Aminophenols
TARGETMOL CHEMICALS INC Biotin-4-aminophenol 10MG
Also available in 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Biotin-4-aminophenol (BP) is a selective and potent biotin-phenol analog that works by generating free radicals and binding to tyrosine residues in proteins. Purity 98.99%
Medchemexpress LLC RS 67333 (hydrochloride) | 168986-60-5 | MFCD00938576 | 99.7% | 389.36 | C19H30Cl2N2O2 | 25 MG
RS 67333 hydrochloride is a research-grade, selective 5-HT4 receptor partial agonist used in preclinical and in vitro neuroscience studies to investigate serotonergic signaling and neuroprotective mechanisms.
- Potent, selective 5-HT4 receptor partial agonist for neuroscience research.
- High purity, 99.7% (as listed by manufacturer).
- Molecular weight 389.36 g/mol; formula C19H30Cl2N2O2.
- Solid, light yellow to yellow appearance supplied as a dry powder.
- Storage: 4°C, sealed and away from moisture; in solvent store at -80°C for long-term.
- Available as a 25 MG vial for laboratory use.
- CAS number 168986-60-5.
Medchemexpress LLC AM-92016 hydrochloride | 133229-11-5 | MFCD00673947 | 99.3% | 483.84 | C19H25Cl3N2O4S | 1 ML
AM-92016 hydrochloride is a small-molecule blocker of delayed rectifier potassium currents (IK), commonly used in electrophysiology and cardiovascular research to modulate action potential duration. It is supplied both as a solid and as a ready-to-use solution to support in vitro pharmacology and ion-channel assays.
- Blocks delayed rectifier potassium channels (IK) and shortens action potential duration.
- Supplied as a 10 mM solution in DMSO or as a dry solid for custom preparation.
- High purity suitable for research use (reported ~99.3%).
- Molecular weight 483.84 and CAS 133229-11-5 for clear identification.
- Available in small-quantity formats compatible with pharmacological assays.
Medchemexpress LLC Zzw-115 hydrochloride | 10122-45-9 | 98.1 % | 573.97 | 5 MG
ZZW-115 hydrochloride is a potent NUPR1 inhibitor with a Kd of 2.1 μM. It induces tumor cell death through necroptosis and apoptosis, demonstrating anticancer activity. It is efficient in killing various cancer cells with IC50 values ranging from 0.42 μM to 4.93 μM. This compound also induces a decrease in ATP production and a ROS overproduction.
- Efficient in killing cancer cells with IC50 values ranging from 0.42 μM to 7.75 μM
- Induces tumor cell death via necroptosis and apoptosis
- Decreases ATP production and induces ROS overproduction
- Inhibits the growth of pancreatic xenografted tumors in vivo
- Demonstrates potent anticancer activity
Medchemexpress LLC Rhosin hydrochloride | 1281870-42-5 | 99.9% | 394.86 | 100 MG
Rhosin hydrochloride is a potent and specific inhibitor of the RhoA subfamily of Rho GTPases. It specifically binds to RhoA to inhibit RhoA-GEF interaction and does not interact with Cdc42 or Rac1. This compound induces cell apoptosis and promotes stress resiliency by enhancing D1-MSN plasticity and reducing hyperexcitability.
- Potent and specific RhoA subfamily Rho GTPases inhibitor
- Induces cell apoptosis
- Promotes stress resiliency through enhancing D1-MSN plasticity and reducing hyperexcitability
- Dose-dependently reduces RhoA and p-MLC1 activities of mammospheres
- Decreases size and reduces number of mammospheres in cells
- Prevents social avoidance and blocks sucrose preference deficits in mice
- Attenuates stress-induced social avoidance
- Blocks stress-induced hyperexcitability in NAc dopamine 1 receptor medium spiny neurons (D1-MSNs)
Medchemexpress LLC FTI-277 hydrochloride | 180977-34-8 | 98.0% | 484.07 | 5 MG
FTI-277 hydrochloride is an inhibitor of farnesyl transferase (FTase). It is a highly potent Ras CAAX peptidomimetic that antagonizes both H- and K-Ras oncogenic signaling and can inhibit hepatitis delta virus (HDV) infection.
- Inhibits farnesyl transferase (FTase)
- Antagonizes H- and K-Ras oncogenic signaling
- Can inhibit hepatitis delta virus (HDV) infection
- Significantly decreases survival of radioresistant cells expressing the 24-kDa isoform
- Stimulates postmitotic cell death in HeLa 3A cells
- Reduces G(2)/M-phase arrest in both cell types (HeLa 3A and HeLa PINA)
- Inhibits migration and invasion in PC-3 cells
- Prevents increased PTP-1B and PTEN protein expression in burned mice
Selleck Chemical LLC Metamizole sodium hydrate S4435-25mg
Metamizole (Dipyrone) sodium hydrate is a potent inhitior of cyclooxygenase (COX) with strong analgesic as well as antipyretic and spasmolytic properties
Medchemexpress LLC GSK2945 (hydrochloride) | 2517771-89-8 | 98.5% | 457.80 | 1 ML
GSK2945 hydrochloride is a tertiary amine and a highly specific Rev-erbα/REV-ERBα (mouse/human reverse erythroblastosis virus α) antagonist with EC50s of 21.5 μM and 20.8 μM, respectively. It enhances cholesterol 7α-hydroxylase (CYP7A1) levels and cholesterol metabolism. For research use only.
- Highly specific Rev-erbα/REV-ERBα antagonist.
- Enhances cholesterol 7α-hydroxylase (CYP7A1) levels.
- Promotes cholesterol metabolism.
- Suitable for research applications.
![Medchemexpress LLC 5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline, 6,7,7a,8-tetrahydro-7-methyl (7aR) | 548-08-3 | 99.9% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232094.png-250.jpg)
Medchemexpress LLC 5H-benzo[g]-1,3-benzodioxolo[6,5,4-de]quinoline, 6,7,7a,8-tetrahydro-7-methyl (7aR) | 548-08-3 | 99.9% | 10 MG
Roemerine is an aporphine alkaloid small-molecule reagent used in biochemical and pharmacological research. It is supplied in small-mass packs for in vitro studies and is commonly used to probe P-glycoprotein interactions and serotonin receptor activity.
- High purity suitable for analytical and biological assays.
- Available in small pack sizes, including 10 MG.
- Molecular weight 279.33 g/mol and formula C18H17NO2 for reference.
- Store sealed at 4°C; follow low-temperature storage guidelines for solutions.
Apexbio Technology LLC 2,4-Di-tert-butylphenol 96-76-4 1g
2 4-Di-tert-butylphenol (CAS 96-76-4) is an endogenous metabolic compound recognized for its antioxidant and anti-inflammatory properties Mechanistic studies have demonstrated that 2 4-Di-tert-butylphenol modulates the expression of genes involved in apoptotic pathways leading to the induction of apoptosis in cancer cell models Additionally experimental evidence indicates antiviral and antifungal activities supporting its use in investigations of infection mechanisms This compound is therefore relevant for research in oncology inflammation and the study of pathogen-host interactions
Medchemexpress LLC Metixene hydrochloride hydrate | 7081-40-5 | 99.9% | 25 MG
Metixene hydrochloride hydrate is an anticholinergic, antiparkinsonian research standard used as a muscarinic acetylcholine receptor antagonist in pharmacology and neuroscience studies. It is supplied as the hydrochloride hydrate salt for improved stability and solubility and is typically provided in small quantities for laboratory research.
- Acts as a muscarinic acetylcholine receptor (mAChR) antagonist for receptor binding and functional assays.
- High purity suitable for analytical and biochemical applications (≈99.9%).
- Molecular weight 363.94 g/mol and formula C20H26ClNOS.
- Available in small package sizes such as 25 MG for laboratory use.
- Provided as a hydrochloride hydrate salt to aid solubility in common solvents.
eMolecules 1259484-97-3 | Medchem Express | SKI-178 | 5mg | 599150633 | HY-12892 | MFCD01913555 | 394.431 | C21H22N4O4
Ambeed | 7-Chloro-[124]triazolo[15-a]pyridine | 100mg | 601097454 | A515415 | 1427452-48-9 | MFCD23708543 | 153.570 | C6H4ClN3
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Medchemexpress LLC LMP744 hydrochloride | 308246-57-3 | 488.92 | 5 MG
LMP744 hydrochloride (MJ-III65 hydrochloride) is a DNA intercalator and Topoisomerase I (Top1) inhibitor exhibiting antitumor activity. It is a solid, light brown to brown in appearance, with a purity of 99.08%.
- DNA intercalator
- Topoisomerase I (Top1) inhibitor
- Exhibits antitumor activity
- Induces dose-dependent accumulation of cells in the S and G2 phases of the cell cycle
- Moderately active against human A253 and FaDu tumor xenografts in vivo