Dicarboxylic acids and derivatives
![Medchemexpress LLC 1-propanaminium, 3-carboxy-N,N,N-tri(methyl-d3)-2-[(1-oxododecyl)oxy]-, chloride (1:1), (2R)- | 2245711-25-3 | 98.0% | C19H29D9ClNO4 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000260025.png-250.jpg)
Medchemexpress LLC 1-propanaminium, 3-carboxy-N,N,N-tri(methyl-d3)-2-[(1-oxododecyl)oxy]-, chloride (1:1), (2R)- | 2245711-25-3 | 98.0% | C19H29D9ClNO4 | 10MG
Lauroyl-L-carnitine-d9 chloride is the deuterium-labeled (d9) chloride salt of lauroyl-L-carnitine supplied as an isotope-labeled reference standard for analytical and research use. It is intended for use as an internal standard or tracer in mass spectrometry, quantitative assays, and metabolic or pharmacokinetic studies, providing a labeled analog of the unlabeled compound.
- Deuterium-labeled (d9) isotope suitable for use as an internal standard in mass spectrometry.
- Chloride salt form to match common analytical reference materials.
- High purity (98.0%) for reliable analytical performance.
- Provided in small, reference quantities tailored for analytical workflows.
- Stable when stored sealed under refrigerated conditions (≈2-8°C).
Medchemexpress LLC VH 101, acid | 2408341-97-7 | 98.8% | 574.66 | C28H35FN4O6S | 10 MG
VH 101, acid is a functionalized von Hippel-Lindau (VHL) E3 ligase ligand developed for PROTAC research and conjugation chemistry. The molecule includes an E3 ligase recognition motif and an alkyl linker terminating in a primary amine, facilitating attachment to target protein ligands.
- Designed for use as a VHL E3 ligase ligand in PROTAC development.
- Alkyl linker with terminal amine enables straightforward conjugation chemistry.
- High reported purity suitable for research applications.
- Supplied in small research-scale quantities for synthetic work and assay testing.
Medchemexpress LLC Lauroyl-L-carnitine chloride | 6919-91-1 | MFCD00274131 | 98.1% | C19H38ClNO4 | 10MG
Lauroyl-L-carnitine chloride is an orally active absorption enhancer used in research to improve the oral bioavailability of peptide compounds. Supplied as a white to off-white solid with high purity, it is applied in formulation and permeability studies to assess and enhance intestinal uptake of peptide drugs.
- Orally active absorption enhancer for peptide compounds.
- Reported to improve oral bioavailability of peptides.
- White to off-white solid suitable for formulation research.
- High purity (~98.1%) as supplied.
- Supports studies of intestinal permeability and delivery.
- Store sealed at 4°C; in solvent, -80°C (6 months) or -20°C (1 month).
TARGETMOL CHEMICALS INC KYN-101 5MG
Also available in 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. KYN-101 is an orally active and selective aryl hydrocarbon receptor (AHR) inhibitor with anticancer activity. KYN-101 decreases CYP1A1 mRNA expression and can be used in the study of breast cancer and acute myeloid leukemia. KYN-101 is an orally active and selective aryl hydrocarbon receptor (AHR) inhibitor with anticancer activity. Purity 99.39%
![Medchemexpress LLC L-Leucinamide, N-acetyl-L-leucyl-N-[(1S)-1-formylpentyl]- | 110044-82-1 | ≥98.0% | 383.53 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000385191-logo.png-250.jpg){kind=logo}
Medchemexpress LLC L-Leucinamide, N-acetyl-L-leucyl-N-[(1S)-1-formylpentyl]- | 110044-82-1 | ≥98.0% | 383.53 | 100 MG
MG-101 (ALLN) is an inhibitor of cysteine proteases, specifically inhibiting calpain I, calpain II, cathepsin B, and cathepsin L with Kis of 190, 220, 150, and 500 pM, respectively. It induces apoptosis and inhibits tumor growth, making it suitable for research on colon cancer. For research use only.
- Inhibits cysteine proteases: calpain I, calpain II, cathepsin B, and cathepsin L
- Induces apoptosis
- Inhibits tumor growth
- Can be used for colon cancer research
![Medchemexpress LLC 3-cyclopropyl-1-[[4-[6-[(1,1-dioxo-1,4-thiazinan-4-yl)methyl]-5-fluoropyridin-2-yl]phenyl]methyl]imi | 2250025-91-1 | Not found | 99.4% | 508.99 | C23H25FN4O4S·HCl | 25MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000236923.png-250.jpg)
Medchemexpress LLC 3-cyclopropyl-1-[[4-[6-[(1,1-dioxo-1,4-thiazinan-4-yl)methyl]-5-fluoropyridin-2-yl]phenyl]methyl]imi | 2250025-91-1 | Not found | 99.4% | 508.99 | C23H25FN4O4S·HCl | 25MG
LEI-101 hydrochloride is a potent, selective, orally bioavailable cannabinoid CB2 receptor agonist supplied for research use. It demonstrates strong functional activity at human CB2 receptors with substantially lower affinity for CB1 and minimal hERG binding, suitable for in vitro and in vivo pharmacology studies.
- Purity 99.4%.
- Reported activity pEC50 = 8 for human CB2.
- Approximately 100-fold selectivity for CB2 over CB1.
- Low hERG interaction (pKi < 4).
- Soluble in DMSO; available as dry powder and 10 mM solution in DMSO.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC GlyH-101 | 328541-79-3 | 99.7% | 493.15 | 25 MG
GlyH-101 is a potent and reversible inhibitor of CFTR (Cystic Fibrosis Transmembrane conductance Regulator) and VSORC (Volume-Sensitive Outwardly Rectifying Chloride) conductance. It also exhibits antiproliferative activity by inhibiting cell growth in a dose-dependent manner. This compound is suitable for various in vitro and in vivo studies related to cystic fibrosis and other conditions involving chloride channel regulation.
- Potent CFTR inhibitor
- Reversible inhibitor of VSORC conductance
- Exhibits antiproliferative activity in PCT and PS120 cells
- Reduces cholera toxin-induced intestinal fluid secretion in mice
- Soluble in DMSO for in vitro applications
- Available in various solid quantities
![Medchemexpress LLC O=C([C@]1(CO1)CO[Si](C)(C)C(C)(C)C)[C@H](CC(C)C)NC([C@H](C)NC(CCCCCC)=O)=O | 1000313-40-5 | 99.6% | 484.74 | C25H48N2O5Si | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000229462.png-250.jpg)
Medchemexpress LLC O=C([C@]1(CO1)CO[Si](C)(C)C(C)(C)C)[C@H](CC(C)C)NC([C@H](C)NC(CCCCCC)=O)=O | 1000313-40-5 | 99.6% | 484.74 | C25H48N2O5Si | 5 MG
UK-101 is a selective immunoproteasome β1i (LMP2) inhibitor for laboratory research. It shows reported potency with an IC50 of about 104 nM and is supplied as a high-purity solid suitable for in vitro studies; recommended solvent is DMSO.
- Selective immunoproteasome β1i (LMP2) inhibitor with IC50 ≈104 nM.
- High purity (≈99.6%).
- Available in small research quantities, e.g., 5 mg.
- Recommended solvent: DMSO for dissolution.
- Powder storage: -20°C (3 years) or 4°C (2 years); solutions: -80°C (6 months).
- For research use only; not for human or clinical use.
Medchemexpress LLC 1,2-Dilauroyl-sn-glycerol | 60562-15-4 | 98.0% | 100 MG
1,2-Dilauroyl-sn-glycerol is identified as a saturated diacylglycerol that might be involved in second messenger signal transduction. It is available as a solid, appearing white to off-white, with a molecular weight of 456.70 and the chemical formula C27H52O5. This compound is intended strictly for research purposes.
- Saturated diacylglycerol.
- May play a role in second messenger signal transduction.
- Available in solid form.
- Appears white to off-white.
- Strictly for research use.
- High purity of 98.0%.
Medchemexpress LLC FITC-labeled ODN 1018 sodium | 98.7% | 8,171.00 Da | 10 MG
FITC-labeled ODN 1018 sodium is an FITC-conjugated CpG oligodeoxynucleotide that functions as a Toll-like receptor 9 (TLR9) agonist. Supplied as the sodium salt, it is used to evaluate CpG ODN cellular uptake and localization by confocal laser-scanning microscopy or flow cytometry. For research use only.
- FITC label with excitation 495 nm and emission 520 nm.
- CpG oligodeoxynucleotide sequence: d(P-thio)(T-G-A-C-T-G-T-G-A-A-C-G-T-T-C-G-A-G-A-T-G-A).
- Molecular weight approximately 8,171 Da.
- Purity 98.7% as supplied.
- Sodium salt form.
- Available in 1 mg, 5 mg, and 10 mg sizes; larger sizes available by quote.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC 1,2-Dilauroyl-sn-glycerol | 60562-15-4 | 98.0% | 25 MG
1,2-Dilauroyl-sn-glycerol is a saturated diacylglycerol that may participate in second messenger signal transduction. It is intended for research use only and is not sold to patients.
- Potential role in second messenger signal transduction.
- Crucial intracellular signaling molecules involved in regulating various physiological processes.
- Specifically designated for research purposes.