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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
T14352 Autotaxin-IN-1
化合物 T14352
1619971-30-0 98%
TargetMol Chemical Structure Autotaxin-IN-1
Autotaxin-IN-1 is a potent autotaxin inhibitor, which has favorable potency (IC50=2.2 nM), PK properties, and a robust PK/PD relationship and it is used in treat...
T10481L BAY 73-6691
化合物 T10481L
794568-92-6 98%
TargetMol Chemical Structure BAY 73-6691
BAY 73-6691 is an inhibitor of brain penetrant PDE9A.
T13232 TyK2-IN-2
化合物 T13232
2098466-94-3 98%
TargetMol Chemical Structure TyK2-IN-2
TyK2-IN-2 is a selective inhibitor of TYK2 (IC50s: 7 nM, 0.1 μM, and 0.05 μM for TYK2 JH2, IL-23, and IFNα).
T38108 Fulvic Acid
黄腐酸
479-66-3 98%
TargetMol Chemical Structure Fulvic Acid
Fulvic Acid 是一种来自土壤、沉积物或水生环境中微生物产生的腐殖质的天然产物,是一种首次青霉菌中分离出的酚酸和真菌代谢产物。Fulvic Acid 抑制淀粉样蛋白b (17-42) (AB17-42)二聚化,破坏预先形成的AB17-42三聚体,并结合到磷酸二酯酶5A (PDE5A)的催化位点,可以调节机体免疫系...
T15766 Lirimilast
化合物 T15766
329306-27-6 98%
TargetMol Chemical Structure Lirimilast
Lirimilast is an effective, selective, and orally active phosphodiesterase-4 (PDE4) inhibitor (IC50: 49 nM). Lirimilast has potently anti-inflammatory properties...
TN1843 Kushenol K
苦参醇K
101236-49-1 98%
TargetMol Chemical Structure Kushenol K
Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT). Kushenol K s...
T16976 TAK-915
化合物 T16976
1476727-50-0 98%
TargetMol Chemical Structure TAK-915
TAK-915 is a potent, selective, and brain-penetrant phosphodiesterase 2A (PDE2A) inhibitor (IC50: 0.61 nM). TAK-915 is >4100-fold more selectivity for PDE2A than...
T10416 Autotaxin-IN-4
化合物 T10416
2156655-86-4 98%
TargetMol Chemical Structure Autotaxin-IN-4
Autotaxin-IN-4 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.
T10417 Autotaxin-IN-5
化合物 T10417
2156655-99-9 98%
TargetMol Chemical Structure Autotaxin-IN-5
Autotaxin-IN-5 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.
T15640 K134
化合物 T15640
189362-06-9 98%
TargetMol Chemical Structure K134
K134 is an inhibitor of phosphodiesterase 3. The IC50s of K134 for PDE3A, PDE3B, PDE5, PDE2 and PDE4 are 0.1, 0.28, 12.1, >300 and >300 μM, respectively.
T16272 Naproxen etemesil
化合物 T16272
385800-16-8 98%
TargetMol Chemical Structure Naproxen etemesil
Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naprox...
T10994L2 Deltasonamide 2 (TFA)
化合物 T10994L2
2235358-74-2 98%
TargetMol Chemical Structure Deltasonamide 2 (TFA)
Deltasonamide 2 TFA is competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
T10350 Apremilast-d5
化合物 T10350
1258597-47-5 98%
TargetMol Chemical Structure Apremilast-d5
Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast. Apremilast is an orally available inhibitor of PDE-4 (IC50: 74 nM). Apremilast inhibits TNF-α rele...
T9805 BAY 2666605
化合物BAY 2666605
2275774-60-0 99.98%
TargetMol Chemical Structure BAY 2666605
BAY 2666605 是一种具有口服活性的 PDE3A 和 PDE3B 抑制剂,IC50 分别为 87 nM 和 50 nM。 BAY 2666605 具有抗癌作用。
TN2159 Robustine
大叶桉亭
2255-50-7 99.97%
TargetMol Chemical Structure Robustine
Robustine 是一种从 Dictamnus albus 获得的呋喃喹啉生物碱,在体外对人磷酸二酯酶 5 (hPDE5A) 具有抑制作用。
T0080 Trapidil
唑嘧胺
15421-84-8 99.96%
TargetMol Chemical Structure Trapidil
Trapidil (Avantrin) 是一种抗血小板药物,是一种血管扩张剂,有特异性血小板衍生生长因子。
T2205 Acefylline
茶碱乙酸
652-37-9 99.95%
TargetMol Chemical Structure Acefylline
Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。
T1681 Aminophylline
氨茶碱
317-34-0 99.94%
TargetMol Chemical Structure Aminophylline
Aminophylline (Phyllocontin) 是一种竞争性非选择性磷酸二酯酶抑制剂,具有支气管扩张作用。它是竞争性的腺苷受体拮抗剂,有用于哮喘研究的潜力。
T1096 Milrinone
米力农
78415-72-2 99.93%
TargetMol Chemical Structure Milrinone
Milrinone (Win 47203) 是一种 PDE3抑制剂,也是一种强心药、血管舒张药。
TN6120 Nauclefine
牛蒡子苷
57103-51-2 99.92%
TargetMol Chemical Structure Nauclefine
Nauclefine (Parvine) 是一种植物吲哚生物碱天然产物,可通过 PDE3A-SLFN12 依赖性死亡途径诱导多种癌细胞的凋亡。 Nauclefine 结合 PDE3A 但不抑制 PDE3A 的磷酸二酯酶活性。
Autotaxin-IN-1
T14352
Autotaxin-IN-1 is a potent autotaxin inhibitor, which has favorable potency (IC50=2.2 nM), PK properties, and a robust PK/PD relationship and it is used in treat...
BAY 73-6691
T10481L
BAY 73-6691 is an inhibitor of brain penetrant PDE9A.
TyK2-IN-2
T13232
TyK2-IN-2 is a selective inhibitor of TYK2 (IC50s: 7 nM, 0.1 μM, and 0.05 μM for TYK2 JH2, IL-23, and IFNα).
Fulvic Acid
T38108
Fulvic Acid 是一种来自土壤、沉积物或水生环境中微生物产生的腐殖质的天然产物,是一种首次青霉菌中分离出的酚酸和真菌代谢产物。Fulvic Acid 抑制淀粉样蛋白b (17-42) (AB17-42)二聚化,破坏预先形成的AB17-42三聚体,并结合到磷酸二酯酶5A (PDE5A)的催化位点,可以调节机体免疫系...
Lirimilast
T15766
Lirimilast is an effective, selective, and orally active phosphodiesterase-4 (PDE4) inhibitor (IC50: 49 nM). Lirimilast has potently anti-inflammatory properties...
Kushenol K
TN1843
Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT). Kushenol K s...
TAK-915
T16976
TAK-915 is a potent, selective, and brain-penetrant phosphodiesterase 2A (PDE2A) inhibitor (IC50: 0.61 nM). TAK-915 is >4100-fold more selectivity for PDE2A than...
Autotaxin-IN-4
T10416
Autotaxin-IN-4 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.
Autotaxin-IN-5
T10417
Autotaxin-IN-5 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.
K134
T15640
K134 is an inhibitor of phosphodiesterase 3. The IC50s of K134 for PDE3A, PDE3B, PDE5, PDE2 and PDE4 are 0.1, 0.28, 12.1, >300 and >300 μM, respectively.
Naproxen etemesil
T16272
Naproxen is a COX-1 and COX-2 inhibitor (IC50s: 8.72 and 5.15 μM, respectively in cell assay). Naproxen etemesil is a lipophilic and non-acidic prodrug of naprox...
Deltasonamide 2 (TFA)
T10994L2
Deltasonamide 2 TFA is competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM.
Apremilast-d5
T10350
Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast. Apremilast is an orally available inhibitor of PDE-4 (IC50: 74 nM). Apremilast inhibits TNF-α rele...
BAY 2666605
T9805
BAY 2666605 是一种具有口服活性的 PDE3A 和 PDE3B 抑制剂,IC50 分别为 87 nM 和 50 nM。 BAY 2666605 具有抗癌作用。
Robustine
TN2159
Robustine 是一种从 Dictamnus albus 获得的呋喃喹啉生物碱,在体外对人磷酸二酯酶 5 (hPDE5A) 具有抑制作用。
Trapidil
T0080
Trapidil (Avantrin) 是一种抗血小板药物,是一种血管扩张剂,有特异性血小板衍生生长因子。
Acefylline
T2205
Acefylline (Theophylline-7-acetic acid) 是黄嘌呤衍生物,是一种腺苷受体拮抗剂。它是蛋白质精氨酸脱亚氨酶 (PAD) 激活剂,也是一种支气管扩张剂,可抑制大鼠肺 cAMP 磷酸二酯酶同工酶。
Aminophylline
T1681
Aminophylline (Phyllocontin) 是一种竞争性非选择性磷酸二酯酶抑制剂,具有支气管扩张作用。它是竞争性的腺苷受体拮抗剂,有用于哮喘研究的潜力。
Milrinone
T1096
Milrinone (Win 47203) 是一种 PDE3抑制剂,也是一种强心药、血管舒张药。
Nauclefine
TN6120
Nauclefine (Parvine) 是一种植物吲哚生物碱天然产物,可通过 PDE3A-SLFN12 依赖性死亡途径诱导多种癌细胞的凋亡。 Nauclefine 结合 PDE3A 但不抑制 PDE3A 的磷酸二酯酶活性。
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