162 Results for "

pde5 1

" in MedChemExpress (MCE) Product Catalog:
Products (162)

162 Results for "pde5 1" in MCE Product Catalog:

75
75 Publications Verification
製品番号: HY-12318
CAS 番号: 28822-58-4
純度:  99.99%
別名: 3-Isobutyl-1-methylxanthine; Isobutylmethylxanthine
研究分野:  

Inflammation/Immunology

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.
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29
29 Cited Publications
製品番号: HY-N0014
CAS 番号: 489-32-7
別名: Ieariline
Icariin is a flavonol glycoside. Icariin inhibits PDE5 and PDE4 activities with IC50s of 432 nM and 73.50 μM, respectively. Icariin also is a PPARα activator.
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16
16 Cited Publications
製品番号: HY-15025
CAS 番号: 139755-83-2
純度:  99.90%
別名: UK-92480
Sildenafil (UK-92480) is a potent phosphodiesterase type 5 (PDE5) inhibitor with an IC50 of 5.22 nM.
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16
16 Cited Publications
製品番号: HY-15025A
CAS 番号: 171599-83-0
純度:  99.86%
別名: UK-92480 citrate
Sildenafil citrate is a potent phosphodiesterase type 5 (PDE5) inhibitor with IC50 of 5.22 nM.
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14
14 Cited Publications
製品番号: HY-15455
CAS 番号: 162401-32-3
純度:  99.98%
別名: APTA-2217; BYK 20869; B9302-107
研究分野:  

Inflammation/Immunology

Roflumilast (APTA-2217) is a selective PDE4 inhibitor with IC50s of 0.7, 0.9, 0.7, and 0.2 nM for PDE4A1, PDE4A4, PDE4B1, and PDE4B2, respectively, without affecting PDE1, PDE2, PDE3 or PDE5 isoenzymes from various cells.
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9
9 Cited Publications
製品番号: HY-90009A
CAS 番号: 171596-29-5
別名: IC-351
Tadalafil (IC-351) is a PDE5 inhibitor with an IC50 value of 1.8 nM.
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6
6 Cited Publications
製品番号: HY-B0442
CAS 番号: 224785-90-4
Vardenafil is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. Vardenafil shows inhibitory towards PDE1, PDE6 with IC50s of 180 nM, and 11 nM, while IC50s are >1000 nM for PDE3 and PDE4 . Vardenafil competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels . Vardenafil can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6].
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6
6 Cited Publications
製品番号: HY-B0442A
CAS 番号: 224785-91-5
Vardenafil hydrochloride is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. Vardenafil hydrochloride shows inhibitory towards PDE1, PDE6 with IC50s of 180 nM, and 11 nM, while IC50s are >1000 nM for PDE3 and PDE4 . Vardenafil hydrochloride competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels . Vardenafil hydrochloride can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6].
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6
6 Cited Publications
製品番号: HY-B0442B
CAS 番号: 330808-88-3
Vardenafil hydrochloride trihydrate is a selective and orally active inhibitor of phosphodiesterase-5 (PDE5), with an IC50 of 0.7 nM. Vardenafil hydrochloride trihydrate shows inhibitory towards PDE1, PDE6 with IC50s of 180 nM, and 11 nM, while IC50s are >1000 nM for PDE3 and PDE4 . Vardenafil hydrochloride trihydrate competitively inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels . Vardenafil hydrochloride trihydrate can be used for the research of erectile dysfunction, hepatitis, diabetes [1]-[6].
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4
4 Cited Publications
製品番号: HY-122942
CAS 番号: 56317-21-6
純度:  98.90%
Moracin M is a phenolic component that can be isolated from Mori Cortex, is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity .
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3
3 Cited Publications
製品番号: HY-B1816
CAS 番号: 37762-06-4
別名: M&B 22948
Zaprinast (M&B 22948) is a selective inhibitor of cGMP-selective Phosphodiesterase (PDE5). Zaprinast causes a significant increase in cGMP levels in myocytes. Zaprinast is a G protein-coupled receptor 35 (GPR35) agonist which activates rat GPR35 strongly and activates human GPR35 moderately. Zaprinast reduces vessel remodeling through antiproliferative and proapoptotic effects .
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3
3 Cited Publications
製品番号: HY-10790
CAS 番号: 153259-65-5
純度:  99.91%
別名: SB-207499
研究分野:  

Inflammation/Immunology

Cilomilast (SB-207499) is a potent, selective and orally active inhibitor of Phosphodiesterase 4 (PDE4), with IC50s of ~100 and 120 nM for LPDE4 and HPDE4, respectively. Cilomilast shows selectivity for PDE4 over PDE1, PDE2, PDE3 and PDE5 (IC50=74, 65, >100, and 83 μM, respectively). Cilomilast has anti-inflammatory and immunomodulatory effects and can be used for thr research of asthma and chronic obstructive pulmonary disease (COPD) .
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1
1 Cited Publications
製品番号: HY-18252
CAS 番号: 330784-47-9
別名: TA1790
Avanafil (TA-1790) is a potent and selective phosphodiesterase-5 (PDE-5) inhibitor with IC50 values of 5.2 nM, 630 nM, 5700 nM, 6200 nM, 12000 nM, 27000 nM, 51000 nM and 53000 nM for PDE-5, PDE-6, PDE-4, PDE-10, PDE-8, PDE-7, PDE-2 and PDE-1, respectively. Avanafil activates NO/cGMP/PKG signaling-pathway to decrease loss in BMD, bone atrophy, and oxidative stress. Avanafil inhibits cyclic guanosine monophosphate (cGMP) hydrolysis and thus increases cGMP levels. Avanafil can be used for the research of erectile dysfunction and osteoporosis .
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1
1 Cited Publications
製品番号: HY-90009
CAS 番号: 171596-36-4
別名: Demethyl Tadalafil
Nortadalafil (Demethyl Tadalafil) is a phosphodiesterase-5 (PDE-5) inhibitor and Tadalafil (HY-90009A) analog. Nortadalafil exhibits pharmacokinetic properties including a half-life of 5.93-6.21 h after single oral doses of 40-120 mg. Nortadalafil is identified as an adulterant in dietary supplements .
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1
1 Cited Publications
製品番号: HY-100933
CAS 番号: 78351-75-4
純度:  99.86%
MY-5445 is a specific inhibitor of the cyclic GMP phosphodiesterase, phosphodiesterase type 5 (PDE5), with a Ki of 1.3 μM. MY-5445 inhibits human platelet aggregation. MY-5445 is a selective modulator of ATP-binding cassette (ABC) transporter ABCG2, with anti-proliferative effect .
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1
1 Cited Publications
製品番号: HY-15455S
CAS 番号: 1398065-69-4
別名: APTA-2217-d4; BYK 20869-d4; B9302-107-d4
Roflumilast-d4 is the deuterium labeled Roflumilast. Roflumilast is a selective PDE4 inhibitor with IC50s of 0.7, 0.9, 0.7, and 0.2 nM for PDE4A1, PDEA4, PDEB1, and PDEB2, respectively, without affecting PDE1, PDE2, PDE3 or PDE5 isoenzymes from various cells .
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1
1 Cited Publications
製品番号: HY-112831
CAS 番号: 1189767-28-9
純度:  99.88%
別名: BI-409306
研究分野:  

Neurological Disease

Osoresnontrine (BI-409306) is a potent and selective PDE9A inhibitor, with an IC50 of 52 nM, and shows weak activity against other PDEs, such as PDE1A (IC50, 1.4 µM), PDE1C (IC50, 1.0 µM), PDE2A, PDE3A, PDE4B, PDE5A, PDE6AB, PDE7A, and PDE10A (IC50 all > 10 μM); Osoresnontrine can be used in the research of memory enhancement in CNS disorders.
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製品番号: HY-18253
CAS 番号: 268203-93-6
別名: DA8159
研究分野:  

Endocrinology Cancer

Udenafil (DA8159) is a potent, selective and orally active phosphodiesterase type 5 (PDE5) inhibitor. Udenafil also inhibits cGMP hydrolysis and can be used for erectile dysfunction research .
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製品番号: HY-123210
CAS 番号: 139755-85-4
純度:  99.94%
別名: Hydroxyhomosildenafil
研究分野:  

Endocrinology

Lodenafil is a potent phosphodiesterase type 5 (PDE5) inhibitor for the treatment of erectile dysfunction (ED) .
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製品番号: HY-W011336
CAS 番号: 139756-21-1
研究分野:  

Others

PDE5-IN-7 (compound 8) is a selective phosphodiesterase 5 (PDE 5) inhibitor with an IC50 value of 5 nM, while an IC50 of 300 nM for PDE 1 .
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