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Filtered Search Results
Medchemexpress LLC Ilginatinib hydrochloride | 1239358-85-0 | 98.9% | 425.89 | 1 G
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Ilginatinib hydrochloride | 1239358-85-0 | 98.9% | 425.89 | 1 G
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eMolecules 693-03-8 | Butylmagnesium bromide, 1.0 M in THF | Synthonix | MFCD00672091 | 161.325 | C4H9BrMg | 0.000 | [Br-].CCCC[Mg+] | 50ml | 702445845
Butylmagnesium bromide, 1.0 M in THF | Synthonix | 693-03-8 | MFCD00672091 | 161.325 | C4H9BrMg | 0.000 | [Br-].CCCC[Mg+] | 50ml | 702445845
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Medchemexpress LLC 1-(2-(((diphenylmethylene)amino)oxy)ethyl)-1,2,5,6-tetrahydro-3-pyridinecarboxylic acid hydrochloride | 145645-62-1 | MFCD00153853 | 99.8% | 386.87 g/mol | C21H23ClN2O3 | 25 MG
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NNC-711 (NO-711 hydrochloride) is a potent and selective inhibitor of the GABA transporter GAT-1 supplied as a high-purity solid for research applications in neuroscience and pharmacology. It exhibits anticonvulsant and analgesic activity in vivo and is used to study GABA uptake and transporter function.
- Potent and selective GAT-1 inhibitor; IC50 ≈ 0.04 μM for human GAT-1.
- High purity suitable for in vitro and in vivo research.
- White to off-white solid, supplied in small pack sizes for laboratory use.
- Stable when stored sealed at low temperature, away from moisture.
- For research use only; not for human or clinical applications.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 186000-43-1 | 4-(Methoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix327.430 | C8H7IO2Zn | 0.000 | [I-].COC(=O)c1ccc([Zn+])cc1 | 50ml | 532652914
4-(Methoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix | 186000-43-1327.430 | C8H7IO2Zn | 0.000 | [I-].COC(=O)c1ccc([Zn+])cc1 | 50ml | 532652914
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eMolecules 112-40-3 | Dodecane | Oakwood Chemicals | MFCD00008969 | 170.340 | C12H26 | 99.000 | CCCCCCCCCCCC | 10g | 480149873
Dodecane | Oakwood Chemicals | 112-40-3 | MFCD00008969 | 170.340 | C12H26 | 99.000 | CCCCCCCCCCCC | 10g | 480149873
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eMolecules 29046-78-4 | Nickel(II) chloride, dimethoxyethane adduct, min. 97% | Strem Chemicals | MFCD00013481 | 219.720 | C4H10Cl2NiO2 | 97.000 | [Cl-].[Cl-].[Ni++].COCCOC | 25g | 321342037
Nickel(II) chloride, dimethoxyethane adduct, min. 97% | Strem Chemicals | 29046-78-4 | MFCD00013481 | 219.720 | C4H10Cl2NiO2 | 97.000 | [Cl-].[Cl-].[Ni++].COCCOC | 25g | 321342037
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Biomatik Corporation DL-Dithiothreitol [DTT]. Grade Biotechnology. Storage -20C. CAS 3483-12-3
DL-Dithiothreitol [DTT]. Grade Biotechnology. Storage -20C. CAS 3483-12-3
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Medchemexpress LLC Siramesine hydrochloride | 224177-60-0 | 99.7% | C30H32ClFN2O | 2 MG
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Siramesine hydrochloride, also known as Lu 28-179 hydrochloride, is a potent sigma-2 receptor agonist. It demonstrates high selectivity for sigma-2 receptors over sigma-1 receptors. This compound triggers cell death by destabilizing mitochondria and exhibits anti-cancer activity.
- Potent sigma-2 receptor agonist
- High selectivity for sigma-2 receptors
- Triggers cell death via mitochondrial destabilization
- Shows anti-cancer activity
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 131379-40-3 | 2-(Ethoxycarbonyl)phenylzinc bromide, 0.50 M in THF | Synthonix | MFCD01863743 | 294.450 | C9H9BrO2Zn | 0.000 | [Br-].CCOC(=O)c1ccccc1[Zn+] | 50ml | 532652803
2-(Ethoxycarbonyl)phenylzinc bromide, 0.50 M in THF | Synthonix | 131379-40-3 | MFCD01863743 | 294.450 | C9H9BrO2Zn | 0.000 | [Br-].CCOC(=O)c1ccccc1[Zn+] | 50ml | 532652803
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Medchemexpress LLC Selegiline hydrochloride | 14611-52-0 | MFCD00069299 | 99.94% | C13H18ClN | 1 ML
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Selegiline hydrochloride (Deprenyl hydrochloride) is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. It exhibits 450-fold selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline hydrochloride can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder.
- Potent, selective, and irreversible inhibitor of MAO-B
- Exhibits 450-fold selectivity for MAO-B over MAO-A
- Increases efflux of norepinephrine, dopamine, and serotonin from rat hypothalamus
- Inhibits efflux of dihydroxyphenylacetic acid and 5-hydroxyindoleacetic acid
- Reduces cocaine self-administration in mice
- Reduces DOPAC and 5-HIAA concentrations in the frontal cortex
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Medchemexpress LLC Amiselimod hydrochloride | 942398-84-7 | 98.7% | 413.90 | 100 MG
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Amiselimod hydrochloride is converted to its active metabolite Amiselimod phosphate by sphingosine kinases in vivo. It is an orally active and highly selective sphingosine 1-phosphate receptor-1 (S1P1) agonist. This compound is designed to reduce the bradycardia effects associated with fingolimod and other S1P receptor modulators. Amiselimod hydrochloride inhibits chronic colitis by preventing the infiltration of colitogenic Th1 and Th17 cells into the colon and inhibits lupus nephritis by reducing the infiltration of autoreactive T cells into the kidneys. It shows promise for the research of autoimmune diseases.
- Orally active and highly selective sphingosine 1-phosphate receptor-1 (S1P1) agonist.
- Designed to reduce bradycardia effects compared to other S1P receptor modulators.
- Inhibits chronic colitis.
- Inhibits lupus nephritis.
- Promising for research of autoimmune diseases.
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Medchemexpress LLC Milveterol (hydrochloride) | 804518-03-4 | 98.2% | C25H30ClN3O4 | 100 MG
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Milveterol hydrochloride is a long-acting β2-adrenergic receptor agonist. It can be used in the study of asthma and chronic obstructive pulmonary disease (COPD).
- Long-acting β2-adrenergic receptor agonist
- Suitable for asthma research
- Suitable for chronic obstructive pulmonary disease (COPD) research
- Bronchodilator
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 2378318-41-1 | 3-(Benzyloxy)propylzinc bromide, 0.5 M in THF | Synthonix294.500 | C10H13BrOZn | 0.000 | [Br-].[Zn+]CCCOCc1ccccc1 | 100ml | 771375796
3-(Benzyloxy)propylzinc bromide, 0.5 M in THF | Synthonix | 2378318-41-1294.500 | C10H13BrOZn | 0.000 | [Br-].[Zn+]CCCOCc1ccccc1 | 100ml | 771375796
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TARGETMOL CHEMICALS INC BI-2852 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. BI-2852 is a KRAS inhibitor for the switch I/II pocket (SI/II-pocket) with nanomolar affinity. BI-2852 is leading to inhibition of downstream signaling and an antiproliferative effect in KRAS mutant cells. purity: 98%
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eMolecules 308796-24-9 | 2-(Thiomethyl)phenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01863640 | 315.480 | C7H7ISZn | 0.000 | [I-].CSc1ccccc1[Zn+] | 50ml | 532652986
2-(Thiomethyl)phenylzinc iodide, 0.50 M in THF | Synthonix | 308796-24-9 | MFCD01863640 | 315.480 | C7H7ISZn | 0.000 | [I-].CSc1ccccc1[Zn+] | 50ml | 532652986
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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