127 Results for "

Efficacious

" in MedChemExpress (MCE) Product Catalog:
Products (127)

127 Results for "Efficacious" in MCE Product Catalog:

Cat. No.: HY-119934
CAS No.: 1494585-79-3
Purity:  99.65%
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

NaV1.7 inhibitor-1 is an efficacious voltage-gated sodium channel (NaV) 1.7 inhibitor with an IC50 of 0.6 nM for hNaV1.7, exhibits 80-fold selectivity versus hNaV1.5 .
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Cat. No.: HY-P4990
CAS No.: 24327-19-3
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

Pro8-Oxytocin is a a modified oxytocin (OXT) ligand. Pro8-Oxytocin produces more potent and efficacious responses at primate OXTR and stronger behavioral effects than the consensus mammalian OXT ligand (Leu8-Oxytocin). Pro8-Oxytocin produce a less efficacious response than Vasopressin (HY-B1811) (AVP) at human AVPR1a and higher efficacious response than AVP at marmoset AVPR1a .
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Cat. No.: HY-P4990A
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

Pro8-Oxytocin TFA is a a modified oxytocin (OXT) ligand. Pro8-Oxytocin produces more potent and efficacious responses at primate OXTR and stronger behavioral effects than the consensus mammalian OXT ligand (Leu8-Oxytocin). Pro8-Oxytocin TFA produce a less efficacious response than Vasopressin (HY-B1811) (AVP) at human AVPR1a and higher efficacious response than AVP at marmoset AVPR1a .
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Cat. No.: HY-101921
CAS No.: 1911564-39-0
Purity:  99.60%
Target:  

PI3K

Research Areas:  

Inflammation/Immunology

PI3Kδ-IN-1 is a potent, selective, and efficacious PI3Kδ inhibitor with an IC50 of 1.7 nM.
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Cat. No.: HY-47030
CAS No.: 2338-05-8
Ferric citrate hydrate, an orally active iron supplement, is an efficacious phosphate binder. Ferric citrate hydrate can be used for iron deficiency anemia and chronic kidney disease (CKD) research .
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Cat. No.: HY-139179
CAS No.: 2411100-70-2
Target:  

STING

Research Areas:  

Infection Cancer

STING agonist-14 (compound 12b) is a potent STING agonist that is efficacious across species. STING agonist-14 could activate the pathway by directly binding human STING. STING agonist-14 can be used for the research of tumours or viral infections .
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Cat. No.: HY-P3584A
Synonyms: (Pro3) Gastric Inhibitory Peptide, human TFA
Target:  

Insulin Receptor

Research Areas:  

Metabolic Disease

(Pro3) GIP, human TFA is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human TFA has high binding affinity for human GIPR with Ki/ Kd value of 0.90 nM. (Pro3) GIP, human TFA human can be used for the research of obesity-related diabetes .
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Cat. No.: HY-133738
CAS No.: 2377335-74-3
Research Areas:  

Cancer

M-808 is a highly potent and efficacious covalent Menin-MLL interaction inhibitor, with a binding IC50 value of 2.6 nM .
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Cat. No.: HY-130253
CAS No.: 2454244-02-9
Purity:  99.30%
Target:  

IRAK

Research Areas:  

Cancer

IRAK4-IN-6 is an orally efficacious and selective IRAK4 inhibitor with an IC50 of 4 nM, and targetes MyD88 L265P mutant diffuse large B cell lymphoma .
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Cat. No.: HY-135797
CAS No.: 1557397-51-9
Target:  

Apoptosis

Research Areas:  

Cancer

DB1976 is a selenophene analog of DB270 and a potent and cell-permeable fully efficacious transcription factor PU.1 inhibitor. DB1976 potently inhibits PU.1 binding (IC50 of 10 nM) and strongly inhibits the PU.1/DNA complex (with high DB1976-λB affinity, KD of 12 nM) in vitro. DB1976 has apoptosis-inducing effect .
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Cat. No.: HY-15199
CAS No.: 1227678-26-3
Synonyms: CEP-32496 hydrochloride; RXDX-105 hydrochloride
Target:  

Raf

Research Areas:  

Cancer

Agerafenib hydrochloride is a highly potent and orally efficacious inhibitor of BRAF V600E with a Kd of 14 nM.
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Cat. No.: HY-12913
CAS No.: 1227067-61-9
Purity:  99.02%
Research Areas:  

Neurological Disease

AMG 579 is a potent, selective, and efficacious inhibitor of phosphodiesterase 10A (PDE10A) with an IC50 of 0.1 nM.
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Cat. No.: HY-10268S
CAS No.: 2098655-51-5
Purity:  99.02%
Synonyms: PRT054021-d6
Betrixaban-d6 is a deuterium labeled Betrixaban. Betrixaban is a highly potent, selective, and orally efficacious factor Xa (fXa) inhibitor .
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Cat. No.: HY-10268B
CAS No.: 2099719-47-6
Synonyms: PRT054021 hydrochloride
Target:  

Factor Xa

Research Areas:  

Cardiovascular Disease

Betrixaban (PRT054021) hydrochloride is a highly potent, selective, and orally efficacious factor Xa (fXa) inhibitor with an IC50 of 1.5 nM. Betrixaban hydrochloride shows antithrombotic effect .
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Cat. No.: HY-102036
CAS No.: 1346669-54-2
Target:  

Btk

Research Areas:  

Inflammation/Immunology

G-744 is a highly potent, selective and orally active Btk inhibitor with an IC50 of 2 nM. G-744 is metabolically stable, well tolerated and efficacious to treat arthritis .
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Cat. No.: HY-108640
CAS No.: 502137-98-6
Research Areas:  

Infection Cancer

HLI373 is an efficacious Hdm2 inhibitor. HLI373 inhibits the ubiquitin ligase activity of Hdm2. HLI373 is effective in inducing apoptosis of several tumor cells that are sensitive to DNA-damaging agents . Antimalarial activity .
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Cat. No.: HY-10268R
CAS No.: 330942-05-7
Synonyms: PRT054021 (Standard)
Research Areas:  

Cardiovascular Disease

Betrixaban (Standard) is the analytical standard of Betrixaban. This product is intended for research and analytical applications. Betrixaban (PRT054021) is a highly potent, selective, and orally efficacious factor Xa (fXa) inhibitor with an IC50 of 1.5 nM. Betrixaban shows antithrombotic effect .
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Cat. No.: HY-14376R
CAS No.: 1020315-31-4
Synonyms: PF-04457845 (Standard)
Research Areas:  

Neurological Disease

Redafamdastat (Standard) is the analytical standard of Redafamdastat. This product is intended for research and analytical applications. Redafamdastat (PF-04457845) is a highly efficacious and selective FAAH inhibitor with IC50 values is 7.2±0.63 nM and 7.4±0.62 nM for hFAAH and rFAAH, respectively.
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Cat. No.: HY-12738
CAS No.: 1023650-66-9
Purity:  99.90%
PF-3882845 is a remarkably high affinity selective and orally efficacious mineralocorticoid receptor (MR binding IC50=2.7 nM) antagonist for hypertension and nephropathy. PF-3882845 also binds to progesterone receptor (PR) with the binding IC50 of 310 nM .
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Cat. No.: HY-P3584
CAS No.: 299898-52-5
Synonyms: (Pro3) Gastric Inhibitory Peptide, human
Target:  

Insulin Receptor

Research Areas:  

Metabolic Disease

(Pro3) GIP, human ((Pro3) Gastric Inhibitory Peptide, human) is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human has high binding affinity for human GIPR with Ki/ Kd values of 0.90 nM. (Pro3) GIP, human can be used for the research of obesity-related diabetes .
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