Molecular Weight: 387
View Pricing Sep 6, 2010 · Tamoxifen UNII 094ZI81Y45 Molecular formula C 26 H 29 NO Molecular weight 371
31% Standard InChI Tamoxifen | C26H29NO | CID 2733526 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety Tamoxifen citrate | C32H37NO8 | CID 2733525 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and
CLINICAL PHARMACOLOGY Tamoxifen citrate is a
Formula: C 26 H 29 NO
The molecular weight of tamoxifen is available in molecular weight page of tamoxifen, which is calculated as the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element in the molecular formula
85, the equilibrium solubility in water at 37°C is 0
2 mg/mL
9 (in Triton X-100) 7,8 METHOD OF PREPARATION:
62, the pKa’ is 8
CLINICAL PHARMACOLOGY Tamoxifen is a nonsteroidal agent that has demonstrated
Introduction
Tamoxifen citrate has a molecular weight of 563
Tamoxifen citrate is a nonsteroidal agent that
The molecular weight obtained in the mass spectra of Tc-99m-tamoxifen spectra corresponds to the molecular formula [M(CO) 3 XL 2], where X is water and L 2 represents the bidentate tamoxifen
3159 mg/mL and in 0
Although it represents a milestone in the mechanism-based treatment of ER +
In Cas9 variants engineered with ligand-dependent inteins 4-Hydroxytamoxifen was used
Tamoxifen is indicated for the treatment of breast cancer in a variety of settings
Tamoxifen metabolism mostly occurs through two pathways, 4-hydroxylation and N-demethylation
The molecular weight (about 474 for the free base) and the long elimination half life suggest that the drug will cross to the embryo-fetus
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]H341 (25%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]H350 (100%): May cause cancer [Danger Carcinogenicity]H360 (100%): May damage fertility or the unborn child [Danger Reproductive toxicity]H362 (25%): May cause harm to breast-fed children [Reproductive
In molecular biology tamoxifen activates enzymes inactivated by fusion to a modified estrogen receptor (ER)
07 was synthesized with N-hydroxysuccinimide activated ester side chains well suited for facile Tamoxifen found in: Tamoxifen, Tamoxifen Citrate, USP, Tamoxifen Citrate Pharmaceutical Secondary Standard; Certified Reference Material, certified
99; Tamoxifen has been used for analyzing its effects on radiation sensitivity and steroid receptor content in human breast cancer cells ; Molecular Weight: 563
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Ruma Maji, Niladri Shekhar Dey, Bhabani Sankar Satapathy, Biswajit Mukherjee, and these two monomers are endogenous compounds and easily metabolized by the body via the Kreb’s cycle
Select a batch to recalculate based on the batch 4'-Hydroxytamoxifen | C26H29NO2 | CID 5284643 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological Afimoxifene, also known as 4-hydroxytamoxifen ( 4-OHT) and by its tentative brand name TamoGel, is a selective estrogen receptor modulator (SERM) of the triphenylethylene group and an active metabolite of tamoxifen
Furthermore, it has the advantage of increased solubility in a wide range of organic solvents
P-gp is expressed on the cell surface in normal