1717 Results for "

High affinity

" in MedChemExpress (MCE) Product Catalog:
Products (1717)

1717 Results for "High affinity" in MCE Product Catalog:

29
29 Cited Publications
Cat. No.: HY-N0737
CAS No.: 343-27-1
Synonyms: Telepathine hydrochloride
Harmine Hydrochloride (Telepathine Hydrochloride) is a natural DYRK inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM .
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29
29 Cited Publications
Cat. No.: HY-N0737A
CAS No.: 442-51-3
Synonyms: Telepathine
Harmine is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM .
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27
27 Cited Publications
Cat. No.: HY-149179
CAS No.: 1404-26-8
Purity:  ≥91.0%
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Polymyxin B is an antibiotic. Polymyxin B inhibits Gram-negative infections by binding to the LPS of the bacterial wall with high affinity. Polymyxin B neutralizes the effect of endotoxin. Polymyxin B induces bacterial death by increasing its permeability. Polymyxin B is used in endotoxemia research .
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27
27 Cited Publications
Cat. No.: HY-A0248
CAS No.: 1405-20-5
Polymyxin B Sulfate is an antibiotic. Polymyxin B Sulfate inhibits Gram-negative infections by binding to the LPS of the bacterial wall with high affinity. Polymyxin B Sulfate neutralizes the effect of endotoxin. Polymyxin B Sulfate induces bacterial death by increasing its permeability. Polymyxin B Sulfate is used in endotoxemia research .
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23
23 Cited Publications
Cat. No.: HY-14171
CAS No.: 153559-49-0
Purity:  99.92%
Synonyms: LGD1069
Target:  

RAR/RXR Autophagy

Research Areas:  

Cancer

Bexarotene (LGD1069) is a high-affinity and selective retinoid X receptors (RXR) agonist with EC50s of 33, 24, 25 nM for RXRα, RXRβ, and RXRγ, respectively. Bexarotene shows limited affinity for RAR receptors (EC50 >10000 nM) . Bexarotene can be used for the research of cutaneous T-cell lymphoma.
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21
21 Cited Publications
Cat. No.: HY-B0129
CAS No.: 78110-38-0
Synonyms: SQ-26,776
Aztreonam (SQ-26,776) is a synthetic monocyclic beta-lactam antibiotic, which has a very high affinity for penicillin-binding protein 3 (PBP-3).
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20
20 Cited Publications
Cat. No.: HY-15277
CAS No.: 1228690-19-4
Purity:  99.86%
Target:  

LPL Receptor

Research Areas:  

Inflammation/Immunology

AM966 is a high affinity, selective, oral LPA1-antagonist, inhibits LPA-stimulated intracellular calcium release (IC50=17 nM).
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17
17 Cited Publications
Cat. No.: HY-15778A
CAS No.: 306288-04-0
Purity:  99.22%
AVE 0991 sodium salt is a nonpeptide and orally active Ang-(1-7) receptor Mas agonist. AVE 0991 competes for high-affinity binding of [ 125I]-Ang-(1-7) to bovine aortic endothelial cell membranes with IC50 of 21 nM .
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16
16 Cited Publications
Cat. No.: HY-19532
CAS No.: 139180-30-6
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease Cancer

ZM241385 is a potent, high affinity and selective adenosine A2a receptor (A2AR) antagonist with a Ki value of 1.4 nM .
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15
15 Cited Publications
Cat. No.: HY-16993
CAS No.: 1801787-56-3
Target:  

Apoptosis WDR5

Research Areas:  

Cancer

OICR-9429, a chemical probe, is high affinity WD repeat domain 5 (WDR5) inhibitor, competitively blocks WDR5 interaction with MLL protein via binding the central peptide-binding pocket of WDR5. OICR-9429 can suppress histone H3K4 trimethylation and can be used for the research of various cancers including non-MLL-rearranged leukaemia, colon, pancreatic, prostate cancer and bladder cancer (BCa) .
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14
14 Cited Publications
Cat. No.: HY-130246
CAS No.: 2380230-73-7
Purity:  99.92%
Target:  

Succinate Receptor 1

Research Areas:  

Inflammation/Immunology

NF-56-EJ40 is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, and shows almost no activity towards rat SUCNR1. NF-56-EJ40 has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM .
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14
14 Cited Publications
Cat. No.: HY-130246A
CAS No.: 2728500-80-7
Target:  

Succinate Receptor 1

Research Areas:  

Inflammation/Immunology

NF-56-EJ40 hydrochloride is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, and shows almost no activity towards rat SUCNR1. NF-56-EJ40 hydrochloride has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM .
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14
14 Cited Publications
Cat. No.: HY-D1027
CAS No.: 10121-91-2
Synonyms: Monodansyl cadaverine
Target:  

Autophagy

Research Areas:  

Others

Dansylcadaverine (Monodansyl cadaverine) is an autofluorescent compound used for the labeling of autophagic vacuoles. Dansylcadaverine, a high affinity substrate of transglutaminases, can block the receptor-mediated endocytosis of many ligands .
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14
14 Cited Publications
Cat. No.: HY-108682
CAS No.: 680590-49-2
Purity:  99.92%
Research Areas:  

Neurological Disease

EMPA is a high-affinity, reversible and selective orexin OX2 receptor antagonist. [ 3H]EMPA binds to human and rat OX2-HEK293 membranes with KD values of 1.1 and 1.4 nM respectively .
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14
14 Cited Publications
Cat. No.: HY-12467
CAS No.: 1338545-07-5
Purity:  99.74%
Target:  

TOPK CDK Apoptosis

Research Areas:  

Cancer

OTS964 hydrochloride is an orally active, high affinity and selective TOPK (T-lymphokine-activated killer cell-originated protein kinase) inhibitor with an IC50 of 28 nM . OTS964 hydrochloride is also a potent inhibitor of the cyclin-dependent kinase CDK11, which binds to CDK11B with a Kd of 40 nM .
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14
14 Cited Publications
Cat. No.: HY-14539
CAS No.: 5786-21-0
Purity:  99.84%
Synonyms: HF 1854; ZINC000019796155
Clozapine (HF 1854) is an antipsychotic used for the research of schizophrenia. Clozapine has high affinity for a number of neuroreceptors. Clozapine is a potent antagonist of dopamine D2 with a Ki of 75 nM. Clozapine inhibits the muscarinic M1 receptor and serotonin 5HT2A receptor with Kis of 9.5 nM and 4 nM, respectively . Clozapine is also a potent and selective agonist at the muscarinic M4 receptor (EC50=11 nM) .
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14
14 Cited Publications
Cat. No.: HY-14539A
CAS No.: 54241-01-9
Synonyms: HF 1854 hydrochloride
Clozapine hydrochloride (HF 1854 hydrochloride) is an antipsychotic used for the research of schizophrenia. Clozapine hydrochloride has high affinity for a number of neuroreceptors. Clozapine hydrochloride is a potent antagonist of dopamine D2 with a Ki of 75 nM. Clozapine hydrochloride inhibits the muscarinic M1 receptor and serotonin 5HT2A receptor with Kis of 9.5 nM and 4 nM, respectively . Clozapine hydrochloride is also a potent and selective agonist at the muscarinic M4 receptor (EC50=11 nM) .
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14
14 Cited Publications
Cat. No.: HY-129039
CAS No.: 778649-18-6
Purity:  99.58%
Synonyms: MB-3
Butyrolactone 3 (MB-3) is a specifical small-molecule inhibitor of the histone acetyltransferase Gcn5 (IC50=100 μM), which has a high affinity to the Gcn5 enzyme comparable to that of its natural substrate, histone H3. Butyrolactone 3 shows weak inhibitory on CBP (IC50=0.5 mM). Butyrolactone 3 can be used in studies of cancer, metabolic, autoimmune and neurological diseases .
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14
14 Cited Publications
Cat. No.: HY-14541
CAS No.: 132539-06-1
Purity:  99.96%
Synonyms: LY170053
Olanzapine (LY170053) is a selective, orally active monoaminergic antagonist with high affinity binding to serotonin H1, 5HT2A/2C, 5HT3, 5HT6 (Ki=7, 4, 11, 57, and 5 nM, respectively), dopamine D1-4 (Ki=11 to 31 nM), muscarinic M1-5 (Ki=1.9-25 nM), and adrenergic α1 receptor (Ki=19 nM). Olanzapine is an atypical antipsychotic .
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13
13 Cited Publications
Cat. No.: HY-10052
CAS No.: 170729-80-3
Purity:  99.82%
Synonyms: MK-0869; MK-869; L-754030
Aprepitant (MK-0869) is a selective and high-affinity neurokinin 1 receptor antagonist with a Kd of 86 pM.
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