Triazines
eMolecules 238759-98-3 | Ambeed | (4S5R)-45-Diphenyl-2-(pyridin-2-yl)-45-dihydrooxazole | 100mg | 600829190 | A1258481 | 300.361 | C20H16N2O
Ambeed | 3-Cyclopropylacrylic acid | 250mg | 624122669 | A470339 | 5687-78-5 | MFCD03002773 | 112.128 | C6H8O2
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Medchemexpress LLC TRIA-662 iodide | 6456-44-6 | 99.78% | 264.06 | 500 MG
TRIA-662 iodide is a chemical compound from MEDCHEMEXPRESS LLC with a purity of 99.78% and a molecular weight of 264.06.
Selleck Chemical LLC ZM241385-10mg
ZM-241385 is a high affinity antagonist ligand selective for the adenosine A2A receptor.
Medchemexpress LLC 5-aza-4'-thio-2'-deoxycytidine | 169514-76-5 | 99.1% | 244.27 g/mol | C8H12N4O3S | 5 MG
5-Aza-4'-thio-2'-deoxycytidine is a sulfur-containing deoxycytidine analog used as a research reagent that acts as a DNA methyltransferase 1 (DNMT1) inhibitor with DNA hypomethylating and antitumor potential. It is supplied as a powder for laboratory use, with stability data for powder and solution storage.
- High purity (99.09%).
- Orally active DNMT1 inhibitor; useful in DNA hypomethylation studies.
- Sulfur-containing deoxycytidine analog; formula C8H12N4O3S; MW 244.27 g/mol.
- Powder form; powder storage at -20°C (stable ~3 years); in solvent: -80°C for 6 months, -20°C for 1 month.
Chem-Impex International, Inc. 4-(4,6-Dimethoxy-1,3,5-triazine-2-yl)-4-methylmorpholinium chloride | MFCD03613550 | 25G
4-(4,6-Dimethoxy-1,3,5-triazine-2-yl)-4-methylmorpholinium chloride , PURITY LIMIT: 99% (HPLC) , MOLECULAR WEIGHT:276.72 , 3945-69-5 , MFCD03613550 , 25g
Medchemexpress LLC Methyl 1H-1,2,4-triazole-5-carboxylate | 4928-88-5 | 127.10 | 100 G
Methyl 1H-1,2,4-triazole-5-carboxylate is a biochemical reagent suitable for life science related research. It is designed for research use only and is not sold to patients. This product presents as a white to off-white solid.
- Biochemical reagent for life science research
- Solid appearance
- White to off-white color
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In-solvent storage: -80°C for 6 months, -20°C for 1 month
eMolecules 313545-40-3 | 4-Isopropoxy-2-(trifluoromethyl)phenylboronic acid | MFCD04972373 | 1g
Ambeed | 1-(3-(Trifluoromethyl)-56-dihydro-[124]triazolo[43-a]pyrazin-7(8H)-yl)-4-(245-trifluorophenyl)butane-13-dione | 1g | 552525323 | A107286 | 764667-65-4 | MFCD11111443 | 406.288 | C16H12F6N4O2
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TARGETMOL CHEMICALS INC VY-3-135 5MG
Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. VY-3-135 is an orally active, stable and specific acetyl-CoA synthetase 2 (ACSS2) inhibitor with IC50 of 44 nM, showing no inhibitory activity against recombinant human ACSS1 or ACSS3. VY-3-135 can effectively inhibit ACSS2-dependent fatty acid metabolism but has no effect on gene expression in tumors. Purity 99.25%
=O)B1OC(C)(C)C(C)(C)O1 | 1g | 117545527](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502190543.JPG-250.jpg)
eMolecules 1218791-22-0 | 4-N-Butylamino-3-nitrophenylboronic acid, pinacol ester | Combi-Blocks | MFCD12913979 | 320.200 | C16H25BN2O4 | 98.000 | CCCCNc1ccc(cc1[N+]([O-])=O)B1OC(C)(C)C(C)(C)O1 | 1g | 117545527
4-N-Butylamino-3-nitrophenylboronic acid, pinacol ester | Combi-Blocks | 1218791-22-0 | MFCD12913979 | 320.200 | C16H25BN2O4 | 98.000 | CCCCNc1ccc(cc1[N+]([O-])=O)B1OC(C)(C)C(C)(C)O1 | 1g | 117545527
Medchemexpress LLC 5-Aza-4'-thio-2'-deoxycytidine | 169514-76-5 | 99.1% | 244.27 | 25 MG
5-Aza-4'-thio-2'-deoxycytidine (5-Aza-T-dCyd) is an orally active DNA methyltransferase I (DNMT1) inhibitor. It is a sulfur-containing deoxy-cytidine analog with potential for DNA hypomethylating and antitumor effects.
- Orally active DNA methyltransferase I (DNMT1) inhibitor
- Sulfur-containing deoxy-cytidine analog
- Potential for DNA hypomethylating and antitumor effects
- Inhibits leukemia cell lines and decreases viability in carcinoma lines
- Depletes DNMT1 in various cell types
- Induces CpG demethylation and re-expression of the p15 tumor suppressor gene
- Effective against NCI-H23 tumor xenografts
- Decreases DNMT1 levels in tumors and provides modest suppression of tumor growth in certain xenograft models