26 Results for "

NTS

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

26 Results for "NTS" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-124767
CAS No.: 184162-21-8
Purity:  98.90%
Research Areas:  

Neurological Disease

SR 142948A is a blood-brain barrier-permeable, orally active, selective, non-peptide Neurotensin Receptor antagonist. SR 142948A exhibits an IC50 of 4.0 nM at the NTS1 site. SR 142948A competitively antagonizes neurotensin-dependent neurotransmitter release and modulates neurotensin-related dopaminergic and serotonergic signaling, making it useful for research on neurobehavioral mechanisms associated with schizophrenia .
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Cat. No.: HY-130463
CAS No.: 268550-95-4
Purity:  99.23%
Synonyms: PG(16:0/18:1) sodium; 1-Palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1'-rac-glycerol) sodium
POPG (sodium) is a negatively charged phospholipid. POPG (sodium) affects the interactions of membrane proteins with other molecules by changing the charge characteristics of the lipid environment. POPG (sodium) increases the apparent affinity of Gαq and Gβ1γ1 for activated NTS1. POPG (sodium) can interact with the positive charge of peptides. POPG sodium salt can be used in Parkinson's disease research .
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Cat. No.: HY-P10275
Target:  

Apoptosis

Research Areas:  

Neurological Disease

Tat-NTS peptide is a cell-penetrating peptide with neuroprotective effects. Tat-NTS peptide can specifically inhibit the nuclear translocation of ANXA1 and reduce neuronal apoptosis in ischemic areas. Moreover, Tat-NTS peptide can reduce the volume of cerebral ischemic infarction and can be used in the research of ischemic stroke .
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Cat. No.: HY-137002
CAS No.: 913733-27-4
Research Areas:  

Others

Fmoc-N-Me-Arg(Pbf)-OH is an amino acid derivative containing a guanidinium protecting group on the arginine side chain. Fmoc-N-Me-Arg(Pbf)-OH is used in the synthesis of neurotensin-derived NTS1 ligands for PET imaging .
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Cat. No.: HY-P2544
CAS No.: 139026-64-5
Synonyms: JMV438
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

[Lys8, Lys9]-Neurotensin (8-13) (JMV438), a Neurotensin analog, exerts its analgesic effects through activation of the G protein-coupled receptors NTS1 and NTS2, with Ki values of 0.33 nM and 0.95 nM for hNTS1 and hNTS2 receptors, respectively .
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Cat. No.: HY-100851A
CAS No.: 172895-15-7
Purity:  99.54%
LY-272015 hydrochloride is an orally active and selective 5-HT2B receptor antagonist. LY-272015 hydrochloride blocks 5-HT2 receptors and inhibits Fluoxetine (HY-B0102)-induced PDGFβ receptor transactivation. LY-272015 hydrochloride attenuates 5-HT-induced smooth muscle cell migration and proliferation, and inhibits downstream mTOR/p70S6K phosphorylation. LY-272015 hydrochloride reduces 5-HT-induced vasoconstriction. LY-272015 hydrochloride reverses the excitatory effect of BW-723C86 (HY-101369) on NTS neurons. LY-272015 hydrochloride lowers mean arterial blood pressure in severely hypertensive DOCA-salt rats. LY-272015 hydrochloride can be used in research related to diseases such as hypertension and cardiovascular calcification .
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Cat. No.: HY-12436
CAS No.: 1623002-61-8
Purity:  98.2%
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

NTRC-824 (Compound 5) is a potent, selective and neurotensin-like nonpeptide neurotensin receptor type 2 (NTS2) antagonist with an IC50 of 38 nM and a Ki of 202 nM. NTRC-824 is >150-fold selectivity for NTS2 over NTS1 (Ki >30 μM) .
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Cat. No.: HY-124831
CAS No.: 1811503-67-9
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

NTRC-844 (compound 8) is a selective antagonist of neurotensin receptor type 2 (NTS2),with the EC50 of 238 nM. NTRC-844 plays an important role in analgesic animal research .
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Cat. No.: HY-137525
CAS No.: 1643879-88-2
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

NTRC-808 is a nonpeptide selective GPCR neurotensin receptor type 2 (NTS2) partial agonist with an EC50 of 14 nM and Ki of 88 nM. NTRC-808 has higher selectivity for NTS2 than for NTS1. NTRC-808 has antipsychotic and analgesic activity .
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Cat. No.: HY-P991147
CAS No.: 2769743-01-1

Target:  

PD-1/PD-L1

Research Areas:  

Cancer

Ledostomig is an immunoglobulin (H-γ1-scFv-L-κ) dimer monoclonal antibody targeting human netrin-5 (NTS5) and programmed death-1 (PD-1). Ledostomig is promising for research of various cancers .
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Cat. No.: HY-P10767
CAS No.: 2468971-42-6
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

MD01-67 is a selective macrocyclic compound targeting the neurotensin receptor type 2 (NTS2), with Ki of 2.9 nM. MD01-67 exhibits analgesic and tactile hypersensitivity reducing activity in rats acute/persistent/chronic inflammatory pain models .
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Cat. No.: HY-175184
Target:  

Histone Demethylase

Research Areas:  

Infection

LSD1-IN-44 (Compound 19) is a LSD1 inhibitor with an IC50 of 0.02  μM for LSD1-CoREST enzymatic complex. LSD1-IN-44 has significant antischistosomal activity against transformed schistosomula (NTS) and Schistosoma mansoni adult worms while showing a delayed onset of action towards juvenile forms. LSD1-IN-44 has no significant toxicity to human cells. LSD1-IN-44 can be used for schistosomiasis research .
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Cat. No.: HY-RS24084
Research Areas:  

Others

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

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Cat. No.: HY-12217
CAS No.: 1612188-96-1
Target:  

Neurotensin Receptor

Research Areas:  

Neurological Disease

NTRC-739 is a selective nonpeptide partial neurotensin receptor type 2 (NTS2) agonist with an EC50 of 12 nM and a Ki of 153 nM. NTRC-739 is 161-fold selective for NTS2 versus NTS1. NTRC-739 can be used for the study of chronic pain research .
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Cat. No.: HY-175185
Target:  

Histone Demethylase

Research Areas:  

Infection

MC3935 is a LSD1 inhibitor with an IC50 of 0.52  μM for LSD1-CoREST enzymatic complex. MC3935 has significant antischistosomal activity against transformed schistosomula (NTS) and Schistosoma mansoni adult worms while showing a delayed onset of action towards juvenile forms. MC3935 has no significant toxicity to human cells. MC3935 can be used for schistosomiasis research .
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Cat. No.: HY-P2025
CAS No.: 113137-57-8
Research Areas:  

Neurological Disease

JMV 236 is a cholecystokinin antagonist with appetite-suppressing activity. JMV 236 affects the regulation of food intake through the interaction of the intestinal endogenous peptide PrRP and the CCK1 receptor. The administration of JMV 236 activates PrRP neurons located in the NTS, thereby enhancing its appetite-suppressing effect. JMV 236 has significant effects on areas of the central nervous system associated with food intake, especially during states of starvation .
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Cat. No.: HY-RS09637
Research Areas:  

Others

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

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Cat. No.: HY-RS17624
Research Areas:  

Others

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

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Cat. No.: HY-P73743
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: NTS; NMN-125; Neurotensin; NT/N; Neurotensin/Neuromedin N; NTS1; Pro-Neurotensin/Neuromedin; NN; Neuromedin N; NT
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-100851
CAS No.: 159730-07-1
Target:  

5-HT Receptor mTOR PDGFR

LY-272015 is an orally active and selective 5-HT2B receptor antagonist. LY-272015 blocks 5-HT2 receptors and inhibits Fluoxetine (HY-B0102)-induced PDGFβ receptor transactivation. LY-272015 attenuates 5-HT-induced smooth muscle cell migration and proliferation, and inhibits downstream mTOR/p70S6K phosphorylation. LY-272015 reduces 5-HT-induced vasoconstriction. LY-272015 reverses the excitatory effect of BW-723C86 (HY-101369) on NTS neurons. LY-272015 lowers mean arterial blood pressure in severely hypertensive DOCA-salt rats. LY-272015 can be used in research related to diseases such as hypertension and cardiovascular calcification .
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