127 Results for "

Efficacious

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

127 Results for "Efficacious" in MCE Product Catalog:

Cat. No.: HY-B0993A
CAS No.: 155319-91-8
Research Areas:  

Cancer

Mangafodipir, hepatocellular-specific contrast agent, is an efficacious inhibitor of CIPN (chemotherapy-induced peripheral neuropath) and other conditions caused by cellular oxidative stress. Mangafodipir shows no negative interference with the tumoricidal activity of chemotherapy .
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Cat. No.: HY-145704
CAS No.: 2715222-97-0
Target:  

Parasite

Research Areas:  

Infection

Antimalarial agent 8 (Compound 7e) is a novel orally active class of antimalarials. Antimalarial agent 8 is potent in vitro against P. falciparum and is orally efficacious (40 mg/kg) in an in vivo mouse model of malaria .
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Cat. No.: HY-19285AR
CAS No.: 23307-72-4
Synonyms: Sulfachloropyrazine sodium (Standard)
Research Areas:  

Infection

Sulfaclozine (sodium) (Standard) is the analytical standard of Sulfaclozine (sodium). This product is intended for research and analytical applications. Sulfaclozine sodium (Sulfachloropyrazine sodium) is an efficacious sulphonamide derivative with antibacterial and anticoccidial effects. Sulfaclozine sodium is commonly used for the treatment of various poultry diseases (particularly, collibacteriosis, fowl cholera and coccidiosis) .
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Cat. No.: HY-19285R
CAS No.: 102-65-8
Synonyms: Sulfachloropyrazine (Standard)
Research Areas:  

Infection

Sulfaclozine (Standard) is the analytical standard of Sulfaclozine. This product is intended for research and analytical applications. Sulfaclozine (Sulfachloropyrazine) is an efficacious sulphonamide derivative with antibacterial and anticoccidial effects. Sulfaclozine is commonly used for the treatment of various poultry diseases (particularly, collibacteriosis, fowl cholera and coccidiosis) .
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Cat. No.: HY-112542R
CAS No.: 102130-84-7
Synonyms: CL-287088 (Standard); LL-F28249 α (Standard)
Nemadectin (Standard) is the analytical standard of Nemadectin. This product is intended for research and analytical applications. Nemadectin (CL-287088), an orally active broad-spectrum endectocide, is highly efficacious against natural infections of all the major canine gastrointestinal helminthes. Anthelmintic activity .
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Cat. No.: HY-15250R
CAS No.: 1210004-12-8
Target:  

FAAH MAGL Autophagy

Research Areas:  

Neurological Disease

JZL195 (Standard) is the analytical standard of JZL195. This product is intended for research and analytical applications. JZL195 is a selective and efficacious dual fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) inhibitor with IC50s of 2 and 4 nM, respectively .
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Cat. No.: HY-10268S1
CAS No.: 2098655-55-9
Synonyms: PRT054021-dsub>4
Betrixaban-d4 (PRT054021-d4) is deuterium labeled Betrixaban. 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-141535A
CAS No.: 2446803-91-2
Purity:  98.38%
Target:  

Interleukin Related

Research Areas:  

Infection Inflammation/Immunology

IL-17 modulator 1 (disodium) is an orally active, highly efficacious IL-17 modulator extracted from patent WO 2020127685. IL-17 modulator 1 (disodium) can be used for the research of diseases including psoriasis, ankylosing spondylitis and psoriatic arthritis .
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Cat. No.: HY-115987
CAS No.: 2376198-66-0
Target:  

Monoamine Oxidase

Research Areas:  

Neurological Disease

MAO-B-IN-6 is a potent, selective and orally active MAO-B inhibitor with an IC50 of 0.019 µM. MAO-B-IN-6 shows more efficacious than Safinamide in vitro and in vivo. MAO-B-IN-6 has the potential for the research of parkinson's disease (PD) .
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Cat. No.: HY-154910
CAS No.: 1021920-32-0
Purity:  98.49%
Target:  

mTOR

Research Areas:  

Cancer

CC214-1 is a potentially efficacious mTOR inhibitor that induces autophagy ,with an IC50 is 0.002 μM. CC214-1 proved to be useful as an in vitro tool compound for the exploration of mTOR kinase biology. CC214-1 can be used for Glioblastoma study .
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Cat. No.: HY-107096
CAS No.: 534605-78-2
Synonyms: TP3076
Target:  

Topoisomerase

Research Areas:  

Cancer

CH-0793076 (TP3076), a hexacyclic camptothecin analog, is active drug and major metabolite of TP300. CH-0793076 inhibits DNA topoisomerase I with an IC50 of 2.3 μM. CH-0793076 is efficacious against cells expressing BCRP (breast cancer resistance protein) .
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Cat. No.: HY-107096B
CAS No.: 2740278-76-4
Purity:  98.71%
Synonyms: TP3076 TFA
Target:  

Topoisomerase

Research Areas:  

Cancer

CH-0793076 (TP3076) TFA, a hexacyclic camptothecin analog, is active drug and major metabolite of TP300. CH-0793076 TFA inhibits DNA topoisomerase I with an IC50 of 2.3 μM. CH-0793076 TFA is efficacious against cells expressing BCRP (breast cancer resistance protein) .
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Cat. No.: HY-118704
CAS No.: 1112994-35-0
Purity:  99.81%
Target:  

mTOR

Research Areas:  

Inflammation/Immunology Cancer

P-2281 is a mTOR inhibitor with anticancer and anti-inflammatory efficacies. P2281 inhibits mTOR activity in colon cancer cells. P-2281 suppresses Dextran sulfate sodium salt (HY-116282C) (DSS)-induced colitis by inhibiting T cell function and is efficacious in a murine model of human colitis .
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Cat. No.: HY-141535
CAS No.: 2446803-85-4
Target:  

Interleukin Related

Research Areas:  

Infection Inflammation/Immunology

IL-17 modulator 1 is an orally active, highly efficacious small molecule IL-17 modulators extracted from patent WO 2020127685. IL-17 modulator 1 can be used for the research of preventing, researching or ameliorating a variety of diseases including psoriasis, ankylosing spondylitis and psoriatic arthritis .
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Cat. No.: HY-W012634R
CAS No.: 95-16-9
Benzothiazole (Standard) is the analytical standard of Benzothiazole. This product is intended for research and analytical applications. Benzothiazole is a natural occurring heterocyclic nuclei. Benzothiazole nucleus possesses a number of biological activities such as anticancer, antimicrobial, antidiabetic, anti-inflammatory, antileishmanial, and antiviral. Furthermore, Benzothiazole nucleus can function as an efficacious β-amyloid imaging agent .
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Cat. No.: HY-11051
CAS No.: 825649-28-3
Purity:  98.00%
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

JNJ-20788560 is a selective and orally active delta opioid receptor agonist with an affinity of 2.0 nM for DOR (rat brain cortex binding assay). JNJ-20788560 also is a potent and efficacious antihyperalgesic agent that does not produce respiratory depression, pharmacologic tolerance, or physical dependence. JNJ-20788560 can be used for the research of the relief of inflammatory hyperalgesia .
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Cat. No.: HY-B0477AS2
Synonyms: CI-906-d4
Quinapril-d4 (CI-906-d4) is deuterium labeled Quinapril. Quinapril is a potent, orally active, non-peptide and nonsulfhydryl inhibitor of angiotensin-converting enzyme (ACE). Quinapril specifically interrupts the conversion of angiotensin I to angiotensin II in both plasma and tissue. Quinapril is enzymatically hydrolyzed to a pharmacologically active diacid form quinaprilat. Quinapril is efficacious in hypertensive models .
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Cat. No.: HY-B1658S
Synonyms: (R)-Frovatriptan-d3 hydrochloride; SB 209509-d3 hydrochloride; VML 251-d3 hydrochloride
Frovatriptan-d3 (hydrochloride) is the deuterium labeled Frovatriptan . Frovatriptan is a potent 5-HT1B//D receptor agonist and has the highest 5-HT1B potency in the triptan class. Frovatriptan is apparently cerebroselective. Frovatriptan is efficacious and even superior in some endpoints also when taken during the headache phase in migraine attacks with aura .
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Cat. No.: HY-141692A
CAS No.: 2446806-90-0
Target:  

Interleukin Related

Research Areas:  

Inflammation/Immunology

IL-17 modulator 4 sulfate is a proagent of IL-17 modulator 1 (HY-141535). IL-17 modulator 1 is an orally active, highly efficacious IL-17 modulator. IL-17 modulator 4 sulfate is promising for the research of IL-17A mediated diseases, including inflammation, autoimmune diseases, infectious diseases, cancer, and precancerous syndrome .
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Cat. No.: HY-144705
CAS No.: 2851895-01-5
Target:  

Cannabinoid Receptor

Research Areas:  

Neurological Disease

GAT564 (Compound 15d) is a potent allosteric modulator of cannabinoid 1 receptor (CB1R) with EC50s of 87 and 320 nM respectively for cAMP and β-arrestin2. GAT564 markedly promotes orthosteric ligand binding to hCB1R. GAT564 is efficacious as a topical agent that significantly reduces intraocular pressure (IOP) in the ocular normotensive murine model of glaucoma .
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