PDE
As fosfodiesterases (PDEs) são enzimas que hidrolisam nucleotídeos cíclicos, como AMPc e GMPc, em suas formas inativas, desempenhando um papel crucial na regulação das vias de sinalização intracelular. Inibidores de PDE são utilizados no tratamento de diversas condições, incluindo doenças cardiovasculares, disfunção erétil e distúrbios respiratórios, devido à sua capacidade de modular os níveis de nucleotídeos cíclicos. Na CymitQuimica, oferecemos uma variedade de inibidores de PDE para apoiar sua pesquisa em sinalização celular, farmacologia e desenvolvimento terapêutico.
Foram encontrados 166 produtos de "PDE"
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N-Methylbenzamide
CAS:<p>N-Methylbenzamide is a potent phosphodiesterase 10A (PDE10A) inhibitor,with anti-cancer activity.</p>Fórmula:C8H9NOPureza:99.83%Cor e Forma:Physical Description Off-White Crystalline Solid (Ntp 1992)Peso molecular:135.16ITI-214
CAS:<p>ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members, exhibits potent PDE1 inhibitory activity.</p>Fórmula:C29H29FN7O5PPureza:98.21%Cor e Forma:SolidPeso molecular:605.56Roflumilast
CAS:<p>Roflumilast (APTA 2217) is an orally available, long-acting inhibitor of phosphodiesterase (PDE) type 4 (PDE4), with anti-inflammatory and potential</p>Fórmula:C17H14Cl2F2N2O3Pureza:99.76% - 99.86%Cor e Forma:SolidPeso molecular:403.21Pumafentrine
CAS:<p>Pumafentrine（BY 343） is a dual PDE3/PDE4 inhibitor that reduces clinical scores and TNF expression in experimental colitis in mice.</p>Fórmula:C29H39N3O3Pureza:>99.99%Cor e Forma:SolidPeso molecular:477.64Cilostazol
CAS:<p>Cilostazol (OPC 21) is a Phosphodiesterase 3 Inhibitor. The mechanism of action of cilostazol is as a Phosphodiesterase 3 Inhibitor.</p>Fórmula:C20H27N5O2Pureza:99.58% - 99.90%Cor e Forma:Off-White SolidPeso molecular:369.46Pimobendan
CAS:<p>Pimobendan (UD-CG 115 BS) is a selective inhibitor of PDE3 (IC50: 0.32 μM).</p>Fórmula:C19H18N4O2Pureza:99.91%Cor e Forma:SolidPeso molecular:334.37EMD57439
CAS:<p>EMD57439 is a selective PDE-III inhibitor, showing no significant increase in c-AMP concentration and producing little change in Ca(50).</p>Fórmula:C22H23N3O4SPureza:99.38% - 99.57%Cor e Forma:SolidPeso molecular:425.5Zatolmilast
CAS:<p>Zatolmilast (BPN14770) is an allosteric inhibitor of selective phosphodiesterase 4D (PDE4D; IC50s: 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3).</p>Fórmula:C21H15ClF3NO2Pureza:98.20%Cor e Forma:SolidPeso molecular:405.8T-0156
CAS:<p>T-0156 is a PEG5 inhibitor that inhibits the hydrolysis of cyclic guanosine monophosphate (cGMP) with low affinity for PDE6, PDE1, PDE2, PDE3 and PDE4.</p>Fórmula:C31H29N5O7Pureza:98.53% - 98.76%Cor e Forma:SoildPeso molecular:583.59NSP-805
CAS:<p>NSP-805 is a potent and selective guinea pig cardiac phosphodiesterase 3 (PDE3) inhibitor.</p>Fórmula:C17H19N3O2Pureza:99.85%Cor e Forma:SolidPeso molecular:297.35ATX inhibitor 1
CAS:<p>ATX inhibitor 1 is a potent ATX inhibitor (IC50: 1.23 nM, FS-3 and 2.18 nM, bis-pNPP).</p>Fórmula:C21H23Cl2N2O6PPureza:99.52%Cor e Forma:SolidPeso molecular:501.3Carbodenafil
CAS:<p>Carbodenafil is a Sildenafil related compound found in healthy foods. Sildenafil is a PDE5 inhibitor (IC50: 5.22 nM).</p>Fórmula:C24H32N6O3Pureza:98.96% - 99.89%Cor e Forma:SolidPeso molecular:452.55Trapidil
CAS:<p>Trapidil (Avantrin) is a coronary vasodilator agent.</p>Fórmula:C10H15N5Pureza:99.42%Cor e Forma:SolidPeso molecular:205.26Milrinone
CAS:<p>Milrinone (Win 47203) is a Phosphodiesterase 3 Inhibitor. The mechanism of action of milrinone is as a Phosphodiesterase 3 Inhibitor.</p>Fórmula:C12H9N3OPureza:99.22% - 99.92%Cor e Forma:SolidPeso molecular:211.22MR-L2
CAS:<p>MR-L2 is a reversible and noncompetitive allosteric activator of long-isoform phosphodiesterase-4 (PDE4).</p>Fórmula:C19H16Cl3FN4OPureza:98.09% - 98.94%Cor e Forma:SolidPeso molecular:441.71Amrinone
CAS:<p>Amrinone (Inocor) is a positive inotropic cardiotonic (cardiotonic agent) with vasodilator properties, phosphodiesterase 3 inhibitory activity.</p>Fórmula:C10H9N3OPureza:98.88% - 99.45%Cor e Forma:SolidPeso molecular:187.2Enpp-1-IN-14
CAS:<p>Enpp-1-IN-14: potent ENPP1 inhibitor, IC50 = 32.38 nM, exhibits anti-tumor properties.</p>Fórmula:C15H22ClN5O4SPureza:99.83%Cor e Forma:SoildPeso molecular:403.88WAY-313170
CAS:<p>WAY-313170 Inhibits hedgehog signaling and phosphodiesterase.</p>Fórmula:C19H17ClN2O2S2Pureza:99.3%Cor e Forma:SolidPeso molecular:404.93FCPR03
CAS:<p>FCPR03 is a selective inhibitor of phosphodiesterase 4 (PDE4) with IC50s of 31 nM, 47 nM, and 60 nM for PDE4B1, PDE4D7, and PDE4 catalytic domain, respectively.</p>Fórmula:C15H19F2NO3Pureza:99.94%Cor e Forma:SolidPeso molecular:299.31BC 11-38
CAS:<p>BC 11-38 is a potent, selective PDE biodepressant which is mainly effective against PDE11 (IC50 : 0.28 μM).</p>Fórmula:C15H16N2OS2Pureza:98.95% - 99.28%Cor e Forma:SolidPeso molecular:304.43OPC18750 HCl
CAS:<p>OPC18750 HCl is a phosphodiesterase inhibitor with positive inotropic effects that can be used to study asthma, cancer, diabetes, and psychiatric disorders.</p>Fórmula:C20H23ClN2O4Pureza:98.92%Cor e Forma:SoildPeso molecular:390.86PDE10A-IN-5
<p>PDE10A-IN-5 (Compound A30) is an orally active inhibitor of phosphodiesterase 10A (PDE10A) with an IC50 value of 3.5 nM. By inhibiting PDE10A, it activates the cyclic adenosine monophosphate (cAMP)-related signaling pathway, exhibiting activity against pulmonary vascular remodeling. This compound is applicable to research in the field of pulmonary arterial hypertension.</p>Cor e Forma:Odour SolidDazonone
CAS:<p>Dazonone (Imidazo[2,1-b]quinazolin-2(3H)-one, 6-chloro-1,5-dihydro-3-methyl-) is a specific PDE III inhibitors.</p>Fórmula:C11H10ClN3OPureza:99.54% - 99.73%Cor e Forma:SolidPeso molecular:235.67PDE5-IN-9
CAS:<p>WAY-639921 treats cardiovascular and respiratory conditions by inhibiting PDE1c.</p>Fórmula:C18H14N4SPureza:99.98%Cor e Forma:SolidPeso molecular:318.4PDE4B-IN-4
<p>PDE4B-IN-4 is an inhibitor of PDE4B (IC50: 2.82 nM) and TNF-α (IC50: 7.20 nM). It demonstrates anti-inflammatory properties by reducing neutrophilia in a mouse model of lipopolysaccharide (LPS)-induced sepsis.</p>Fórmula:C26H27N5O5Cor e Forma:SolidPeso molecular:489.52Oglemilast
CAS:<p>Oglemilast (GRC 3886) suppresses pulmonary cell infiltration, including eosinophilia and neutrophilia in vitro and in vivo.</p>Fórmula:C20H13Cl2F2N3O5SPureza:99.82%Cor e Forma:SolidPeso molecular:516.3BAY 2666605
CAS:<p>BAY 2666605 is an orally active inhibitor of PDE3A and PDE3B with IC50s of 87 nM and 50 nM, respectively. BAY 2666605 has anticancer effects.</p>Fórmula:C17H12F4N2O2Pureza:99.81%Cor e Forma:SolidPeso molecular:352.28ONO-8430506
CAS:<p>ONO-8430506 is an orally available, potent autotaxin (ATX)/ENPP2 inhibitor (IC90: 100 nM) that inhibits ATX activity in mouse plasma.</p>Fórmula:C27H28FN3O3Pureza:98.34%Cor e Forma:SolidPeso molecular:461.53BI 1015550
CAS:<p>Nerandomilast (BI 1015550) is an orally active PDE4B inhibitor with IC50 of 7.2 nM.Cost-effective and quality-assured.</p>Fórmula:C20H25ClN6O2SPureza:98.06% - 99.71%Cor e Forma:SoildPeso molecular:448.97Arofylline
CAS:<p>Arofylline (LAS 31025) is a PDE4 inhibitor and can be used for asthma studies.</p>Fórmula:C14H13ClN4O2Pureza:98.19%Cor e Forma:SolidPeso molecular:304.73cis-Tadalafil
CAS:<p>Tadalafil: a carboline-based PDE5 inhibitor, treats erectile dysfunction, prostatic hyperplasia, and pulmonary hypertension.</p>Fórmula:C22H19N3O4Pureza:99.89%Cor e Forma:SolidPeso molecular:389.4UK 227786
CAS:<p>UK 227786 is an inhibitor of phosphodiesterase 5 (PDE5), used for treatment of prostatic diseases.</p>Fórmula:C22H22Cl2N4O4Pureza:99.9%Cor e Forma:SoildPeso molecular:477.34(1R,2R)-MK-8189
CAS:<p>(1R,2R)-MK-8189 is an isomer of MK-8189, a potent and selective pyrimidine PDE10A inhibitor.</p>Fórmula:C19H22N6OSPureza:>99.99% - >99.99%Cor e Forma:SoildPeso molecular:382.48Theodrenaline hydrochloride
CAS:<p>Theodrenaline hydrochloride is an inhibitor targeting SARS-CoV-2 for the study of hypotension induced by spinal anesthesia.</p>Fórmula:C17H22ClN5O5Pureza:98% - 98.18%Cor e Forma:SoildPeso molecular:411.84Acetildenafil
CAS:<p>Acetildenafil is an analog of the phosphodiesterase inhibitor sildenafil.</p>Fórmula:C25H34N6O3Cor e Forma:Off-White To Pale Yelow SolidPeso molecular:466.58Anti-ALDH7A1 Antibody (3P955)
<p>Anti-ALDH7A1 Antibody (3P955) is a Rabbit antibody targeting ALDH7A1. Anti-ALDH7A1 Antibody (3P955) can be used in WB,ELISA,IP.</p>Cor e Forma:Odour LiquidALDH7A1 Protein, Human, Recombinant (His)
<p>ALDH7A1 (Aldehyde dehydrogenase 7 family, member A1) is a member of subfamily 7 in the aldehyde dehydrogenase family.</p>Cor e Forma:Lyophilized PowderPeso molecular:56 kDa (predicted); 56 kDa (reducing conditions)PF-05180999
CAS:<p>α-2,3-sialyltransferase-IN-1 (Lith-O-Asp analog) is an α-2,3-sialyltransferase inhibitor with anticancer activity.</p>Fórmula:C19H17F3N8Pureza:99.43% - 99.82%Cor e Forma:SolidPeso molecular:414.39Anti-ALDH7A1 Antibody-FITC (5P692)
<p>Anti-ALDH7A1 Antibody-FITC (5P692) is a FITC-conjugated Rabbit antibody targeting ALDH7A1. Anti-ALDH7A1 Antibody-FITC (5P692) can be used in FCM.</p>Cor e Forma:Odour LiquidBAY 73-6691 racemate
CAS:<p>BAY 73-6691 racemate (Rac-BAY 73-6691) is a phosphodiesterase 9A (PDE9A) inhibitor, useful for studying Parkinson’s disease.</p>Fórmula:C15H12ClF3N4OCor e Forma:SolidPeso molecular:356.73Autotaxin modulator 1
CAS:<p>Autotaxin modulator 1 is a new modulator of Autotaxin.</p>Fórmula:C28H31F6NO3Pureza:99.46%Cor e Forma:SolidPeso molecular:543.54Anti-ALDH7A1 Antibody (6G475)
<p>Anti-ALDH7A1 Antibody (6G475) is a Mouse antibody targeting ALDH7A1. Anti-ALDH7A1 Antibody (6G475) can be used in IHC-P.</p>Cor e Forma:Odour LiquidN-Ethyl tadalafil
CAS:<p>N-Ethyl tadalafil (NEthyl tadalafil) is a PDE inhibitor used in the study of cardiovascular disease.</p>Fórmula:C23H21N3O4Pureza:99.58%Cor e Forma:SolidPeso molecular:403.43ENPP1 Inhibitor C
CAS:<p>ML-354 (VU0099704) is an antagonist with and PAR4 for the study of cardiovascular diseases.</p>Fórmula:C15H18N6Pureza:99.28%Cor e Forma:SolidPeso molecular:282.34Anti-ALDH7A1 Antibody (1G435)
<p>Anti-ALDH7A1 Antibody (1G435) is a Mouse antibody targeting ALDH7A1. Anti-ALDH7A1 Antibody (1G435) can be used in ELISA.</p>Cor e Forma:Odour LiquidDNMDP
CAS:DNMDP is a potent and selective PDE3A inhibitor with anticancer activity. It binds to PDE3A, promoting its interaction with Schlafen 12 (SLFN12).Fórmula:C15H20N4O3Cor e Forma:SolidPeso molecular:304.34Anti-ALDH7A1 Antibody (5P692)
<p>Anti-ALDH7A1 Antibody (5P692) is a Rabbit antibody targeting ALDH7A1. Anti-ALDH7A1 Antibody (5P692) can be used in FCM,ICC/IF.</p>Cor e Forma:Odour LiquidBay 60-7550
CAS:<p>Bay 60-7550 is a PDE2 inhibitor that exerts positive inotropic effects in the rat heart by increasing PKA-mediated phosphorylation.</p>Fórmula:C27H32N4O4Pureza:98.14%Cor e Forma:SolidPeso molecular:476.57PF-05085727
CAS:<p>PF-05085727 inhibits PDE2A >4,000-fold selectivity over PDE1 and PDE3-11.</p>Fórmula:C20H18F3N7Pureza:98%Cor e Forma:SolidPeso molecular:413.4THPP-1
CAS:<p>THPP-1 is a potent and orally bioavailable inhibitor of PDE10A(Ki of 1 nM and 1.3 nM for human and rat PDE10A, respectively).</p>Fórmula:C23H21ClN6O3Pureza:99.46%Cor e Forma:SolidPeso molecular:464.9PF-8380
CAS:<p>PF-8380 is an effective and orally available autotaxin inhibitor (IC50: 2.8 nM, in isolated enzyme assay; 101 nM, in the human whole blood).</p>Fórmula:C22H21Cl2N3O5Pureza:98.70% - 99.25%Cor e Forma:SolidPeso molecular:478.33PQ-10
CAS:<p>PQ-10 (A-844337) is a PDE-10 inhibitor. PQ-10 induces brain glucose metabolism patterns, which may be a potential translational biomarker.</p>Fórmula:C22H21N5O3Pureza:99.86%Cor e Forma:SolidPeso molecular:403.43Roflumilast N-oxide
CAS:<p>Roflumilast N-oxide is an inhibitor of PDE type 4.</p>Fórmula:C17H14Cl2F2N2O4Pureza:98.19% - 99.69%Cor e Forma:SolidPeso molecular:419.21Balipodect
CAS:<p>Balipodect (TAK063) is a highly effective and selective PDE10A inhibitor (IC50: 0.30 nM); Its selectivity is >15000-fold over other PDEs.</p>Fórmula:C23H17FN6O2Pureza:98% - 99.79%Cor e Forma:SolidPeso molecular:428.42Irsogladine
CAS:<p>Irsogladine (Dicloguamine) is an anti-ulcer agent that promotes gap junction intercellular communication via M1 muscarinic acetylcholine receptor binding.</p>Fórmula:C9H7Cl2N5Pureza:99.74% - 99.91%Cor e Forma:White Or Colorless Crystal Or Crystalline Powder Odorless Slightly BitterPeso molecular:256.09K-Ras-PDEδ-IN-1
CAS:<p>K-Ras-PDEδ-IN-1 is a potent inhibitor of competitive K-Ras-PDEδ.It binds to the farnesyl binding pocket of PDEδ(Kd of 8 nM).</p>Fórmula:C25H26FN5O2Pureza:99.48%Cor e Forma:SolidPeso molecular:447.5Cilomilast
CAS:<p>Cilomilast (SB-207499) is a potent PDE4 inhibitor with IC50 of about 110 nM, has anti-inflammatory activity and low central nervous system activity. Phase 3.</p>Fórmula:C20H25NO4Pureza:97.37% - 99.52%Cor e Forma:White SolidPeso molecular:343.42ICI 63197
CAS:<p>ICI 63197 (2-Amino-6-methyl-4-propyl-[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one) is a PDE4 inhibitor.</p>Fórmula:C9H13N5OPureza:99.70%Cor e Forma:White SolidPeso molecular:207.23IBMX
CAS:<p>IBMX (Methylisobutylxanthine) is a broad-spectrum phosphodiesterase (PDE) inhibitor with inhibitory activity against PDE3, PDE4, and PDE5 (IC50=6.5/26.3/31.7 μM</p>Fórmula:C10H14N4O2Pureza:98% - >99.99%Cor e Forma:Off-WhitePeso molecular:222.242,5-dichloro-4-(difluoromethoxy)-N,N-dimethylbenzene-1-sulfonamide
CAS:<p>2,5-dichloro-4-(difluoromethoxy)-N,N-dimethylbenzene-1-sulfonamide is a PDE inhibitor.</p>Fórmula:C9H9Cl2F2NO3SPureza:98.60%Cor e Forma:SolidPeso molecular:320.14Olprinone
CAS:<p>Olprinone (Loprinone)(Loprinone) is a selective phosphodiesterase 3 (PDE3) inhibitor.Olprinone has been reported to improve microcirculation and attenuate</p>Fórmula:C14H10N4OPureza:99.68%Cor e Forma:SolidPeso molecular:250.26HA130
CAS:<p>HA130 is a selective ATX (autotaxin) inhibitor.</p>Fórmula:C24H19BFNO5SPureza:98.26% - ≥95%Cor e Forma:SolidPeso molecular:463.29Ro 20-1724
CAS:<p>Ro 20-1724 (4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone) is a widely used inhibitor of cyclic nucleotide phosphodiesterase with IC50 of 2.0 μM and Ki of 3.1</p>Fórmula:C15H22N2O3Pureza:98.82% - 99.79%Cor e Forma:SolidPeso molecular:278.35Mardepodect
CAS:<p>Mardepodect (PF-2545920) is a phosphodiesterase inhibitor selective for the PDE10A subtype with an IC50 of 0.37 nM, >1000-fold selectivity over PDE.</p>Fórmula:C25H20N4OPureza:99.81% - 99.94%Cor e Forma:SolidPeso molecular:392.45BW-A 78U
CAS:<p>BW-A 78U is a PDE4 inhibitor (IC50: 3 μM). It is not inhibition on the lipopolysaccharide (LPS)-induced TNF-α release.</p>Fórmula:C13H12FN5Pureza:99.45%Cor e Forma:SolidPeso molecular:257.27MBCQ
CAS:<p>MBCQ is an inhibitor of cGMP-specific phosphodiesterase PDE5.</p>Fórmula:C16H12ClN3O2Pureza:99.45%Cor e Forma:SolidPeso molecular:313.74HA 155
CAS:<p>HA 155 (Autotaxin Inhibitor IV) is a boronic acid-based compound, inhibiting ATX with IC50 of 5.7 nM by selectively binding to its catalytic threonine.</p>Fórmula:C24H19BFNO5SPureza:99.88%Cor e Forma:SolidPeso molecular:463.29Ibudilast
CAS:<p>Ibudilast (MN-166)(KC-404;AV-411;MN-166) is a relatively nonselective phosphodiesterase inhibitor. It is approved for use as an anti-inflammatory in Japan.</p>Fórmula:C14H18N2OPureza:99.83% - >99.99%Cor e Forma:White SolidPeso molecular:230.31ML-030
CAS:<p>ML-030 is a potent PDE4 inhibitor, selective for subtypes (A1, B1, B2, C1, D2) with IC50 ranging from 6.7 to 452 nM.</p>Fórmula:C20H20N4O4SPureza:97.93%Cor e Forma:SolidPeso molecular:412.46SEP-0372814
CAS:<p>SEP-0372814 is a potent inhibitor of PDE10.</p>Fórmula:C21H19N7Pureza:99.29%Cor e Forma:SolidPeso molecular:369.42YM976
CAS:<p>YM976 is an orally active PDE4 inhibitor (IC50:2.2 nM)</p>Fórmula:C17H16ClN3OPureza:99.84%Cor e Forma:SolidPeso molecular:313.78Cilostamide
CAS:<p>Cilostamide (OPC3689) is a selective phosphodiesterase (PDE)3A and PDE3B inhibitor(IC50 values of 27 and 50 nM, respectively)</p>Fórmula:C20H26N2O3Pureza:98.87%Cor e Forma:White To Off-White SolidPeso molecular:342.43D159687
CAS:<p>D159687 is a selective PDE4D inhibitor,had a procognitive profile as it improved memory in the novel object recognition test but had no antidepressant benefit.</p>Fórmula:C21H19ClN2O2Pureza:97.57%Cor e Forma:SolidPeso molecular:366.84RS-25344 hydrochloride
CAS:<p>RS 25344 hydrochloride is a phosphodiesterase (PDE) 4 inhibitor</p>Fórmula:C19H14ClN5O4Pureza:99.25%Cor e Forma:SolidPeso molecular:411.8BRL-50481
CAS:<p>BRL-50481 is a novel and selective inhibitor of PDE7 with IC50s of 0.15, 12.1, 62 and 490 μM for PDE7A, PDE7B, PDE4 and PDE3, respectively.</p>Fórmula:C9H12N2O4SPureza:99.66%Cor e Forma:SolidPeso molecular:244.27Piclamilast
CAS:<p>Piclamilast (RP 73401) is a PDE4 inhibitor.</p>Fórmula:C18H18Cl2N2O3Pureza:98.28% - 99.57%Cor e Forma:SolidPeso molecular:381.25Ensifentrine
CAS:<p>Ensifentrine (Ensifentrinum) is a PDE3/4 inhibitor, although its affinity for PDE3(IC50: 0.4 nM) is 3,440 times higher than that for PDE4(IC50: 1479 nM), that</p>Fórmula:C26H31N5O4Pureza:99.76% - 99.94%Cor e Forma:SolidPeso molecular:477.56Z-HA155
CAS:<p>Z-HA155 (CS-963) selectively and potently inhibits autotaxin with an IC50 of 5.7 nM.</p>Fórmula:C24H19BFNO5SPureza:99.18%Cor e Forma:SolidPeso molecular:463.29Crisaborole
CAS:<p>Crisaborole (AN-2728) is a Phosphodiesterase 4 Inhibitor.</p>Fórmula:C14H10BNO3Pureza:99.70%Cor e Forma:SolidPeso molecular:251.05Udenafil
CAS:<p>Udenafil is an inhibitor of PDE5 .</p>Fórmula:C25H36N6O4SPureza:99.90%Cor e Forma:Off-White SolidPeso molecular:516.66GSK256066
CAS:<p>GSK256066 is a selective PDE4B(equal affinity to isoforms A-D) inhibitor with IC50 of 3.2 pM, >380, 000-fold selectivity versus PDE1/2/3/5/6 and >2500-fold</p>Fórmula:C27H26N4O5SPureza:99.60% - 99.66%Cor e Forma:SolidPeso molecular:518.58Nortadalafil
CAS:<p>Nortadalafil, a demethylated form of Tadalafil, is a PDE5 inhibitor used to treat ED and pulmonary arterial hypertension as Adcirca.</p>Fórmula:C21H17N3O4Pureza:99.42%Cor e Forma:SolidPeso molecular:375.38Homo Sildenafil
CAS:<p>Homo Sildenafil is an analog of Sildenafil, It acts as a phosphodiesterase inhibitor.</p>Fórmula:C23H32N6O4SPureza:99.88%Cor e Forma:White SolidPeso molecular:488.6GEBR-7b
CAS:<p>GEBR-7b (3-(Cyclopentyloxy)-4-methoxybenzaldehyde) is a phosphodiesterase-4 (PDE4) inhibitor.</p>Fórmula:C13H16O3Pureza:99.533%Cor e Forma:SolidPeso molecular:220.26Enoximone
CAS:<p>Enoximone is a selective inhibitor of phosphodiesterase III (PDE3), with treatment of congestive heart failure.</p>Fórmula:C12H12N2O2SPureza:98.53%Cor e Forma:SolidPeso molecular:248.3MY-5445
CAS:<p>MY-5445 (N-(3-chlorophenyl)-4-phenylphthalazin-1-amine) is a specific inhibitor of phosphodiesterase type 5 (PDE5).</p>Fórmula:C20H14ClN3Pureza:99.77%Cor e Forma:SolidPeso molecular:331.8Amino Tadalafil
CAS:<p>Amino tadalafil is a potent phosphodiesterase 5 (PDE5) inhibitor.</p>Fórmula:C21H18N4O4Pureza:99.85%Cor e Forma:White PowderPeso molecular:390.39Sildenafil Mesylate
CAS:<p>Sildenafil Mesylate is a mesylate form of Sildenafil, an inhibitor of Phosphodiesterase 5.</p>Fórmula:C22H30N6O4S·xCH4O3SPureza:99.84%Cor e Forma:SolidPeso molecular:570.68Lodenafil
CAS:<p>Lodenafil (Hydroxyhomosildenafil) is a potent PDE5 inhibitor, with treatment of erectile dysfunction (ED)</p>Fórmula:C23H32N6O5SPureza:99.92%Cor e Forma:SolidPeso molecular:504.6[11C]MP 10
CAS:<p>[11C]MP 10 (PF-2545920), a specific and effective PDE10A inhibitor (IC50=0.37 nM), is with more than1000-fold specificity activity over the PDE.</p>Fórmula:C25H20N4OPureza:99.5%Cor e Forma:SolidPeso molecular:391.45Osoresnontrine
CAS:<p>Osoresnontrine is a potent and selective inhibitor of PDE9A (IC50 of 52 nM),and can be used in the research of memory.</p>Fórmula:C16H17N5O2Pureza:99.93%Cor e Forma:SolidPeso molecular:311.34CP671305
CAS:<p>CP671305 is an orally active, potent and selective inhibitor of phosphodiesterase-4-D.</p>Fórmula:C23H19FN2O7Pureza:99.39%Cor e Forma:SolidPeso molecular:454.4Ziritaxestat
CAS:<p>Ziritaxestat (GLPG1690), an autotaxin inhibitor, currently being evaluated in an exploratory phase 2 study in idiopathic pulmonary fibrosis patients.</p>Fórmula:C30H33FN8O2SPureza:97% - 99.85%Cor e Forma:SolidPeso molecular:588.7PDE10-IN-1
CAS:<p>PDE10-IN-1 (SEP-0372814) is used for treating CNS and metabolic disorders.</p>Fórmula:C21H19N7Pureza:99.65%Cor e Forma:SolidPeso molecular:369.42RS-25344
CAS:<p>RS-25344: a strong PDE4 blocker, curbs eosinophil movement, boosts sperm motility in vitro.</p>Fórmula:C19H13N5O4Pureza:98.98%Cor e Forma:SolidPeso molecular:375.34Lotamilast
CAS:<p>Lotamilast (RVT-501) is a phosphodiesterase 4 (PDE-4) inhibitor (IC50: 2.8 nM) potentially for the treatment of atopic dermatitis.</p>Fórmula:C26H24N4O5Pureza:97.03% - 99.29%Cor e Forma:SolidPeso molecular:472.49Enpp-1-IN-1
CAS:<p>Enpp-1-IN-1 is an inhibitor of Ectonucleotide pyrophosphatase-phosphodiesterase 1 (enpp-1)</p>Fórmula:C17H17N3O3SPureza:97.52%Cor e Forma:SolidPeso molecular:343.4GSK256066 Trifluoroacetate
CAS:<p>GSK 256066 Trifluoroacetate: selective PDE4 inhibitor, IC50: 3.2 pM for PDE4B, treats COPD.</p>Fórmula:C29H27F3N4O7SCor e Forma:SolidPeso molecular:632.61Crisaborole-d4
<p>Crisaborole-d4 (AN-2728-d4) is the deuterated form of Crisaborole. Crisaborole is a PDE4 inhibitor and also a cytokine release inhibitor.</p>Fórmula:C14H6D4BNO3Cor e Forma:SolidPeso molecular:255.07ent-Tadalafil
CAS:<p>ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).</p>Fórmula:C22H19N3O4Pureza:98%Cor e Forma:SolidPeso molecular:389.4
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