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Filtered Search Results
Apexbio Technology LLC AS 2034178 10MG
AS 2034178 10MG APEXBIO TECHNOLOGIES
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eMolecules 3946-91-6 | 2,2'-((1,2-Phenylenebis(azanylylidene))bis(methanylylidene))diphenol | MFCD00009995 | 25g
Medchem Express | Imidapril (hydrochloride) | 10mg | 446273910 | HY-B1451 | 89396-94-1 | MFCD00923828 | 441.910 | C20H28ClN3O6
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eMolecules Building Block Tool<|a>
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Medchemexpress LLC TRPV4 agonist-1 free 10mg | 2314467-59-7 | 10 MG
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TRPV4 agonist-1 free base is a small-molecule agonist of the transient receptor potential vanilloid 4 (TRPV4) ion channel. It activates human TRPV4 with an EC50 of 60 nM in calcium mobilization assays and is supplied for research use only.
- Activates human TRPV4 with EC50 of 60 nM in calcium mobilization assay.
- Measured by intracellular Ca2+ increase in HEK293 cells using Fura-2 AM probe.
- Molecular formula C25H22F2N4O2; molecular weight 448.46 g/mol.
- High reported purity (~99.7%).
- Available in multiple mg-scale sizes for laboratory research applications.
- Intended for laboratory research use only, not for human use.
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Medchemexpress LLC Nitroflurbiprofen 100mg | 100mg
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Nitroflurbiprofen is a cyclooxygenase (COX) inhibitor with nitric oxide (NO)-donating properties modulates the increased intrahepatic vascular tone in portal hypertensive cirrhotic rats
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Medchemexpress LLC HY-112125A 5mg Medchemexpress, KRN2 (bromide) CAS:1390654-28-0 Purity:>98%
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Medchemexpress, HY-112125A 5mg KRN2 (bromide) CAS:1390654-28-0 KRN2 (bromide) is a selective inhibitor of nuclear factor of activated T cells (NFAT5), with an IC50 of 0.1 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 SLMP53-2 | 1826116-38-4 | C26H22N2O2 | 5 MG
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SLMP53-2 is a mutant p53 reactivator that restores wild-type-like conformation and DNA-binding ability of mutp53-Y220C by enhancing its interaction with Hsp70, leading to the reestablishment of p53 transcriptional activity. It can induce cell cycle arrest, apoptosis, and endoplasmic reticulum (ER) stress, and exhibits antitumor activity.
- Restores wild-type-like function to mutant p53.
- Enhances interaction with Hsp70 to reestablish p53 transcriptional activity.
- Induces cell cycle arrest, apoptosis, and endoplasmic reticulum (ER) stress.
- Exhibits antitumor activity.
- Inhibits growth of various cancer cell lines.
- Reduces tumor volume and weight in xenograft mouse models.
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eMolecules 176317-02-5 | 1-Bromo-2,3,4-trifluorobenzene | Ambeed | MFCD00013248 | 210.981 | C6H2BrF3 | 98.000 | Fc1ccc(Br)c(F)c1F | 5g | 552750317
1-Bromo-2,3,4-trifluorobenzene | Ambeed | 176317-02-5 | MFCD00013248 | 210.981 | C6H2BrF3 | 98.000 | Fc1ccc(Br)c(F)c1F | 5g | 552750317
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![eMolecules ChemScene / Chlorodimethyl[3-(23456-pentafluorophenyl)propyl]silane / 1g / 717420346 / CS-0214166 / 0.000 / 157499-19-9 / MFCD00054911 / 302.740 / C11H12ClF5Si](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502482562.JPG-250.jpg)
eMolecules ChemScene / Chlorodimethyl[3-(23456-pentafluorophenyl)propyl]silane / 1g / 717420346 / CS-0214166 / 0.000 / 157499-19-9 / MFCD00054911 / 302.740 / C11H12ClF5Si
ChemScene / Chlorodimethyl[3-(23456-pentafluorophenyl)propyl]silane / 1g / 717420346 / CS-0214166 / 0.000 / 157499-19-9 / MFCD00054911 / 302.740 / C11H12ClF5Si
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Medchemexpress LLC Tetrahydrodeoxycorticosterone | 567-03-3 | MFCD00067604 | 99.5% | 334.49 g/mol | C21H34O3 | 5 MG
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Tetrahydrodeoxycorticosterone (THDOC) is an endogenous neurosteroid and a potent positive allosteric modulator of the GABAA receptor. It demonstrates strong neuroinhibitory effects and is used in biochemical and pharmacological research to investigate GABAergic signaling, neurosteroid modulation, and central nervous system activity. Handle according to safety data sheet recommendations and store protected from light.
- Potent positive allosteric modulator of GABAA receptor.
- Used to study GABAergic signaling and neurosteroid mechanisms.
- Exhibits neuroinhibitory, sedative, and anxiolytic activity.
- Supplied as a research-grade solid with specified purity (≈99.5%).
- Store protected from light at 4°C; in solvent: -80°C up to 6 months.
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eMolecules 765917-27-9 | 4-chloro-2-fluorophenylboronic aicd, pinacol ester | Combi-Blocks | MFCD18729919 | 256.510 | C12H15BClFO2 | 98.000 | CC1(C)OB(OC1(C)C)c1ccc(Cl)cc1F | 1g | 117544455
4-chloro-2-fluorophenylboronic aicd, pinacol ester | Combi-Blocks | 765917-27-9 | MFCD18729919 | 256.510 | C12H15BClFO2 | 98.000 | CC1(C)OB(OC1(C)C)c1ccc(Cl)cc1F | 1g | 117544455
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Medchemexpress LLC 2-chloro-6-fluorobenzaldehyde | 387-45-1 | MFCD00003306 | 99.7% | 158.56 | C7H4ClFO | 50 G
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2-Chloro-6-fluorobenzaldehyde (CAS 387-45-1) is a halogenated benzaldehyde used as an intermediate and reagent in organic and medicinal chemistry. It is provided as a high-purity material suitable for research and synthesis.
- High purity appropriate for research use (99.7%).
- Molecular formula C7H4ClFO; molecular weight 158.56.
- Commonly used as an intermediate in organic synthesis and medicinal chemistry.
- Available in multiple pack sizes to support small-scale and scaled-up needs.
- Product documentation available including certificate of analysis.
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Medchemexpress LLC Racemic MEM 1003 | 165187-25-7 | 99.6% | 10 MG
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(Rac)-MEM 1003 is the racemate of MEM 1003, a dihydropyridine L-type calcium channel antagonist (CAS 165187-25-7) used in neuroscience research. The compound has formula C22H25ClN2O5 and molecular weight 432.9 g·mol⁻¹, and is supplied at high purity for research applications.
- Racemic form of MEM 1003, a dihydropyridine calcium channel antagonist.
- Potent L-type Ca2+ channel antagonist; useful in neuronal signaling studies.
- High purity suitable for research use.
- Available in small-scale quantities (e.g., 5 mg-100 mg) with larger sizes by request.
- Certificate of analysis, datasheet, and safety data sheet available.
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Medchemexpress LLC Canertinib dihydrochloride | 289499-45-2 | MFCD09954112 | 558.86 g/mol | C24H27Cl3FN5O3 | 500 MG
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Canertinib dihydrochloride is an irreversible inhibitor of epidermal growth factor receptor (EGFR) and ErbB2 (HER2) tyrosine kinases used in preclinical biochemical and cellular studies to probe receptor signaling and kinase inhibition mechanisms.
- Irreversible EGFR and ErbB2 inhibition suitable for kinase studies.
- Applicable to biochemical and cellular assay workflows.
- Molecular formula C24H27Cl3FN5O3; molecular weight 558.86 g/mol.
- Storage: keep sealed and away from moisture; in solution, store frozen as recommended.
- Provided as a research-grade reagent; consult the product datasheet for handling and safety information.
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eMolecules 94010-78-3 | 2,2-Difluoro-2-(4-fluorophenyl)acetic acid | ChemScene | MFCD11167795 | 190.121 | C8H5F3O2 | 98.000 | OC(=O)C(F)(F)c1ccc(F)cc1 | 1g | 582648183
2,2-Difluoro-2-(4-fluorophenyl)acetic acid | ChemScene | 94010-78-3 | MFCD11167795 | 190.121 | C8H5F3O2 | 98.000 | OC(=O)C(F)(F)c1ccc(F)cc1 | 1g | 582648183
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Matrix Scientific 4-FLUOROPHENETHYL ALCOHOL4-F-5
4-fluorophenethyl Alcohol Mf C8h9fo Mw 140.16 Cas 7589-27-7 Mdl MFCD00002898
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