49 Results for "

high-affinity binding sites

" in MedChemExpress (MCE) Product Catalog:
Products (49)

49 Results for "high-affinity binding sites" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-15419
CAS No.: 199864-86-3
Purity:  99.78%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

RS-127445 hydrochloride is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist with a pKi of 9.5. RS-127445 hydrochloride shows 1000 fold selectivity for this receptor as compared to numerous other receptor and ion channel binding sites .
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5
5 Cited Publications
Cat. No.: HY-15419A
CAS No.: 199864-87-4
Purity:  99.62%
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

RS-127445 is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist with a pKi of 9.5. RS-127445 shows 1000 fold selectivity for this receptor as compared to numerous other receptor and ion channel binding sites .
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4
4 Cited Publications
Cat. No.: HY-109012
CAS No.: 1293281-49-8
Purity:  99.86%
Synonyms: JNJ-42847922
Seltorexant (JNJ-42847922) is an orally active, high-affinity, and selective orexin-2 receptor (OX2R) antagonist (pKi values of 8.0 and 8.1 for human and rat OX2R). Seltorexant (JNJ-42847922) crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain .
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4
4 Cited Publications
Cat. No.: HY-109012A
CAS No.: 1293284-49-7
Purity:  99.90%
Synonyms: JNJ-42847922 hydrochloride
Seltorexant hydrochloride (JNJ-42847922 hydrochloride) is an orally active, high-affinity, and selective OX2R antagonist (pKi values of 8.0 and 8.1 for human and rat OX2R). Seltorexant hydrochloride crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain .
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3
3 Cited Publications
Cat. No.: HY-P99037
CAS No.: 2211985-36-1
Synonyms: M281

Target:  

Fc Receptor (FcR)

Research Areas:  

Inflammation/Immunology

Nipocalimab (M281) is a fully humanized, recombinant, and non-glycosylated IgG1 monoclonal antibody. Nipocalimab can bind to the IgG-binding site of FcRn with high affinity and inhibit the transplacental transfer of IgG. Nipocalimab can be used in the research of fetal and neonatal hemolytic disease, myasthenia gravis, and various IgG-mediated autoimmune diseases .
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3
3 Cited Publications
Cat. No.: HY-P0185
CAS No.: 189388-22-5
Endomorphin 1, a high affinity, highly selective agonist of the μ-opioid receptor (Ki: 1.11 nM), displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. Endomorphin 1 has antinociceptive properties .
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3
3 Cited Publications
Cat. No.: HY-P0185A
CAS No.: 1276123-71-7
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor (Ki: 1.11 nM), displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive properties .
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1
1 Cited Publications
Cat. No.: HY-150654
CAS No.: 2417012-26-9
Purity:  99.56%
Target:  

WDR5

Research Areas:  

Cancer

WDR5-IN-5 is an orally active and selective inhibitor of WIN site of WD repeat domain 5 (WDR5). WDR5-IN-5 exhibits anti-proliferative activity towards cancer cells and good pharmacokinetics profile in mice. WDR5-IN-5 shows high affinity to WDR5 and the binding affinity Ki value <0.02 nM .
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Cat. No.: HY-P99009
CAS No.: 2187430-05-1
Synonyms: RVT-1401; HBM9161; IMVT-1401

Target:  

Fc Receptor (FcR)

Research Areas:  

Inflammation/Immunology

Batoclimab (RVT-1401) is a fully humanized IgG1 monoclonal antibody targeting FcRn. Batoclimab has high affinity for the IgG-binding site on FcRn. By competitively binding to the IgG binding site on FcRn, Batoclimab blocks FcRn-mediated recycling of IgG, resulting in enhanced degradation and subsequent reductions in IgG levels. Batoclimab can be used in the research of autoimmune diseases such as myasthenia gravis and thyroid eye disease .
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Cat. No.: HY-18698
CAS No.: 142326-59-8
Target:  

iGluR

Research Areas:  

Neurological Disease

L-701324 is a potent, orally active NMDA receptor antagonist that antagonizes the activity of the NMDA receptor by blocking its glycine B binding site. L-701324 binds with high affinity to rat brain membranes (IC50=2 nM). L-701324 has antidepressant activity .
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Cat. No.: HY-107322
CAS No.: 104757-53-1
Purity:  99.96%
Synonyms: Mepirodipine hydrochloride; YM-09730-5
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

Barnidipine (Mepirodipine) hydrochloride is an L-type calcium antagonist (CaA) with high affinity for [ 3H] initrendipine binding sites (Ki = 0.21 nmol/L, has selective action against CaA receptors. Barnidipine hydrochloride is an orally active antihypertensive agent that can reduce the level of platelet-derived growth factor B-chain mRNA and peripheral vascular resistance .
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Cat. No.: HY-100982
CAS No.: 24587-49-3
Purity:  ≥98.0%
Synonyms: trans-4-Hydroxycrotonic acid; trans-γ-Hydroxycrotonic acid; T‐HCA
(E)-4-Hydroxycrotonic acid (trans-4-Hydroxycrotonic acid) is a semirigid linear analog of γ-Hydroxybutyric acid. (E)-4-Hydroxycrotonic acid can be present in the mammalian central nervous system. (E)-4-Hydroxycrotonic acid binds to high-affinity γ-Hydroxybutyric acid binding sites and displaces radioligands .
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Cat. No.: HY-P0186A
CAS No.: 1276124-00-5
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

Endomorphin 2 TFA, a high affinity, highly selective agonist of the μ-opioid receptor, displays reasonable affinities for kappa3 binding sites, with Ki value between 20 and 30 nM .
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Cat. No.: HY-107322A
CAS No.: 104713-75-9
Synonyms: Mepirodipine; YM-09730-5 Free base
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

Barnidipine (Mepirodipine) is an L-type calcium antagonist (CaA) with high affinity for [ 3H] initrendipine binding sites (Ki = 0.21 nmol/L), has selective action against CaA receptors. Barnidipine is an orally effective antihypertensive agent that can reduce the level of platelet-derived growth factor B-chain mRNA and peripheral vascular resistance .
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Cat. No.: HY-136280
CAS No.: 139225-22-2
Purity:  99.43%
Synonyms: EMD 57445
Target:  

Sigma Receptor

Research Areas:  

Neurological Disease

Panamesine (EMD 57445) is a sigma receptor ligand, which has a high affinity (IC50 6 nM) and selectivity for sigma binding sites. Panamesine is a potential atypical neuroleptic agent .
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Cat. No.: HY-P1076A
Target:  

Calmodulin

Research Areas:  

Inflammation/Immunology

CALP2 TFA is a calmodulin (CaM) antagonist (Kd of 7.9 µM) with high affinity for binding to the CaM EF-hand/Ca 2+-binding site. CALP2 TFA inhibits CaM-dependent phosphodiesterase activity and increases intracellular Ca 2+ concentrations. CALP2 TFA potently inhibits of adhesion and degranulation. CALP2 TFA is also a strong activator of alveolar macrophages .
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Cat. No.: HY-15419R
CAS No.: 199864-86-3
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

RS-127445 (hydrochloride) (Standard) is the analytical standard of RS-127445 (hydrochloride). This product is intended for research and analytical applications. RS-127445 hydrochloride is a selective, high affinity, orally bioavailable 5-HT2B receptor antagonist with a pKi of 9.5. RS-127445 hydrochloride shows 1000 fold selectivity for this receptor as compared to numerous other receptor and ion channel binding sites .
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Cat. No.: HY-107322S
CAS No.: 2930289-02-2
Purity:  ≥98.0%
Synonyms: Mepirodipine-d5 hydrochloride; YM-09730-5-d5 hydrochloride
Barnidipine-d5 (hydrochloride) is the deuterium labeled Barnidipine hydrochloride. Barnidipine hydrochloride (Mepirodipine hydrochloride) is an L-type calcium antagonist (CaA) with high affinity for [3H] initrendipine binding sites (Ki=0.21 nmol/l), has selective action against CaA receptors .Barnidipine hydrochloride (Mepirodipine hydrochloride) is an antihypertensive agent and acts by the reduction of peripheral vascular resistance secondary to its vasodilatory action .
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Cat. No.: HY-107322AS1
CAS No.: 2771469-19-1
Purity:  98.97%
Synonyms: Mepirodipine-d5; YM-09730-5-d5 Free base
Barnidipine-d5 is the deuterium-labeled Barnidipine (HY-107322A). Barnidipine-d5 (Mepirodipine) is an L-type calcium antagonist (CaA) with high affinity for [ 3H] initrendipine binding sites (Ki=0.21 nmol/l), has selective action against CaA receptors . Barnidipine-d5 (Mepirodipine) is an antihypertensive agent and acts by the reduction of peripheral vascular resistance secondary to its vasodilatory action .
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Cat. No.: HY-P11131
Synonyms: Human lactoferrin (28-34)
Target:  

Bacterial

Research Areas:  

Infection

hLF (28-34) (Human lactoferrin (28-34)) is a loop region of human lactoferrin (hLF) that is essential for the high-affinity binding of LPS. hLF (28-34) is a key site responsible for its high-affinity binding to E. coli 055B5 lipopolysaccharide. hLF (28-34) can be used for antibacterial research .
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