44 Results for "

PDE10A

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "PDE10A" in MCE Product Catalog:

3
3 Cited Publications
Referencia número: HY-50098
No. CAS: 898562-94-2
Synonyms: PF-2545920
Áreas de investigación:  

Neurological Disease Cancer

Mardepodect is a potent, selective orally active, and brain-penetrant PDE10A inhibitor with an IC50 of 0.37 nM, with >1000-fold selectivity over other PDEs .
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3
3 Cited Publications
Referencia número: HY-50098A
No. CAS: 2070014-78-5
Synonyms: PF-2545920 hydrochloride
Áreas de investigación:  

Cancer

Mardepodect hydrochloride (PF-2545920 hydrochloride) is a potent, orally active and selective PDE10A inhibitor with an IC50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect hydrochloride can cross the blood-brain barrier .
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2
2 Cited Publications
Referencia número: HY-12472
No. CAS: 1238697-26-1
Pureza:  99.47%
Synonyms: TAK-063
Áreas de investigación:  

Infection Neurological Disease Cancer

Balipodect (TAK-063) is a selective, brain-penetrant and orally active PDE10A inhibitor with an IC50 of 0.30 nM. Balipodect shows >15000-fold selectivity over other PDEs. Balipodect elevates striatal cAMP and cGMP levels in mice. Balipodect can be used for the study of schizophrenia[1].
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2
2 Cited Publications
Referencia número: HY-14550
No. CAS: 898563-00-3
Pureza:  99.88%
TP-10 is a selective PDE10A inhibitor with an IC50 value of 0.8 nM. TP-10 shows an antioxidant activity with IC50s of 31.72 and 16.04 μg/ml for DPPH and CUPRAC, respectively. TP-10 can be used for the research of neuropathy .
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1
1 Cited Publications
Referencia número: HY-112831
No. CAS: 1189767-28-9
Pureza:  99.88%
Synonyms: BI-409306
Áreas de investigación:  

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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1
1 Cited Publications
Referencia número: HY-117604
No. CAS: 1257051-63-0
Pureza:  98.75%
Áreas de investigación:  

Neurological Disease

THPP-1, a SGC chemical probe, is a potent and orally bioavailable phosphodiesterase 10A (PDE10A) inhibitor, with Ki values of 1 nM and 1.3 nM for human and rat PDE10A, respectively. THPP-1 has excellent pharmacokinetic properties in preclinical species .
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Referencia número: HY-153093
No. CAS: 1424371-93-6
Pureza:  98.95%
Synonyms: MK-8189
Áreas de investigación:  

Neurological Disease

Elpipodect (MK-8189) is an orally active and selective PDE10A inhibitor with a Ki value of 29 pM. Elpipodect can be used in research of schizophrenia .
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Referencia número: HY-W003486
No. CAS: 57489-77-7
Áreas de investigación:  

Neurological Disease Cancer

5,7-Dichloropyrazolo[1,5-a]pyrimidine is a PDE10A inhibitor with a Ki of 24 μM. 5,7-Dichloropyrazolo[1,5-a]pyrimidine serves as a key intermediate in the synthesis of 5,7-disubstituted pyrazolo[1,5-a]pyrimidine derivatives (HIV-1 non-nucleoside reverse transcriptase inhibitors). 5,7-Dichloropyrazolo[1,5-a]pyrimidine can be used for the research of schizophrenia .
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Referencia número: HY-135848
No. CAS: 613-93-4
Pureza:  99.93%
Áreas de investigación:  

Cancer

N-Methylbenzamide is a potent phosphodiesterase 10A (PDE10A) inhibitor. N-Methylbenzamide has anti-cancer activity .
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Referencia número: HY-18078
No. CAS: 927691-21-2
Áreas de investigación:  

Neurological Disease

PQ-10 is a potent inhibitor of Phosphodiesterase 10A (PDE10A) with IC50 andED50 of 4.6 nM and 13 mg/kg, respectively. PQ-10 induces patterns of brain glucose metabolism which can be a potential translational biomarker. PQ-10 has the potential for researching psychiatric disorders like schizophrenia .
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Referencia número: HY-RS10199
Áreas de investigación:  

Others

PDE10A Human Pre-designed siRNA Set A contains three designed siRNAs for PDE10A gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Referencia número: HY-RS10200
Áreas de investigación:  

Others

Pde10a Mouse Pre-designed siRNA Set A contains three designed siRNAs for Pde10a gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Referencia número: HY-RS10201
Áreas de investigación:  

Others

Pde10a Rat Pre-designed siRNA Set A contains three designed siRNAs for Pde10a gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Referencia número: HY-10568
No. CAS: 959705-64-7
Áreas de investigación:  

Metabolic Disease

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. TC-E 5005 inhibits adrenergic and neurogenic smooth muscle contractions in the human prostate .
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Referencia número: HY-12913
No. CAS: 1227067-61-9
Pureza:  99.02%
Áreas de investigación:  

Neurological Disease

AMG 579 is a potent, selective, and efficacious inhibitor of phosphodiesterase 10A (PDE10A) with an IC50 of 0.1 nM.
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Referencia número: HY-152838
No. CAS: 1380329-87-2
Synonyms: RO554965
Áreas de investigación:  

Neurological Disease

Gemlapodect (RO554965) is an inhibitor of phosphodiesterase 10A (PDE10A). Gemlapodect can be used for researching schizophrenia .
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Referencia número: HY-148954
No. CAS: 1620909-95-6
Áreas de investigación:  

Cancer

PBF-999 is a phosphodiesterase10A (PDE-10A) and adenosine A2A receptor (A2AR) dual antagonist.
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Referencia número: HY-131973
Pureza:  98.43%
Áreas de investigación:  

Cardiovascular Disease Metabolic Disease

PDE10A-IN-2 hydrochloride is a potent, highly selective and orally active phosphodiesterase 10A (PDE10A) inhibitor with an IC50 of 2.8 nM. PDE10A-IN-2 hydrochloride shows selectivity of >3500-fold against other PDE subtypes. PDE10A-IN-2 hydrochloride can be used for pulmonary arterial hypertension (PAH) research .
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Referencia número: HY-153093A
No. CAS: 1424378-99-3
Synonyms: (1R,2R)-MK-8189
Áreas de investigación:  

Neurological Disease

(1R,2R)-Elpipodect ((1R,2R)-MK-8189) is the (1R,2R) enantiomer of Elpipodect (HY-153093). Elpipodect (MK-8189) is an orally active and selective PDE10A inhibitor with a Ki of 29 pM. Elpipodect can be used in research of schizophrenia .
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Referencia número: HY-178987
No. CAS: 3067849-10-6
Áreas de investigación:  

Cancer

BJH-86 is a soluble mitochondrial complex 1 inhibitor (oxygen consumption rate inhibition IC50 = 5 μM). BJH-86 exhibits weak inhibitory activity against phosphodiesterase 10A (PDE10A) (IC50 >10 μM). BJH-86 can reduce cellular oxygen consumption and inhibit cancer cell proliferation. BJH-86 can be used for the research of cancer, such as lung cancer .
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