Carboxylic acids and derivatives
eMolecules 36679-81-9 | 4-Hydroxymethyl-dihydro-furan-2-one | J & W PharmLab LLC | MFCD21099409 | 116.116 | C5H8O3 | 96.000 | OCC1COC(=O)C1 | 1g | 309209384
4-Hydroxymethyl-dihydro-furan-2-one | J & W PharmLab LLC | 36679-81-9 | MFCD21099409 | 116.116 | C5H8O3 | 96.000 | OCC1COC(=O)C1 | 1g | 309209384
Sigma Aldrich Fine Chemicals Biosciences 3-Acetyldeoxynivalenol from Fusarium roseum | 50722-38-8 | MFCD00135964 | 1MG
3-Acetyldeoxynivalenol from Fusarium roseum | Mol Wt: 338.35 | 50722-38-8 | MFCD00135964 | 1MG
Sigma Aldrich Fine Chemicals Biosciences 4-Acetoxy-2,5-dimethyl-3(2H)furanone >=95%, FG | 4166-20-5 | MFCD00799462 | 100G
4-Acetoxy-2,5-dimethyl-3(2H)furanone >=95%, FG | Purity: >=95% | Mol Wt: 170.16 | 4166-20-5 | MFCD00799462 | 100G
eMolecules 922-67-8 | Methyl propiolate | Ochem Incorporation | MFCD00008572 | 84.074 | C4H4O2 | 95.000 | COC(=O)C#C | 50g | 773165771
Methyl propiolate | Ochem Incorporation | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 95.000 | COC(=O)C#C | 50g | 773165771
Medchemexpress LLC NB-598 (Maleate) | 155294-62-5 | 99.4% | 565.74 | 50 MG
NB-598 Maleate is a potent and competitive inhibitor of squalene epoxidase (SE), and it suppresses triglyceride biosynthesis through the farnesol pathway. It is also a click chemistry reagent, containing an Alkyne group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules that contain Azide groups.
- Potent and competitive inhibitor of squalene epoxidase (SE)
- Suppresses triglyceride biosynthesis through the farnesol pathway
- Functions as a click chemistry reagent
- Contains an Alkyne group
- Capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide groups
eMolecules 922-67-8 | Methyl propiolate | Synthonix | MFCD00008572 | 84.074 | C4H4O2 | 95.000 | COC(=O)C#C | 10g | 649430196
Methyl propiolate | Synthonix | 922-67-8 | MFCD00008572 | 84.074 | C4H4O2 | 95.000 | COC(=O)C#C | 10g | 649430196
Selleck Chemical LLC Rosiglitazone maleate S2505-1g
Rosiglitazone maleate a member of the thiazolidinedione class of antihyperglycaemic agents is a high-affinity selective agonist of the peroxisome proliferator-activated receptor- (PPAR- ) with IC50 of 42 nM Rosiglitazone maleate also modulates TRP channels and induces autophagy Rosiglitazone prevents ferroptosis
Pfaltz & Bauer Diethylacetylene dicarboxylate 5G | 762-21-0
Diethylacetylene dicarboxylate 5G | 762-21-0
Chem-Impex International, Inc. Propargylic acid ethyl ester | 623-47-2 | MFCD00009184 | 100G
Propargylic acid ethyl ester, 623-47-2, MFCD00009184, 100G
Medchemexpress LLC Cediranib maleate | 857036-77-2 | 99.9% | 50 MG
Cediranib maleate is a highly potent, orally available VEGFR inhibitor. It effectively inhibits VEGF-stimulated proliferation and KDR phosphorylation in human umbilical vein endothelial cells and reduces vessel sprouting in coculture models. In vivo, it ablates experimental angiogenesis and inhibits the growth of various human tumor xenografts.
- Highly potent, orally available VEGFR inhibitor
- Inhibits VEGF-stimulated proliferation and KDR phosphorylation
- Reduces vessel area, length, and branching at subnanomolar concentrations
- Ablates experimental angiogenesis
- Inhibits growth of established human tumor xenografts
Medchemexpress LLC Cipralisant maleate | 223420-20-0 | 99.8% | 332.39 | C18H24N2O4 | 1 MG
Cipralisant maleate is a research-grade histamine H3 receptor ligand used in pharmacology and neuroscience research. It acts as a potent, selective H3 receptor antagonist in vivo and may display agonist activity in certain in vitro assays. The material is supplied as a high-purity solid and is intended for experimental use under appropriate laboratory conditions.
- Potent, selective histamine H3 receptor ligand.
- Suitable for in vitro and in vivo pharmacology studies.
- High reported purity (≈99.8%).
- Stable as a powder when stored under recommended cold conditions.
- Available in small package sizes for research, including 1 mg.
- White to off-white solid appearance.