9, CYP2D6, and CYP3A. Anastrozole is widely used in studies of estrogen receptor-positive (ER+) breast cancer, endocrine resistance and hormone regulation. It is a standard reference compound in preclinical drug screening and mechanistic studies targeting estrogen biosynthesis. Compound can be used as analytical reference material in relation to doping analytics.

Product-specific References
(1) P.V. Plourde, et al.; Breast Cancer Res. Treat. 30(1), 103-111 (1994) | (2) S.W. Grimm & M.C. Dyroff; Drug Metab. Dispos. 25, 598 (1997) | (3) P.E. Goss & L.M. Tye; Oncology 11, 1697 (1997) | (4) P.E. Lonning, et al.; Breast Cancer Res. Treat. 49, S53 (1998) | (5) A.U. Buzdar; Br. J. Cancer 85, 6 (2001) | (6) P. Kubatka, et al.; Anticancer Res. 28, 28193 (2008) | (7) J. Cairns, et al.; Mol. Cancer Ther. 21, 206 (2022) | (8) O. Alomar, et al.; Clin. Ther. 44, 1214 (2022) | (9) J. Sternberg, et al.; Metabolites 15, 452 (2025)
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