Carboxylic acids and derivatives
Medchemexpress LLC SU14813 maleate | 849643-15-8 | MFCD24682713 | 99.0% | 558.56 g/mol | C27H31FN4O8 | 50 MG
SU14813 maleate is the maleate salt of SU14813, a small-molecule multi-targeted receptor tyrosine kinase inhibitor with nanomolar potency against VEGFR1, VEGFR2, PDGFRβ, and KIT. It is supplied for research use and characterized by a defined chemical formula and high purity suitable for biochemical and cellular studies.
- Potent inhibition of VEGFR1 (IC50 2 nM), VEGFR2 (IC50 50 nM), PDGFRβ (IC50 4 nM), and KIT (IC50 15 nM).
- Maleate salt form to aid solubility and handling in aqueous systems.
- High purity suitable for research-grade experiments.
- Applicable to biochemical kinase assays and cellular target validation studies.
- Provided in small, laboratory-scale quantities for research applications.
eMolecules Sodium valproate | 1069-66-5 | MFCD00078604 | 25g
Combi-Blocks | Sodium valproate | 25g | 232311152 | QA-1100 | 97.000 | 1069-66-5 | MFCD00078604 | 166.196 | C8H15NaO2
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![Medchemexpress LLC L-methionine N-[(5-(imidazol-5-ylmethyl)amino)methyl-2'-methylbiphenyl-2-yl]carbonyl methyl ester | 344900-92-1 | 99.8% | 466.60 | C25H30N4O3S | 25MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000239529.png-250.jpg)
Medchemexpress LLC L-methionine N-[(5-(imidazol-5-ylmethyl)amino)methyl-2'-methylbiphenyl-2-yl]carbonyl methyl ester | 344900-92-1 | 99.8% | 466.60 | C25H30N4O3S | 25MG
FTI-2153 is a potent, highly selective farnesyltransferase (FTase) inhibitor used in research to study Ras processing and mitotic spindle formation. It demonstrates low-nanomolar FTase inhibition and is applied in cell biology and oncology research to probe Ras-dependent signaling and mitotic effects.
- Potent, selective inhibition of farnesyltransferase (IC50 ≈ 1.4 nM).
- Inhibits H-Ras processing and affects mitotic spindle formation in cell assays.
- Suitable for cell-based and biochemical studies of Ras signaling.
- High purity appropriate for research applications (HPLC purity: 99.77%).
- Supplied as a solid, convenient for storage and formulation.
- Available in 25 MG quantities for laboratory use.
Medchemexpress LLC N-(3-propylcarbamoyloxirane-2-carbonyl)-isoleucyl-proline | 134448-10-5 | MFCD00797531 | >98.0% | 383.44 g/mol | C18H29N3O6 | 100 MG
CA-074 is a potent, selective inhibitor of cathepsin B with a reported Ki of 2-5 nM, used in biochemical and cell-based research to study cysteine protease activity. It is an epoxysuccinyl peptide derivative with typical purity over 98% and a molecular weight of 383.44 g/mol.
- Potent cathepsin B inhibition with Ki of 2-5 nM.
- Suitable for biochemical and cell-based assays.
- Typical purity greater than 98% (HPLC).
- Molecular formula C18H29N3O6 and molecular weight 383.44 g/mol.
- Available in multiple pack sizes, including 100 MG, for research use.
eMolecules 3-N-DI-BOC-2-METHYL-PROPIONIC ACID | 357610-29-8 | MFCD24475052 | 5g
AstaTech | 3-N-DI-BOC-2-METHYL-PROPIONIC ACID | 5g | 338839279 | 70023 | 95.000 | 357610-29-8 | MFCD24475052 | 303.355 | C14H25NO6
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Medchemexpress LLC Flupirtine (maleate) | 75507-68-5 | 100.0% | 420.39 | 5 MG
Flupirtine (maleate) | 75507-68-5 | 100.0% | 420.39 | 5 MG
Medchemexpress LLC Pd-168077 maleate | 630117-19-0 | 99.6% | 450.49 | 1 ML
PD-168077 maleate is a selective dopamine D4 receptor agonist with a Ki of 9 nM. It is intended for research use only. It exhibits intrinsic activity at the D4 receptor, leading to quinpirole-like inhibition of forskolin-stimulated cAMP accumulation or stimulation of [3H]thymidine uptake.
- Shows >100-fold selectivity over other D2-like receptor family members and D1-like counterparts.
- Demonstrates 20-fold selectivity over α1 and α2 receptors.
- Exhibits 45-fold selectivity over 5-HT1A.
- Shows 460-fold selectivity over 5-HT2A receptors.
- Induces synaptic translocation of Ca2+/calmodulin-dependent protein kinase II in cultured prefrontal cortical neurons.
eMolecules Ambeed / Dibutyltin diacetate / 25g / 742299394 / A158384 / / 1067-33-0 / MFCD00008697 / 351.030 / C12H24O4Sn
Ambeed / Dibutyltin diacetate / 25g / 742299394 / A158384 / / 1067-33-0 / MFCD00008697 / 351.030 / C12H24O4Sn
Cayman Chemical FluoresceIn dIacetate 25g
A cell-permeable fluorogenic cell viability probe; cleaved by intracellular esterases to produce fluorescein which displays excitation/emission maxima of 490/520 nm, respectively
eMolecules 1-Isopropenyl-1,3-dihydro-2H-1,3-benzimidazol-2-one | 72798-66-4 | 500MG | Purity: 95%
Matrix Scientific | 1-Isopropenyl-1,3-dihydro-2H-1,3-benzimidazol-2-one | 500MG | 72798-66-4 | MFCD00218253
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eMolecules Isobutyl cinnamate | 122-67-8 | MFCD00038289 | 25g
Ambeed | Isobutyl cinnamate | 25g | 587278964 | A802989 | | 122-67-8 | MFCD00038289 | 204.269 | C13H16O2
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Apexbio Technology LLC (+)-MK 801 Maleate 77086-22-7 10mM (in 1mL DMSO)
( )-MK 801 Maleate is a non-competitive antagonist of the N-methyl-D-aspartate (NMDA) receptor exhibiting a Ki value of approximately 30 5 nM By blocking the NMDA receptor-mediated ion channel MK 801 disrupts glutamate-associated excitatory neurotransmission In experimental models MK 801 demonstrates anticonvulsant and anxiolytic properties through modulation of NMDA receptor activity This compound readily penetrates the central nervous system binding reversibly and region-specifically to cortical and hippocampal membranes MK 801 effectively inhibits NMDA-triggered depolarization responses in neuronal preparations making it applicable in studies focused on epilepsy excitotoxicity and neuronal signaling pathways
Accela Chembio Inc Sodium Trimethylacetate Hydrate | 25g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
Sodium Trimethylacetate Hydrate | 25g | 143174-36-1 | MFCD00150782 | 99% | Shelf Life: 1620 Days | Light Sensitive
