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AKR1C1-IN-1

Cat. No.:YN480602

  • CAS No. :4906-68-7

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    • 产品名称: AKR1C1-IN-1
      CAS No.: 4906-68-7
      Chemical Name: 5-bromo-4-hydroxy-[1,1'-biphenyl]-3-carboxylic acid
      Synonyms:
      分子量:293.11
      分子式:C₁₃H₉BrO₃
      SMILES:O=C(C1=CC(C2=CC=CC=C2)=CC(Br)=C1O)O
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: AKR1C1-IN-1 是一种高效、选择性的AKR1C1抑制剂,其Ki值为 4 nM。
      IC50和靶点:
      In Vitro:
      In Vivo:
      Clinical Trial:
      Solvent & Solubility:
    • Zhang, Y., Dufort, I., Rheault, P., et al.Characterization of a human 20α-hydroxysteroid dehydrogenaseJ. Mol. Endocrinol.25(2),221-228(2000)

      Lewis, M.J., Wiebe, J.P., and Heathcote, J.G.Expression of progesterone metabolizing enzyme genes (AKR1C1, AKR1C2, AKR1C3, SRD5A1, SRD5A2) is altered in human breast carcinomaBMC Cancer4,27(2004)

      Wang, H.W., Lin, C.P., Chiu, J.H., et al.Reversal of inflammation-associated dihydrodiol dehydrogenases (AKR1C1 and AKR1C2) overexpression and drug resistance in nonsmall cell lung cancer cells by wogonin and chrysinInt. J. Cancer120(9),2019-2027(2007)

      Belelli, D., Herd, M.B., Mitchell, E.A., et al.Neuroactive steroids and inhibitory neurotransmission: Mechanisms of action and physiological relevanceNeuroscience138(3),821-829(2006)

      Usami, N., Yamamoto, T., Shintani, S., et al.Substrate specificity of human 3(20)α-hydroxysteroid dehydrogenase for neurosteroids and its inhibition by benzodiazepinesBiol. Pharm. Bull.25(4),441-445(2002)

      El-Kabbani, O., Scammells, P.J., Gosling, J., et al.Structure-guided design, synthesis, and evaluation of salicylic acid-based inhibitors targeting a selectivity pocket in the active site of human 20α-hydroxysteroid dehydrogenase (AKR1C1)J. Med. Chem.52(10),3259-3264(2009)

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