Phenols
Medchemexpress LLC Ethyl phenyl(2,4,6-trimethylbenzoyl)phosphinate | 84434-11-7 | MFCD08692488 | 97.0% | 316.33 g/mol | C18H21O3P | 500 G
Ethyl phenyl(2,4,6-trimethylbenzoyl)phosphinate is a liquid Norrish Type I photoinitiator used to generate free radicals under UV and near-UV exposure to initiate rapid polymerization in resins, coatings, adhesives, inks, and photopolymerization-based 3D printing. It is suitable for both clear and pigmented formulations and supports two-photon induced polymerization applications.
- Liquid form for easy incorporation into resin formulations.
- Efficient radical generation under UV/near-UV light for fast cure.
- Suitable for two-photon polymerization and stereolithography processes.
- Performs well in pigmented and clear UV-curable systems for good through-cure.
- High polymerization quantum yield for effective conversion.
Medchemexpress LLC Tris(hydroxymethyl)aminomethane | 77-86-1 | 99.9% | 500 G
THAM (Tris) is a biologically inert amino alcohol with low toxicity that buffers carbon dioxide and acids both in vitro and in vivo. It is an effective amine compound for pH control in the physiological range. It has been shown to reduce arterial carbon dioxide tension (PaCO2) levels and increase pH above 7.4 during infusion in pigs.
- Biologically inert amino alcohol with low toxicity
- Buffers carbon dioxide and acids
- Effective for pH control in the physiological range
- Reduces arterial carbon dioxide tension
- Increases pH during infusion
Medchemexpress LLC Ethylhexylglycerin 1kg
Ethylhexylglycerin has antimicrobial activity inhibiting the growth of Acinetobacter spp Pseudomonas aeruginosa complex and Stenotrophomonas maltophilia Ethylhexylglycerin can cause pigmentary contact dermatitis[1][2]
Medchemexpress LLC Arl67156 trisodium | 1021868-83-6 | MFCD08544552 | 99.9% | 785.05 g/mol | C15H21Br2N5Na3O12P3 | 5 MG
ARL67156 trisodium is the trisodium salt of ARL67156, a small-molecule inhibitor of ecto-ATPases (NTPDases) including CD39, NTPDase3, and NPP1. It is used in purinergic signaling research and disease models such as calcific aortic valve disease and asthma.
- selective ecto-ATPase inhibitor targeting CD39, NTPDase3, and NPP1.
- reported Ki values of ~11 μM, 18 μM, and 12 μM for respective targets.
- high purity suitable for research (99.94% by HPLC).
- small-scale research quantity (5 mg) for exploratory studies.
- storage guidelines: sealed and dry; in solvent store at -80°C up to 6 months, -20°C up to 1 month.
Medchemexpress LLC Zika virus E/envelope protein (438 a.a., Sf9, His) | >90.0% | 10 UG
Recombinant Zika virus envelope (E) protein expressed in Sf9 insect cells as a partial sequence (residues F257-G694) with a C-terminal His tag. Supplied as a 0.22 μm filtered solution in Tris/NaCl/glycerol, the protein is >90% pure by reducing SDS-PAGE and intended for biochemical, immunological, and assay development applications. Store frozen and avoid repeated freeze-thaw cycles.
- Partial E protein covering residues F257-G694.
- Produced in Sf9 insect cells with a C-terminal His tag.
- Supplied in Tris/NaCl/glycerol buffer, 0.22 μm filtered.
- Purity greater than 90% by reducing SDS-PAGE.
- Predicted molecular mass 45.53 kDa.
- Suitable for ELISA, antibody validation, and biochemical assays.
- Store at -80°C and avoid repeated freeze-thaw cycles.
Medchemexpress LLC BCR-ABL1-IN-1 | 1488090-21-6 | 99.82% | C18H12F3N3O2 | 1 ML
BCR-ABL1-IN-1 is a potent ABL1 inhibitor with an IC50 of 8.7 nM. This compound is suitable for research applications related to central nervous system (CNS) diseases. It has demonstrated effectiveness in inhibiting the proliferation of Ba/F3-BCR-ABL1-WT cells.
- Inhibitor for ABL1 (64-515)
- IC50 of 8.7 nM against ABL1
- Suitable for CNS disease research
- Inhibits Ba/F3-BCR-ABL1-WT cell proliferation with an IC50 of 30 nM
- Purity of 99.82%
- Stable under recommended storage conditions
- Powder storage: -20°C for 3 years, 4°C for 2 years
- Solution storage: -80°C for 6 months, -20°C for 1 month
Apexbio Technology LLC Agatolimod sodium 541547-35-7 1mg
Agatolimod sodium (CAS 541547-35-7) also known as ODN 2006 is a synthetic oligodeoxynucleotide classified as a B-type CpG ODN It selectively activates Toll-like receptor 9 (TLR9) by binding to specific CpG motifs leading to the induction of various cytokines and chemokines in immune cells This immunostimulatory activity enhances host immune responses and modulates immune function Agatolimod sodium is widely investigated as an immunomodulatory agent in preclinical and clinical research with applications as a vaccine adjuvant and in studies of antitumor and anti-infective therapies
Medchemexpress LLC Bromoacetamido-C2-PEG2-NH-Boc | 182244-33-3 | C13H25BrN2O5 | 5 G
Bromoacetamido-C2-PEG2-NH-Boc is a PEG-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.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Medchemexpress LLC Ard-2051 | 2632305-17-8 | 98.6% | 789.32 | C43H45ClN8O5 | 10 MG
ARD-2051 is a selective, orally active androgen receptor proteolysis-targeting chimera (PROTAC) degrader developed for preclinical research into AR-dependent cancers. It induces potent AR protein degradation in cell-based assays and has demonstrated favorable pharmacokinetics and oral efficacy in animal models.
- Potent AR protein degradation (DC50 ~0.6 nM).
- Orally active with demonstrated in vivo efficacy in preclinical models.
- Effective in AR-positive prostate cancer cell lines, including LNCaP and VCaP.
- Characterized pharmacokinetic profile and oral bioavailability in rodent and canine studies.
- High chemical purity suitable for research applications.
- Supplied as a solid with defined storage recommendations for stability.
Medchemexpress LLC Methyl 2-fluoro-4-((1-methoxy-2-methyl-1-oxopropan-2-yl)amino)benzoate | 1802242-47-2 | MFCD00006432 | 25g
Enzalutamide impurity 4 is an impurity of Enzalutamide (HY-70002)
Medchemexpress LLC Ethylhexylglycerin 25g
Ethylhexylglycerin has antimicrobial activity inhibiting the growth of Acinetobacter spp Pseudomonas aeruginosa complex and Stenotrophomonas maltophilia Ethylhexylglycerin can cause pigmentary contact dermatitis[1][2]
![Medchemexpress LLC Quinoxaline, 6-[3-(6-methyl-2-pyridinyl)-1H-pyrazol-4-yl] | 746667-48-1 | 99.6% | 287.32 g·mol⁻¹ | C17H13N5 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000307903.png-250.jpg)
Medchemexpress LLC Quinoxaline, 6-[3-(6-methyl-2-pyridinyl)-1H-pyrazol-4-yl] | 746667-48-1 | 99.6% | 287.32 g·mol⁻¹ | C17H13N5 | 1 ML
BIO-013077-01 is a pyrazole-based small-molecule inhibitor of the transforming growth factor-beta (TGF-β) receptor family for in vitro research use. The compound has molecular formula C17H13N5 and molecular weight 287.32 g·mol⁻¹ and is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) or as solid aliquots.
- Potent inhibition of TGF-β receptor signaling in cellular assays.
- Available as a 10 mM solution in DMSO for immediate use.
- Also available as solid forms for long-term storage or bulk use.
- Well-characterized molecular properties (C17H13N5, 287.32 g·mol⁻¹).
- High purity suitable for research applications.
- For laboratory research use only; not for human or veterinary use.
Apexbio Technology LLC Adrenalone HCl 62-13-5 10mM (in 1mL DMSO)
Adrenalone hydrochloride (CAS 62-13-5) is a synthetic adrenergic agonist primarily targeting alpha-1 adrenergic receptors Through activation of these receptors Adrenalone induces vasoconstriction leading to reduced local blood flow This pharmacological property underpins its utility as a topical hemostatic agent in research settings where precise modulation of vascular tone is required Adrenalone is frequently employed to investigate adrenergic receptor signaling pathways and the physiological mechanisms underlying vascular constriction