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Filtered Search Results
Medchemexpress LLC HY-16639 5mg Medchemexpress, ML314 CAS:1448895-09-7 Purity:>98%
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Medchemexpress, HY-16639 5mg ML314 CAS:1448895-09-7 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-14958A 5mg Medchemexpress, Pardoprunox (hydrochloride) CAS:269718-83-4 Purity:>98%
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Medchemexpress, HY-14958A 5mg Pardoprunox (hydrochloride) CAS:269718-83-4 Pardoprunox (SLV-308) hydrochloride is a partial dopamine D2 and D3 receptor partial agonist and a serotonin 5-HT1A receptor agonist, with pEC50s of 8, 9.2, and 6.3, respectively. 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-13032A 5mg Medchemexpress, GSK 525768A CAS:1260530-25-3 Purity:>98%
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Medchemexpress, HY-13032A 5mg GSK 525768A CAS:1260530-25-3 GSK 525768A is the inactive enantiomer of GSK525762A. GSK 525768A has no activity towards BET. 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-B0942 100mg Medchemexpress, Benzethonium chloride CAS:121-54-0 Purity:>98%
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Medchemexpress, HY-B0942 100mg Benzethonium chloride CAS:121-54-0 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-19998 5mg Medchemexpress, Taprenepag isopropyl CAS:1005549-94-9 Purity:>98%
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Medchemexpress, HY-19998 5mg Taprenepag isopropyl CAS:1005549-94-9 Taprenepag isopropyl is a highly selective EP2 receptor agonist. 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-18771 10mg Medchemexpress, O4I1 CAS:175135-47-4 Purity:>98%
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Medchemexpress, HY-18771 10mg O4I1 CAS:175135-47-4 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 Phenoxybenzamine hydrochloride | 63-92-3 | 99.5% | 50 MG
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Phenoxybenzamine hydrochloride is a nonselective, irreversible, orally active α-adrenoceptor antagonist. It is commonly used for the research of hypertension, specifically that caused by pheochromocytoma. It also demonstrates antitumor activity.
- Nonselective, irreversible, orally active α-adrenoceptor antagonist
- Used for research on hypertension caused by pheochromocytoma
- Demonstrates antitumor activity
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eMolecules 34574-69-1 | 3-Hydroxydodecanedioic Acid | Toronto Research Chemicals | MFCD16619163 | 246.303 | C12H22O5 | 95.000 | OC(CCCCCCCCC(O)=O)CC(O)=O | 100mg | 483413311
3-Hydroxydodecanedioic Acid | Toronto Research Chemicals | 34574-69-1 | MFCD16619163 | 246.303 | C12H22O5 | 95.000 | OC(CCCCCCCCC(O)=O)CC(O)=O | 100mg | 483413311
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Medchemexpress LLC 1-(5-chloronaphthalen-1-yl)sulfonyl-1,4-diazepane hydrochloride | 105637-50-1 | MFCD00065525 | 99.9% | 361.29 g/mol | C15H18Cl2N2O2S | 100 MG
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ML-9 is a small-molecule research inhibitor of Akt kinase that also inhibits myosin light-chain kinase (MLCK) and STIM1. It shows reported Ki values of 4 μM (MLCK), 32 μM (PKA), and 54 μM (PKC), and can induce autophagy by stimulating autophagosome formation. Intended for laboratory research use; handle and store under dry, sealed conditions.
- Inhibits Akt kinase, MLCK, and STIM1.
- Induces autophagy by stimulating autophagosome formation.
- High purity: 99.86%.
- Molecular weight: 361.29 g/mol.
- Chemical formula: C15H18Cl2N2O2S.
- Available as solids (including 100 mg) and 10 mM solutions in DMSO.
- Storage: solid at 4°C; in solvent -80°C (up to 6 months) or -20°C (up to 1 month).
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![Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000238246.png-250.jpg)
Medchemexpress LLC β-[4-([4-methyl-2-(4-(trifluoromethyl)phenyl)-5-thiazolyl]methoxy)phenyl]-3-isoxazolepropanoic acid | 1011531-27-3 | 99.0% | 488.48 | C24H19F3N2O4S | 10MG
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AM-4668 is a research-grade small-molecule agonist of GPR40 (FFAR1) used in preclinical studies relevant to type 2 diabetes. It activates human GPR40 with low-nanomolar potency in cell-based functional assays and is supplied as a solid for in vitro pharmacology and biochemical studies.
- Low-nanomolar potency at GPR40 (EC50 3.6 nM in A9 cells, 36 nM in CHO cells).
- Suitable for in vitro receptor activation and pharmacology studies.
- High purity solid (99.0%).
- Molecular weight 488.48 and formula C24H19F3N2O4S.
- Available in milligram quantities for laboratory use.
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Medchemexpress LLC Tibenelast sodium | 105102-18-9 | MFCD00864802 | >98.0% | 288.29 g·mol⁻¹ | C13H13NaO4S | 25 MG
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Tibenelast sodium is a small-molecule phosphodiesterase inhibitor supplied as the sodium salt for preclinical research. It is used to modulate cyclic nucleotide signaling in biochemical and cellular studies and is typically provided as a white to off-white solid suitable for dissolution in common organic solvents.
- Phosphodiesterase inhibition activity for PDE-related studies.
- Suitable for biochemical and cellular assays.
- Provided as a stable sodium salt to aid solubility in DMSO and other solvents.
- Commonly available in small research pack sizes for lab-scale experiments.
- Chemical identity confirmed (CAS 105102-18-9); consult the certificate of analysis for lot-specific purity.
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Medchemexpress LLC 1,3-Dimethoxybenzene | 151-10-0 | 99.99% | 138.17 | 100 MG
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1,3-Dimethoxybenzene is a volatile compound with a sweet, medicinal odor, carrying hazelnut, resinous, and woody notes. It has been identified as a new volatile component of Douro region grape musts and port wines.
- Possesses sweet medicinal, hazelnut, resinous, and woody aromas.
- Can be isolated from grape juice and Port wine.
- Maximum content reaches up to 19.4 μg/L in 1999 vintage Port wine.
- Primarily eluted in 60% hexane/40% diethyl ether fraction by flash chromatography.
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Strem, An Ascensus Company PHOSPHORUS (11AR)-10,11 50MG
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Phosphorus (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-bis[2,4,6-trisisopropylphenyl]-5-oxide-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin, 95% (99% ee)50mg
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![eMolecules 58546-54-6 | (6S,7S,13aR)-1,2,3,13-Tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[3',4']cycloocta[1',2':4,5]benzo[1,2-d][1,3]dioxol-6-ol | MFCD00865153 | 10mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502134040.JPG-250.jpg)
eMolecules 58546-54-6 | (6S,7S,13aR)-1,2,3,13-Tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[3',4']cycloocta[1',2':4,5]benzo[1,2-d][1,3]dioxol-6-ol | MFCD00865153 | 10mg
Ambeed | (6S,7S,13aR)-1,2,3,13-Tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[3',4']cycloocta[1',2':4,5]benzo[1,2-d][1,3]dioxol-6-ol | 10mg | 525041252 | A134812 | 58546-54-6 | MFCD00865153 | 416.470 | C23H28O7
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Medchemexpress LLC N-(3-((3-(5-chlorothiophene-2-sulfonamido)-4-methoxyindazol-1-yl)methyl)benzyl)-2-hydroxy-2-methylpropanamide | 1240516-71-5 | 99.8% | 549.06 | C24H25ClN4O5S2 | 25 MG
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GSK2239633A is a small-molecule CC-chemokine receptor 4 (CCR4) antagonist supplied for research use. It inhibits [125I]-TARC binding to human CCR4 with a reported pIC50 of 7.96 and shows activity in human CD4+ CCR4+ T-cells. The compound is provided as a solid with high reported purity and defined molecular formula and weight, suitable for in vitro pharmacology and analytical studies.
- Allosteric CCR4 antagonist with reported pIC50 ~7.96.
- Validated in vitro activity on human CD4+ CCR4+ T-cells.
- High reported purity suitable for research assays.
- Solid form, stable for analytical use.
- Contains defined molecular formula and molecular weight for characterization.
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