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PDE

PDE

PDE related products

Structure Cat No. Product Name CAS No. Product Description
(S)-(+)-咯利普兰 V0787 S- (+)-Rolipram (ME-3167; SB95952; ZK-62711) 85416-73-5 S-(+)-Rolipram, theS-isomer of rolipram (ME3167;SB-95952; ZK62711), isa potent phosphodiesterase PDE4-inhibitor with potent anti-inflammatory and anti-depressant activity.
Enpp-1-IN-30 V135116 Enpp-1-IN-30 Enpp-1-IN-30 is an ENPP1 inhibitor with high oral bioavailability, and its human IC50 value is 13.1 nM.
GSK-256066 V0783 GSK256066 801312-28-7 GSK256066 (GSK-256066; GSK 256066) is a novel, potent and selective inhibitor of PDE4B (phosphodiesterase 4B) with important biological activity (e.
Mardepodect (PF-2545920; MP-10) V0792 Mardepodect (PF-2545920; MP-10) 898562-94-2 Mardepodect (formerly known as PF-2545920, PF2545920, MP10; MP-10) is a novel, potent and selective PDE10A (phosphodiesterase) inhibitor with antipsychotic activity.
Mardepodect盐酸盐 V2648 Mardepodect HCl (PF-2545920 HCl) 2070014-78-5 Mardepodect HCl, the hydrochloric acid salt of PF-2545920 (Also known as Mardepodect,MP-10), is a novel, potent and selective PDE10A (phosphodiesterase) inhibitor with IC50 of 0.37 nM, andwith >1000-fold selectivity over the PDE.
PAT-078 V142262 PAT-078 1682644-84-3 PAT-078 is a type II autosecretin (ATX) inhibitor.
PDE3/4-IN-2 V142333 PDE3/4-IN-2 2857007-03-3 PDE3/4-IN-2 is a dual inhibitor of PDE3A and PDE4B1, with an IC50 of 0.13 nM for PDE3A and 50 nM for PDE4B1.
PDE3/4-IN-3 V142334 PDE3/4-IN-3 2939748-69-1 PDE3/4-IN-3 is an orally effective dual PDE3/4 inhibitor with IC50 values of 0.17 nM for PDE3A and ≤50 nM for PDE4B2.
Phosphodiesterase-IN-4 V142632 Phosphodiesterase-IN-4 Phosphodiesterase-IN-4 is a potent inhibitor of tyrosyl-DNA phosphodiesterase 1 (TDP1).
RX-RA-69 V144433 RX-RA-69 77749-49-6 RX-RA-69 is an orally effective platelet phosphodiesterase (PDE) inhibitor with an IC50 of 1 nM.
Sildenafil chlorosulfonyl V144915 Sildenafil chlorosulfonyl 139756-22-2 Sildenafil chlorosulfonyl is an intermediate in the synthesis of sildenafil, a phosphodiesterase 5 (PDE5) inhibitor.
SMQ-03-20 V145068 SMQ-03-20 SMQ-03-20 is a highly bioavailable, selective, and potent PDE11A4 inhibitor that can cross the blood-brain barrier.
TAK-063 (Balipodect) V2623 TAK-063 (Balipodect) 1238697-26-1 Balipodect (formerly also known as TAK-063) is a novel,highly potent, orally bioavailable and selective phosphodiesterase 10A (PDE10A) inhibitor with potential usefulness inthe treatment of schizophrenia.
V11294 V146830 V11294 162278-10-6 V11294 is a phosphodiesterase 4 (PDE4) inhibitor with a Ki value of 436 nM for human lung PDE4.
乌地那非 V4577 Udenafil 268203-93-6 Udenafil (formerly known as DA8159) isa novel and potent PDE5 inhibitor used in urology to treat erectile dysfunction.
二羟丙茶碱 V0793 Dyphylline 479-18-5 Dyphylline (also named as Diprophylline; Corphyllin;Lufyllin; Neothylline), a xanthine derivative with bronchodilator and vasodilator effects,is used in the treatment of respiratory disorders like cardiac dyspnea,asthma, and bronchitis.
他达那非 V0780 Tadalafil (IC 351; Cialis) 171596-29-5 Tadalafil (formerly known as IC351; IC-351;trade name Cialis) is a potent, orally bioavailable, reversible and competitive small-molecule inhibitor of PDE-5 (phosphodiesterase 5) with the potential to treat erectile dysfunction (ED), benign prostatic hyperplasia (BPH), and pulmonary arterial hypertension.
伊索拉定 V0796 Irsogladine 57381-26-7 Irsogladine (MN1695; MN 1695; Gaslon; MN-1695; Dicloguamine),a mucosal protective drug, is a novel and potent PDE4 inhibitor and muscarinic acetylcholine receptor binder with anti-ulceric activity.
匹莫苯 V0782 Pimobendan 74150-27-9 Pimobendan (UD-CG115; UDCG115;Trade names Vetmedin, Acardi), a veterinary medication approvedto treat CHF-congestive heart failure in dogs, is a potent and selective inhibitor ofphosphodiesterasePDE3 with positive inotropic and vasodilator effects.
双嘧达莫 V0790 Dipyridamole ( NSC-515776; RA-8; Persantine) 58-32-2 Dipyridamole (also known as NSC515776; RA8; Persantine) is a pyrimido-pyrimidine based phosphodiesterase (PDE) inhibitor with antiplatelet properties.
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