810 Results for "

PDE

" in MedChemExpress (MCE) Product Catalog:
Products (810)

810 Results for "PDE" in MCE Product Catalog:

75
75 Publications Verification
Art. -Nr.: HY-12318
CAS. Nr.: 28822-58-4
Reinheit:  99.99%
Synonyms: 3-Isobutyl-1-methylxanthine; Isobutylmethylxanthine
Forschungsgebiete:  

Inflammation/Immunology

IBMX is a broad-spectrum phosphodiesterase (PDE) inhibitor, with IC50s of 6.5, 26.3 and 31.7 μM for PDE3, PDE4 and PDE5, respectively.
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33
33 Cited Publications
Art. -Nr.: HY-14252
CAS. Nr.: 78415-72-2
Reinheit:  99.80%
Synonyms: Win 47203
Forschungsgebiete:  

Cardiovascular Disease

Milrinone is a PDE3 inhibitor, and also an inotrope and vasodilator.
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29
29 Cited Publications
Art. -Nr.: HY-N0014
CAS. Nr.: 489-32-7
Synonyms: Ieariline
Icariin is a flavonol glycoside. Icariin inhibits PDE5 and PDE4 activities with IC50s of 432 nM and 73.50 μM, respectively. Icariin also is a PPARα activator.
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19
19 Cited Publications
Art. -Nr.: HY-16900
CAS. Nr.: 61413-54-5
Synonyms: (R,S)-Rolipram; (±)-Rolipram; ZK 62711
Rolipram is a PDE4 inhibitor, with blood-brain barrier permeability, that reverses β-amyloid-induced learning and memory impairment in rats. Rolipram elevates intracellular cAMP and clevels and regulates the cAMP/CREB signaling pathway, thereby alleviating neuroinflammation and apoptotic responses. Rolipram promotes neuronal differentiation of human bone marrow mesenchymal stem cells and inhibits Methamphetamine- and morphine-induced hyperlocomotion in mice. Rolipram also reduces the viability of glioblastoma stem-like cells and enhances Bevacizumab (HY-P9906)-induced cell death. Rolipram inhibits the expression of proinflammatory cytokines and enhances central noradrenergic transmission. Rolipram is mainly used in studies related to various central nervous system diseases including Alzheimer's disease, major depressive disorder, glioblastoma multiforme, and multiple sclerosis .
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16
16 Cited Publications
Art. -Nr.: HY-15025A
CAS. Nr.: 171599-83-0
Reinheit:  99.86%
Synonyms: UK-92480 citrate
Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM.
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16
16 Cited Publications
Art. -Nr.: HY-15025
CAS. Nr.: 139755-83-2
Reinheit:  99.90%
Synonyms: UK-92480
Sildenafil (UK-92480) is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM.
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14
14 Cited Publications
Art. -Nr.: HY-15455
CAS. Nr.: 162401-32-3
Reinheit:  99.98%
Synonyms: APTA-2217; BYK 20869; B9302-107
Forschungsgebiete:  

Inflammation/Immunology

Roflumilast (APTA-2217) is a selective PDE4 inhibitor with IC50s of 0.7, 0.9, 0.7, and 0.2 nM for PDE4A1, PDE4A4, PDE4B1, and PDE4B2, respectively, without affecting PDE1, PDE2, PDE3 or PDE5 isoenzymes from various cells.
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13
13 Cited Publications
Art. -Nr.: HY-15426
CAS. Nr.: 1305115-80-3
Reinheit:  99.55%
Forschungsgebiete:  

Cancer

PF-04957325 is a highly potent and selective PDE8 inhibitor, with IC50s of 0.7 nM and 0.3 nM for PDE8A and PDE8B, respectively.
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13
13 Cited Publications
Art. -Nr.: HY-B0140
CAS. Nr.: 317-34-0
Aminophylline is a competitive and non-selective phosphodiesterase (PDE) inhibitor. Aminophylline is a competitive adenosine receptor antagonist. Aminophylline has apulmonary vasodilator action as well as a bronchodilator action and has the potential for asthma research .
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13
13 Cited Publications
Art. -Nr.: HY-B0809
CAS. Nr.: 58-55-9
Synonyms: 1,3-Dimethylxanthine; Theo-24
Theophylline (1,3-Dimethylxanthine) is a potent phosphodiesterase (PDE) inhibitor, adenosine receptor antagonist, and histone deacetylase (HDAC) activator. Theophylline (1,3-Dimethylxanthine) inhibits PDE3 activity to relax airway smooth muscle. Theophylline (1,3-Dimethylxanthine) has anti-inflammatory activity by increase IL-10 and inhibit NF-κB into the nucleus. Theophylline (1,3-Dimethylxanthine) induces apoptosis. Theophylline (1,3-Dimethylxanthine) can be used for asthma and chronic obstructive pulmonary disease (COPD) research .
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13
13 Cited Publications
Art. -Nr.: HY-B0715
CAS. Nr.: 6493-05-6
Synonyms: BL-191; PTX; Oxpentifylline
Pentoxifylline (BL-191), a haemorheological agent, is an orally active non-selective phosphodiesterase (PDE) inhibitor, with immune modulation, anti-inflammatory, hemorheological, anti-fibrinolytic and anti-proliferation effects. Pentoxifylline can be used for the research of peripheral vascular disease, cerebrovascular disease and a number of other conditions involving a defective regional microcirculation .
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12
12 Cited Publications
Art. -Nr.: HY-B0312
CAS. Nr.: 58-32-2
Forschungsgebiete:  

Cardiovascular Disease Cancer

Dipyridamole is an orally active phosphodiesterase (PDE) inhibitor. Dipyridamole also is an antiplatelet agent used in secondary prophylaxis against stroke. Dipyridamole can induce cancer cell-specific apoptosis .
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11
11 Cited Publications
Art. -Nr.: HY-B0809A
CAS. Nr.: 5967-84-0
Synonyms: 1,3-Dimethylxanthine monohydrate; Theo-24 monohydrate
Theophylline (1,3-Dimethylxanthine) monohydrate is a potent phosphodiesterase (PDE) inhibitor, adenosine receptor antagonist, and histone deacetylase (HDAC) activator. Theophylline (1,3-Dimethylxanthine) monohydrate inhibits PDE3 activity to relax airway smooth muscle. Theophylline (1,3-Dimethylxanthine) monohydrate has anti-inflammatory activity by increase IL-10 and inhibit NF-κB into the nucleus. Theophylline (1,3-Dimethylxanthine) monohydrate induces apoptosis. Theophylline (1,3-Dimethylxanthine) monohydrate can be used for asthma and chronic obstructive pulmonary disease (COPD) research .
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10
10 Cited Publications
Art. -Nr.: HY-B0763
CAS. Nr.: 50847-11-5
Synonyms: KC-404; AV-411; MN-166
Forschungsgebiete:  

Inflammation/Immunology Cancer

Ibudilast (KC-404; AV-411; MN-166) is a cyclic AMP phosphodiesterase (PDE) inhibitor. Ibudilast has platelet anti-aggregatory effects. Ibudilast can be used for the research of asthma for its inhibitory effects on tracheal smooth muscle contractility. Ibudilast may be a useful neuroprotective and anti-dementia agent counteracting neurotoxicity in activated microglia .
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10
10 Cited Publications
Art. -Nr.: HY-12085
CAS. Nr.: 608141-41-9
Reinheit:  99.91%
Synonyms: CC-10004
Apremilast (CC-10004) is an orally available inhibitor of type-4 cyclic nucleotide phosphodiesterase (PDE-4) with an IC50 of 74 nM. Apremilast inhibits TNF-α release by lipopolysaccharide (LPS) with an IC50 of 104 nM .
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9
9 Cited Publications
Art. -Nr.: HY-90009A
CAS. Nr.: 171596-29-5
Synonyms: IC-351
Forschungsgebiete:  

Cardiovascular Disease Cancer

Tadalafil (IC-351) is a PDE5 inhibitor with an IC50 value of 1.8 nM.
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8
8 Cited Publications
Art. -Nr.: HY-113556
CAS. Nr.: 102067-84-5
Reinheit:  99.87%
Sappanone A is an orally active homoisoflavone found in sappan L. Sappanone A is a PDE4 and NF-κB inhibitor with anti-inflammatory and antioxidant effect. Sappanone A induces HO-1 expression through activation of Nrf2 pathway. Sappanone A also inhibits RANKL-induced osteoclastogenesis. Sappanone A has great potential in the research of inflammation-related and cardiovascular .
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8
8 Cited Publications
Art. -Nr.: HY-13295
CAS. Nr.: 42971-09-5
Reinheit:  99.57%
Synonyms: Ethyl apovincaminate
Vinpocetine (Ethyl apovincaminate) is a derivative of the alkaloid Vincamine that blocks voltage-gated Na + channels. The IC50 value of Vinpocetine on direct IKK inhibition in the cell-free system is 17.17 μM. Vinpocetine is a phosphodiesterase (PDE) inhibitor and inhibits NF-κB-dependent inflammatory responses by directly targeting IκB kinase complex (IKK), and has been widely used for the treatment of cerebrovascular disorders .
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7
7 Cited Publications
Art. -Nr.: HY-16558
CAS. Nr.: 487-52-5
Synonyms: 2’,3,4,4’-tetrahydroxy Chalcone
Butein is a cAMP-specific PDE inhibitor with an IC50 of 10.4 μM for PDE4 . Butein is a specific protein tyrosine kinase inhibitor with IC50s of 16 and 65 μM for EGFR and p60 c-src in HepG2 cells . Butein sensitizes HeLa cells to Cisplatin through AKT and ERK/p38 MAPK pathways by targeting FoxO3a . Butein is a SIRT1 activator (STAC).
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6
6 Cited Publications
Art. -Nr.: HY-B0442
CAS. Nr.: 224785-90-4
Vardenafil is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. Vardenafil shows inhibitory towards PDE1, PDE6 with IC50s of 180 nM, and 11 nM, while IC50s are >1000 nM for PDE3 and PDE4 . Vardenafil competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels . Vardenafil can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6].
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