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Filtered Search Results
MEDCHEMEXPRESS LLC L-CYSTEINE METHYL ESTER HYDRO
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501874312 L-CYSTEINE METHYL ESTER HYDRO
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eMolecules 25134-21-8 | METHYL-5-NORBORNENE-2,3-DICARBOXYLIC ANHYDRIDE (MIXTURE OF ISOMERS) | AstaTech | MFCD00135202 | 178.187 | C10H10O3 | 95.000 | CC12C3CC(C=C3)C1C(=O)OC2=O | 25g | 718076220
METHYL-5-NORBORNENE-2,3-DICARBOXYLIC ANHYDRIDE (MIXTURE OF ISOMERS) | AstaTech | 25134-21-8 | MFCD00135202 | 178.187 | C10H10O3 | 95.000 | CC12C3CC(C=C3)C1C(=O)OC2=O | 25g | 718076220
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Apexbio Technology LLC CA-074 Me 147859-80-1 25mg
CA-074 Me (CAS 147859-80-1) is a cell-permeable methyl ester derivative of CA-074 functioning primarily as a selective inhibitor of cathepsin B It exhibits potent inhibitory activity against cathepsin B (IC50 36 3 nM) In cultured human gingival fibroblasts CA-074 Me effectively suppresses cathepsin B activity while moderately reducing combined cathepsin B and L activities Under strong reducing conditions (e g presence of DTT or GSH) CA-074 Me inhibits cathepsin L substantially Thus it is widely utilized in biomedical research to study lysosomal enzyme functions and roles of cathepsins in cellular processes
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eMolecules 868-84-8 | S,S'-Dimethyl dithiocarbonate | Combi-Blocks, Inc. | MFCD00144163 | 122.200 | C3H6OS2 | 97.000 | CSC(=O)SC | 5g | 603153628
S,S'-Dimethyl dithiocarbonate | Combi-Blocks, Inc. | 868-84-8 | MFCD00144163 | 122.200 | C3H6OS2 | 97.000 | CSC(=O)SC | 5g | 603153628
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Medchemexpress LLC HY-N0480A 100mg Medchemexpress, Reserpine (hydrochloride) CAS:16994-56-2 Purity:>98%
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Medchemexpress, HY-N0480A 100mg Reserpine (hydrochloride) CAS:16994-56-2 Reserpine hydrochloride is an inhibitor of the vesicular monoamine transporter 2 ( VMAT2 ). 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 Sulfadiazine sodium | 547-32-0 | 98.0% | 500 MG
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Sulfadiazine sodium is a sulfonamide antibiotic with antimalarial activity. It is used for toxoplasmosis research, targeting bacteria and parasites in anti-infection pathways.
- Sulfonamide antibiotic
- Antimalarial activity
- Used for toxoplasmosis research
- Targets bacteria and parasites
- Involved in anti-infection pathways
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eMolecules 13110-37-7 | Pentyl 4-aminobenzoate | Combi-Blocks | MFCD00455845 | 207.273 | C12H17NO2 | 98.000 | CCCCCOC(=O)c1ccc(N)cc1 | 1g | 415500556
Pentyl 4-aminobenzoate | Combi-Blocks | 13110-37-7 | MFCD00455845 | 207.273 | C12H17NO2 | 98.000 | CCCCCOC(=O)c1ccc(N)cc1 | 1g | 415500556
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Medchemexpress LLC Diethyl maleate | 141-05-9 | MFCD00009191 | 98.1% | 172.18 | C8H12O4 | 10g
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Diethyl maleate (DEM) is an orally available effective glutathione (GSH) depletor that crosses the blood-brain barrier Diethyl maleate covalently binds irreversibly to GSH via glutathione S-transferase with an in vitro IC50 of 0 1-0 5 mM Diethyl maleate selectively depletes GSH in liver lung and brain tissues exacerbating oxidative stress and enhancing hyperbaric oxygen toxicity Diethyl maleate promotes precursor amino acid uptake and in turn promotes GSH synthesis by upregulating the activity of the cystine-glutamate transporter XO- Diethyl maleate can be used to study redox homeostasis and GSH protection mechanisms in oxidative stress-related diseases such as hyperbaric oxygen injury and metabolic diseases[1][2][3]
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Apexbio Technology LLC Mepyramine maleate 59-33-6 10mM (in 1mL DMSO)
Mepyramine maleate (CAS 59-33-6) is a selective antagonist of the histamine H1 receptor exhibiting dissociation constants of 0 8 nM for H1 5200 nM for H2 and over 3000 nM for H3 receptors By blocking H1 receptor-mediated signaling it modulates pathways involved in allergic responses Mepyramine maleate is commonly utilized in experimental models of allergic diseases to investigate histamine-related mechanisms and to delineate the role of H1 receptor activity in immunological and inflammatory processes
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Medchemexpress LLC Bgt226 maleate | 1245537-68-1 | MFCD22124895 | 99.9% | C32H29F3N6O6 | 10MG
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BGT226 maleate is a research-grade small-molecule inhibitor of class I PI3K isoforms and mTOR, used to probe PI3K/mTOR signaling in cellular and biochemical studies. The compound is supplied as a high-purity solid salt for laboratory research use only and is provided with recommended storage conditions and analytical quality data.
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Apexbio Technology LLC Timolol Maleate 26921-17-5 10mM (in 1mL DMSO)
Timolol Maleate (CAS 26921-17-5) is the maleate salt form of the (S)-enantiomer of Timolol a potent non-selective -adrenergic receptor antagonist It exhibits high binding affinity toward both 1 and 2 adrenergic receptor subtypes with reported Ki values of approximately 1 97 nM ( 1) and 2 0 nM ( 2) Timolol maleate functions by competitively blocking adrenergic signaling pathways thus modulating sympathetic nervous system activities It is widely utilized in biomedical research to investigate -adrenergic signal transduction mechanisms and associated physiological processes including cardiac function and ophthalmic conditions
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Medchemexpress LLC Tris (maleate) | 72200-76-1 | MFCD00082442 | 98.0% | 237.21 g/mol | C8H15NO7 | 10 G
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Tris (maleate) is the maleate salt of tris(hydroxymethyl)aminomethane used as a buffering agent in biochemical and cell biology applications. It stabilizes pH in growth media, tissue preparations, and washing or diluent solutions, and is supplied as a highly soluble reagent to support reproducible experimental workflows.
- Buffered pH support for media and tissue preparations.
- Water-soluble; also soluble in DMSO with sonication if needed.
- High purity: 98.0%.
- Suitable for use as a diluent or washing buffer.
- Available in laboratory-scale package sizes such as 10 G.
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Apexbio Technology LLC L-693,403 maleate 207455-21-8 10mg
L-693 403 maleate (CAS 207455-21-8) is a small molecule exhibiting high affinity and selectivity for sigma ( ) receptors By modulating receptor-mediated signaling pathways it influences neuronal signal transduction at the molecular level Preclinical studies indicate that L-693 403 maleate possesses analgesic properties likely through its regulatory effects on neural activity Owing to these pharmacological characteristics it is utilized in exploratory research on neurological disorders supporting its value as a tool compound in the investigation of neural modulation mechanisms
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eMolecules 628-48-8 | TRANS-GLUTACONIC ACID | AstaTech | MFCD00002784 | 130.099 | C5H6O4 | 95.000 | OC(=O)C\C=C\C(O)=O | 0.25g | 718059738
TRANS-GLUTACONIC ACID | AstaTech | 628-48-8 | MFCD00002784 | 130.099 | C5H6O4 | 95.000 | OC(=O)C\C=C\C(O)=O | 0.25g | 718059738
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Medchemexpress LLC Ciproxifan (maleate) | 184025-19-2 | MFCD06411563 | 99.7% | 386.40 g/mol | C20H22N2O6 | 10 MG
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Ciproxifan maleate is a potent, selective, orally bioavailable competitive antagonist of the histamine H3 receptor supplied as a white to off-white powder for research use. It is used as an analytical standard and research reagent in neuroscience and aging-disease studies, with reported nanomolar potency.
- Potent H3 receptor antagonist (IC50 ≈ 9.2 nM)
- High purity (≈ 99.7%)
- Provided as a powdered maleate salt for stability and handling
- Suitable for neuroscience and Alzheimer's disease research
- Available in small pack sizes for analytical and screening use
- Includes CAS number 184025-19-2 and molecular weight 386.40 g/mol
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