Azoles
Medchemexpress LLC HY-101524 100mg Medchemexpress, TC13172 CAS:2093393-05-4 Purity:>98%
Medchemexpress, HY-101524 100mg TC13172 CAS:2093393-05-4 TC13172 is a mixed lineage kinase domain-like protein ( MLKL ) inhibitor with an EC 50 value of 2 nM for HT-29 cells. 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.
Medchemexpress LLC SGC-CK2-1 | 2470424-39-4 | 99.7% | 375.43 | 50 MG
SGC-CK2-1 is a highly potent, ATP-competitive, and cell-active CK2 chemical probe. It shows exclusive selectivity for both human CK2 isoforms, with IC50s of 36 nM for CK2α and 16 nM for CK2α′ in the nanoBRET assay. This compound can be utilized for research into neurodegenerative diseases.
- Highly potent, ATP-competitive, and cell-active
- Exclusive selectivity for human CK2 isoforms
- Useful for neurodegenerative disease research
Medchemexpress LLC Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
Contezolid (MRX-I) | 1112968-42-9 | 99.2% | 408.33 | 50 MG
Medchemexpress LLC 7-BIA 10mg | 1313403-49-4 | 294.30 g/mol | C15H18O6 | 10 MG
7-BIA is a small-molecule inhibitor of receptor-type protein tyrosine phosphatase D (PTPRD) used for biochemical and cellular research. Reported activity: PTPRD IC50 ≈ 1-3 μM; PTPRS IC50 = 40 μM. Molecular formula C15H18O6; molecular weight 294.30 g/mol; purity 98.0%.
- Potent PTPRD inhibition (IC50 ≈ 1-3 μM)
- Also inhibits PTPRS (IC50 = 40 μM)
- High stated purity of 98.0%
- Supplied as solid and solution formats for flexible use
- Suitable for biochemical and cellular research applications
Accela Chembio Inc 1-butyl-2 | 3-dimethylimidazolium Tetrafluoroborate | 100g | 402846-78-0 | MFCD03427618 | 97+% | D: 1.198 | Shelf Life: 1260 Days | Light Sensitive/+4
1-butyl-2 | 3-dimethylimidazolium Tetrafluoroborate | 100g | 402846-78-0 | MFCD03427618 | 97+% | D: 1.198 | Shelf Life: 1260 Days | Light Sensitive/+4
Medchemexpress LLC HY-112302 5mg Medchemexpress, HC-070 CAS:1628291-95-1 Purity:>98%
Medchemexpress, HY-112302 5mg HC-070 CAS:1628291-95-1 HC-070 is an antagonist of TRPC4/TRPC5, with IC50s of 9.3 nM and 46 nM for hTRPC5 and hTRPC4 in cells, 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.
Medchemexpress LLC 1-Methylinosine | 2140-73-0 | 99.7% | 282.25 | 50 MG
1-Methylinosine is a modified nucleotide that plays a role in eukaryotic tRNA, specifically at position 37. As a metabolite derived from inosine, its elevated levels have been observed in urine samples from breast cancer models.
- Modified nucleotide for eukaryotic tRNA
- Metabolite derived from inosine
- Elevated levels observed in breast cancer models
- White to off-white solid appearance
Medchemexpress LLC (2R,4R)-2-(2-hydroxyphenyl)-3-(3-sulfanylpropanoyl)-1,3-thiazolidine-4-carboxylic acid | 80830-42-8 | MFCD00868438 | 99.6% | 313.39 g·mol⁻¹ | C13H15NO4S2 | 50 MG
Rentiapril is an orally active angiotensin-converting enzyme (ACE) inhibitor supplied for research and analytical applications. It is provided as a research reagent (not for human or clinical use) and is identified by CAS 80830-42-8. The compound has molecular formula C13H15NO4S2 and molecular weight 313.39 g·mol⁻¹.
- Orally active ACE inhibitor with antihypertensive activity.
- Supplied for research and analytical applications (not for human use).
- High purity reported (99.59%).
- Molecular weight 313.39 g·mol⁻¹.
- Chemical formula C13H15NO4S2.
- Available in multiple small pack sizes (5 mg-100 mg).
![eMolecules 163080-99-7 | 1-Carbobenzoxy-3-methylimidazolium triflate | J & W PharmLab, LLC | MFCD20265581 | 366.310 | C13H13F3N2O5S | 96.000 | [O-]S(=O)(=O)C(F)(F)F.C[n+]1ccn(c1)C(=O)OCc1ccccc1 | 5g | 250006001](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502155982.JPG-250.jpg)
eMolecules 163080-99-7 | 1-Carbobenzoxy-3-methylimidazolium triflate | J & W PharmLab, LLC | MFCD20265581 | 366.310 | C13H13F3N2O5S | 96.000 | [O-]S(=O)(=O)C(F)(F)F.C[n+]1ccn(c1)C(=O)OCc1ccccc1 | 5g | 250006001
1-Carbobenzoxy-3-methylimidazolium triflate | J & W PharmLab, LLC | 163080-99-7 | MFCD20265581 | 366.310 | C13H13F3N2O5S | 96.000 | [O-]S(=O)(=O)C(F)(F)F.C[n+]1ccn(c1)C(=O)OCc1ccccc1 | 5g | 250006001
eMolecules 23516-79-2 | 1-(4-Aminophenyl)-2,2,2-trifluoroethanone | MFCD05663790 | 1g
Medchem Express | Reynoutrin | 5mg | 451965818 | HY-N1354 | 549-32-6 | MFCD29050264 | 434.353 | C20H18O11
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Medchemexpress LLC SR2640 hydrochloride 50mg | 146662-42-2 | 50MG
SR2640 (hydrochloride) is a potent and selective competitive leukotriene D4/leukotriene E4 antagonist SR2640 can be used for researching the role of leukotrienes in human asthma[1
Medchemexpress LLC Sec61-IN-1 (compound A317) | 2484865-42-9 | 99.7% | 430.53 g/mol | C23H22N6OS | 5 MG
Sec61-IN-1 (compound A317) is a small-molecule inhibitor of the Sec61 translocon used as a research tool to study protein translocation and Sec61-mediated pathways. Manufacturer documentation reports molecular formula C23H22N6OS, molecular weight 430.53 g/mol, and purity of 99.7%. The compound has been reported to target glioma cells and to enhance T cell cytotoxic effects in experimental studies.
- High purity (99.7%) suitable for research use.
- Selective inhibition of Sec61-mediated protein translocation.
- Reported activity against glioma cells and enhancement of T cell cytotoxicity.
- Supplied as a five mg vial for small-scale in vitro or in vivo preparation.
- Includes supporting documentation: data sheet, certificate of analysis, and safety data sheet.
eMolecules 1965305-17-2 | 11,11,11-Trifluoro-undecylamine | Oakwood Chemical | MFCD29915583 | 225.299 | C11H22F3N | 90.000 | NCCCCCCCCCCC(F)(F)F | 1g | 537707874
11,11,11-Trifluoro-undecylamine | Oakwood Chemical | 1965305-17-2 | MFCD29915583 | 225.299 | C11H22F3N | 90.000 | NCCCCCCCCCCC(F)(F)F | 1g | 537707874
Medchemexpress LLC 2'3'-c-di-AM(PS)2 (Rp,Rp) enantiomer (ammonium salt) | 98.9% | 1 MG
This product is the less active enantiomer of 2'3'-c-di-AM(PS)2 (Rp,Rp). It is an activator of stimulator of interferon genes (STING) and is intended for research use only.
- Less active enantiomer
- Activates stimulator of interferon genes (STING)
- High purity of 98.9%
- Intended for research use only
- Ships at room temperature
- Solid form for storage