221 Results for "

inhibitory peptide

" in MedChemExpress (MCE) Product Catalog:
Products (221)

221 Results for "inhibitory peptide" in MCE Product Catalog:

44
44 Publications Verification
製品番号: HY-10235
CAS 番号: 402957-28-2
純度:  99.54%
別名: VX-950
Target:  

HCV Protease HCV SARS-CoV

研究分野:  

Infection

Telaprevir (VX-950) is a highly selective, reversible, and potent peptidomimetic inhibitor of the HCV NS3-4A protease, the steady-state inhibitory constant (Ki) of Telaprevir is 7 nM against a genotype 1 (H strain) NS3 protease domain plus a NS4A cofactor peptide . Telaprevir inhibits SARS-CoV-2 3CL pro activity .
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7
7 Cited Publications
製品番号: HY-18962
CAS 番号: 20324-87-2
研究分野:  

Cancer

AMI-1 is a potent, cell-permeable and reversible inhibitor of protein arginine N-methyltransferases (PRMTs), with IC50s of 8.8 μM and 3.0 μM for human PRMT1 and yeast-Hmt1p, respectively. AMI-1 exerts PRMTs inhibitory effects by blocking peptide-substrate binding .
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7
7 Cited Publications
製品番号: HY-18962A
CAS 番号: 134-47-4
研究分野:  

Cancer

AMI-1 free acid is a potent, cell-permeable and reversible inhibitor of protein arginine N-methyltransferases (PRMTs), with IC50s of 8.8 μM and 3.0 μM for human PRMT1 and yeast-Hmt1p, respectively. AMI-1 free acid exerts PRMTs inhibitory effects by blocking peptide-substrate binding .
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5
5 Cited Publications
製品番号: HY-B1190
CAS 番号: 50370-12-2
別名: BL-S 578
Target:  

Bacterial Antibiotic EAAT

研究分野:  

Infection Neurological Disease

Cefadroxil is an orally active broad-spectrum cephalosporin antibiotic. Cefadroxil inhibits bacterial cell wall synthesis and enhances the expression of glutamate transporter-1. Cefadroxil is dependent on the intestinal peptide transporter PepT1 for small intestinal absorption. Cefadroxil has inhibitory and bactericidal activity against a variety of Gram-positive and Gram-negative bacteria and has analgesic effects on neuropathic pain .
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5
5 Cited Publications
製品番号: HY-B1190A
CAS 番号: 66592-87-8
別名: BL-S 578 hydrate
Target:  

Bacterial Antibiotic EAAT

研究分野:  

Infection Neurological Disease

Cefadroxil hydrate is an orally active broad-spectrum cephalosporin antibiotic. Cefadroxil hydrate inhibits bacterial cell wall synthesis and enhances the expression of glutamate transporter-1. Cefadroxil hydrate is dependent on the intestinal peptide transporter PepT1 for small intestinal absorption. Cefadroxil hydrate has inhibitory and bactericidal activity against a variety of Gram-positive and Gram-negative bacteria and has analgesic effects on neuropathic pain .
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3
3 Cited Publications
製品番号: HY-P3400
CAS 番号: 887255-16-5
別名: LQVTDSGLYRCVIYHPP
Target:  

ペプチド

研究分野:  

Neurological Disease

LP17 (LQVTDSGLYRCVIYHPP) is a BBB-penetrable triggering receptor expressed on myeloid cells (TREM-1) inhibitory peptide. LP17 substantially alleviates ischemia-induced infarction and neuronal injury. LP17 can get access into brain and block TREM-1 .
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3
3 Cited Publications
製品番号: HY-P3400A
別名: LQVTDSGLYRCVIYHPP TFA
Target:  

ペプチド

研究分野:  

Neurological Disease

LP17 (LQVTDSGLYRCVIYHPP) TFA is a BBB-penetrable triggering receptor expressed on myeloid cells (TREM-1) inhibitory peptide. LP17 TFA substantially alleviates ischemia-induced infarction and neuronal injury. LP17 TFA can get access into brain and block TREM-1 .
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2
2 Cited Publications
製品番号: HY-P0276
CAS 番号: 100040-31-1
別名: Gastric inhibitory peptide (GIP), human
Target:  

Insulin Receptor

研究分野:  

Metabolic Disease

GIP, human, a peptide hormone consisting of 42 amino acids, is a stimulator of glucose-dependent insulin secretion and a weak inhibitor of gastric acid secretion. GIP, human acts as an incretin hormone released from intestinal K cells in response to nutrient ingestion .
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2
2 Cited Publications
製品番号: HY-P0276A
別名: Gastric inhibitory peptide (GIP), human TFA
Target:  

Insulin Receptor

研究分野:  

Metabolic Disease

GIP, human TFA, a peptide hormone consisting of 42 amino acids, is a stimulator of glucose-dependent insulin secretion and a weak inhibitor of gastric acid secretion. GIP, human TFA acts as an incretin hormone released from intestinal K cells in response to nutrient ingestion .
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2
2 Cited Publications
製品番号: HY-P0214A
Target:  

CaMK Autophagy

研究分野:  

Neurological Disease

Autocamtide-2-related inhibitory peptide (TFA) is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.
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2
2 Cited Publications
製品番号: HY-112862
CAS 番号: 301351-95-1
純度:  ≥98.0%
研究分野:  

Infection

Arg-AMS (compound 24) is a potent nanomolar inhibitor of arginyl tRNA synthetase, which displays tightly bound inhibitory characteristics for the A-domains in non-ribosomal peptide synthetases (NRPS) enzymes .
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2
2 Cited Publications
製品番号: HY-P1333
CAS 番号: 80448-90-4
Dynorphin A is an endogenous opioid peptide involved in inhibitory neurotransmission in the central nervous system (CNS). Dynorphin A is a highy potent kappa opioid receptor (KOR) agonist, and is also an agonist for other opioid receptors, such as mu (MOR) and delta (DOR). Dynorphin A can induce neuronal death, and can be used in the research of neurological disease .
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2
2 Cited Publications
製品番号: HY-107648
CAS 番号: 55-45-8
純度:  99.81%
Target:  

mAChR

McN-A-343 is a selective M1 muscarinic agonist that stimulates muscarinic transmission in sympathetic ganglia. McN-A-343 produces a significant inhibitory effect on Muscarine (HY-121404)-evoked catecholamine secretion from the isolated perfused rat adrenal gland. McN-A-343 is involved in the regulation of neuronal firing and activates enteroendocrine L cells to release glucagon-like peptide 1 (GLP-1) and modulates the secretion of α-melanocyte stimulating hormone (α-MSH) from the pituitary gland in the central nervous system. McN-A-343 reduces colonic inflammation and oxidative stress in Acetic acid (HY-Y0319)-induced ulcerative colitis (UC) mice. McN-A-343 can be used for the study of ulcerative colitis .
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2
2 Cited Publications
製品番号: HY-P2259
CAS 番号: 1404188-93-7
TAT-GluA2 3Y is a blood-brain barrier-permeable AMPA receptor inhibitory peptide that crosses cell membranes via the HIV-1 TAT protein domain. TAT-GluA2 3Y blocks the endocytosis of AMPA receptors, including the internalization of GluA1/GluA2 subunits, by disrupting interactions with the AP2, Brag2 and Syt3-GluA2 complexes, while also inhibiting long-term depression. TAT-GluA2 3Y blocks hypoxia-mediated AMPAR internalization, alleviates A1R-induced persistent synaptic inhibition, and reduces cerebral ischemic volume, neurological deficits and spatial memory deficits. TAT-GluA2 3Y blocks the effect of NLRP3 deficiency on fear generalization, inhibits amphetamine-induced behavioral/neurochemical sensitization, weakens the unconditioned stimulus-conditioned stimulus association of morphine, and promotes the extinction of morphine CPP. TAT-GluA2 3Y can be used in studies related to fear generalization, ischemic stroke, hypoxia, drug addiction and opioid addiction .
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1
1 Cited Publications
製品番号: HY-W012479
CAS 番号: 153-94-6
別名: D-Tryptophan
H-D-Trp-OH (D-Tryptophan) is the D-isomer of tryptophan, which is occasionally found in natural peptides, such as marine toxin peptides. H-D-Trp-OH can increase intestinal microbial diversity and counteract the inhibitory effect of allergic airway inflammation on intestinal microbial diversity .
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1
1 Cited Publications
製品番号: HY-P10086
CAS 番号: 1289375-12-7
別名: Human TREM-1(213-221)
TREM-1 inhibitory peptide GF9 (Human TREM-1 (213-221)) is a TREM-1 inhibitor. TREM-1 inhibitory peptide GF9 blocks the TREM-1 signaling pathway via a ligand-independent mechanism, spontaneously inserts into the cell membrane to dissociate TREM-1 from DAP-12, and functions through the Signaling Chain Homooligomerization (SCHOOL) model. TREM-1 inhibitory peptide GF9 reduces the levels of TNFα, IL-1β, IL-6, and M-CSF. TREM-1 inhibitory peptide GF9 inhibits tumor growth, prolongs the survival of mice with pancreatic cancer models, ameliorates collagen-induced arthritis, and exerts protective effects on bone and cartilage simultaneously. TREM-1 inhibitory peptide GF9 can be used in research related to arthritis, pancreatic cancer, retinopathy, alcoholic liver disease, and liver cancer .
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1
1 Cited Publications
製品番号: HY-P1369
CAS 番号: 251634-22-7
Target:  

Dynamin

研究分野:  

Neurological Disease

DynaMin inhibitory peptide, myristoylated is a DynaMin inhibitor to interfere with the binding of amphiphysin with dynamin. DynaMin inhibitory peptide, myristoylated is a membrane-permeant form of the peptide that prevents endocytosis .
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1
1 Cited Publications
製品番号: HY-P1083
CAS 番号: 251634-21-6
Target:  

Dynamin

研究分野:  

Neurological Disease

Dynamin inhibitory peptide competitively blocks binding of dynamin to amphiphysin, thus preventing endocytosis. Dynamin inhibitory peptide blocks the dopamine D3 effect on GABAA receptors .
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1
1 Cited Publications
製品番号: HY-P5521
CAS 番号: 3033299-76-9
Target:  

ペプチド

研究分野:  

Cardiovascular Disease

mLR12 is a Trem1 inhibitory peptide. mLR12 decreases aortic rupture rate in BAPN-induced Thoracic aortic aneurysm and dissection (TAAD) mice model .
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1
1 Cited Publications
製品番号: HY-P1138
CAS 番号: 1315378-72-3
別名: FSVYWAQADR
研究分野:  

Others

Scrambled 10Panx (FSVYWAQADR) is an inactive scrambled control peptide of the Pannexin-1 hemichannel inhibitory peptide 10panx .
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