Organophosphorus compounds
Medchemexpress LLC Achra(97-116) | 663154-30-1 | 99.4% | 2252.56 | 1 MG
AChRα(97-116) is a synthetic peptide corresponding to the 97-116 region of the rat acetylcholine receptor α-subunit, and also an inducer of autoimmune diseases. It can be used in studies related to experimental autoimmune myasthenia gravis.
- Does not induce significant proliferation of lymphocytes.
- Maintains antigen-specific immune cell phenotype responsive to dopaminergic modulation.
- Effectively detects elevated antibody levels in serum.
- Stimulates T cells to differentiate into Tfh cells.
- Stimulates lymph node-derived mononuclear cells to produce elevated percentages of pre-Tfh cells.
- Induces experimental autoimmune myasthenia gravis in Lewis rats.
- Drives elevated antibody production, reduced muscle clusters, and expansion of Tfh cells.
Medchemexpress LLC Fc-116 | 2417298-29-2 | MFCD20612185 | 98.0% | 369.39 g/mol | C21H20FNO4 | 10 MG
FC-116 is a small-molecule tubulin inhibitor supplied for research use with demonstrated antitumor activity in preclinical models. It is provided as a high-purity solid (approx. 98.0%) and includes batch-specific analytical documentation for laboratory research. Handle according to institutional safety procedures; not for human use.
- Acts as a tubulin inhibitor with reported antitumor activity.
- High analytical purity (98.0%).
- Supplied as an off-white to light yellow solid.
- Suitable for in vitro and preclinical research applications.
- Provided with a certificate of analysis for batch-specific data.
- Identified by CAS number 2417298-29-2 for unambiguous reference.
BIOHIPPO miR-29a-3p-GFP-Puro
miR-29a-3p-GFP-Puro lentiviral vector expressing microRNA 29a with GFP reporter and Puromycin selection for studies in Human/mouse Each vial provides a nominal titer of 1x10E6 transducing units TU miR-29a-3p Lentivirus miRNA lentiviral particles for expression of human/mouse miR-29a (3p) The lentiviral vector contains the entire human miRNA stem-loop which leads to expression of the human/mouse common mature miRNA sequence in transduced cells The miRNA lentivirus is ultra-purified and concentrated by PEG precipitation and sucrose gradient centrifugation ideal for in vitro or in vivo use and transduction of difficult-to-transfect (e g thawed and/or primary) cells
Medchemexpress LLC 5-pyrimidinecarboxamide, N-(2-chloro-6-methylphenyl)-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-[[2-[(1-oxo-2-propen-1-yl)amino]phenyl]amino]- | 2556836-50-9 | 98.6% | 597.11 | 25 MG
DGY-06-116 is an irreversible covalent, selective Src inhibitor with an IC50 of 3 nM. It also inhibits FGFR1 with an IC50 of 8340 nM. This product is for research use only.
- Selective Src inhibitor
- Inhibits FGFR1
- White to off-white solid appearance
Medchemexpress LLC Trimethylolpropane ethoxylate triacrylate | 28961-43-5 | 428 | 5 G
Trimethylolpropane ethoxylate triacrylate (ETPTA) is a plasticizer utilized in the synthesis of nanocomposites. It can be used to fabricate photonic crystals with varying stop band positions through photopolymerization of its photocurable resin. Gold nanoparticles can then be embedded into inverse ETPTA films via multiple infiltration.
- Utilized as a plasticizer
- Suitable for synthesizing nanocomposites
- Enables fabrication of photonic crystals
- Supports embedding of gold nanoparticles into films
Medchemexpress LLC hsa-miR-214-3p mimic 20nmol | 20nmol
hsa-miR-214-3p mimics are small chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity
TARGETMOL CHEMICALS INC CYC-116 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM is less potent to VEGFR2 (Ki of 44 nM) with 50-fold greater potency than CDKs not active against PKA Akt/PKB PKC no effect on GSK-3(alpha)/(beta) CK2 Plk1 and SAPK2A. Phase 1. purity: 96%
TARGETMOL CHEMICALS INC BSJ-4-116 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BSJ-4-116 is a highly potent and selective CDK12 degrader (PROTAC) with an IC50 of 6 nM. It downregulates DDR genes through a premature termination of transcription primarily through increasing poly(adenylation). purity: 99%
Apexbio Technology LLC LEP (116-130) (mouse) 258276-95-8 1mg
LEP 116-130 (mouse) is an amidated peptide fragment derived from mouse leptin It is designed to mimic leptin-like biological activities thereby contributing to the regulation of energy balance and appetite through hypothalamic signaling pathways LEP 116-130 (mouse) exerts its biological activity by engaging pathways associated with body weight homeostasis and food consumption Based on these pharmacological properties LEP 116-130 (mouse) holds research potential in the fields of obesity metabolism regulation and related signaling pathologies
Medchemexpress LLC Triethyl phosphate-d15 | 135942-11-9 | MFCD08705044 | 99.6% | 197.25 g/mol | C6D15O4P | 25 MG
Triethyl phosphate-d15 is the deuterium-labeled isotopologue of triethyl phosphate used as an analytical standard and tracer for LC-MS and other mass spectrometry applications. Supplied as a high-purity reference material for quantitative analysis and method development (research use only).
- Deuterium-labeled internal standard for LC-MS quantification.
- High isotopic enrichment, reducing interference in mass spectra.
- High chemical purity suitable for analytical standards.
- Available in small milligram pack sizes for trace-level work.
- Stable when stored under recommended conditions, preserving integrity.
Medchemexpress LLC mmu-miR-378a-3p inhi 20nmol | 20nmol
mmu-miR-378a-3p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs The miRNA inhibitors have full-length nucleotide 2 -methoxy modification The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes thereby inhibiting miRNAs from functioning
![Medchemexpress LLC 4-methyl-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-1,3-thiazol-2-amine | 693228-63-6 | MFCD14155805 | 99.1% | 368.46 g/mol | C18H20N6OS | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240176.png-250.jpg)
Medchemexpress LLC 4-methyl-5-[2-(4-morpholin-4-ylanilino)pyrimidin-4-yl]-1,3-thiazol-2-amine | 693228-63-6 | MFCD14155805 | 99.1% | 368.46 g/mol | C18H20N6OS | 1 ML
CYC-116 is a small-molecule inhibitor of Aurora A and Aurora B kinases for laboratory research. It exhibits low-nanomolar affinity (Ki ≈ 8 nM for Aurora A; 9 nM for Aurora B) and is supplied as a high-purity solid or as a 10 mM solution in DMSO for in vitro studies. Intended for research use only.
- Potent Aurora A and B inhibition with Kis of 8 nM and 9 nM.
- High purity (≈99.1%) suitable for biochemical assays.
- Available as solid and 10 mM 1 mL solution in DMSO.
- Molecular formula C18H20N6OS; molecular weight 368.46 g/mol.
- Storage: powder -20°C (up to 3 years); solution -80°C (recommended).
- Intended for in vitro research use only.