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Filtered Search Results
eMolecules 1209287-84-2 | 1-Methylpyrrolidin-3-amine dihydrochloride | Combi-Blocks | MFCD13195986 | 173.080 | C5H14Cl2N2 | 96.000 | Cl.Cl.CN1CCC(N)C1 | 1g | 388718244
1-Methylpyrrolidin-3-amine dihydrochloride | Combi-Blocks | 1209287-84-2 | MFCD13195986 | 173.080 | C5H14Cl2N2 | 96.000 | Cl.Cl.CN1CCC(N)C1 | 1g | 388718244
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Medchemexpress LLC 2-pyrrolidinemethanol, 1-methyl-, (2S)- | 34381-71-0 | MFCD00011727 | 99.3% | 115.17 g/mol | C6H13NO | 25 G
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(S)-N-Methylpyrrolidine-2-methanol is a chiral small-molecule research reagent used as the (S)-enantiomer of N-methyl-2-pyrrolidinemethanol. It is employed as a building block, intermediate, or reference standard in organic synthesis and life-science research, and is provided with analytical documentation validating purity and identity.
- Chiral (S)-enantiomer suitable for stereospecific synthesis.
- High purity (99.3% by GC) for analytical and synthetic applications.
- Chemical formula C6H13NO; molecular weight 115.17 g/mol.
- Commonly used as a building block, intermediate, or reference standard.
- Available in 25 g and 50 g packages for laboratory-scale work.
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Medchemexpress LLC C12-iE-DAP hydrochloride | 1269619-57-9 | 538.07 | 5 MG
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C12-iE-DAP hydrochloride is the hydrochloride salt form of C12-iE-DAP. This biologically active peptide functions as an agonist for NOD1, formed by adding a lauroyl (C12) group to the glutamic residue of iE-DAP.
- Biologically active peptide
- Functions as a NOD1 agonist
- Targets NOD-like receptor (NLR)
- Relevant to immunology and inflammation pathways
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Medchemexpress LLC Caroverine hydrochlo 100mg | 55750-05-5 | 100MG
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Caroverine hydrochloride is a potent competitive and reversible antagonist of NMDA and AMPA glutamate receptor Caroverine hydrochloride is also an antioxidant and calcium-blocking agent that exhibits vasorelaxant action Caroverine hydrochloride can be used for the research of inner ear tinnitus[1 [2 [3
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000746770 NH-BISC1-PEG1-BOC 1G
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![Medchemexpress LLC (2S)-N-(3,5-Dimethylphenyl)-1-[(4-methoxyphenyl)sulfonyl]-2-pyrrolidinecarboxamide | 1361321-96-1 | MFCD28502270 | 99.5% | 388.48 g/mol | C20H24N2O4S | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000248208.png-250.jpg)
Medchemexpress LLC (2S)-N-(3,5-Dimethylphenyl)-1-[(4-methoxyphenyl)sulfonyl]-2-pyrrolidinecarboxamide | 1361321-96-1 | MFCD28502270 | 99.5% | 388.48 g/mol | C20H24N2O4S | 100 MG
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ACT-462206 is a brain-penetrant dual orexin receptor antagonist used in preclinical research on insomnia, anxiety-related disorders, and addiction. It exhibits potent activity at orexin receptors and is supplied as a high-purity research chemical for laboratory studies. Not for human or veterinary use.
- Dual orexin receptor antagonist (OX1 and OX2)
- Brain-penetrant compound suitable for CNS research
- Potent activity: IC50 ≈ 60 nM (OX1), ≈ 11 nM (OX2)
- High purity suitable for laboratory use
- Storage: protect from light; in solvent store at -80°C (6 months) or -20°C (1 month)
- Available as solid or as 10 mM solution in DMSO
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000743990 BOC-NH-PEG8-CH2CH2CO 1G
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5000743992 AZIDO-PEG6-ACID 1G
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Medchemexpress LLC Tyrphostin AG490 | 134036-52-5 | MFCD00236452 | 99.7% | 294.30 | C17H14N2O3 | 1 ML
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(E/Z)-AG490 is a racemic mixture of the E and Z isomers of AG490, a small-molecule tyrosine kinase inhibitor used in biochemical and cellular research. It is employed to probe JAK/STAT signaling and related pathways due to reported inhibition of JAK2/3, STAT3, and EGFR.
- Racemic mixture of E and Z isomers.
- Small-molecule tyrosine kinase inhibitor for signaling research.
- Reported to inhibit JAK2/3, STAT3, and EGFR.
- Available as a concentrated solution for cell-based assays (10 mM in DMSO).
- High purity, 99.71%.
- Molecular weight 294.30 and formula C17H14N2O3.
- Offered in multiple solid and solution formats for assay flexibility.
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Medchemexpress LLC Boc-AEVD-CHO | 220094-15-5 | MFCD00210086 | 98.3% | 516.54 | 5 MG
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Boc-AEVD-CHO is a Caspase 8 inhibitor useful in the study of apoptosis and immune and inflammatory diseases. This compound is a white to off-white solid with a purity of 98.34%, intended for research use only.
- Caspase 8 inhibitor
- Useful for research into apoptosis
- Useful for research into immune and inflammatory diseases
- White to off-white solid appearance
- High purity of 98.34%
- Molecular weight of 516.54
- Sequence: Boc-Ala-Glu-Val-Asp-CHO
- Good solubility in DMSO (66.67 mg/mL)
- Stable storage conditions for powder and solvent forms
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Ambeed AMBEED
5000892684 S-N-METHYLPYRROLIDINE-2- 250MG
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Medchemexpress LLC BMS-1166 (hydrochloride) | 2113650-05-6 | 100.0% | 677.57 g/mol | C36H34Cl2N2O7 | 5 MG
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BMS-1166 hydrochloride is a small-molecule PD-1/PD-L1 immune checkpoint inhibitor that induces PD-L1 dimerization and blocks PD-1 binding. It exhibits potent biochemical activity in the low-nanomolar range and is supplied as a stable hydrochloride salt in solid form for research use in biochemical and cellular assays.
- Potent PD-1/PD-L1 interaction inhibitor with low-nanomolar activity.
- Hydrochloride salt, solid, white to off-white, suitable for handling.
- High purity appropriate for research applications.
- Stable as a powder under recommended storage conditions for extended shelf life.
- Intended for use in biochemical and cell-based immune checkpoint studies.
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5000733562 BOC-C17-COOH 250MG
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![Medchemexpress LLC 3-[4-methyl-2-[(Z)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid | 215543-92-3 | MFCD08235144 | >97.0% | 296.32 Da | C17H16N2O3 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000242563.png-250.jpg)
Medchemexpress LLC 3-[4-methyl-2-[(Z)-(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrol-3-yl]propanoic acid | 215543-92-3 | MFCD08235144 | >97.0% | 296.32 Da | C17H16N2O3 | 10 MG
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SU 5402 is a small-molecule, multi-targeted receptor tyrosine kinase inhibitor used in research to block VEGFR2, FGFR1, and PDGFRβ signaling. It exhibits nanomolar potency against VEGFR2 and FGFR1 and sub-micromolar activity against PDGFRβ, and is commonly used to study angiogenesis and growth factor pathways in vitro.
- Potent inhibition of VEGFR2, FGFR1, and PDGFRβ (IC50: 20 nM, 30 nM, 510 nM).
- Useful for studying angiogenesis and growth factor signaling in cell-based assays.
- Cell-permeable, ATP-competitive tyrosine kinase inhibitor.
- Molecular weight 296.32 Da and formula C17H16N2O3.
- Provided as a high-purity research reagent suitable for biochemical and cellular studies.
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Medchemexpress LLC Boc-Met-Leu-Phe-OH | 67247-12-5 | MFCD00037435 | 99.9% | 509.66 | C25H39N3O6S | 25 MG
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Boc-Met-Leu-Phe-OH is a formyl peptide receptor (FPR) antagonist that reduces superoxide production induced by fMLF, with an IC50 of 0.63 μM. It is supplied as a high-purity peptide for research use in studies of FPR signaling and neutrophil activation.
- Reduces fMLF-induced superoxide production (IC50 = 0.63 μM)
- High purity (99.9%)
- Molecular weight 509.66 g/mol
- Molecular formula C25H39N3O6S
- Available in small mg quantities for lab-scale studies
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