26 Results for "

TP-H

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "TP-H" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-14454
CAS No.: 21306-65-0
Purity:  99.81%
Synonyms: Triphenyl Compound A
Research Areas:  

Cancer

TPh A (Triphenyl Compound A) is a potent inhibitor of the nuclear protein pirin and binds specifically to pirin with a Ki of 0.6 uM. TPh A disrupts the formation of the bcl3–pirin complex. TPh A can be used as a novel small molecule tool to regulate pirin in cells .
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1
1 Cited Publications
Cat. No.: HY-13041
CAS No.: 945976-76-1
Purity:  99.14%
Research Areas:  

Neurological Disease

LX-1031 is a potent, orally available tryptophan 5-hydroxylase (TPH) inhibitor that reduces serotonin (5-HT) synthesis peripherally.
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1
1 Cited Publications
Cat. No.: HY-23460
CAS No.: 278605-15-5
Synonyms: 4-Ethynyl-L-phenylalanine
Research Areas:  

Neurological Disease

p-Ethynylphenylalanine (4-Ethynyl-L-phenylalanine) is a potent, selective, reversible and competitive inhibitor of tryptophan hydroxylase (TPH), with a Ki of 32.6 μM . p-Ethynylphenylalanine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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1
1 Cited Publications
Cat. No.: HY-23460A
CAS No.: 188640-63-3
Synonyms: 4-Ethynyl-L-phenylalanine hydrochloride
Research Areas:  

Neurological Disease

p-Ethynylphenylalanine hydrochloride (4-Ethynyl-L-phenylalanine hydrochloride) is a potent, selective, reversible and competitive inhibitor of tryptophan hydroxylase (TPH), with a Ki of 32.6 μM . p-Ethynylphenylalanine (hydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-W019599
CAS No.: 14173-39-8
Synonyms: L-PCPA
4-Chloro-L-phenylalanine (L-PCPA) is a tryptophan hydroxylase inhibitor targeting TPH1 and TPH2, with the activity of blocking serotonin biosynthesis. 4-Chloro-L-phenylalanine reduces the levels of serotonin and its metabolites in the brain without impairing the survival of serotonergic neurons. 4-Chloro-L-phenylalanine enhances anhedonic, depression-like and anxiety-like behaviors in mice with depleted noradrenergic and dopaminergic neurons. 4-Chloro-L-phenylalanine acts as a decarboxylation substrate for aromatic L-amino acid decarboxylase from Bacillus atrophaeus. 4-Chloro-L-phenylalanine can be used in studies related to Parkinson's disease .
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Cat. No.: HY-101124
CAS No.: 1673571-51-1
Purity:  97.25%
Synonyms: KAR5585
Rodatristat ethyl (KAR5585) is a first-in-class oral tryptophan hydroxylase 1 (TPH1) Inhibitor with nanomolar in vitro potency. Rodatristat ethyl reduces the level of 5-HT and significantly reduces pulmonary arterial hypertension (PAH) .
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Cat. No.: HY-N0137
CAS No.: 6429-04-5
Research Areas:  

Neurological Disease

Tetrahydropapaverine hydrochloride is a tetrahydroisoquinoline (TIQ) compound with inhibitory effects on tryptophan hydroxylase (TPH) (IC50 = 5.7 μM). Tetrahydropapaverine hydrochloride decreases intracellular serotonin content in murine mastocytoma P815 cells, with an IC50 value of 6.2 μM. Tetrahydropapaverine hydrochloride can be used for studies on potential neurotoxicity in monoaminergic neurons .
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Cat. No.: HY-157014
CAS No.: 3032648-15-7
Purity:  99.90%
Research Areas:  

Cancer

TPT-004 is a selective and oraly active tryptophan hydroxylases (TPH) inhibitor with IC50s of 77 nM and 16 nM for TPH1 and TPH2, repsectively. TPT-004 exhibits exceptional selectivity for TPH1 compared with other members of the AAAH family. TPT-004 shows efficacy peripheral serotonin attenuation and colorectal tumor growth in mice[1][2].
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Cat. No.: HY-120083
CAS No.: 1673568-73-4
Purity:  99.11%
Synonyms: KAR5417
Rodatristat (KAR5417) is a potent tryptophan hydroxylase 1 (TPH1) and TPH2 inhibitor with IC50s value of 33 nM and 7 nM, respectively, and shows robust reduction of intestinal serotonin (5-HT) levels in mice .
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Cat. No.: HY-106429
CAS No.: 627085-11-4
Research Areas:  

Others

OT-551 (free base) is a lipophilic, disubstituted hydroxylamine with antioxidant properties. OT-551 can be used as an eye drop and can be converted by intraocular esterases to its active metabolite, Tempol-H (TP-H). OT-551 can be utilized in geographic atrophy and macular degeneration research .
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Cat. No.: HY-156093
CAS No.: 3040015-86-6
Research Areas:  

Metabolic Disease

TPH1-IN-1 (compound 40) is a xanthine derivative and an inhibitor of tryptophan hydroxylase TPH1 (IC50: 110.1 nM). TPH1-IN-1 has good in vitro activity and liver microsome stability, and effectively inhibits adipocyte differentiation of T3-L1 cells .
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Cat. No.: HY-RS14932
Research Areas:  

Others

TPH1 Human Pre-designed siRNA Set A contains three designed siRNAs for TPH1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS14933
Research Areas:  

Others

TPH2 Human Pre-designed siRNA Set A contains three designed siRNAs for TPH2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS24111
Research Areas:  

Others

Tph2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tph2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS17127
Research Areas:  

Others

Tph1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Tph1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS23572
Research Areas:  

Others

Tph1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Tph1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-19572
CAS No.: 1783256-96-1
Research Areas:  

Inflammation/Immunology

ACT-678689 (Compound Example 1.53.4) is a tryptophan hydroxylase (TPH) inhibitor with an IC50 of 8 nM .
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Cat. No.: HY-181575
Research Areas:  

Neurological Disease

TPH2 agonist-1 (compound 20e) is an orally active, blood-brain barrier permeable, 1,3,4-oxadiazol-2 (3H)-one-derived TPH2 agonist. TPH2 agonist-1 upregulates TPH2 expression, elevates 5-HT and GABA levels, and exhibits antiepileptic activity in SCN1A-deficient models. TPH2 agonist-1 stabilizes the electrophysiological activity of neuronal networks and inhibits abnormal spike and burst activities. TPH2 agonist-1 shows no significant hERG inhibition or cytotoxicity, and it can be used in studies related to severe myoclonic epilepsy of infancy (Dravet syndrome) .
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Cat. No.: HY-RS17651
Research Areas:  

Others

Tph2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Tph2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P73566
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TPH; TPH-1; TPRH; Tryptophan 5-hydroxylase 1; Tryptophan Hydroxylase 1
Species:  
Source:  
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