48 Results for "

NPS

" in MedChemExpress (MCE) Product Catalog:
Products (48)

48 Results for "NPS" in MCE Product Catalog:

Cat. No.: HY-17633
CAS No.: 515138-06-4
Synonyms: NPS-005; SJP-0035
Target:  

PPAR

Research Areas:  

Neurological Disease

Fonadelpar is a PPARδ agonist, used in the research of neuroparalytic keratopathy.
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Cat. No.: HY-10167
CAS No.: 148717-54-8
Synonyms: R-568; NPS R-568 free base
Target:  

CaSR

Research Areas:  

Others

Tecalcet (R 568), an orally active calcimimetic compound, allosterically and positively modulates the calcium-sensing receptor (CaSR). Tecalcet (R 568) increases the sensitivity to activation by extracellular Ca 2+ .
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Cat. No.: HY-121870A
CAS No.: 553-63-9
Purity:  99.36%
Synonyms: Larocaine hydrochloride
Target:  

Dopamine Receptor

Research Areas:  

Neurological Disease

Dimethocaine (Larocaine) hydrochloride is distributed and consumed as "new psychoactive substance" (NPS) without any safety testing
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Cat. No.: HY-158220C
Synonyms: HAMA (MW 50000)
Hyaluronic acid methacryloyl (HAMA) (MW 50000) is a methacrylate-modified hyaluronic acid that serves as a hydrogel former, hydrolysis-resistant material, photocrosslinkable hydrogel scaffold, and drug delivery carrier for tissue engineering. Hyaluronic acid methacryloyl (MW 50000) forms hydrogels via photocrosslinking; when combined with AuMA NPs through a one-step photocrosslinking method, its effective swelling ratio increases, and the mechanical reinforcement effect of Au NPs compensates for the impact caused by reduced crosslinking density. Hyaluronic acid methacryloyl (MW 50000) can be combined with AuMA NPs via a one-step photocrosslinking method, enabling non-invasive monitoring of hydrogel degradation with contrast-enhanced micro-CT .
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Cat. No.: HY-178794
CAS No.: 3038861-75-2
Target:  

PGE synthase

Research Areas:  

Inflammation/Immunology

AGU661 is a Microsomal prostaglandin E2 synthase 1 (mPGES-1) inhibitor with an IC50 of 0.22  nM. AGU661 lowers PGE2 formation in human pro-inflammatory M1 macrophages and activated monocytes without affecting other lipid mediator pathways. AGU661 has unfavorable physicochemical properties with poor metabolic stability and strong plasma protein binding tendencies. AGU661 into PLGA-based NPs significantly enhances its bioactivity. AGU661 can be used for inflammatory disorders research .
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Cat. No.: HY-W423643
CAS No.: 1225617-75-3
Target:  

Drug Derivative

Research Areas:  

Neurological Disease

Benzedrone is a synthetic drug derivative. Benzedrone can increase the levels of neurotransmitters such as dopamine, serotonin and norepinephrine in the brain, thus producing a stimulant effect. Benzedrone can be used in the research of new psychoactive substances (NPS) .
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Cat. No.: HY-W767865
Cyclic GMP sodium- 13C5 is the 13C-labeled Cyclic GMP sodium (HY-113469A). Cyclic GMP (cGMP) sodium, an important second messenger, is a major intracellular mediator of extracellular signals such as nitric oxide (NO) and natriuretic peptides (NPs). Effects of Cyclic GMP sodium occur through three main groups of cellular targets: cGMP-dependent protein kinases (PKGs), cGMP-gated cation channels, and PDEs. Cyclic GMP can inhibit both platelet adhesion and aggregation. cGAMP (Cyclic-GMP-AMP) (HY-12512), a conjugate of Cyclic GMP and AMP, can induce IRF3 phosphorylation and nuclear translocation, enhancing antiviral immune responses .
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Cat. No.: HY-RS09502
Research Areas:  

Others

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

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Cat. No.: HY-138232
CAS No.: 141365-20-0
Synonyms: LTNAM
Target:  

Aminopeptidase

Research Areas:  

Neurological Disease

Lys-psi(CH2NH)-Trp(Nps)-OMe is a lysine-tryptophan (Nps) pseudodipeptide analog. It is obtained by replacing the peptide bond in the Lys-Trp(Nps) molecule with an aminomethylene bond and has analgesic activity. Lys-psi(CH2NH)-Trp(Nps)-OMe induces a dose-dependent and naloxone-reversible analgesia after intracerebroventricular administration in mice, and its analgesic effect lasts longer than that of the original compound. It protects methionine enkephalin from degradation in rat striatal slices and binds to low-dose opioid peptides to produce analgesia. Lys-psi(CH2NH)-Trp(Nps)-OMe effectively inhibits brain aminopeptidase activity both in vitro and in vivo. The enhanced resistance of this pseudodipeptide to proteolysis may explain its prolonged analgesic activity.
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Cat. No.: HY-103090
CAS No.: 299433-10-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

NPS ALX Compound 4a is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM .
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Cat. No.: HY-103090A
CAS No.: 1781934-44-8
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

NPS ALX Compound 4a dihydrochloride is a potent and selective 5-hydroxytryptamine6 (5-HT6) receptor antagonist, with an IC50 of 7.2 nM and a Ki of 0.2 nM .
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Cat. No.: HY-106397
CAS No.: 186495-49-8
Synonyms: NPS-1506
Research Areas:  

Neurological Disease

Delucemine is a selective serotonin reuptake inhibitor (SSRI) and NMDAR antagonist. Delucemine can be used as an antidepressant .
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Cat. No.: HY-106397A
CAS No.: 186495-99-8
Synonyms: NPS-1506 hydrochloride
Research Areas:  

Neurological Disease

Delucemine hydrochloride is a selective serotonin reuptake inhibitor (SSRI) and NMDAR antagonist. Delucemine hydrochloride can be used as an antidepressant .
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Cat. No.: HY-W010713
CAS No.: 2669-65-0
Synonyms: Fimaporfin free base
Target:  

Photosensitizer

Research Areas:  

Cancer

Meso-tetraphenylchlorin (TPCS2a) is a photosensitizer with poor water solubility, which limits its use in the blood circulation. However, TPCS2a@NPs nanoparticles can be prepared based on polylactic-co-polyethylene glycol acid (PLGA) polymer core loaded with TPCS2. Such nanoparticles can be coated with mesenchymal stem cell-derived plasma membranes (mMSCs) to form mMSC-TPCS2a@NPs, which prolongs blood circulation time and improves tumor targeting ability. Compared with uncoated TPCS2a@NPs, mMSC-TPCS2a@NPs can reduce macrophage uptake by 54% to 70% under different conditions. Both nanoparticle forms are effectively accumulated in MCF7 and MDA-MB-231 breast cancer cells, while uptake in normal breast epithelial cells MCF10A is significantly lower .
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Cat. No.: HY-D2314
CAS No.: 1650559-73-1
Cyanine 7-amine (chloride hydrochloride) can be used to label cationic nanoparticles (NPs) or to NP conjugates (NPCs). It can track the residence time and clearance of nanoparticles in the body .
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Cat. No.: HY-11095R
CAS No.: 226878-01-9
NPS 2390 (Standard) is the analytical standard of NPS 2390 (HY-11095). This product is intended for research and analytical applications. NPS 2390 is a noncompetitive antagonist of mGluR1 and mGluR5 . NPS 2390 is also a potent CaSR (calcium-sensing receptor) inhibitor .
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Cat. No.: HY-182543
CAS No.: 148717-47-9
Target:  

CaSR

Research Areas:  

Others

NPS-467 is a calcium-sensing receptor (CaR) activator and stereospecific agent with only its R-enantiomer active. NPS-467 increases the sensitivity of the CaR to activation by extracellular calcium. NPS-467 stimulates stanniocalcin (STC) secretion in trout and induces inhibition of gill calcium transport in trout. NPS-467 has no effect on serum calcitonin levels in trout .
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Cat. No.: HY-100509R
CAS No.: 1221713-92-3
Research Areas:  

Cancer

NPS-1034 (Standard) is the analytical standard of NPS-1034 (HY-100509). This product is intended for research and analytical applications. NPS-1034 is a dual inhibitor of AXL and MET with IC50s of 10.3 and 48 nM, respectively.
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Cat. No.: HY-169434
Synonyms: Lon-TK-BMS-1
Target:  

PD-1/PD-L1

Research Areas:  

Cancer

LTB is a prodrug formed by coupling glycolysis inhibitor (Lonidamine (HY-B0486)) with PD1/PDL1 blocker (BMS-1 (HY-19991)) by thioketal linkage. LTB can further encapsulate photosensitizer chlorine e6 (Ce6) (HY-13594) to construct a co-delivery photodynamic nanoplatform (LTB-6 NPs) by self-assembly .
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Cat. No.: HY-10007R
CAS No.: 284035-33-2
Synonyms: SB-262470A (Standard)
Research Areas:  

Metabolic Disease

NPS-2143 (Standard) is the analytical standard of NPS-2143 (HY-10007). This product is intended for research and analytical applications. NPS-2143 (SB-262470A), an orally active calcilytic agent, is a selective and potent calcium ion-sensing receptor (CaSR) antagonist. NPS-2143 (SB-262470A) blocks increases in cytoplasmic Ca2+ concentrations (IC50=43 nM) elicited by activating the Ca2+ receptor in HEK 293 cells expressing the human Ca2+ receptor .
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