Pyridazines and derivatives
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Filtered Search Results
Aobchem AOBCHEM
5000932081 2-BROMO-4-ISOPROPYLPHENYL CY
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Aobchem AOBCHEM
5000932978 4-BROMO-2-ISOPROPYLPHENYL PH
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Aobchem AOBCHEM
5000932712 1- 4-ETHOXY-3-ISOPROPYLPHENYL
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Aobchem AOBCHEM
5000875539 1- 4-CHLORO-3-ISOPROPYLPHENYL
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Aobchem AOBCHEM
5001022372 N- 2-BROMO-4-ISOPROPYLPHENYL -
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Aobchem AOBCHEM
5000944895 1- 2-CHLORO-5-ISOPROPYLPHENYL
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Aobchem AOBCHEM
5001032779 ETHYL 2- 2-ISOPROPYLPHENYL -2-
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Medchemexpress LLC Phthalazine | 253-52-1 | 130.15 | 5 G
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This organic heterocyclic compound serves as a substrate for human aldehyde oxidase 1, potentially generating reactive oxygen species and leading to enzyme inactivation. It has shown promising activity against various cancers, including blood, breast, colon, lung, and renal cancers.
- Substrate for human aldehyde oxidase 1.
- Nitrogen-containing organic heterocyclic compound.
- Exhibits antitumor activity.
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Crescent Chemical Co Inc LUMINOL RESEARCH GRADE
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Luminol research grade For microdetermination of superoxide dismutase (2). Peroxidase reagent (1). Size - 5G Storage Conditions - +15 °C TO +30 °C Catalog Number - 28085.02 CAS 521-31-3
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Aobchem AOBCHEM
5000941860 4-FLUORO-3-ISOPROPYLPHENYL BO
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Chem-Impex International, Inc. Luminol | MFCD00006890 | 5G
Luminol, MFCD00006890, 5G
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Aobchem AOBCHEM
5000931057 3-FLUORO-4-ISOPROPYLPHENYL TR
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Aobchem AOBCHEM
5000932509 2-BROMO-4-ISOPROPYLPHENYL CY
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Aobchem AOBCHEM
5000935738 1- 4-CHLORO-3-ISOPROPYLPHENYL
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Medchemexpress LLC Zardaverine | 101975-10-4 | C12H10F2N2O3 | 50 MG
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Zardaverine is an orally active and selective PDE3/4 inhibitor with IC50 values of 0.58 uM for PDE3 and 0.17 uM for PDE4. It exhibits potent bronchodilator activity and is effective in reducing inflammation in asthma. Zardaverine also shows antitumor potential by selectively inhibiting the proliferation of HCC cells, inducing apoptosis, and causing cell cycle arrest (G0/G1 phase).
- Orally active and selective PDE3/4 inhibitor
- Potent bronchodilator activity
- Effective in reducing inflammation in asthma
- Selectively inhibits proliferation of HCC cells
- Induces apoptosis and cell cycle arrest (G0/G1 phase)
- Antitumor potential
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