84243-58-3

Imazodan Chemical Structure
84243-58-3

Chemical Structure

Imazodan

Synonym(s): CI 914 free base

  • CAS No.: 84243-58-3
  • Formula:C13H12N4O
  • Molecular Weight:240.26

IUPAC Name: 6-(4-(1H-imidazol-1-yl)phenyl)-4,5-dihydropyridazin-3(2H)-one

InChIKey: VXMYWVMXSWJFCV-UHFFFAOYSA-N

SMILES: O=C1CCC(C2=CC=C(N3C=CN=C3)C=C2)=NN1

Biological Activity: Imazodan is a selective inhibitor for phosphodiesterase III (PDE III), which increases myocardial contractility by blocking the cAMP degradation, and improves the contractile function of heart. Imazodan serves also as a peripheral vasodilator[1].

Cat. No. Product Name Purity Description Pricing
HY-106045
Imazodan 99.38% Imazodan is a selective inhibitor for phosphodiesterase III (PDE III), which increases myocardial contractility by blocking the cAMP degradation, and improves the contractile function of heart. Imazodan serves also as a peripheral vasodilator.
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HY-101693
Senazodan Senazodan (MCI 154) is a Ca2+ sensitiser, and also shows inhibition effect on PDE III.
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HY-101693AR
Senazodan hydrochloride (Standard) ≥98% Senazodan (hydrochloride) (Standard) is the analytical standard of Senazodan (hydrochloride) (HY-101693A). This product is intended for research and analytical applications. Senazodan (MCI 154) (hydrochloride), as a Ca2+ sensitiser, shows inhibition effect on PDE III.
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HY-106045A
Imazodan hydrochloride Imazodan hydrochloride is the hydrochloride form of Imazodan (HY-106045). Imazodan hydrochloride is a selective inhibitor for phosphodiesterase III (PDE III), which increases myocardial contractility by blocking the cAMP degradation, and improves the contractile function of heart. Imazodan hydrochloride serves also as a peripheral vasodilator.
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HY-106739
Motapizone 96.25% Motapizone (NAT 05-239) is a selective PDE3 inhibitor. Motapizone moderately inhibits cytokine release in lipopolysaccharide (LPS)-induced alveolar macrophages. Motapizone also inhibits human platelet aggregation by increasing intracellular cAMP.
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HY-147853
B-Raf IN 8 B-Raf IN 8 (compound 7g) is a potent B-Raf inhibitor, with an IC50 of 70.65 nM. B-Raf IN 8 exhibits antitumor activity against hepatocellular carcinoma (HEPG-2), colon carcinoma (HCT-116), mammary gland (MCF-7) and human prostate cancer (PC-3) cells, with IC50 values of 9.78, 13.78, 18.52 and 29.85 µM.
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HY-183455
CI-930 CI-930 is a selective, orally active phosphodiesterase 3 (PDE3) inhibitor with an IC50 value of 0.0.84 μM. CI-930 exerts positive inotropic and vasodilatory effects by inhibiting cAMP hydrolysis. CI-930 also regulates hemodynamics, inhibits the proliferation of coronary artery smooth muscle cells, and suppresses the proliferation of mouse splenocytes. CI-930 can be used in research related to heart failure, atherosclerosis, and asthma.
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HY-W004645R
Ozagrel methyl ester (Standard) ≥98% (E)-methyl 3-(4-((1H-imidazol-1-yl)methyl)phenyl)acrylate (Standard) is the analytical standard of (E)-methyl 3-(4-((1H-imidazol-1-yl)methyl)phenyl)acrylate. This product is intended for research and analytical applications.
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HY-W075136
1,4-Di(1H-imidazol-1-yl)benzene 1,4-Di(1H-imidazol-1-yl)benzene is a metal-organic framework (MOF).
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HY-W112861
1-(Imidazol-1-yl)-4-(1,2,4-triazole-1-yl-methyl)benzene 1-(Imidazol-1-yl)-4-(1,2,4-triazole-1-yl-methyl)benzene is a metal-organic framework (MOF).
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HY-W456587
4'-(1H-Imidazol-1-yl)-[1,1'-biphenyl]-4-carboxylic acid 4'-(1H-Imidazol-1-yl)-[1,1'-biphenyl]-4-carboxylic acid is a metal-organic framework (MOF).
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References