PDE3

PDE3 Related Products (22):

By Type:	Pan (15) Selective (5)
By Effects:	Inhibitors (21) Modulator (1)

Cat. No.	Product Name	Effect	Purity

HY-B0809

Theophylline	Inhibitor	99.94%
Theophylline (1,3-Dimethylxanthine) is a potent phosphodiesterase (PDE) inhibitor, adenosine receptor antagonist, and histone deacetylase (HDAC) activator.

HY-B0442A

Vardenafil hydrochloride	Inhibitor	99.48%
Vardenafil hydrochloride is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC₅₀ of 0.7 nM.

HY-15485

Zardaverine	Inhibitor	98.73%
Zardaverine is an orally active and selective PDE3/4 inhibitor (IC₅₀)=0.58 uM/0.17 uM) with potent bronchodilator activity.

HY-B0442

Vardenafil	Inhibitor	99.58%
Vardenafil is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC₅₀ of 0.7 nM.

HY-135746

OR-1896	Inhibitor	99.03%
OR-1896 is an active long-lived metabolite of Levosimendan.

HY-110005

Sp-cAMPS triethylamine	Inhibitor
Sp-cAMPS triethylamine, a cAMP analog, is potent activator of cAMP-dependent PKA I and PKA II.

HY-10568

TC-E 5005	Inhibitor
TC-E 5005 is a potent and selective PDE10A inhibitor with IC₅₀ values of 7.28, 239, 779, 919, 3,100, and 3,700 nM for PDE10A, 2A, 11A, 5A, 7B and 3A, respectively.

HY-145924

BAY 2666605	Inhibitor	99.64%
BAY 2666605 is an orally active PDE3A and PDE3B inhibitor with IC₅₀s of 87 nM and 50 nM, respectively.

HY-B1639

Enoximone	Inhibitor	98.05%
Enoximone is an inotropic vasodilating agent and a selective and orally active phosphodiesterase III (PDE3) inhibitor with an IC₅₀ of 5.9 μM.

HY-119708

Ensifentrine	Inhibitor	99.47%
Ensifentrine (RPL-554) is an inhaled first-in-class dual inhibitor of phosphodiesterase 3 (PDE3) and PDE4 with IC₅₀s of 0.4 nM and 1479 nM, respectively.

HY-100530C

Sp-cAMPS sodium salt	Inhibitor	98.73%
Sp-cAMPS sodium salt, a cAMP analog, is potent activator of cAMP-dependent PKA I and PKA II.

HY-136350

BRD9500	Modulator	99.60%
BRD9500 is an orally active phosphodiesterases 3 (PDE3) inhibitor with IC₅₀s of 10 and 27 nM for PDE3A and PDE3B, respectively.

HY-114672

MBCQ	Inhibitor	99.37%
MBCQ is a potent and selective cGMP-specific phosphodiesterase (PDE V; PDE5) inhibitor with an IC₅₀ of 19 nM.

HY-108621

RS-25344 hydrochloride	Inhibitor	99.50%
RS-25344 hydrochloride is a selective cAMP-phosphodiesterase 4 (PDE 4; PDE IV) inhibitor with an IC₅₀ of 0.28 nM in human lymphocytes.

HY-12887

Piclamilast	Inhibitor	99.09%
Piclamilast (RP 73401) is a phosphodiesterase 4 (PDE4) inhibitor, with IC₅₀ values of 16 nM and 2 nM in pig aorta and eosinophil soluble, respectively.

HY-100530B

Sp-cAMPS	Inhibitor
Sp-cAMPS, a cAMP analog, is potent activator of cAMP-dependent PKA I and PKA II.

HY-119611A

Thioquinapiperifil dihydrochloride	Inhibitor	99.18%
Thioquinapiperifil dihydrochloride (KF31327), a potent, selective and non-competitive phosphodiesterase-5 (PDE-5, IC₅₀ of 0.074 nM) inhibitor, is used for sexual enhancement study.

HY-119611

Thioquinapiperifil	Inhibitor
Thioquinapiperifil (KF31327 free base), a potent, selective and non-competitive phosphodiesterase-5 (PDE-5, IC₅₀ of 0.074 nM) inhibitor, is used for sexual enhancement study.

HY-B0442B

Vardenafil hydrochloride trihydrate	Inhibitor
Vardenafil hydrochloride trihydrate is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC₅₀ of 0.7 nM.

HY-105349

T-0156	Inhibitor
T-0156 is a potent and selective phosphodiesterase type 5 (PDE5) inhibitor.

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