Cell Metabolism

产品 101 到 150 共 623个

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  1. VCE-004.8

    Catalog No. A18549
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    PPARγ and CB2 receptor dual agonist
    VCE-004.8, a semi-synthetic multitarget cannabinoquinoid, is a specific PPARγ and CB2 receptor dual agonist with potent anti-inflammatory activity. 了解更多
  2. LJ570

    Catalog No. A20081
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    PPARα/PPARγ dual agonist
    LJ570 is a PPARα/PPARγ dual agonist with EC50s of 1.05 and 0.12 μM, respectively. 了解更多
  3. MA-0204

    Catalog No. A19031
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    PPARδ modulator
    MA-0204 is a potent, highly selective and orally available peroxisome proliferator activated receptor δ (PPARδ) modulator with EC50s of 0.4 nM, 7.9 nM and 10 nM for human, mouse and rat PPARδ, respectively. Potential treatment for Duchene Muscular Dystrophy (DMD). 了解更多
  4. Leriglitazone

    Catalog No. A18636
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    PPAR gamma agonist
    Leriglitazone is a peroxisome proliferator activated receptor (PPAR) gamma agonist. 了解更多
  5. Chiglitazar

    Catalog No. A12701
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    PPARα/γ dual agonist
    Chiglitazar is a PPARα/γ dual agonist, with EC50s of 1.2, 0.08, 1.7 μM for PPARα, PPARγ and PPARδ, respectively. 了解更多
  6. Vinpocetine

    Catalog No. A11602
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    PDE1 抑制剂
    Vinpocetine是一种Ca2+钙调蛋白依赖性磷酸二酯酶I(PDE1)抑制剂。 了解更多
  7. Cilostamide

    Catalog No. A13596
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    PDE3 抑制剂
    Cilostamide是磷酸二酯酶(PDE)3A和PDE3B的选择性抑制剂,IC50值分别为27和50 nM。 了解更多
  8. MK-0359

    Catalog No. A13467
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    PDE4 抑制剂
    MK-0359是一种选择性和有效的口服PDE4抑制剂,用于慢性哮喘。 了解更多
  9. GSK256066 2,2,2-trifluoroacetic acid

    Catalog No. A15097
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    PDE 抑制剂
    GSK256066是一种选择性PDE4B(与A-D型同等亲和力)抑制剂,IC50为3.2 pM,对PDE1/2/3/5/6的选择性> 380,000倍,对PDE4B与PDE7的选择性> 2500倍。 了解更多
  10. Nortadalafil

    Catalog No. A15191
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    PDE5 抑制剂
    Nortadalafil是去甲基他达拉非,它是一种PDE5抑制剂,目前以药丸形式销售,用于治疗勃起功能障碍(ED),名称为Cialis。并以Adcirca为名,用于治疗肺动脉高压。 了解更多
  11. Oglemilast

    Catalog No. A15197
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    PDE4 抑制剂
    Oglemilast是PDE4的有效抑制剂。 了解更多
  12. Olprinone Hydrochloride

    Catalog No. A15198
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    PDE3 抑制剂
    Olprinone Hydrochloride是一种选择性磷酸二酯酶3(PDE3)抑制剂。 了解更多
  13. TAK-063

    Catalog No. A15799
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    PDE10A 抑制剂?
    TAK-063是一种高效,选择性和口服活性的PDE10A抑制剂,IC50为0.30 nM。选择性是其他PDE的15000倍以上。 了解更多
  14. Sildenafil

    Catalog No. A12631
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    PDE5 抑制剂
    Sildenafil是选择性磷酸二酯酶5(PDE5)抑制剂之一(IC50 = 5.22 nM),被认为是治疗勃起功能障碍的最佳方法。 了解更多
  15. PDE-9 inhibitor

    Catalog No. A11532
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    PDE-9 inhibitor
    PDE-9 inhibitor is useful for neurodegenerative diseases. 了解更多
  16. AN3199

    Catalog No. A12228
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    PDE4 inhibitor
    AN3199 is a PDE4 inhibitor with IC50 of 94.5 nM. 了解更多
  17. PF-05180999

    Catalog No. A13006
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    PDE2A inhibitor
    PF-05180999 is a phosphodiesterase 2A (PDE2A) inhibitor, with an IC50 of 1.6 nM. 了解更多
  18. BI-409306

    Catalog No. A12970
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    PDE9A inhibitor
    BI-409306 is a potent and selective PDE9A inhibitor, with an IC50 of 52 nM. 了解更多
  19. Sildenafil citrate

    Catalog No. A10841
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    PDE5 inhibitor
    Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM. 了解更多
  20. Mirodenafil dihydrochloride

    Catalog No. A18047
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    PDE-5 inhibitor
    Mirodenafil dihydrochloride (SK3530 dihydrochloride) is a phosphodiesterase type 5 (PDE-5) inhibitor developed for the treatment of erectile dysfunction. 了解更多
  21. D159687

    Catalog No. A21228
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    PDE4D inhibitor
    D159687 is a selective PDE4D inhibitor. 了解更多
  22. PF-04957325

    Catalog No. A21246
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    PDE8 inhibitor
    PF-04957325 is a highly potent and selective PDE8 inhibitor, with IC50s of 0.7 nM and 0.3 nM for PDE8A and PDE8B, respectively. 了解更多
  23. Mirodenafil

    Catalog No. A21260
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    PDE-5 inhibitor
    Mirodenafil(SK3530) is a phosphodiesterase type 5 (PDE-5) inhibitor developed for the treatment of erectile dysfunction. 了解更多
  24. Saterinone hydrochloride

    Catalog No. A21402
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    PDE3 inhibitor
    Saterinone hydrochloride is a phosphodiesterase III (PDE III) inhibitor. 了解更多
  25. ITI214

    Catalog No. A21422
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    PDE1 inhibitor
    ITI-214 is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM). 了解更多
  26. AMG 579

    Catalog No. A21478
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    PDE10A inhibitor
    AMG 579 is a potent, selective, and efficacious inhibitor of phosphodiesterase 10A (PDE10A) with an IC50 of 0.1 nM. 了解更多
  27. BAY 73-6691 racemate

    Catalog No. A21745
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    PDE9 inhibitor
    BAY 73-6691 racemate is a phosphodiesterase 9 inhibitor extracted from patent WO 2017070293 A1. 了解更多
  28. VP3.15 dihydrobromide

    Catalog No. A21789
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    PDE7/GSK3 inhibitor
    VP3.15 dihydrobromide is a potent, orally bioavailable and CNS-penetrant dual phosphodiesterase (PDE)7- glycogen synthase kinase (GSK)3 inhibitor, with IC50s of 1.59 μM and 0.88 μM for PDE7 and GSK-3, respectively. 了解更多
  29. IBMX

    Catalog No. A21847
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    PDE inhibitor
    IBMX is a broad-spectrum phosphodiesterase (PDE) inhibitor, with IC50s of 6.5, 26.3 and 31.7 μM for PDE3, PDE4 and PDE5, respectively. 了解更多
  30. Olprinone

    Catalog No. A21869
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    PDE3 inhibitor
    Olprinone(Loprinone) is a selective phosphodiesterase 3 (PDE3) inhibitor. 了解更多
  31. TP-10

    Catalog No. A21935
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    PDE10A inhibitor
    TP-10 is a PDE10A inhibitor with IC50 of 0.8 nM. 了解更多
  32. ITI214 free base

    Catalog No. A21947
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    picomolar PDE1 inhibitor
    ITI-214 (free base) is a picomolar PDE1 inhibitor with excellent selectivity against other PDE family members and against a panel of enzymes, receptors, transporters, and ion channels, exhibits potent PDE1 inhibitory activity (Ki = 58 pM). 了解更多
  33. Deltasonamide 2

    Catalog No. A21970
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    PDEδ inhibitor
    Deltasonamide 2 is a competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM. 了解更多
  34. Deltasonamide 2 (TFA)

    Catalog No. A21979
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    PDEδ inhibitor
    Deltasonamide 2 TFA is competitive, high affinity PDEδ inhibitor with a Kd of ~385 pM. 了解更多
  35. Cilostazol

    Catalog No. A10217
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    PDE3 抑制剂
    Cilostazol是3型磷酸二酯酶(PDE3)的选择性抑制剂,IC50为0.2 μM,其治疗重点是cAMP。 了解更多
  36. Rolipram

    Catalog No. A10805
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    PDE4 抑制剂
    Rolipram是一种PDE4抑制剂,IC50 = 2.0μM。 了解更多
  37. Icariin

    Catalog No. A10464
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    PDE5 抑制剂
    Icariin对抑制PDE5A1、PDE5A2和PDE5A3的所有三种PDE5A亚型均有抑制作用,IC50值分别为1.0、0.75和1.1 μM。 了解更多
  38. Pimobendan (Vetmedin)

    Catalog No. A10733
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    PDE 抑制剂
    Pimobendan (Vetmedin)是一种钙增敏剂,具有正性肌力和血管舒张作用。它也是磷酸二酯酶III(PDE3)的选择性抑制剂。 了解更多
  39. GSK256066

    Catalog No. A11073
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    PDE 抑制剂
    GSK256066是PDE4的极高亲和力和选择性抑制剂,它以相等的亲和力抑制PDE4亚型A-D,并具有很高的HARBS(高亲和力利普兰结合位点)比率(> 17)。 了解更多
  40. PF-2545920

    Catalog No. A11191
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    PDE10A 抑制剂
    PF-2545920是对PDE10A亚型具有选择性的磷酸二酯酶抑制剂。 了解更多
  41. Ibudilast (KC-404)

    Catalog No. A11019
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    PDE 抑制剂
    Ibudilast (KC-404)是一种相对非选择性的phosphodiesterase抑制剂,具有抗炎和神经保护活性。 了解更多
  42. Cilomilast (SB-207499)

    Catalog No. A10216
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    PDE-4 抑制剂
    Cilomilast (SB-207499)可作为选择性磷酸二酯酶4抑制剂,具有抗炎作用。可针对与COPD相关的支气管收缩,粘液分泌过多和气道重塑。 了解更多
  43. Hesperetin

    Catalog No. A10449
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    PDE4 抑制剂
    Hesperetin是一种选择性磷酸二酯酶(PDE)4抑制剂,存在于中药“陈皮”中。橙皮素是一种柑橘类黄酮,据报道可以降低血浆胆固醇。橙皮素降低Hep-G2细胞中ACAT-2 mRNA的转录,并以剂量依赖的方式降低ApoB蛋白的合成。它也是类癌的潜在疗法。 了解更多
  44. Luteolin

    Catalog No. A10541
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    PDE4 抑制剂
    Luteolin是PDE4抑制剂、磷酸二酯酶抑制剂和白细胞介素6抑制剂,影响木聚嗪/氯胺酮诱导的小鼠麻醉。Luteolin作为单胺转运蛋白激活剂,是少数证明具有这种性质的化学物质之一。 了解更多
  45. Apremilast (CC 10004)

    Catalog No. A11289
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    PDE4 抑制剂
    Apremilast (CC 10004)是一种新型的PDE4抑制剂,可抑制人类风湿性滑膜细胞自发产生肿瘤坏死因子-α,并改善实验性关节炎。 了解更多
  46. Vardenafil

    Catalog No. A10965
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    PDE-5 抑制剂
    Vardenafil是用于治疗勃起功能障碍的PDE5抑制剂。 了解更多
  47. Roflumilast

    Catalog No. A10804
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    PDE 抑制剂
    Roflumilast可作为PDE-4酶的选择性长效抑制剂,无细胞试验中IC50为0.2-4.3 nM。 了解更多
  48. Bay 60-7550

    Catalog No. A11326
    PDE-2 抑制剂
    Bay 60-7550是一种强效PDE2抑制剂,IC50值为2.0 nM(牛)和4.7 nM(人)。 了解更多
  49. Aminophylline

    Catalog No. A10066
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    Adenosine receptor 拮抗剂
    Aminophylline是一种非选择性的腺苷受体拮抗剂和磷酸二酯酶抑制剂,能够逆转局部缺血引起的bradyasystole。 了解更多
  50. Dipyridamole

    Catalog No. A10319
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    PDE 抑制剂
    Dipyridamole (Persantine)是一种磷酸二酯酶抑制剂,可阻止红细胞和血管内皮细胞摄取和代谢腺苷。 了解更多

产品 101 到 150 共 623个

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