Carboxylic acid esters
L-Ascorbic acid sodium salt, 99%
CAS: 134-03-2 Molecular Formula: C6H7NaO6 Molecular Weight (g/mol): 198.11 MDL Number: MFCD00082340 InChI Key: IFVCRSPJFHGFCG-HXPAKLQESA-N Synonym: sodium ascorbate,l-ascorbic acid sodium salt,sodium l-ascorbate,vitamin c sodium,ascorbicin,sodascorbate,cebitate,aminofenitrooxon,natrii ascorbas,monosodium l-ascorbate PubChem CID: 131674100 IUPAC Name: sodium 5-[(1S)-1,2-dihydroxyethyl]-3-hydroxy-2,4-dioxooxolan-3-ide SMILES: [Na+].OC[C@H](O)C1OC(=O)[C-](O)C1=O
Isopropenyl Acetate 98.0+%, TCI America™
CAS: 108-22-5 Molecular Formula: C5H8O2 Molecular Weight (g/mol): 100.12 MDL Number: MFCD00008709 InChI Key: HETCEOQFVDFGSY-UHFFFAOYSA-N Synonym: isopropenyl acetate,2-acetoxypropene,1-methylvinyl acetate,2-acetoxypropylene,methylvinyl acetate,1-propen-2-ol, acetate,propen-2-yl acetate,acetic acid isopropenyl ester,1-acetoxy-1-methylethylene,1-propen-2-yl acetate PubChem CID: 7916 IUPAC Name: prop-1-en-2-yl acetate SMILES: CC(=C)OC(C)=O
Medchemexpress LLC Dizocilpine (maleate) | 77086-22-7 | C20H19NO4 | 5 MG
Dizocilpine maleate (MK-801 maleate) is a potent, selective, and non-competitive NMDA receptor antagonist. It targets iGluR, involved in Membrane Transporter/Ion Channel and Neuronal Signaling pathways. This compound has a Kd of 37.2 nM in rat brain membranes and a molecular weight of 337.37.
- Potent, selective, non-competitive NMDA receptor antagonist
- Targets iGluR, Membrane Transporter/Ion Channel, and Neuronal Signaling
- Soluble in DMSO, ethanol, and water (requires ultrasonic)
- Can be used to induce schizophrenia models
- Inhibits activation of microglia induced by LPS
- Reduces microglial TNF-α output
- Recommended storage at 4°C, sealed, away from moisture
- In solvent, store at -80°C for 2 years or -20°C for 1 year
Medchemexpress LLC Neratinib (maleate) | 915942-22-2 | 99.7% | 673.11 | 5 MG
Neratinib maleate is an orally available, irreversible, and highly selective inhibitor of HER2 and EGFR. It effectively inhibits the proliferation of cell lines expressing high levels of HER-2 and shows anticancer activities in tumor xenograft models. This compound induces G1-S phase arrest and leads to inhibition of MAPK and Akt phosphorylation.
- Orally available
- Irreversible, highly selective HER2 and EGFR inhibitor
- Inhibits proliferation of HER-2 expressing cell lines
- Induces G1-S phase arrest
- Inhibits MAPK and Akt phosphorylation
- Shows anticancer activity in tumor xenograft models
Sigma Aldrich Isopropenyl acetate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Selleck Chemical LLC Pimethixene maleate S3913-5mg
Pimethixene (Pimetixene) maleate an antihistamine anntimigraine agent and antiserotonergic compound is a highly potent antagonist of a broad range of monoamine receptors including a variety of serotonin receptors Pimethixene maleate inhibits 5-HT2A 5-HT2B 5-HT2C 5-HT1A 5-HT1B 5-HT6 5-HT7 Adrenergic -1A Dopamine D1 Receptor Dopamine D2 Receptor Dopamine D4 4 Receptor Histamine H1 Receptor Muscarinic M1 and Muscarinic M2 with pKi of 10 22 10 44 8 42 7 63 5 7 30 7 28 7 61 6 37 8 19 7 54 10 14 8 61 and 9 38 respectively