Molecular weight of tamoxifen

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  • nih
  • Average mass 371
  • 02 N HCl at 37°C, it is 0
  • 85, the equilibrium solubility in water at 37°C is 0
  • 85, the equilibrium solubility in water at 37°C is 0
  • 5 mg/mL and in 0
  • 62, the pKa' is 8
  • Monoisotopic mass 371
  • Tamoxifen citrate has a molecular weight of 563
  • 6 E-isomer (cis-form) content: less than 0
  • 02 N HCl at 37°C, it is 0
  • 2 mg or 30
  • 85, the equilibrium solubility in water at 37°C is 0
  • The
  • 4 mg, respectively, of tamoxifen citrate, USP)
  • Molecular weight: 371
  • Tamoxifen
  • 02 N HCl at 37°C, it is 0
  • 6381 Monoisotopic: 563
  • 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

    Copy Sheet of paper on top of another sheet

    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

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