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PDE

PDE

A phosphodiesterase (PDE) is an enzyme that breaks a phosphodiester bond. Usually, phosphodiesterase refers to cyclic nucleotide phosphodiesterases, which have great clinical significance and are described below. However, there are many other families of phosphodiesterases, including phospholipases C and D, autotaxin, sphingomyelin phosphodiesterase, DNases, RNases, and restriction endonucleases (which all break the phosphodiester backbone of DNA or RNA), as well as numerous less-well-characterized small-molecule phosphodiesterases.The cyclic nucleotide phosphodiesterases comprise a group of enzymes that degrade the phosphodiester bond in the second messenger molecules cAMP and cGMP. They regulate the localization, duration, and amplitude of cyclic nucleotide signaling within subcellular domains. PDEs are therefore important regulators of signal transduction mediated by these second messenger molecules.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
T4480 Vardenafil dihydrochloride
二盐酸伐地那非
224789-15-5 99.77%
TargetMol Chemical Structure Vardenafil dihydrochloride
Vardenafil dihydrochloride (Levitra) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。
TN2217 Sophoflavescenol
槐苦参醇
216450-65-6 99.65%
TargetMol Chemical Structure Sophoflavescenol
Sophoflavescenol 是异戊烯基黄酮类化合物,能够抑制PDE5的活性,IC50=0.013 μM。它也抑制 RLAR,HRAR,BACE1,AChE 和 BChE,IC50值分别为 0.30 µM,0.17 µM,10.98 µM,8.37 µM 和 8.21 µM。
T19706 Ro 20-1724
化合物Ro20-1724
29925-17-5 98.82%
TargetMol Chemical Structure Ro 20-1724
Ro 20-1724 (4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone) 是 cAMP 特异性磷酸二酯酶抑制剂 b>(PDE4/PDE IV),其 Ki=1930 nM,具有神经保护作用。
T12315 OR-1896
化合物 T12315
220246-81-1 98%
TargetMol Chemical Structure OR-1896
OR-1896 is an active long-lived Levosimendan metabolite, is a highly selective inhibitor of phosphodiesterase (PDE) III isoformand a powerful vasodilator.
T22491 PDE7-IN-2
化合物 PDE7-IN-2
107522-19-0 98%
TargetMol Chemical Structure PDE7-IN-2
PDE7-IN-2 是磷酸二酯酶 7 (IC50 = 2.1 µM) 的抑制剂,可用于帕金森病研究。
T10994 Deltasonamide 2
化合物 T10994
2088485-34-9 98%
TargetMol Chemical Structure Deltasonamide 2
Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
T12394 PDE5-IN-2
化合物 T12394
2244517-61-9 98%
TargetMol Chemical Structure PDE5-IN-2
PDE5-IN-2 is a potent, highly selective, and orally active inhibitor of PDE5(IC50 of 0.31 nM)
T16484 PF-05180999
化合物 T16484
1394033-54-5 98%
TargetMol Chemical Structure PF-05180999
PF-05180999 is an inhibitor of phosphodiesterase 2A (IC50: 1.6 nM).
TN2095 Pomiferin
橙桑黄酮
572-03-2 98%
TargetMol Chemical Structure Pomiferin
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has a...
T16434 PAT-048
化合物 T16434
1359983-15-5 98%
TargetMol Chemical Structure PAT-048
PAT-048 is an effective and selective autotaxin inhibitor. PAT-048 reduces dermal fibrosis in vivo. PAT-048 also inhibits IL-6 mRNA expression but displays no ef...
TN2974 3-O-Methylquercetin tetraacetate
化合物 TN2974
1486-69-7 98%
TargetMol Chemical Structure 3-O-Methylquercetin tetraacetate
Quercetin 3-O-methyl ether is a potent phosphodiesterase (PDE)3/4 inhibitor, it has potential for treating asthma against ovalbumin-induced airway hyperresponsiv...
T10994L Deltasonamide 2 hydrochloride
化合物 T10994L
T10994L 98%
TargetMol Chemical Structure Deltasonamide 2 hydrochloride
Deltasonamide 2 hydrochloride is a competitive high-affinity PDEδ inhibitor with a Kd of approximately 385 pM.
TN4317 Isopedicin
化合物 TN4317
4431-42-9 98%
TargetMol Chemical Structure Isopedicin
Isopedicin has anti-inflammatory functions, it inhibits the O(2)(*)(-) production in human neutrophils by an elevation of cellular cAMP and activation of PKA thr...
T14962 CI-1044
化合物 T14962
197894-84-1 98%
TargetMol Chemical Structure CI-1044
CI-1044 is an inhibitor of PDE4 (IC50s: 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3).
TN4397 Kuraridine
次苦参素
34981-25-4 98%
TargetMol Chemical Structure Kuraridine
Kuraridine is measured against cGMP PDE5 to identify potent cGMP specific phosphodiesterase type 5 inhibitory constituents.
T11483 GSK256066 Trifluoroacetate
化合物 T11483
1415560-64-3 98%
TargetMol Chemical Structure GSK256066 Trifluoroacetate
GSK 256066 Trifluoroacetate is a selective and high-affinity phosphodiesterase 4 (PDE) inhibitor (IC50: 3.2 pM for PDE4B). It can be used for the treatment of ch...
T11206 Ent-Tadalafil
化合物 T11206
629652-72-8 98%
TargetMol Chemical Structure ent-Tadalafil
ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).
T16482 PF-05085727
化合物 T16482
1415637-72-7 98%
TargetMol Chemical Structure PF-05085727
PF-05085727 inhibits PDE2A >4,000-fold selectivity over PDE1 and PDE3-11. PF-05085727 is an effective, selective and brain penetrant inhibitor of cGMP-dependent ...
T10418 Autotaxin modulator 1
化合物 T10418
1548743-69-6 98%
TargetMol Chemical Structure Autotaxin modulator 1
Autotaxin modulator 1 is a new modulator of Autotaxin.
TN4665 Norbraylin
化合物 TN4665
60796-64-7 98%
TargetMol Chemical Structure Norbraylin
Norbraylin is a natural product from Toddalia asiatica.
Vardenafil dihydrochloride
T4480
Vardenafil dihydrochloride (Levitra) 是一种新型 PDE 抑制剂,对 PDE5 和 PDE1 的 IC50 分别为 0.7 和 180 nM。
Sophoflavescenol
TN2217
Sophoflavescenol 是异戊烯基黄酮类化合物,能够抑制PDE5的活性,IC50=0.013 μM。它也抑制 RLAR,HRAR,BACE1,AChE 和 BChE,IC50值分别为 0.30 µM,0.17 µM,10.98 µM,8.37 µM 和 8.21 µM。
Ro 20-1724
T19706
Ro 20-1724 (4-(3-Butoxy-4-methoxybenzyl)-2-imidazolidinone) 是 cAMP 特异性磷酸二酯酶抑制剂 b>(PDE4/PDE IV),其 Ki=1930 nM,具有神经保护作用。
OR-1896
T12315
OR-1896 is an active long-lived Levosimendan metabolite, is a highly selective inhibitor of phosphodiesterase (PDE) III isoformand a powerful vasodilator.
PDE7-IN-2
T22491
PDE7-IN-2 是磷酸二酯酶 7 (IC50 = 2.1 µM) 的抑制剂,可用于帕金森病研究。
Deltasonamide 2
T10994
Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
PDE5-IN-2
T12394
PDE5-IN-2 is a potent, highly selective, and orally active inhibitor of PDE5(IC50 of 0.31 nM)
PF-05180999
T16484
PF-05180999 is an inhibitor of phosphodiesterase 2A (IC50: 1.6 nM).
Pomiferin
TN2095
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has a...
PAT-048
T16434
PAT-048 is an effective and selective autotaxin inhibitor. PAT-048 reduces dermal fibrosis in vivo. PAT-048 also inhibits IL-6 mRNA expression but displays no ef...
3-O-Methylquercetin tetraacetate
TN2974
Quercetin 3-O-methyl ether is a potent phosphodiesterase (PDE)3/4 inhibitor, it has potential for treating asthma against ovalbumin-induced airway hyperresponsiv...
Deltasonamide 2 hydrochloride
T10994L
Deltasonamide 2 hydrochloride is a competitive high-affinity PDEδ inhibitor with a Kd of approximately 385 pM.
Isopedicin
TN4317
Isopedicin has anti-inflammatory functions, it inhibits the O(2)(*)(-) production in human neutrophils by an elevation of cellular cAMP and activation of PKA thr...
CI-1044
T14962
CI-1044 is an inhibitor of PDE4 (IC50s: 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3).
Kuraridine
TN4397
Kuraridine is measured against cGMP PDE5 to identify potent cGMP specific phosphodiesterase type 5 inhibitory constituents.
GSK256066 Trifluoroacetate
T11483
GSK 256066 Trifluoroacetate is a selective and high-affinity phosphodiesterase 4 (PDE) inhibitor (IC50: 3.2 pM for PDE4B). It can be used for the treatment of ch...
ent-Tadalafil
T11206
ent-Tadalafil (ent-IC-351), compound (6S,12aS), is a inactive cis-enantiomer of compound (6R,12aS).
PF-05085727
T16482
PF-05085727 inhibits PDE2A >4,000-fold selectivity over PDE1 and PDE3-11. PF-05085727 is an effective, selective and brain penetrant inhibitor of cGMP-dependent ...
Autotaxin modulator 1
T10418
Autotaxin modulator 1 is a new modulator of Autotaxin.
Norbraylin
TN4665
Norbraylin is a natural product from Toddalia asiatica.
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