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Filtered Search Results
Medchemexpress LLC Droxidopa | 23651-95-8 | MFCD00799030 | 98.8% | C9H11NO5 | 10MG
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Droxidopa (L-DOPS) is an orally active precursor of norepinephrine used in research to evaluate orthostatic hypotension, noradrenergic pathways, and related pharmacology. Supplied as an analytical-grade reagent for biochemical, pharmacological, and assay-development applications.
- Orally active norepinephrine precursor for research use.
- High purity suitable for analytical and pharmacological studies.
- Chemical formula C9H11NO5; molecular weight 213.19 g·mol-1.
- CAS 23651-95-8 for unambiguous identification.
- Packaged in small sizes convenient for assay development and standards.
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eMolecules 8015-61-0 | Aloin (Mixture of A and B) | MFCD00151160 | 25g
Ambeed | Aloin (Mixture of A and B) | 25g | 600833537 | A201696 | 8015-61-0 | MFCD00151160 | 418.398 | C21H22O9
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000370391 SWTX-143 25MG
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Medchemexpress LLC Dehydroxymethylepoxyquinomicin | 287194-40-5 | 99.8% | 261.23 | 2 MG
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Dehydroxymethylepoxyquinomicin, also known as (-)-DHMEQ, is a potent, selective, and irreversible NF-κB inhibitor that covalently binds to a cysteine residue. This chemical compound is known to inhibit the nuclear translocation of NF-κB, which plays a crucial role in various cellular processes. It exhibits significant anti-inflammatory and anticancer activities.
- Potent and selective NF-κB inhibitor
- Irreversibly binds to a cysteine residue
- Inhibits nuclear translocation of NF-κB
- Exhibits anti-inflammatory activity
- Demonstrates anticancer activity
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Medchemexpress LLC ML-109 | 1186649-91-1 | 99.0% | 523.58 | 50 MG
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ML-109 is identified as a potent and full agonist of the thyroid stimulating hormone receptor (TSHR), exhibiting an EC50 of 40 nM. While being surprisingly stable under neutral and basic conditions with a half-life of approximately 16 hours, it degrades at lower pH levels, with a half-life of about 3 hours. It shows no activity at FSHR or LHCGR.
- Potent and full thyroid stimulating hormone receptor (TSHR) agonist
- EC50 of 40 nM for TSHR
- No activity at FSHR or LHCGR
- Stable at neutral and basic conditions (t1/2 of ~16 h)
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Selleck Chemical LLC 2 4-Dihydroxybenzoic acid
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2 4-Dihydroxybenzoic acid ( -resorcylic acid p-Hydroxysalicylic acid) is a degradation product of cyanidin glycosides from tart cherries in cell cultures and a metabolite found in human plasma after cranberry juice consumption
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000427383 -10-HYDROXYCAMPTO 50MG
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Cospheric LLC MICROSPHRS0.96G/CC75-90UM-10G
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NC3822453 MICROSPHRS0.96G/CC75-90UM-10G
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eMolecules 110623-72-8 | Medchem Express | Epimedin A | 5mg | 446274882 | HY-N0257 | MFCD30496681 | 838.809 | C39H50O20
Medchem Express | Fodipir | 10mg | 536983846 | HY-108869 | 118248-91-2 | MFCD00868476 | 638.460 | C22H32N4O14P2
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eMolecules 693288-97-0 | Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | MFCD12912405 | 406.82 | C22H15ClN2O4
Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | 693288-97-0 | MFCD12912405 | 406.820 | C22H15ClN2O4
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eMolecules 116183-66-5 | Medchem Express | Complanatuside | 5mg | 446275595 | HY-N1444 | MFCD20527287 | 624.548 | C28H32O16
Ambeed | 4-Chloro-2-methyl-18-naphthyridine | 100mg | 525877529 | A423508 | 1221272-96-3 | MFCD16140201 | 178.620 | C9H7ClN2
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eMolecules 57852-57-0 | Medchem Express | Idarubicin (hydrochloride) | 5mg | 446268293 | HY-17381 | MFCD00897212 | 533.96 | C26H28ClNO9
Medchem Express | Idarubicin (hydrochloride) | 5mg | 446268293 | HY-17381 | 57852-57-0 | MFCD00897212 | 533.960 | C26H28ClNO9
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Enzo Life Sciences Tyrphostin AG 527 (25mg). CAS: 133550-32-0
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Alternative name: Tyrphostin B44, (-)-(R)-N-(alpha-Methylbenzyl)-3,4-dihydroxybenzylidenecyanoacetamide. Formula: C18H16N2O3. MW: 308.3. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO or 100% ethanol. Long Term Storage: -20°C. Handling: Store tightly sealed in the dark. Protect from light.
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ALADDIN SCIENTIFIC CORPORATION Phenol, 100g
Phenol 99%Cas-108-95-2
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Medchemexpress LLC 4-O-Methyl honokiol | 68592-15-4 | 280.36 | 100 MG
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4-O-Methyl honokiol is a natural neolignan isolated from *Magnolia officinalis*. It acts as a PPARγ agonist and inhibits NF-κB activity, making it suitable for cancer and inflammation research.
- Natural neolignan isolated from *Magnolia officinalis*.
- Functions as a PPARγ agonist.
- Inhibits NF-κB activity.
- Suitable for cancer and inflammation research.
- Available in various quantities and formulations.
- Detailed information on solubility and stock solution preparation for experiments.
- Supports research with related antibodies and screening libraries.
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