Furans
Medchemexpress LLC 2-isopropylphenyl (2-(naphthalen-2-yl)ethyl)carbamate | 1354359-53-7 | MFCD20926355 | 99.5% | 333.42 g/mol | C22H23NO2 | 50 MG
JW480 is a potent, selective small-molecule inhibitor of the serine hydrolase KIAA1363 (AADACL1) used in biochemical and cell-based research to probe enzyme function and related pathways. This compound is supplied for research use only.
- Potent, selective inhibitor of KIAA1363.
- Intended for research use only.
- High purity: 99.54%.
- Chemical formula: C22H23NO2.
- Molecular weight: 333.42 g/mol.
- CAS number: 1354359-53-7.
- Supplied as a 50 mg quantity.
Medchemexpress LLC Gunagratinib | 2211082-53-8 | 98.5% | C22H25N5O4 | 10MG
Gunagratinib is a research small molecule that irreversibly and covalently inhibits fibroblast growth factor receptors (FGFR). It is orally active in preclinical models and is used in cancer research and biochemical studies; the molecule also contains an alkyne handle that allows copper-catalyzed azide-alkyne cycloaddition (click chemistry) applications.
Medchemexpress LLC PF-06456384 trihydrochloride | 1834610-75-1 | 99.4% | 829.18 g/mol | C35H35Cl3F3N7O3S2 | 100 MG
PF-06456384 trihydrochloride is a potent, selective small-molecule inhibitor of the voltage-gated sodium channel NaV1.7 for laboratory research use. Provided as the trihydrochloride salt, it appears as a white to off-white solid with high listed purity and is used in preclinical pain-model studies. Available in solid and solution formats for flexible assay setup.
- Potent NaV1.7 inhibition (IC50 = 0.01 nM), enabling high-sensitivity pharmacology studies.
- Trihydrochloride salt form for improved solubility and handling.
- High listed purity for reproducible experimental results.
- Available in multiple pack sizes and as a 10 mM DMSO solution for assay flexibility.
- Intended for laboratory research use only; not for human or veterinary use.
Medchemexpress LLC Inx-sm-56 | 2734878-18-1 | 99.5% | 576.70 g/mol | C32H36N2O6S | 5 MG
INX-SM-56 is an ADC cytotoxin intended for use in the synthesis of anti-VISTA antibody-agent conjugates. It is supplied as a solid (white to yellow) with high reported purity, and it has defined solubility and storage profiles suitable for research applications.
- Cas number 2734878-18-1.
- Purity 99.5%.
- Molecular formula C32H36N2O6S.
- Molecular weight 576.70 g/mol.
- Form solid, white to yellow.
- Soluble in DMSO ≥ 50 mg/mL; in vivo formulation ≥ 1.25 mg/mL in 10% DMSO/90% corn oil.
- Store sealed, away from moisture and light; in solvent: -80°C up to 6 months, -20°C up to 1 month.
- Available pack sizes include 1 mg and 5 mg.
Medchemexpress LLC C-021 | 864289-85-0 | 100.0% | 467.65 g/mol | C27H41N5O2 | 5 MG
C-021 is a small-molecule antagonist of the CC chemokine receptor 4 (CCR4) used for research into GPCR signaling and immunology. It inhibits CCR4-mediated chemotaxis in human and mouse systems and is supplied as a solid for laboratory studies.
- Target CCR4.
- Molecular formula C27H41N5O2.
- Molecular weight 467.65 g/mol.
- Purity 99.95%.
- Appearance solid, off-white to light yellow.
- Storage powder: -20°C (up to 3 years); in solvent: -80°C (short-term).
- Supplied in small research quantities.
Medchemexpress LLC TCS PrP Inhibitor 13 25mg | 34320-83-7 | 25MG
TCS PrP Inhibitor 13 an antiprion agent is a cellular prion protein (PrPC) inhibitor TCS PrP Inhibitor 13 as a protease-resistant form of prion protein (PrP-res) accumulation inhibitor shows an IC50 value of 3 nM in both ScN2a and F3 cell lines TCS PrP Inhibitor 13 induces Schwannoma cells apoptosis[1
Apexbio Technology LLC Ethynodiol diacetate 297-76-7 500mg
Ethynodiol diacetate (297-76-7) is a small-molecule agonist targeting progesterone receptors It is designed to selectively bind and activate these receptors thereby modulating gene transcription pathways and influencing reproductive tissue responses Ethynodiol diacetate exerts its biological activity primarily through selective activation of progesterone receptors Based on these pharmacological properties Ethynodiol diacetate holds research potential in studies investigating hormonal regulation contraceptive mechanisms and modulation of the reproductive system
Medchemexpress LLC Furazolidone (Standard) | 67-45-8 | 99.95% | 50 MG
Furazolidone (Standard) is the analytical standard of Furazolidone, intended for research and analytical applications. It is a nitrofuran derivative with antiprotozoal and antibacterial activity, inhibiting AML1-ETO transformed cells with an IC50 of 12.7 μM.
- Analytical standard of Furazolidone.
- Intended for research and analytical applications.
- Nitrofuran derivative.
- Antiprotozoal and antibacterial activity.
- Inhibits AML1-ETO transformed cells with an IC50 of 12.7 μM.
- Commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
![Medchemexpress LLC 2-(4-hydroxyphenyl)-1-(1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl)-ethanone | 1373764-75-0 | 98.3% | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000234533.png-250.jpg)
Medchemexpress LLC 2-(4-hydroxyphenyl)-1-(1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl)-ethanone | 1373764-75-0 | 98.3% | 10 MG
YH-306 is a small-molecule focal adhesion kinase (FAK) inhibitor used in research to study tumor growth, migration, and metastasis. It shows antitumor activity in colorectal cancer models and is supplied at high purity for biochemical and cellular assays.
- Small-molecule FAK inhibitor for pathway and oncology research.
- Demonstrated suppression of colorectal tumor growth and metastasis in preclinical studies.
- High purity suitable for biochemical and cellular assays.
- Available in small research pack sizes for screening and dose-response studies.
- Chemical formula C19H18N2O2; molecular weight 306.36 g/mol.
Medchemexpress LLC 1-aminohydantoin hydrochloride | 2827-56-7 | MFCD02181047 | ≥98.0% | 151.55 | C3H6ClN3O2 | 1mL
1-Aminohydantoin hydrochloride is a major metabolite of Nitrofurantoin (HY-A0090) in animal tissues and can be used as a standard for the determination of residues of veterinary agents in meat milk et al 1-Aminohydantoin hydrochloride covalently binds to tissue proteins and is released from the tissues under slightly acidic conditions and derivatized with 2-nitrobenzaldehyde to form nitrophenyl derivatives of 1-Aminohydantoin hydrochloride before detection[1][2]