Aminophenols
eMolecules 3-Chloro-N-(3-hydroxyphenyl)-2,2-dimethylpropanamide | 303986-05-2 | MFCD00793397 | 100mg
Oakwood Chemical | 3-Chloro-N-(3-hydroxyphenyl)-2,2-dimethylpropanamide | 100mg | 537712736 | 181182 | | 303986-05-2 | MFCD00793397 | 227.690 | C11H14ClNO2
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Medchemexpress LLC DI-82 | 1638148-50-1 | MFCD28386371 | 98.0% | 510.65 g·mol⁻¹ | C20H26N6O4S3 | 5 MG
DI-82 is a small-molecule inhibitor of deoxycytidine kinase (dCK) with reported biochemical potency and observed antitumor activity. It is supplied for research use in biochemical assays and preclinical studies as a powder form for laboratory workflows.
- Potent dCK inhibition: IC50app 27.8 nM; Kiapp 9.2 nM.
- High purity (98.0%) suitable for research applications.
- Soluble in DMSO at 120 mg/mL; ultrasonic assistance may be needed.
- Provided as a powder with recommended storage: -20°C for powder; -80°C for long-term storage in solvent.
- Intended for in vitro studies and preclinical antitumor research.
Medchemexpress LLC Bn82002 hydrochloride | 1049740-43-3 | MFCD08276983 | 99.4% | 395.88 | C19H26ClN3O4 | 5 MG
BN82002 hydrochloride is an irreversible inhibitor of the CDC25 phosphatase family for laboratory research. It is supplied as the hydrochloride salt and is available as a solid or as a 10 mM solution in DMSO (CAS 1049740-43-3).
- Potent, selective inhibitor of CDC25 phosphatases.
- Available as solid and 10 mM solution in DMSO for convenience.
- High purity: 99.4% (RP-HPLC).
- Chemical formula C19H26ClN3O4; molecular weight 395.88.
- Storage: solid at 4°C; in solvent at -80°C (up to 6 months) or -20°C (1 month).
- For research use only; not for human or clinical use.
Medchemexpress LLC Rs100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 10 MG
RS100329 hydrochloride is a selective α1A-adrenoceptor antagonist supplied as the hydrochloride salt for research use. It is reported to have high affinity for α1A (pKi ≈ 9.6) with lower affinity for α1D and α1B, and is used in preclinical studies including investigations of urethral reflex contractions and benign prostatic hyperplasia.
- Selective α1A-adrenoceptor antagonist for receptor pharmacology research.
- High reported purity suitable for preclinical assays.
- Supplied as a stable hydrochloride salt in solid form.
- Available in small milligram pack sizes for early-stage studies.
Medchemexpress LLC BIIL-260 hydrochlori 10mM 1mL | 192581-24-1 | 1 ML
Biil-260 hydrochloride is a potent leukotriene B4 (LTB4) receptor antagonist used in research to investigate inflammatory signaling pathways. It is typically supplied at high purity and commonly provided as a 10 mM solution in DMSO for in vitro applications.
- Potent LTB4 receptor antagonist
- High purity (99.4%)
- Molecular weight 503.03 g/mol
- Supplied as a 10 mM solution in DMSO, 1 mL
- Appearance: solid, white to off-white
- Storage: solids sealed at 4°C; in solution store at -80°C for long term
TARGETMOL CHEMICALS INC CGS 15435 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. CGS 15435 is a potent thromboxen (TxA2) synthetase inhibitor (IC50 1 nM). CGS 15435 acts on PGI2 synthase cyclooxygenase and liposynthase with much less selectivity than on thromboxin synthase. purity: 99%
TARGETMOL CHEMICALS INC ECOPLADIB 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ecopladib (PLA 725) is a sub-micromolar inhibitor of cytosolic phospholipase A2(alpha) (cPLA2(alpha)) with IC50s of 0.15 uM and 0.11 uM in the GLU micelle and rat whole blood assays respectively. purity: 99%
TARGETMOL CHEMICALS INC GLPG0492 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. GLPG0492 is a novel selective androgen receptor modulator. After oral dosing it showed anabolic activity on muscle strongly dissociated from the androgenic activity on the prostate. purity: 98%
TARGETMOL CHEMICALS INC JHU395 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. JHU395 is an orally-bioavailable prodrug of a lipophilic glutamine antagonist (GA) 6-diazo-5-oxo-L-norleucine (DON). It demonstrates delivery of DON to malignant peripheral nerve sheath tumor (MPNST) both in vitro and in vivo resulting in significant antitumor activity in MPNST. Additionally JHU395 exhibits plasma stability. purity: 99%
![eMolecules ChemScene / 1-(5-Ethynyl-2-hydroxyphenyl)ethanone / 100mg / 726025579 / CS-0566511 / 0.000 / 1350803-03-0 / [null] / 160.172 / C10H8O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502469533.JPG-250.jpg)
eMolecules ChemScene / 1-(5-Ethynyl-2-hydroxyphenyl)ethanone / 100mg / 726025579 / CS-0566511 / 0.000 / 1350803-03-0 / [null] / 160.172 / C10H8O2
ChemScene / 1-(5-Ethynyl-2-hydroxyphenyl)ethanone / 100mg / 726025579 / CS-0566511 / 0.000 / 1350803-03-0 / [null] / 160.172 / C10H8O2
![Medchemexpress LLC N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-α,α-dimethyl-1H-indole-3-ethanamine HCl | 169505-93-5 | 99.9% | 449.41 | C24H30Cl2N2O2 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000211386.png-250.jpg)
Medchemexpress LLC N-[2-(2-cyclopropylmethoxyphenoxy)ethyl]-5-chloro-α,α-dimethyl-1H-indole-3-ethanamine HCl | 169505-93-5 | 99.9% | 449.41 | C24H30Cl2N2O2 | 1 ML
A selective α1A adrenoceptor antagonist supplied as a ready-to-use 10 mM solution in DMSO for in vitro pharmacology and receptor signaling studies. Demonstrates high potency and is provided at high purity for research applications.
- Supplied as a 10 mM solution in DMSO, 1 mL.
- High potency: pKi 9.1 and pA2 9.8.
- High purity: 99.9%.
- Molecular weight: 449.41.
- CAS number: 169505-93-5.
- Storage: store sealed, away from moisture; in solvent: -80°C up to 6 months, -20°C up to 1 month.