95 Results for "

NPY

" in MedChemExpress (MCE) Product Catalog:
Products (95)

95 Results for "NPY" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-P0221
CAS No.: 137061-48-4
Synonyms: Pituitary Adenylate Cyclase Activating Polypeptide 38
PACAP (1-38), human, ovine, rat is a PAC1 receptor agonist. PACAP (1-38), human, ovine, rat binds to PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 with IC50s of 4 nM, 2 nM, and 1 nM, respectively. PACAP (1-38), human, ovine, rat increases the α-secretase activity. PACAP (1-38), human, ovine, rat elevates cytosolic Ca 2+, increases proliferation and increases phosphorylation of extracellular regulates kinase (ERK) and the epidermal growth factor receptor (EGFR). PACAP (1-38), human, ovine, rat demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production. PACAP (1-38), human, ovine, rat can be used for neurotrophic and neuroprotective research .
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4
4 Cited Publications
Cat. No.: HY-107725
CAS No.: 191868-14-1
Purity:  99.81%
Research Areas:  

Metabolic Disease

BIBO3304, a chemical probe, is a potent, orally active, and selective neuropeptide Y (NPY) Y1 receptor antagonist, with subnanomolar affinity for both the human and the rat Y1 receptor (IC50=0.38 and 0.72 nM, respectively) .
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2
2 Cited Publications
Cat. No.: HY-101986
CAS No.: 246146-55-4
Purity:  99.10%
Synonyms: AR-H 053591
Research Areas:  

Metabolic Disease Endocrinology

BIIE-0246 (AR-H 053591) is a potent and selective NPY2R (neuropeptide Y receptor 2) antagonist with an IC50 value of 15 nM for rat [ 125I]PYY3-36. BIIE-0246 decreases the expression of p-AKT S473, P-p44/42 MAPK under the NPY-stimulated. BIIE-0246 reduces albuminuria in ADR nephropathy .
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2
2 Cited Publications
Cat. No.: HY-101986A
Purity:  ≥99.0%
Synonyms: AR-H 053591 hydrochloride
Research Areas:  

Metabolic Disease

BIIE-0246 hydrochloride (AR-H 053591 hydrochloride) is a potent and selective NPY2R (neuropeptide Y receptor 2) antagonist with an IC50 value of 15 nM for rat [ 125I]PYY3-36. BIIE-0246 hydrochloride decreases the expression of p-AKT S473, P-p44/42 MAPK under the NPY-stimulated. BIIE-0246 hydrochloride reduces albuminuria in ADR nephropathy .
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2
2 Cited Publications
Cat. No.: HY-P71063
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Pro-Neuropeptide Y; Neuropeptide Y; Neuropeptide Tyrosine; NPY; C-Flanking Peptide of NPY; CPON; NPY
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-120619
CAS No.: 186185-03-5
Purity:  99.08%
BMS-193885 is a selective neuropeptide Y1 receptor antagonist (Ki=3.3 nM) that competitively blocks the receptor to inhibit NPY-mediated appetite regulation signaling pathways, reduce food intake and inhibit weight gain. BMS-193885 has good blood-brain barrier penetration and is mainly used in the study of obesity and related metabolic diseases .
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1
1 Cited Publications
Cat. No.: HY-P0208
CAS No.: 125580-28-1
Research Areas:  

Neurological Disease

[Leu31,Pro34]- Neuropeptide Y (porcine), a Neuropeptide Y (NPY) analog, is a selective NPY Y1 receptor agonist. [Leu31,Pro34]- Neuropeptide Y (porcine) exhibits anxiolytic effects .
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1
1 Cited Publications
Cat. No.: HY-14423
CAS No.: 342577-38-2
Purity:  99.21%
Synonyms: S2367
Velneperit (S-2367) is an orally active neuropeptide Y (NPY) Y5 receptor antagonist that can penetrate the blood-brain barrier. Velneperit inhibits the appetite-stimulating and metabolism-inhibiting effects mediated by NPY. Velneperit selectively improves diet-induced obesity in mice. Velneperit enhances the expression of fear acutely by removing the inhibition of CeA Drd2 neurons. Velneperit can be used for the study of obesity .
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1
1 Cited Publications
Cat. No.: HY-107726
CAS No.: 1068148-47-9
Purity:  99.25%
Research Areas:  

Neurological Disease

BIBP3226 TFA is a potent and selective neuropeptide Y Y1 (NPY Y1) and neuropeptide FF (NPFF) receptor antagonist, with Kis of 1.1, 79, and 108 nM for rNPY Y1, hNPFF2, and rNPFF, respectively. BIBP3226 TFA displays anxiogenic-like effect .
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Cat. No.: HY-116797
CAS No.: 73912-52-4
Purity:  99.51%
Synonyms: MS0015203
Target:  

GPR171

Research Areas:  

Metabolic Disease

MS15203 is a potent and selective GPR171 agonist. MS15203 increases food intake and body weight. MS15203 increases neuronal activity. MS15203 significantly increases the abundance of the mRNAs encoding proSAAS, NPY, AgRP .
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Cat. No.: HY-107734
CAS No.: 6508-43-6
Purity:  99.89%
Research Areas:  

Metabolic Disease Endocrinology

L 152804 is an orally active and selective neuropeptide Y Y5 receptor (NPY5-R) antagonist, with a Ki of 26 nM for hY5. L 152804 causes weight loss in diet-induced obese mice by modulating food intake and energy expenditure .
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Cat. No.: HY-P0199
CAS No.: 75976-10-2
Synonyms: Human pancreatic polypeptide
Research Areas:  

Metabolic Disease Endocrinology

Pancreatic Polypeptide, human is a C-terminally amidated 36 amino acid peptide, which acts as a neuropeptide Y (NPY) Y4/Y5 receptor agonist.
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Cat. No.: HY-P10026
CAS No.: 2663844-45-7
Synonyms: LY-3457263
Research Areas:  

Metabolic Disease

Nisotirotide (LY-3457263) is a subcutaneous injectable NPY2 receptor agonist. By mimicking peptide YY (PYY), Nisotirotide inhibits appetite and can be used in the research of diseases such as obesity and diabetes .
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Cat. No.: HY-P10000
CAS No.: 123583-37-9
Research Areas:  

Metabolic Disease

Peptide YY (PYY) (3-36), Human is an endogenous appetite suppressing peptide. Peptide YY (PYY) (3-36), Human, a neuropeptide Y (NPY) Y2 receptor agonist, is a powerful inhibitor of intestinal secretion .
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Cat. No.: HY-107730
CAS No.: 439861-56-0
Purity:  98.86%
Research Areas:  

Neurological Disease

NPY5RA-972 is an orally active, central nervous system (CNS) penetrating, potent and selective NPY Y5 receptor antagonist that prevents feeding driven by activation of this receptor .
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Cat. No.: HY-P1845
CAS No.: 138764-85-9
Research Areas:  

Others

PACAP-38 (31-38), human, mouse, rat is a fragment containing the C-terminal 31-38 fragment of PACAP (1-38), human, ovine, rat (HY-P0221). PACAP-38 (31-38), human, mouse, rat does not bind to the PACAP receptor .
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Cat. No.: HY-107735
CAS No.: 1383478-94-1
Purity:  99.43%
Research Areas:  

Neurological Disease

CYM 9484 is a selective and highly potent neuropeptide Y (NPY) Y2 receptor antagonist with an IC50 value of 19 nM .
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Cat. No.: HY-107733
CAS No.: 191931-56-3
Purity:  98.36%
Research Areas:  

Neurological Disease

NTNCB (Compound 11) hydrochloride is a potent and selective neuropeptide Y Y5 (NPY Y5) receptor antagonist with a Ki of 8 nM against human Y5 .
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Cat. No.: HY-P4087
CAS No.: 1417221-06-7
Target:  

HIV

Research Areas:  

Infection Cancer

Cys(Npys)-(Arg)9 is a synthetic cationic cell-penetrating peptide with a reversible thiol-reactive nitropyridyl (Npys) group. Cys(Npys)-(Arg)9 efficiently mediates the internalization and delivery of various "cargo" such as proteins and antibodies by forming reversible disulfide bonds with surface-exposed cysteine residues. Cys(Npys)-(Arg)9 endows TALEN proteins with cell-penetrating activity, enabling gene knockout in mammalian cells and protein transduction in wheat microspores. Cys(Npys)-(Arg)9 can be conjugated with antibodies to form cationized IgG for enhancing endosomal escape of oligonucleotides, or form siRNA delivery complexes. When the molar ratio of Cys(Npys)-(Arg)9 to loaded molecules is higher than 1:1, it exerts certain cytotoxic effects on cells. Cys(Npys)-(Arg)9 can be used in studies related to oral squamous cell carcinoma and HIV infection .
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Cat. No.: HY-P4123
CAS No.: 1231898-26-2
Target:  

MMP

TAT (47-57) GGG-Cys (Npys) is a cell-penetrating peptide and delivery carrier derived from TAT. TAT (47-57) GGG-Cys (Npys) facilitates the translocation of conjugated drug molecules across cell membranes. TAT (47-57) GGG-Cys (Npys) acts as a delivery carrier for MT1-MMP inhibitors. TAT (47-57) GGG-Cys (Npys) is applicable to research on diseases associated with MT1-MMP activity, such as cancer, arthritis, heart disease, and vascular disorders .
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