Phenols
Medchemexpress LLC P-hydroxybenzaldehyde-d4 | 284474-52-8 | 99.7% | 126.15 | C7H2D4O2 | 10mg
p-Hydroxybenzaldehyde-d4 is the deuterium labeled p-Hydroxybenzaldehyde p-Hydroxybenzaldehyde is a one of the major components in Dendrocalamus asper bamboo shoots with antagonistic effect on GABAA receptor of the 1 2 2S subtype at high concentrations
![eMolecules Pharmablock 3-fluorobicyclo[1 1 1]pentane-1-carboxylic acid 500mg 551107224 PBHM9062 0 000 146038-53-1 MFCD19228680 130 118 C6H7FO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
eMolecules Pharmablock 3-fluorobicyclo[1 1 1]pentane-1-carboxylic acid 500mg 551107224 PBHM9062 0 000 146038-53-1 MFCD19228680 130 118 C6H7FO2
Pharmablock 3-fluorobicyclo[1 1 1]pentane-1-carboxylic acid 500mg 551107224 PBHM9062 0 000 146038-53-1 MFCD19228680 130 118 C6H7FO2
Cayman Chemical p-Cresol GlucuronIde 1mg
A metabolite of p-cresol; formed from p-cresol primarily by UGT1A6, but also by UGT1A9, in human liver and kidney microsomes; accumulates in feces, blood, and urine of patients with CKD
Medchemexpress LLC 3-(2-Pyridyldithio)propanoic Acid | 68617-64-1 | 99.5% | 10 G
3-(2-Pyridyldithio)propanoic Acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Target: PROTAC linkers
- Pathway: PROTAC
- Molecular weight: 215.29
- Formula: C8H9NO2S2
- Appearance: Solid
- Color: White to off-white
- Solubility (in vitro): DMSO: 250 mg/mL
TARGETMOL CHEMICALS INC NMS-E973 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. NMS-E973 is a potent and selective Hsp90 inhibitor with DC50 of <10 nM for Hsp90 binding no activiy against a panel of 52 diverse protein kinases. purity: 99%
Medchemexpress LLC p-Tolylmaleimide | 1631-28-3 | 98.0% | 100 MG
p-Tolylmaleimide (compound 9) is a naphthalimide derivative with cytotoxic effects on cancer cells. It can arrest the cell cycle of human acute myeloid leukemia cells K562 in the sub-G0/G1 phase and induce apoptosis.
- Inhibits human acute myeloid leukemia cell K562 with IC50s of 24.99 μM (24 h), 6.61 μM (48 h), and 12.10 μM (72 h).
- Inhibits human acute myeloid leukemia cell Jurkat with IC50s of 27.16 μM (24 h), 15.51 μM (48 h), and 3.94 μM (72 h).
- Cytotoxicity against human MCF7, NCI-H460, and SF-268 cells (GI50 > 10 μg/mL).
Medchemexpress LLC Amyloid P-IN-1 | 1819986-22-5 | MFCD30489728 | 99.6% | 656.68 g/mol | C30H44N2O14 | 10 MG
Amyloid P-IN-1 is a research-grade small-molecule inhibitor used to study depletion of serum amyloid P component (SAP) in models of amyloidosis, Alzheimer's disease, type 2 diabetes mellitus, and osteoarthritis. It is supplied for laboratory research use only and is not intended for clinical use or human administration.
- High purity: 99.6% by assay.
- Molecular weight: 656.68 g/mol.
- Chemical formula: C30H44N2O14.
- Available as milligram quantities or as a 10 mM solution in DMSO.
- Solid appearance: white to off-white powder.
- Storage recommendations for powder and solutions to maintain stability.
Medchemexpress LLC P-Selectin Rat HEK 50ug
P-Selectin a Ca(2 )-dependent receptor on myeloid cells binds to neutrophils and monocytes via carbohydrates It interacts with SELPLG to enable rapid leukocyte rolling over vascular surfaces in early inflammation P-Selectin also interacts with SNX17 and promotes neutrophil adhesion and rolling requiring SELPLG s sialyl-Lewis X and tyrosine sulfation P-Selectin Protein Rat (HEK293 His) is the recombinant rat-derived P-Selectin protein expressed by HEK293 with C-His labeled tag
Medchemexpress LLC N-(p-Coumaroyl) Serotonin | 68573-24-0 | 99.0% | 10 MG
N-(p-Coumaroyl) Serotonin is a selective inhibitor of PDGFRβ, ERK1/2, and caspase-8, exhibiting antioxidant, anti-atherosclerotic, and anti-inflammatory properties. It inhibits glioblastoma cells and can improve atherosclerosis and aortic wall enlargement.
- Selective inhibitor of PDGFRβ, ERK1/2, and caspase-8
- Exhibits antioxidant, anti-atherosclerotic, and anti-inflammatory properties
- Inhibits glioblastoma cells
- Blocks calcium influx
- Induces apoptosis by activating caspase-8
- Can improve atherosclerosis and aortic wall enlargement
- Used in glioblastoma research
Medchemexpress LLC Tris(2-(4-fluorophenyl)pyridine)iridium | 370878-69-6 | MFCD70878696 | 98.0% | 708.75 g/mol | C33H21F3IrN3 | 5 MG
Ir(p-F-ppy)3 is an iridium(III) cyclometalated complex used as a photocatalyst in photoredox chemistry and as a phosphorescent emitter in optoelectronic research. It facilitates electron-transfer processes in organic synthesis and is applied in studies aimed at improving display and photovoltaic device performance.
- High photocatalytic activity for photoredox reactions.
- Suitable as a phosphorescent emitter in optoelectronic studies.
- Supplied at 98.0% purity for reproducible results.
- Available in milligram-scale quantities for research applications.
- Chemical formula C33H21F3IrN3; molecular weight 708.75 g/mol.
Medchemexpress LLC Dehydrothio-p-toluidine | 92-36-4 | MFCD00005780 | 99.9% | 240.32 g/mol | C14H12N2S | 10 G
Dehydrothio-p-toluidine (DHPT) is a solid chemical intermediate used primarily in the production of dyestuffs and related organic syntheses. It is supplied at high purity for research and industrial use; consult the safety data sheet for handling and inhalation hazard information.
- Chemical intermediate for dyestuff production.
- High purity supports synthetic and research applications.
- Available in lab-scale pack sizes for scalable use.
- Comes with SDS and COA documentation for safety and quality assurance.
- Handle with measures to prevent inhalation exposure.
TARGETMOL CHEMICALS INC LONAFARNIB 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Lonafarnib (Sch66336) is an orally bioavailable FPTase inhibitor for H-ras K-ras-4B and N-ras (IC50 1.9/5.2/2.8 nM). purity: 98%
Medchemexpress LLC o,p'-DDE (2,4'-DDE) | 3424-82-6 | 98.0% | 1 MG
o,p'-DDE (2,4'-DDE) is an organochlorine pesticide metabolite and degradation product of DDT used as an analytical reference in environmental and toxicology research. It is a persistent organic pollutant with documented endocrine-disrupting activity; handle and dispose according to institutional and regulatory safety guidance.
- Analytical reference standard for environmental and toxicology studies.
- Chemical formula C14H8Cl4; molecular weight 318.03 g/mol.
- Available in milligram pack sizes suitable for trace-level analyses.
- Useful for method development, calibration, and toxicological assays.
- Persistent organic pollutant; requires appropriate handling and disposal.
Cayman Chemical p-Cresol sulfatepotasIM100mg
A sulfate conjugate of p-cresol; increases migration and proliferation of isolated rat aortic VSMCs at 500 µM; increases aortic atherosclerotic plaques lesion area in nephrectomized ApoE-/- mice fed a high-fat diet when administered at 100 mg/kg per day via the drinking water; serum levels are increased in patients with advanced stage chronic kidney disease and positively associated with vascular calcification