Triazines
eMolecules J W PharmLab LLC 9-Hydroxy-3-aza-spiro[5 5]undecane-3-carboxylic acid tert-butyl ester 250mg 491379838 60R0759 96 000 918644-73-2 MFCD12755293 269 385 C15H27NO3
J W PharmLab LLC 9-Hydroxy-3-aza-spiro[5 5]undecane-3-carboxylic acid tert-butyl ester 250mg 491379838 60R0759 96 000 918644-73-2 MFCD12755293 269 385 C15H27NO3
Medchemexpress LLC Aza-cybz | 95.2% | 802.23 | C43H49ClIN3O2 | 10 MG
Aza-CyBz is a NaCl-responsive near-infrared fluorescent probe used to detect and visualize salt-induced stress in plant samples. It forms ordered J-aggregates with NaCl through electrostatic interaction, producing near-infrared fluorescence quenching with a reported detection limit of 170 μM. Supplied for research use, the compound is provided in milligram-scale quantities for laboratory studies.
- Responds selectively to NaCl via J-aggregate formation.
- Near-infrared fluorescence quenching enables imaging of salt stress.
- Detection limit approximately 170 μM.
- Molecular formula C43H49ClIN3O2; molecular weight 802.23.
- Purity approximately 95.2% as supplied.
- Store sealed at 4°C, protected from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
Selleck Chemical LLC VY-3-135-E1147-1G
VY-3-135 a potent ACSS2 inhibitor with IC50 of 44 3 85 nM potently inhibits ACSS2 dependent fatty acid metabolism but has no effect on gene expression in tumors
![Medchemexpress LLC Imidazo[1,2-a]-1,3,5-triazin-4(3H)-one, 2-amino- | 67410-64-4 | 99.86% | 151.13 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000439488-Logo.png-250.jpg){kind=logo}
Medchemexpress LLC Imidazo[1,2-a]-1,3,5-triazin-4(3H)-one, 2-amino- | 67410-64-4 | 99.86% | 151.13 | 25 MG
5-Aza-7-deazaguanine is a substrate for wild-type (WT) E. coli purine nucleoside phosphorylase and its Ser90Ala mutant in the synthesis of base-modified nucleosides. It is for research use only.
- For research use only
- Substrate for wild-type (WT) E. coli purine nucleoside phosphorylase
- Substrate for Ser90Ala mutant in the synthesis of base-modified nucleosides
eMolecules J W PharmLab LLC 9-Hydroxy-3-aza-spiro[5 5]undecane-3-carboxylic acid tert-butyl ester 500mg 491379837 60R0759 96 000 918644-73-2 MFCD12755293 269 385 C15H27NO3
J W PharmLab LLC 9-Hydroxy-3-aza-spiro[5 5]undecane-3-carboxylic acid tert-butyl ester 500mg 491379837 60R0759 96 000 918644-73-2 MFCD12755293 269 385 C15H27NO3
Medchemexpress LLC 5-aza-4'-thio-2'-deoxycytidine | 169514-76-5 | 99.1% | C8H12N4O3S | 10MG
5-Aza-4'-thio-2'-deoxycytidine is a sulfur-containing deoxycytidine analog and DNA methyltransferase inhibitor used in preclinical research to induce DNA hypomethylation and evaluate antitumor activity. It is supplied as a high-purity solid suitable for laboratory studies and requires low-temperature storage for stability.
- High purity (99.09%) for research applications.
- White to off-white solid appearance.
- Molecular formula C8H12N4O3S; molecular weight 244.27 g/mol.
- Powder stable at -20°C for long-term storage.
- In-solution storage: -80°C for 6 months, -20°C for 1 month.
Medchemexpress LLC NS-638 | 150493-34-8 | 99.8% | 325.72 g/mol | C15H11ClF3N3 | 50 MG
NS-638 is a small nonpeptide calcium channel blocker used in research to inhibit K+-stimulated intracellular Ca2+ elevation (IC50 = 3.4 μM). It is supplied with high reported purity and is available as a powder or ready-to-use DMSO solutions for use in biochemical and cellular assays.
- High purity suitable for biochemical and cellular assays.
- Blocks K+-stimulated intracellular Ca2+ elevation (IC50 3.4 μM).
- Available as powder and as DMSO solution for easy reconstitution.
- Provides long-term stability when stored under recommended conditions.
- Intended for in vitro pharmacology and calcium channel studies.
Medchemexpress LLC 2-amino-1-(4-chlorobenzyl)-5-trifluoromethylbenzimidazole | 150493-34-8 | 99.8% | 325.72 g·mol⁻1 | C15H11ClF3N3 | 1 ML
NS-638 is a small nonpeptide Ca2+-channel blocker used in research to inhibit K+-stimulated intracellular calcium elevation. It is commonly employed in in vitro pharmacology studies of voltage-gated calcium channels and calcium-dependent cellular responses.
- Small nonpeptide Ca2+-channel blocker suitable for in vitro studies.
- Blocks K+-stimulated intracellular Ca2+ elevation with IC50 = 3.4 μM.
- Molecular formula C15H11ClF3N3; molecular weight 325.72 g·mol⁻1.
- High reported purity (≈99.8%).
- Available as a 10 mM solution in DMSO (1 mL) and in multiple solid weights for flexibility.