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Filtered Search Results
Medchemexpress LLC Nα,Nα-bis(carboxymethyl)-L-lysine | 113231-05-3 | MFCD00237437 | 98.8% | 262.26 | C10H18N2O6 | 10 G
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Nα,Nα-Bis(carboxymethyl)-L-lysine is a research-grade small molecule that competitively inhibits the bitter taste receptor T2R4, with a reported IC50 of approximately 59 nM. It is used in receptor pharmacology and cell-based assays to probe T2R4-mediated signaling; in vitro studies show reduction of basal receptor activity, while limited in vivo effects on bitter taste behavior have been reported.
- Competitive inhibitor of bitter taste receptor 4 (IC50 ≈59 nM).
- Suitable for receptor pharmacology and cell-based assays.
- Shown in vitro to reduce basal activity of constitutively active T2R4 mutants.
- Reported minimal in vivo effect on bitter taste licking behavior at 10 μM.
- High purity material (98.8%) for research use.
- Molecular weight 262.26; formula C10H18N2O6.
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eMolecules Ambeed / Methyl 3-amino-56-dichloropyrazine-2-carboxylate / 250mg / 552526635 / A108171 / / 1458-18-0 / MFCD00010431 / 222.030 / C6H5Cl2N3O2
Ambeed / Methyl 3-amino-56-dichloropyrazine-2-carboxylate / 250mg / 552526635 / A108171 / / 1458-18-0 / MFCD00010431 / 222.030 / C6H5Cl2N3O2
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Medchemexpress LLC HY-N3513 5mg Medchemexpress, Mulberrin CAS:62949-79-5 Purity:>98%
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Medchemexpress, HY-N3513 5mg Mulberrin CAS:62949-79-5 Mulberrin is a strong inhibitor of organic anion-transporting polypeptide 2B1 (OATP2B1)-mediated estrone-3-sulfate (E3S) uptake with an IC50 value being 1.8 ±1.5 μM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-N0339 100mg Medchemexpress, Syringic acid CAS:530-57-4 Purity:>98%
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Medchemexpress, HY-N0339 100mg Syringic acid CAS:530-57-4 Syringic acid is correlated with high antioxidant activity and inhibition of LDL oxidation. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Aobchem Phenol 2-bromo-4-methyl- 1-propanoate | ≥95% | CAS 939533-80-9 | C10H11BrO2 | 250mg
Phenol 2-bromo-4-methyl- 1-propanoate | ≥95% | CAS 939533-80-9 | C10H11BrO2 | 250mg
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Medchemexpress LLC GINKGOLIC ACID C13 5 mg
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GINKGOLIC ACID C13 5MG
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Aobchem 2-Fluoro-3-(methylthio)phenol | ≥97% | CAS 1243283-09-1 | C7H7FOS | 500mg
2-Fluoro-3-(methylthio)phenol | ≥97% | CAS 1243283-09-1 | C7H7FOS | 500mg
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Cospheric LLC MICROSPHRS0.96G/CC75-90UM-10G
NC3822453 MICROSPHRS0.96G/CC75-90UM-10G
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Medchemexpress LLC I-OME-TYRPHOSTIN AG 100 mg
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I-OME-TYRPHOSTIN AG 100MG
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Apexbio Technology LLC Salidroside 10338-51-9 20mg
Salidroside (CAS 10338-51-9) is a naturally occurring phenylpropanoid glycoside isolated primarily from Rhodiola species It exerts multiple biological effects through modulation of cellular pathways related to oxidative stress inflammation and apoptosis including activation of the PI3K/Akt signaling pathway and inhibition of pro-inflammatory mediators Salidroside has been shown to protect cells from oxidative damage modulate mitochondrial function and suppress inflammatory responses in various in vitro and in vivo models This compound is widely utilized in biomedical research investigating neuroprotection cardioprotection and potential therapeutic strategies targeting metabolic and neurodegenerative disorders
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Medchemexpress LLC Ko 143 | 461054-93-3 | MFCD19053160 | 99.9% | 469.57 g·mol⁻¹ | C26H35N3O5 | 50 MG
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Ko 143 is a potent, selective inhibitor of the ATP-binding cassette subfamily G member 2 (ABCG2/BCRP) used as a research reagent to investigate transporter-mediated drug efflux and multidrug resistance. It exhibits nanomolar activity in biochemical and cell-based assays and shows substantial selectivity versus other transporters. Supplied as a research-grade small molecule for laboratory use only.
- Potent ABCG2 inhibition at nanomolar concentrations.
- High selectivity over P-gp and MRP-1.
- Suitable for studies of transporter activity and drug resistance.
- Supplied in milligram quantities for laboratory experiments.
- Stable as powder when stored appropriately at low temperature.
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Medchemexpress LLC Tyrphostin AG1433 | 168835-90-3 | 99.1% | 5 MG
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Tyrphostin AG1433 is a small-molecule tyrosine kinase inhibitor used in preclinical research to selectively inhibit PDGFRβ and VEGFR-2. It is supplied as a high-purity research chemical suitable for biochemical and cell-based assays, with documented solubility in DMSO and common in vivo vehicle formulations.
- High purity suitable for sensitive assays.
- Molecular weight 266.29 g/mol and formula C16H14N2O2.
- High DMSO solubility (~62.5 mg/mL) and in vivo vehicle solubility ≥ 2.08 mg/mL.
- Useful for probing PDGFR and VEGFR signaling in vitro and in vivo models.
- Typically stored as a powder at low temperature to preserve stability.
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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 Topotecan HCl | 119413-54-6 | MFCD00866235 | 1g
Combi-Blocks | Topotecan HCl | 1g | 401042320 | QA-7182 | 97.000 | 119413-54-6 | MFCD00866235 | 457.910 | C23H24ClN3O5
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Medchemexpress LLC Honokiol dichloroacetate | 1620160-42-0 | 99.1% | 488.19 g/mol | C22H18Cl4O4 | 100MG
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Honokiol dichloroacetate is a bis-dichloroacetate ester analog of honokiol used as a small-molecule research reagent. It has demonstrated in vitro activity against human prostate cancer cells and is used as a biochemical tool compound to study mitochondrial and androgen receptor-related pathways.
- Dichloroacetate ester of honokiol.
- Reported to inhibit prostate cancer cell growth in vitro.
- Reduces androgen receptor (AR) protein levels in cell studies.
- High purity (99.1%) determined by RP-HPLC.
- Molecular weight 488.19 g/mol; formula C22H18Cl4O4.
- Available in multiple pack sizes, including 100 mg.
- Intended for research use only.
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