| | Phosphodiesterase Inhibitors
- 1,3-Dipropylxanthine
A caffeine analog and phosphodiesterase inhibitor that has some selectivity for A2 adenosine receptors. UV lmax = 273 nm, log e=3.98.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-213513 | 31542-62-8 | C11H16N4O2 | 50 mg |
- 4-{[3',4'-(Methylenedioxy)benzyl]amino}-6-methoxyquinazoline
This substance has been demonstrated to be a specific and potent inhibitor of cGMP-specific phosphodiesterase. It is not shown to have an effect on other PDE isozymes. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-352371 | 150450-42-3 | C17H15N3O3 | 1 mg |
- 7-(β-Hydroxyethyl)-theophylline
Weak phosphodiesterase inhibitor resembling theophylline in its pharmacological profile. Used as an intermediate in the preparation of 7-substituted xanthines.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202836 | 519-37-9 | C9H12N4O3 | 5 g |
- 8-Methoxymethyl-IBMX
Shown to inhibit Cam-PDE which results in an increase in cGMP but not cAMP levels in rabbit aortic slices. Also reported to potentially cause vasodilation and relieve pulmonary artery pressure in rabbits. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201192 | 78033-08-6 | C12H18N4O3 | 10 mg/50 mg |
- Amrinone
This compound is a selective cAMP phosphodiesterase (PDE-3) inhibitor with positive inotropic and vasodilatory activity. It is also cardiotonic.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-207288 | 60719-84-8 | C10H9N3O | 1 g |
- Anagrelide hydrochloride
Potent type III phosphodiesterase (PDE3) inhibitor (IC50 = 36 nM). Produces potent thrombocytopenic effects via inhibition of megakaryocyte maturation and inhibits platelet aggregation .| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203513 | 58579-51-4 | C10H7Cl2N3O.HCl | 10 mg/50 mg |
- BRL-50481
The first selective PDE7 inhibitor (Ki=180 nM).| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201178 | 433695-36-4 | C9H12N2O4S | 10 mg/50 mg |
- Caffeine
CNS stimulant. Blocks adenosine A1 and A2A receptors. cAMP phosphodiesterase inhibitor. Interferes with the uptake and storage of Ca2+ by the sarcoplasmic reticulum in skeletal muscle. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202514 | 58-08-2 | C8H10N4O2 | 5 g |
- CDP 840 hydrochloride
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-362723 | 162542-90-7 | C25H27NO2.HCl | 10 mg/50 mg |
- Chlorpromazine, Hydrochloride
Calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase inhibitor. A peripheral vasodilator. Inhibitor of lysosomal sphingomyelinase and of TNF-α production. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202537 | 69-09-0 | C17H19ClN2S•HCl | 500 mg |
- Cilostamide (OPC 3689)
A specific phosphodiesterase 3 (PDE3) inhibitor. The compound has been shown to block DNA binding of p-Stat3, increase cAMP levels, and block the effects of insulin and IGF-1 on meiosis| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201180 | 68550-75-4 | C20H26N2O3 | 5 mg/25 mg |
- Cilostazol
Contains vasodilator, antimitogenic, andtithrombotic, and cardiotonic properties. Also been observed to inhibit mitogenesis, migration of vascular smooth muscle cells, and platelet aggregation.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201182 | 73963-72-1 | C20H27N5O2 | 10 mg/50 mg |
- CP 80633
Selective inhibitor of phosphodiesterase type 4 which does not display significant isozyme selectivity of PDE4. Inhibits hydrolysis of cAMP in isolated monocytes, eosinophils, human peripheral blood and T cells. Exhibits anti-inflammatory and bronchodilatory activity in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-205276 | 135637-46-6 | C18H24N2O3 | 10 mg/50 mg |
- Denbufylline
Selective xanthine derivative that inhibits PDE IV. Has bronchodilatory properties. Exhibits negative inotropic effects by acting on verapamil-sensitive sites of Ca2+ channels in guinea pig ventricle papillary muscle independently of its PDE inhibitory activity.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203915 | 57076-71-8 | C16H24N4O3 | 5 mg |
- Dipyridamole
A phosphodiester, cGMP, and non-specific nucleoside transport inhibitor with antioxidant properties. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-200717 | 58-32-2 | C24H40N8O4 | 1 g/5 g |
- EHNA
An inhibitor of adenosine deaminase (ADA) and a selective inhibitor of cyclic nucleotide phosphodiesterase- 2 (PDE2).| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201184 | 51350-19-7 | C14H23N5O•HCl | 10 mg/50 mg |
- Etazolate Hydrochloride
Selective inhibitor of cAMP-specific phosphodiesterase (PDE IV, IC50=2 µM).| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201186 | 51022-77-6 | C14H19N5O2 ·HCl | 5 mg/25 mg |
- Gisadenafil besylate
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-361185 | 334827-98-4 | C23H33N7O5S.C6H6O3S | 10 mg/50 mg |
- IBMX
A nonspecific inhibitor of cyclic nucleotide phosphodiesterases. Raises intracellular cyclic AMP levels.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201188 | 28822-58-4 | C10H14N4O2 | 200 mg/1 g |
- Ibudilast
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203080 | 50847-11-5 | C14H18N2O | 10 mg |
- ICI 63197
Potent phosphodiesterase (PDE) 4 inhibitor (IC50 = 35 nM for inhibition of [3H]-rolipram binding to rat brain). Antidepressant following systemic administration in vivo.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203600 | 27277-00-5 | C9H13N5O | 10 mg/50 mg |
- Mesopram
Orally active phosphodiesterase (PDE) 4 inhibitor. Inhibits Th1 cell proliferation and decreases production of IFN-γ, TNF-α, IL-10 and iNOS in vitro. Triggers ovulation and exhibits efficacy against experimental autoimmune encephalomyelitis and murine colitis in vivo.
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204077 | 189940-24-7 | C14H19NO4 | 10 mg/50 mg |
- Milrinone
A PDE3 inhibitor that exhibits vasodilator and positive inotropic effects. Can be inhibited by carbachol (sc-202092). | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201193 | 78415-72-2 | C12H9N3O | 10 mg/50 mg |
- MY-5445
An inhibitor of platelet aggregation via an increase in cyclic GMP. Shown to affect cyclic GMP phosphodiesterase and cause relaxation of rat aorta.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201195 | 78351-75-4 | C20H14ClN3 | 10 mg |
- Obscurolide A1
Weak phosphodiesterase inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203167 | 144397-99-9 | C15H17NO5 | 1 mg/5 mg |
- Pentoxifylline
Non-selective phosphodiesterase inhibitor. Inhibits endotoxin-induced synthesis of TNF-α.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203184 | 6493-05-6 | C13H18N4O3 | 1 g |
- Phosphodiesterase 4 Inhibitor
Pyrazole compound with a high-affinity active site binding inhibitor of phosphodiesterases IVB and IVD (IC50 = 33 nM and 21 nM). More potent than Rolipram (IC50 = 570 nM and 1.1 µM for PDEIVB and PDEIVD), respectively and greater selectivity over PDEIB, PDEIIA, PDEIIIB, PDEVA, PDEVIIB, PDEVIIIA, PDEIXA and PDEXIA (IC50 > 30 µM) and minimally inhibit PDEXA with an IC50 of 6.9 µM.
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204190 | 346440-86-6 | C14H15N3O4 | 10 mg/50 mg |
- Phosphodiesterase V Inhibitor II
A cell-permeable tetrahydro-β-carboline-hydantoin compound. Acts as a potent and highly selective phosphodiesterase V inhibitor.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-222167 | n.n. | C24H25N3O3 | 5 mg |
- Quazinone (Ro 13-6438)
Selective inhibitor of cGMP-inhibited phosphodiesterase (PDE III, IC50=0.6 µM). | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201196 | 70018-51-8 | C11H10ClN3O | 10 mg/50 mg |
- R-(-)-Rolipram
Shown to specifically inhibit PDE IV and affect cellular functions. Also reported to demonstrate anti-inflammatory characteristics via reduction of antigen-induced prostaglandin D2 release.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201199 | 85416-75-7 | C16H21NO3 | 5 mg |
- Ro 20-1724
A selective inhibitor of cGMP-insensitive PDE4 (type IV phosphodiesterase, PDE IV) found in immune cells which increase endothelial cAMP levels and stabilize the endothelial barrier.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-200709 | 29925-17-5 | C15H22N2O3 | 100 mg/1 g |
- Rolipram
Selective inhibitor of cAMP-specific phosphodiesterase (PDE4); promotes apoptosis in HL60 cells through a cAMP-independent mechanism.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-3563 | 61413-54-5 | C16H21NO3 | 5 mg/50 mg |
- RS 25344 hydrochloride
A potent and selective phosphodiesterase (PDE) 4 inhibitor (IC50 values are 0.28, > 100, 160 and 330 nM at PDE4, PDE1, PDE2 and PDE3 respectively). Has been shown to inhibit eosinophil chemotaxis and increase progressive motility of spermatozoa in vitro. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-296280 | 152814-89-6 | C19H13N5O4•HCl•xH2O | 10 mg/50 mg |
- S-(+)-Rolipram
An inhibitor of cyclic AMP-specific phosphodiesterase. Ten times less potent than the (R)-(-)-Rolipram isomer. Presents neuroprotection against excitotoxic insult.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201200 | 85416-73-5 | C16H21NO3 | 5 mg |
- Siguazodan
PDE III inhibitor, inotropic, vasodilator and antiplatelet agent with sustained activity. Synergizes with PDE IV inhibitors (Roliprams) in blocking antigen-induced bronchospasm in the guinea pig. | Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201201 | 115344-47-3 | C14H16N6O | 5 mg/25 mg |
- Theobromine
Weak phosphodiesterase inhibitor and adenosine receptor blocker. Diuretic and smooth-muscle relaxant.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-203296 | 83-67-0 | C7H8N4O2 | 5 g/25 g |
- Theophylline
Cyclic phosphodiesterase inhibitor. Weakly inhibits alkaline phosphodiesterases and 5’-nucleotidase. Muscle relaxant, cardiac stimulant and diuretic. Used for the treatment of asthma.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-202835 | 58-55-9 | C7H8N4O2 | 5 g/25 g |
- Trequinsin hydrochloride
Ultrapotent, highly selective inhibitor of cGMP-inhibited phosphodiesterase (PDE lll) in vitro. Potentiates adenosine-stimulated cAMP accumulation.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-358713 | 78416-81-6 | C24H27N3O3 ·HCl | 10 mg |
- Vinpocetine
Selective inhibitor of Ca2+/CaM-PDE with potential neuroprotective and vasodialative properties.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201204 | 42971-09-5 | C22H26N2O2 | 20 mg/100 mg |
- YM 976
Orally active inhibits PDE4 (IC50 = 2.2 nM). Low emetogenic activity, suggested to be due to poor brain penetration.| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-204411 | 191219-80-4 | C17H16ClN3O | 10 mg/50 mg |
- Zaprinast (M&B 22948)
| Katalog # | CAS Nummer | Summenformel | Menge |
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| sc-201206 | 37762-06-4 | C13H13N5O2 | 20 mg/100 mg |
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