
Benzimidazoles
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Filtered Search Results

1-Methyl-2-(methylsulfonyl)benzimidazole 98.0+%, TCI America™
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CAS: 61078-14-6 Molecular Formula: C9H10N2O2S Molecular Weight (g/mol): 210.251 InChI Key: VDZVTXFWEKBHBV-UHFFFAOYSA-N PubChem CID: 640715 IUPAC Name: 1-methyl-2-methylsulfonylbenzimidazole SMILES: CN1C2=CC=CC=C2N=C1S(=O)(=O)C
PubChem CID | 640715 |
---|---|
CAS | 61078-14-6 |
Molecular Weight (g/mol) | 210.251 |
SMILES | CN1C2=CC=CC=C2N=C1S(=O)(=O)C |
IUPAC Name | 1-methyl-2-methylsulfonylbenzimidazole |
InChI Key | VDZVTXFWEKBHBV-UHFFFAOYSA-N |
Molecular Formula | C9H10N2O2S |
Rabeprazole Sodium Salt 98.0+%, TCI America™
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CAS: 117976-90-6 Molecular Formula: C18H20N3NaO3S Molecular Weight (g/mol): 381.43 MDL Number: MFCD02092688 InChI Key: KRCQSTCYZUOBHN-UHFFFAOYNA-N PubChem CID: 14720269 ChEBI: CHEBI:8769 IUPAC Name: sodium 2-{[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methanesulfinyl}-1H-1,3-benzodiazol-1-ide SMILES: [Na+].COCCCOC1=CC=NC(CS(=O)C2=NC3=CC=CC=C3[N-]2)=C1C
PubChem CID | 14720269 |
---|---|
CAS | 117976-90-6 |
Molecular Weight (g/mol) | 381.43 |
ChEBI | CHEBI:8769 |
MDL Number | MFCD02092688 |
SMILES | [Na+].COCCCOC1=CC=NC(CS(=O)C2=NC3=CC=CC=C3[N-]2)=C1C |
IUPAC Name | sodium 2-{[4-(3-methoxypropoxy)-3-methylpyridin-2-yl]methanesulfinyl}-1H-1,3-benzodiazol-1-ide |
InChI Key | KRCQSTCYZUOBHN-UHFFFAOYNA-N |
Molecular Formula | C18H20N3NaO3S |
Cayman Chemical Albendazole 5g
An anticonvulsant inhibits the activation of Nav1 1 at 100 UM inhibits Nav1 1 but not Nav1 2 Nav1 3 and Nav1 6 opening and increases the action potential threshold in primary rat hippocampal neurons inhibits CAVA (Ki 343 8 nM) but not CAI and CAII (Kis 10000 nM for both) prolongs the preictal phase and reduces seizure-like event frequency in an in vitro model of epileptiform activity in rat hippocampal slices at 100 UM inhibits pentylenetetrazole-induced seizures in a mouse model of epilepsy (ED50 54 mg/kg i p ) reduces kainic acid-induced neuronal cell death in the mouse hippocampal CA3 region when used at doses of 25 50 and 100 mg/kg

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Cayman Chemical Albendazole sulfon 25mg
A GPR52 antagonist (IC50 0 63 UM) reduces mHTT protein levels in STHdhQ7/Q111 cells in a concentration-dependent manner reduces apoptosis induced by growth factor deprivation in primary striatal neurons isolated from HdhQ7/Q140 mice decreases striatal levels of soluble and insoluble mHTT as well as increases the latency to fall in the rotarod test in the HdhQ140 mouse model of Huntingtons disease at 5 mg/kg

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Cayman Chemical Omeprazole N-oxIde 25mg
A deoxyribonucleotide oral administration in combination with dTMP increases lifespan in a Tk2 H126N knock-in mouse model of TK2 deficiency

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Med Vet International Omeprazole Delayed Release Caplets, 20mg, 1000ct.
Omeprazole is a proton pump inhibitor that helps decrease the amount of acid produced in the stomach.

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eMolecules Ambeed / N-Methyl Omeprazole / 100mg / 600851645 / A638530 / / 89352-76-1 / MFCD19441777 / 359.440 / C18H21N3O3S
Ambeed / N-Methyl Omeprazole / 100mg / 600851645 / A638530 / / 89352-76-1 / MFCD19441777 / 359.440 / C18H21N3O3S

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Cayman Chemical Albendazole sulfon-d3 5mg
A carbenapenem antibiotic active against a panel of clinical isolates from a variety of bacterial species (MIC50s 0 0039-8 Ug/ml) inhibitsBlactamase decreases the number of CFUs in the lungs in a mouse model of penicillin-resistant S pneumoniae infection at doses ranging from 0 32 to 3 2 mg/kg

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Cayman Chemical Albendazole sulfon-d3 10mg
Preparation This antibody which contains a mouse IgG1 isoform was produced as a recombinant protein expressed in HEK293 cells using an engineered construct based on a monoclonal scavenger receptor B2/CD36 antibody Host HEK293 cells Species Reactivity ( ) Human mouse rat Cross Reactivity ( ) CD36 Applications FC

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Cayman Chemical Omeprazole sulfon 50mg
A serotonin synthesis inhibitor that is used for tracing pools of neuronal serotonin as a competitive inhibitor of tryptophan binding to albumin and as a substrate for the serotonin neural transporter

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Albendazole Oxide 54029-12-8 10mM (in 1mL DMSO)
Albendazole Oxide (CAS 54029-12-8) is a small-molecule inhibitor targeting beta-tubulin It is designed to inhibit beta-tubulin polymerization in parasites thereby disrupting cytoplasmic microtubule structure and interfering with glucose metabolic pathways Albendazole Oxide exerts its biological activity primarily through inhibition of beta-tubulin polymerization In both in vitro and in vivo studies Albendazole Oxide demonstrates anti-parasitic activity with reported IC50 values typically ranging from nanomolar to micromolar concentrations depending on the parasite species and assay system Based on these pharmacological properties Albendazole Oxide holds research potential in the exploration of anti-parasitic pharmacodynamics notably for studies involving Echinococcus spp and other parasitic infections

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Cayman Chemical 4-desmethoxy Omeprazole 10mg
A suppressor of IQ electron leak (IC50 70 nM) diminishes endogenous oxidative damage in primary astrocytes reduces stress-induced signaling in a cardiomyocyte cell model and protects against ischemia-reperfusion injury in perfused mouse heart

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eMolecules Medchem Express / Omeprazole sulfide / 100mg / 446274382 / HY-G0006 / / 73590-85-9 / [null] / 329.420 / C17H19N3O2S
Medchem Express / Omeprazole sulfide / 100mg / 446274382 / HY-G0006 / / 73590-85-9 / [null] / 329.420 / C17H19N3O2S

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Cayman Chemical Albendazole 10g
An inactive metabolite of TXA2 serum levels positively correlate with platelet COX-1 activation urinary levels reflect intrarenal TXA2 synthesis

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TARGETMOL CHEMICALS INC Albendazole sulfoxide 500MG
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Albendazole sulfoxide (Ricobendazole) is a metabolite of Albendazole, an anthelmintic. Purity 98.04%

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