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S81726

FADROZOLE

源葉(MedMol) 99%
  • 英文名:
  • FADROZOLE
  • 別名:
  • 法倔唑;4-(5,6,7,8-四氫咪唑并[1,5-Α]吡啶-5-基)苯腈;FADROZOLE;4-(5,6,7,8-Tetrahydroimidazo[1,5-α]pyridin-5-y1)benzonitrile;Afema;CGS-169494;4-(5,6,7,8-Tetrahydroimidazo[1,5-a]pyridine-5-yl)benzonitrile;4-[(5,6,7,8-T
  • CAS號:
  • 102676-47-1
  • 分子式:
  • C14H13N3
  • 分子量:
  • 223.273
  • 核磁/質(zhì)譜:
品牌貨號產(chǎn)品規(guī)格價格(RMB) 庫存(上海) 北京 武漢 南京 數(shù)量計量單位 加入購物車...
源葉(MedMol) S81726-5mg 99% ¥335.00元 9 - - - EA 加入購物車
源葉(MedMol) S81726-10mg 99% ¥540.00元 7 - - - EA 加入購物車
源葉(MedMol) S81726-25mg 99% ¥980.00元 8 - - - EA 加入購物車
源葉(MedMol) S81726-50mg 99% ¥1540.00元 3 - - - EA 加入購物車
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參考文獻(xiàn)

質(zhì)檢證書(COA)

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  • 提示:詳情請下載說明書。
  • 產(chǎn)品描述: Fadrozole (CGS 16949A free base) is a potent, selective and nonsteroidal inhibitor of aromatase with an IC50 of 6.4 nM.
  • 靶點: Aromatase
  • 體內(nèi)研究:
    Fadrozole hydrochloride is able to inhibit the aromatase-mediated androstenedione-induced uterine hypertrophy in immature female rats with an ED50 of 0.03 mg/kg when given orally. In the same model, aminoglutethimide elicits the same effect with an ED50 of 30 mg/kg when given orally. Fadrozole hydrochloride prevents the development of both benign and malignant spontaneus mammary neoplasns in female Sprague-Dawley rats. It also slows the spontaneous development of ptuitary pars dta mas in female rats, and reduces the of spontaneous hcu ar tumours in male and female rats. Administration of fadrozole in male and female mice suppresses the production of 17b-estradiol, accompanied with a 70% reduction in parasite burden. This protective effect is associated in male mice with a recovery of the specific cellular immune response. Interleukin-6 (IL-6) serum levels, and its production by splenocytes, is augmented by 80%, together with a 10-fold increase in its expression in testes of infected male mice. Fadrozole treatment returns these levels to baseline values
  • 參考文獻(xiàn):
    1. Browne LJ, et al. Fadrozole hydrochloride: a potent, selective, nonsteroidal inhibitor of aromatase for the treatment of estrogen-dependent disease. J Med Chem. 1991 Feb;34(2):725-36. 2. Gunson DE, et al. Prevention of spontaneous tumours in female rats by fadrozole hydrochloride, an aromatase inhibitor. Br J Cancer. 1995 Jul;72(1):72-5. 3. Morales-Montor J, et al. Inhibition of p-450 aromatase prevents feminisation and induces protection during cysticercosis. Int J Parasitol. 2002 Oct;32(11):1379-87.
  • 溶解性: Soluble  in  DMSO
  • 保存條件: 2-8℃
  • 配置溶液濃度參考:
    1mg 5mg 10mg
    1 mM 4.479 ml 22.394 ml 44.788 ml
    5 mM 0.896 ml 4.479 ml 8.958 ml
    10 mM 0.448 ml 2.239 ml 4.479 ml
    50 mM 0.09 ml 0.448 ml 0.896 ml
  • 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
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