126 Results for "

Tolerated

" in MedChemExpress (MCE) Product Catalog:
Products (126)

126 Results for "Tolerated" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-B0265B
CAS No.: 77940-93-3
Synonyms: (S)-BAY-e 9736
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

(S)-Nimodipine ((S)-BAY-e 9736) is an enantiomer of Nimodipine. Nimodipine (BAY-e 9736) is an orally active, well-tolerated and light-sensitive dihydropyridine calcium antagonist. Nimodipine can be used for the research of cerebrovascular disorders .
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Cat. No.: HY-16700
CAS No.: 202350-68-3
Research Areas:  

Cancer

PNU-159682, a metabolite of the anthracycline Nemorubicin, is a highly potent DNA topoisomerase II inhibitor with excellent cytotoxicity. PNU-159682 acts as a more potent and tolerated ADC cytotoxin than Doxorubicin for ADC synthesis. PNU-159682 can be used in EDV-nanocell technology to overcome agent resistance.
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Cat. No.: HY-174406
MT-125 is a specific and well-tolerated inhibitor of non-muscle myosin IIA (Ki,NMIIA = 2.7 μM) and IIB (EC50 = 1.7 μM). MT-125 can pass through the blood-brain barrier. MT-125 induces ferroptosis and DNA damage by increasing the levels of reactive oxygen species (ROS) within tumor cells. MT-125 can enhance the PDGFR signaling pathway. MT-125 can be used for research on glioblastoma.
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Cat. No.: HY-114237
CAS No.: 1494581-70-2
Purity:  99.69%
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

GDC-0276 is a potent, selective, reversible and orally active NaV1.7 inhibitor with an IC50 value of 0.4 nM. GDC-0276 is well tolerated and exhibits a good pharmacokinetic profile. GDC-0276 has the potential for the treatment of pain and to address shortcomings of existing pain medications, such as addiction and off-target side effects .
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Cat. No.: HY-P99665
CAS No.: 2131038-11-2
Synonyms: LY-3209590

Target:  

Insulin Receptor

Research Areas:  

Metabolic Disease

Insulin efsitora alfa (LY-3209590) is a selective agonist of insulin receptor (IR). Insulin efsitora alfa is a fusion protein composed of human IR agonists fused with the crystallizable (Fc) domain of human immunoglobulin G2 (IgG2) fragment, with a molecular weight of 64.1 kDa. Insulin efsitora alfa is well tolerated and has potential applications in diabetes .
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Cat. No.: HY-B1895
CAS No.: 99291-25-5
Synonyms: (S)-(-)-Dropropizine; DF-526
Levodropropizine (DF-526) is an orally active histamine receptor inhibitor, Levodropropizine is an effective and very well tolerated peripheral antitussive agent .
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Cat. No.: HY-16487
CAS No.: 108319-06-8
Synonyms: TMFX; TA-167 free acid; A-62254 free acid
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Temafloxacin (TMFX) is an orally active quinolone broad-spectrum antibacterial agent. Temafloxacin is well tolerated in lower respiratory and genitourinary tract infections .
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Cat. No.: HY-N7393
CAS No.: 64519-82-0
Synonyms: Palatinitol
Isomalt (Palatinitol), a well-tolerated, non-toxic polyol and a protein-stabilizing excipient, stabilizes lactate dehydrogenase (LDH) moderately during freeze-drying, and performs better during storage. Isomalt is traditionally used as a sweetening agent in the food industry and as a tabletting excipient for pharmaceutical purposes .
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Cat. No.: HY-B1804
CAS No.: 538-23-8
Synonyms: Trioctanoin; Glyceryl trioctanoate
Tricaprilin (Trioctanoin) is an orally active and well tolerated ketogenic agent that safely induces ketosis. Tricaprilin restores brain electrical activity and metabolism to help counteract neuroinflammation in migraine. Tricaprilin is promising for research of migraine prevention and Alzheimer’s disease (AD). Tricaprilin is a pure C8 medium chain triglyceride (MCT) .
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Cat. No.: HY-148772
CAS No.: 2476724-74-8
Purity:  98.72%
Target:  

DNA/RNA Synthesis

Research Areas:  

Neurological Disease

PTC258 is a specific and orally active splicing modulator of Elongator complex protein 1 gene (ELP1). PTC258 increases the expression of ELP1 in vitro and in vivo. PTC258 is well tolerated in mouse model .
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Cat. No.: HY-126810A
Purity:  99.80%
Target:  

Fungal

Research Areas:  

Infection

NP213 TFA is a rapidly acting, novel, first-in-class synthetic antimicrobial peptide (AMP), has anti-fungal activities. NP213 TFA targets the fungal cytoplasmic membrane and plays it role via membrane perturbation and disruption. NP213 TFA is effective and well-tolerated in resolving nail fungal infections .
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Cat. No.: HY-112163A
CAS No.: 2098191-54-7
Purity:  97.32%
Synonyms: rel-eFT226
rel-Zotatifin is the racemic isomer of Zotatifin, acts as an eIF4A inhibitor with activity less than Zotatifin. Zotatifin (eFT226) is a potent, selective, and well-tolerated eIF4A inhibitor. Zotatifin promotes eIF4A binding to specific mRNA sequences with recognition motifs in the 5’-UTRs (IC50=2 nM) and interferes with the assembly of the eIF4F initiation complex .
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Cat. No.: HY-18060
CAS No.: 639489-84-2
Synonyms: TC-5619
Target:  

nAChR

Research Areas:  

Neurological Disease

Bradanicline (TC-5619) is an orally active agonist of α7 nAChR with moderate blood-brain barrier penetration. Bradanicline exhibits high affinity and subtype selectivity for human α7 nAChR. Bradanicline possesses antitussive activity that depends on sustained receptor binding and activation. Bradanicline requires systemic administration to dose-dependently inhibit cough induced by citric acid, bradykinin and inhaled nicotine. Bradanicline is well tolerated in preclinical studies and is widely used in research related to chronic refractory cough .
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Cat. No.: HY-161672
CAS No.: 2413455-99-7
Target:  

IRE1

Research Areas:  

Cancer

G-5758 is a selective and orally effective IRE1α inhibitor with an IC50 of 38 nM (detected by the XBP1s luciferase reporter cell assay). G-5758 is still well tolerated in rats at oral doses up to 500 mg/kg. G-5758 can be used in the research of multiple myeloma .
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Cat. No.: HY-122347A
CAS No.: 579475-24-4
Purity:  99.99%
Synonyms: GW823296 maleate
Orvepitant maleate (GW823296 maleate) is potent, selective, orally active and well-tolerated neurokinin-1 receptor (NK-1) antagonist with a pKi of 10.2 for human neurokinin-1 receptor. Orvepitant maleate can across the blood-brain barrier. Orvepitant maleate has the potential for depressive disorder and chronic refractory cough (CRC) treatment .
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Cat. No.: HY-112081
CAS No.: 2109805-96-9
Purity:  99.64%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

BAY-707, a chemical probe, is a substrate-competitive, highly potent and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. BAY-707 has a good pharmacokinetic (PK) profile to other MTH1 compounds and is well-tolerated in mice, but shows a clear lack of in vitro or in vivo anticancer efficacy .
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Cat. No.: HY-107345
CAS No.: 90101-16-9
Synonyms: Ombolan
Research Areas:  

Inflammation/Immunology

Droxicam (Ombolan) is a non-steroidal anti-inflammatory agent, with strong analgesic activity. Droxicam acts by inhibiting PGE2 varies, and is characterised by being a pro-drug of Piroxicam (HY-B0253). Droxicam is well tolerated with slight side effects in the said mucosa. Droxicam does not show cardiovascular or respiratory effects in cats, and inhibits peritoneal capillary permeability in mouse .
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Cat. No.: HY-125999
CAS No.: 1147883-03-1
Purity:  99.53%
Research Areas:  

Neurological Disease

EPI-589, a quinone derivative, is a safe and well tolerated oxidoreductase enzyme inhibitor and a free radical scavenger, with blood-brain barrier permeable and orally available. EPI-589 is a redox-active neuroprotectant that effectively delays the symptoms of motor neuron disease in wobbler mice. EPI-589 can be used in amyotrophic lateral sclerosis (ALS) research .
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Cat. No.: HY-34222
CAS No.: 7355-55-7
Target:  

DYRK

Research Areas:  

Cancer

7-Deazaguanine (Compound 1) is a highly selective, well-tolerated, brain-penetrant DYRK1A inhibitor. 7-Deazaguanine is promising for research of cancers and Down’s syndrome .
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Cat. No.: HY-126810
CAS No.: 942577-31-3
Target:  

Fungal

Research Areas:  

Infection

NP213 is a rapidly acting, novel, first-in-class synthetic antimicrobial peptide (AMP), has anti-fungal activities. NP213 targets the fungal cytoplasmic membrane and plays it role via membrane perturbation and disruption. NP213 is effective and well-tolerated in resolving nail fungal infections .
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