Anastrozole (ZD-1033) - Moligand™, 10mM in DMSO , Cytochrome P450 19A1 inhibitor, CAS No.120511-73-1, Cytochrome P450 19A1 inhibitor

CAS: 120511-73-1 Cat. No.: A409166 Molecular Weight: 293.37 EC Number: 601-715-6
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO
Synonyms
α1,​α1,​α3,​α3-​tetramethyl-​5-​(1H-​1,​2,​4-​triazol-​1-​ylmethyl)​- 1,​3-​benzenediacetonitril​e
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
A409166-1ml
1
$70.90
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Why this grade

Moligand™, 10mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Anastrozole (ZD-1033) Anastrozole (ZD-1033) is a third-generation nonsteroidal selective aromatase inhibitor. It may offer greater selectivity compared with other aromatase inhibitors, being without any intrinsic endocrine effects and with no apparent e
In vitro

Anastrozole has high intrinsic potency in vitro and inhibits human placental aromatase with an IC50 of 15 nM. Anastrozole it is 200 times as potent as AG, twice as potent as 4-OHA and one third as potent as fadrozole. . Anastrozole inhibits aromatase by binding competitively to the hem group of the CYP unit of the enzyme thereby reducing estrogen biosynthesis in the periphery and the breast. Anastrozole has little or no effect on other steroid hormones.

In vivo

Anastrozole (0.1 mg/kg) given orally to mature rats on Day 2 or 3 of the estrous cycle, blocked ovulation in mature females; in pubertal rats, the same dose given for 3 days completely blocks androstenedione-stimulated uterine development. These effects may be attributes to inhibition of the normal preovulatory rise in ovarian follicular estrogen synthesis in mature females and to inhibition of metabolism of the exogenous androstenedione by the immature ovary in prepubertal females. Twice-daily administration of >9.1 mg/kg of Anastrozole given orally to male pigtailed monkeys inhibits peripheral aromatase, thereby reducing circulating estradiol concentrations by 50% to 60%.
Cell Data

cell lines:Neurons

Concentrations:

Incubation Time:

Powder Purity:≥97%

Specifications

Synonyms
α1, ​α1, ​α3, ​α3-​tetramethyl-​5-​(1H-​1, ​2, ​4-​triazol-​1-​ylmethyl)​- 1, ​3-​benzenediacetonitril​e
Specifications & Purity
Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms
Anastrozole (ZD-1033) is a third-generation nonsteroidal selective aromatase inhibitor. It may offer greater selectivity compared with other aromatase inhibitors, being without any intrinsic endocrine effects and with no apparent effect on the synthesis o
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
INHIBITOR
Mechanism of action
Cytochrome P450 19A1 inhibitor
Product Properties
ALogP2.1
Names and Identifiers
Isomeric SMILES CC(C)(C#N)C1=CC(=CC(=C1)CN2C=NC=N2)C(C)(C)C#N
WGK Germany 3
RTECS CZ1465000
Molecular Weight 293.37
Reaxy-Rn 8005958
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8005958&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Associated Targets(Human)
CYP19A1 Tclin Aromatase (12 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Documents & Articles
Citations of This Product
References
1. Luo Yu-Wei, Zhou Jiang-Peng, Ji Hongyu, Xu Doudou, Zheng Anqi, Wang Xin, Dai Zhizheng, Luo Zhicheng, Cao Fang, Wang Xing-Yue, Bai Yunfang, Chen Di, Chen Yueming, Wang Qi, Yang Yaying, Zhang Xinghai, Chiu Sandra, Peng Xiaozhong, Huang Ai-Long, Tang Kai-Fu.  (2024)  SARS-CoV-2 N protein-induced Dicer, XPO5, SRSF3, and hnRNPA3 downregulation causes pneumonia.  Nature Communications,  15  (1): (1-23).  [PMID:39138195] [10.1038/s41467-024-51192-1]
2. Tiantian Fu, Bingyi Yao, Yuanqing Guo, Yujia Yang, Junze Huang, Chenmeizi Liang, Yuanjin Zhang, Xin Wang.  (2025)  Metabolism of nifedipine by placental CYP19A1 and competitive inhibition by chlorpromazine.  BIOCHEMICAL PHARMACOLOGY,      [PMID:41110490] [10.1016/j.bcp.2025.117425]
3. Le-hao Jin, Zhe-yan Zhang, Xiao-yu Xu, Zhong-xi Chen, Jing Chen, Yu-bin Lan, Liu-liu Pan, Xiao-dan Zhang.  (2026)  The Inhibitory Effect of Anastrozole on the Metabolism of Abemaciclib In Vitro and In Vivo.  ACS Omega,      [PMID:] [10.1021/acsomega.6c00144]
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