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T176

Supelco

4-idrossitamoxifene

analytical standard, (E) and (Z) isomers (50:50)

Sinonimo/i:

4-(1-[4-(dimetilaminoetossi)fenil]-2-fenil-1-butenil)fenolo, 4-OHT, cis/trans4-idrossitamoxifene

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About This Item

Formula empirica (notazione di Hill):
C26H29NO2
Numero CAS:
Peso molecolare:
387.51
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Forma fisica

powder

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Solubilità

ethanol: 20 mg/mL

Spettro attività antibiotica

neoplastics

applicazioni

forensics and toxicology
pharmaceutical (small molecule)

Formato

neat

Modalità d’azione

enzyme | inhibits

Stringa SMILE

CC\C(c1ccccc1)=C(/c2ccc(O)cc2)c3ccc(OCCN(C)C)cc3.CC\C(c4ccccc4)=C(\c5ccc(O)cc5)c6ccc(OCCN(C)C)cc6

InChI

1S/2C26H29NO2/c2*1-4-25(20-8-6-5-7-9-20)26(21-10-14-23(28)15-11-21)22-12-16-24(17-13-22)29-19-18-27(2)3/h2*5-17,28H,4,18-19H2,1-3H3/b26-25+;26-25-
ZJLDABGSDWXVGE-BDSXMVAQSA-N

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Descrizione generale

4-Hydroxytamoxifen is an antiestrogenic agent and one of the active metabolites of tamoxifen, formed upon its hydroxylation cytochrome P4502D6 (CYP2D6). Tamoxifen is used significantly in breast cancer as hormonal therapy.

Applicazioni

The 4-Hydroxytamoxifen analytical standard can be used as follows:
  • Determination of tamoxifen and its three metabolites from dried blood spot (DBS) discs by ultra-high performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-ESI-MS/MS)
  • Simultaneous estimation of tamoxifen, 4-hydroxytamoxifen, and endoxifen from DBS samples by UHPLC-MS/MS
  • Development and validation of a non-aqueous capillary electrophoretic (NACE) method coupled with capacitively coupled contactless conductivity detection (C4D) to analyze tamoxifen and its three main metabolites after their liquid-liquid extraction (LLE) from human plasma samples obtained from breast cancer patients
  • Multi-residue analysis of human plasma samples to quantify tamoxifen and its degradation products using the non-aqueous capillary electrophoretic (NACE) method combined with UV-detection
  • Combined detection of tamoxifen and centchroman, along with their degradation products in human plasma samples by LC-ESI-MS/MS

Azioni biochim/fisiol

Metabolita del farmaco chemioterapico tamoxifene, mostra un′attività agonista/antagonista nei confronti degli estrogeni più potente rispetto al farmaco progenitore. È attivo anche come inibitore intramembranoso della perossidazione dei lipidi.

Altre note

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

Health hazardExclamation mark

Avvertenze

Warning

Classi di pericolo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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