58 Results for "

PDE4D

" in MedChemExpress (MCE) Product Catalog:
Products (58)

58 Results for "PDE4D" in MCE Product Catalog:

4
4 Cited Publications
Cat. No.: HY-122942
CAS No.: 56317-21-6
Purity:  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
Cat. No.: HY-117571
CAS No.: 1606974-33-7
Purity:  99.50%
Synonyms: BPN14770
Research Areas:  

Neurological Disease

Zatolmilast (BPN14770) is a selective phosphodiesterase 4D (PDE4D) allosteric inhibitor with IC50s of 7.8 nM and 7.4 nM for PDE4D7 and PDE4D3, respectively .
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2
2 Cited Publications
Cat. No.: HY-16900A
CAS No.: 85416-75-7
Synonyms: (R)-Rolipram; (-)-Rolipram
Research Areas:  

Neurological Disease

(R)-(-)-Rolipram is the R-enantiomer of Rolipram. Rolipram is a selective inhibitor of phosphodiesterases PDE4 with IC50 of 3 nM, 130 nM and 240 nM for PDE4A, PDE4B, and PDE4D, respectively.
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2
2 Cited Publications
Cat. No.: HY-128358
CAS No.: 2374703-19-0
Purity:  98.37%
Research Areas:  

Neurological Disease

MR-L2 is a reversible and noncompetitive allosteric activator of long-isoform phosphodiesterase-4 (PDE4), activates representative PDE4 long-isoform variants (PDE4A4, PDE4B1, PDE4C3, PDE4D5). MR-L2 suppresses PGE2-induced MDCK cell cyst formation with an EC50 of 1.2 μM .
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1
1 Cited Publications
Cat. No.: HY-103050
CAS No.: 1013750-77-0
Purity:  99.50%
Research Areas:  

Inflammation/Immunology

ML-030 is a potent PDE4 inhibitor, with IC50 of 6.7 nM, 12.9 nM, 48.2 nM, 37.2 nM, 452 nM and 49.2 nM for PDE4A, PDE4A1, PDE4B1, PDE4B2, PDE4C1,and PDE4D2, respectively.
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Cat. No.: HY-115687
CAS No.: 915082-52-9
Purity:  99.59%
Research Areas:  

Inflammation/Immunology

PDE4B-IN-2 is an orally active and selective PDE4B inhibitor with an IC50 of 15 nM. PDE4B-IN-2 inhibits PDE4D (IC50=1.7 μM). PDE4B-IN-2 exhibits potent anti-inflammatory effects .
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Cat. No.: HY-15444
CAS No.: 1155877-97-6
Purity:  98.34%
Research Areas:  

Neurological Disease

D159687 is a selective PDE4D inhibitor .
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Cat. No.: HY-119190
CAS No.: 2055776-17-3
Purity:  98.23%
Research Areas:  

Neurological Disease

PF-06445974, a promising positron emission tomography (PET) lead, has exquisite potency at PDE4B with an IC50 <1 nM. The IC50 values are 36, 4.7 and 17 nM for PDE4D, PDE4A and PDE4C, respectively. PF-06445974 has good selectivity over PDE4D, excellent brain permeability, and a high level of specific binding in the "cold tracer" study .
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Cat. No.: HY-117960
CAS No.: 1353546-86-7
Purity:  99.37%
Synonyms: LEO-32731
Research Areas:  

Inflammation/Immunology

Orismilast (LEO-32731) is an orally active and selective PDE4 inhibitor used for the research of inflammatory diseases. Orismilast demonstrates potent inhibition of PDE4B and PDE4D subtype splice variants .
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Cat. No.: HY-100246
CAS No.: 197894-84-1
Purity:  98.02%
Synonyms: PD-189659
Research Areas:  

Inflammation/Immunology

CI-1044 is an orally active PDE4 inhibitor with IC50s of 0.29, 0.08, 0.56, 0.09 μM for PDE4A5, PDE4B2, PDE4C2 and PDE4D3, respectively.
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Cat. No.: HY-RS10225
Research Areas:  

Others

PDE4D Human Pre-designed siRNA Set A contains three designed siRNAs for PDE4D gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-139178
CAS No.: 2410550-31-9
Purity:  99.81%
Research Areas:  

Neurological Disease

KVA-D-88 is a blood-brain barrier-permeable PDE4 inhibitor with IC50 values of 140 and 880 nM for PDE4B and PDE4D, respectively. KVA-D-88 induces cAMP accumulation and inhibits neuroactive substance-mediated hyperlocomotion, locomotor sensitization. KVA-D-88 can be used for the research of drug addiction .
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Cat. No.: HY-106003
CAS No.: 720704-34-7
Purity:  99.82%
GSK356278 is a potent, selective, orally bioavailable and brain-penetrant inhibitor of phosphodiesterase 4 (PDE4), with pIC50s of 8.6, 8.8, and 8.7 for human PDE4A, PDE4B, and PDE4D, respectively. GSK356278 has anti-inflammatory activity, and exhibits anxiolytic and cognition-enhancing effects .
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Cat. No.: HY-15178
CAS No.: 778576-62-8
Purity:  98.00%
Synonyms: GRC 3886
Research Areas:  

Inflammation/Immunology

Oglemilast (GRC 3886) is a potent and orally active phosphodiesterase-4 (PDE4) inhibitor with an IC50 of 0.5 nM for PDE4D3. Oglemilast inhibits pulmonary cell infiltration, including eosinophilia and neutrophilia in vitro and in vivo. Oglemilast has the potential for inflammatory airway diseases .
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Cat. No.: HY-169981
CAS No.: 3087059-29-5
Research Areas:  

Inflammation/Immunology

PDE4-IN-24 (compoud 14h) is a potent inhibitor of PDE4D with the IC50 of 0.57 nM and >4100-fold selectivity over other PDE families. PDE4-IN-24 plays an important role in inflammatory disease .
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Cat. No.: HY-108047
CAS No.: 500355-52-2
MK-0873 is a selective phosphodiesterase-4 (PDE4) inhibitor with an IC50 value of < 38 nM. MK-0873 inhibits LPS-induced TNF-α production. MK-0873 suppresses bronchoconstriction. MK-0873 is applicable to research related to chronic obstructive pulmonary disease, plaque psoriasis and asthma .
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Cat. No.: HY-155830
CAS No.: 2231329-25-0
Purity:  98.92%
Synonyms: ME3183; PDE4-IN-14
Morcamilast (ME3183) is a potent, orally active, selective phosphodiesterase 4 (PDE4) inhibitor, with IC50 values of 1.28 nM, 2.33 nM and 1.63 nM against human PDE4A1A, PDE4B1 and PDE4D2, respectively. Morcamilast inhibits the production of TNF-α, IL-12/23p40, IL-23, IL-17A, IL-4, IL-5 and IL-13 in human PBMCs and T cells, and alleviates chronic Oxazolone (HY-126360)-induced dermatitis, Substance P (HY-P0201)-induced pruritus, Imiquimod (HY-B0180)-induced psoriasis-like dermatitis and LPS (HY-D1056)-induced arthritis . Morcamilast is used for the research of psoriasis, atopic dermatitis, psoriatic arthritis and other inflammatory and immune-related diseases [4] .
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Cat. No.: HY-RS24072
Research Areas:  

Others

Pde4d Rat Pre-designed siRNA Set A contains three designed siRNAs for Pde4d gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-170397
CAS No.: 1321513-73-8
ADORA2A/PDE4D-IN-1 (Compound 9) is a dual inhibitor for adenosine A2a receptor (ADORA2A) and phosphodiesterase 4D (PDE4D). ADORA2A/PDE4D-IN-1 can be used in research of bronchial asthma .
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Cat. No.: HY-161772
CAS No.: 3055162-32-5
Research Areas:  

Neurological Disease

(S)-Gebr32a is a potent PDE4 inhibitor with IC50 values of 19.5, 2.1 µM for PDE4 cat; PDE4D3, respectively .
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