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A2736

Anastrozole

≥98% (HPLC), aromatase inhibitor, solid

Offerta disponibile

Sinonimo/i:

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

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Utilizza il codice SAVE15 nel carrello. Accedi per verificare l'idoneità. Acquista Prodotti

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Cambia visualizzazione
Voi/SKUDisponibilitàPrezzo
10 mg
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CHF 99.40
50 mg
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CHF 393.00

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C17H19N5
Numero CAS:
Peso molecolare:
293.37
MDL number:
UNSPSC Code:
51111800
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
solid

CHF 99.40

Salva 15% con il codice SAVE15
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Nome del prodotto

Anastrozole, ≥98% (HPLC)

Quality Segment

assay

≥98% (HPLC)

form

solid

solubility

DMSO: 40 mg/mL

originator

AstraZeneca

storage temp.

room temp

SMILES string

[n]2(ncnc2)Cc1cc(cc(c1)C(C)(C)C#N)C(C)(C)C#N

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

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.
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.
Anastrozole is a nonsteroidal aromatase inhibitor.

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.
This compound was developed by AstraZeneca. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Questo articolo
1034807Y0001522PHR1783
Anastrozole ≥98% (HPLC)

Sigma-Aldrich

A2736

Anastrozole

USP

USP

1034807

Anastrozole

vibrant-m

Y0001522

Anastrozole

Anastrozole Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1783

Anastrozole

description

≥98% (HPLC)

description

United States Pharmacopeia (USP) Reference Standard

description

European Pharmacopoeia (EP) Reference Standard

description

Pharmaceutical Secondary Standard; Certified Reference Material

assay

≥98% (HPLC)

assay

-

assay

-

assay

-

form

solid

form

-

form

-

form

-

Quality Level

100

Quality Level

-

Quality Level

-

Quality Level

300

storage temp.

room temp

storage temp.

-

storage temp.

2-8°C

storage temp.

2-30°C

solubility

DMSO: 40 mg/mL

solubility

-

solubility

-

solubility

-

originator

AstraZeneca

originator

-

originator

-

originator

-


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Parola di avvertenza

Danger

Classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Punto di infiammabilità (°F)

Not applicable

Punto di infiammabilità (°C)

Not applicable

Organi bersaglio

Liver,Kidney,Testes,ovaries

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 1 - Carc. 2 - Repr. 1B - STOT RE 1 Oral



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