Benzenoids
eMolecules 1-(2-Amino-4-fluorophenyl)ethanone | 159305-15-4 | MFCD20621031 | 1g
Ambeed | 1-(2-Amino-4-fluorophenyl)ethanone | 1g | 600840196 | A430032 | | 159305-15-4 | MFCD20621031 | 153.156 | C8H8FNO
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eMolecules 4-(3-Chloro-4-fluorophenyl)-1H-1,2,4-triazol-5(4H)-one | 1346235-03-7 | | 1g
Apollo Scientific | 4-(3-Chloro-4-fluorophenyl)-1H-1,2,4-triazol-5(4H)-one | 1g | 562430660 | PC32900 | | 1346235-03-7 | | 213.600 | C8H5ClFN3O
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eMolecules Medchem Express / AZ960 / 1mg / 446258578 / HY-10411 / / 905586-69-8 / MFCD16621127 / 354.365 / C18H16F2N6
Medchem Express / AZ960 / 1mg / 446258578 / HY-10411 / / 905586-69-8 / MFCD16621127 / 354.365 / C18H16F2N6
eMolecules Medchem Express / Relugolix / 5mg / 446267437 / HY-16474 / / 737789-87-6 / MFCD25976856 / 623.640 / C29H27F2N7O5S
Medchem Express / Relugolix / 5mg / 446267437 / HY-16474 / / 737789-87-6 / MFCD25976856 / 623.640 / C29H27F2N7O5S
Medchemexpress LLC N-(4-chloro-3-nitrophenyl)-4-nitro-2,1,3-benzoxadiazol-5-amine | 313964-19-1 | 99.9% | 335.66 g/mol | C12H6ClN5O5 | 10 MG
HIF-2α-IN-3 is a small-molecule allosteric inhibitor of hypoxia-inducible factor-2α (HIF-2α) used as a research reagent in studies of hypoxia signaling and oncology. Reported biochemical activity includes an IC50 of 0.4 μM and a KD of 1.1 μM; the compound is supplied as a high-purity solid for laboratory use.
- Allosteric HIF-2α inhibition with reported IC50 0.4 μM and KD 1.1 μM.
- Suitable for in vitro studies of hypoxia signaling and cancer biology.
- High purity suitable for research applications.
- Supplied as a light yellow solid for standard laboratory handling.
Medchemexpress LLC EGFR-IN-17 10mg | 2817679-31-3 | 568.01 | C27H31ClN7O3P | 10 MG
EGFR-IN-17 is a potent, selective small-molecule inhibitor of the epidermal growth factor receptor (EGFR), active against resistance-associated mutants such as C797S, T790M, and L858R. Supplied as a 10 mg research-use compound, it is used to study EGFR signaling and mechanisms of drug resistance in biochemical and cellular assays.
- Potent EGFR inhibition (IC50 0.0002 μM).
- Active against resistance-associated mutants C797S, T790M, and L858R.
- High purity suitable for research applications (98.18%).
- Well-characterized chemical identity (MW 568.01; formula C27H31ClN7O3P).
- Available in small quantities convenient for assay development.
- Accompanied by a product data sheet with experimental and handling information.
eMolecules AstaTech / 4-FLUOROPHENETHYL ALCOHOL / 5g / 296375959 / 67685 / 98.000 / 7589-27-7 / MFCD00002898 / 140.157 / C8H9FO
AstaTech / 4-FLUOROPHENETHYL ALCOHOL / 5g / 296375959 / 67685 / 98.000 / 7589-27-7 / MFCD00002898 / 140.157 / C8H9FO
Medchemexpress LLC PRX-08066 | 866206-54-4 | C19H17ClFN5S | 1 MG
PRX-08066 is a selective and orally active 5-hydroxytryptamine receptor 2B (5-HT2BR) antagonist. It inhibits the MAPK pathway, 5-HT release, and the expression of fibrotic factors. This product can be used for research related to pulmonary Arterial Hypertension (PAH) and neuroendocrine tumors (NET).
- Selective and orally active 5-HT2BR antagonist (Ki of 3.4 nM)
- Inhibits MAPK pathway and 5-HT release
- Inhibits expression of fibrotic factors (TGFβ1, CTGF, and FGF2)
- Inhibits proliferation of KRJ-I cells
- Induces apoptosis via caspase-3 activation
- Inhibits pulmonary vascular remodeling
Medchemexpress LLC N1,N3,N5-tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide | 2922283-38-1 | >98.0% | C93H177N3O3 | 10MG
N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide is an ionizable lipid-like compound used for research on lipid nanoparticle (LNP) formulations and nucleic acid delivery. It is applied in formulation optimization and preclinical mRNA delivery studies, and is supplied as a high-molecular-weight solid with supporting documentation for laboratory use.
- Ionizable lipid-like structure suitable for LNP formulation.
- Supports mRNA delivery and nucleic acid encapsulation studies.
- High molecular weight and long alkyl chains enhance membrane interaction.
- Provided as a research-grade solid with documentation for reproducible use.
![eMolecules Medchem Express / CDK9-IN-15 / 5mg / 719836183 / HY-147026 / / 852678-17-2 / [null] / 293.340 / C16H11N3OS](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502458333.PNG-250.jpg)
eMolecules Medchem Express / CDK9-IN-15 / 5mg / 719836183 / HY-147026 / / 852678-17-2 / [null] / 293.340 / C16H11N3OS
Medchem Express / CDK9-IN-15 / 5mg / 719836183 / HY-147026 / / 852678-17-2 / [null] / 293.340 / C16H11N3OS
Medchemexpress LLC Relamorelin TFA | 2863659-22-5 | 99.8% | 905.00 | C45H51F3N8O7S | 10 MG
Relamorelin TFA is the trifluoroacetate salt of Relamorelin (RM-131), a pentapeptide ghrelin/growth hormone secretagogue receptor agonist supplied as a solid for laboratory research. It stimulates growth hormone release and accelerates gastric emptying, and is used in preclinical investigations of gastrointestinal motility and cachexia.
- High purity of 99.8%.
- Molecular weight of 905.00 g/mol.
- CAS number 2863659-22-5.
- Supplied as a solid suitable for bench-top handling and formulation.
- Selective GHSR agonist that increases growth hormone release and accelerates gastric emptying.
- Intended for preclinical research into gastroparesis and cachexia models.
eMolecules Nonanamide | 1120-07-6 | MFCD00025540 | 50mg
Toronto Research Chemicals | Nonanamide | 50mg | 601591012 | B504368 | | 1120-07-6 | MFCD00025540 | 157.257 | C9H19NO
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Medchemexpress LLC α-Spinasterol | 481-18-5 | MFCD00200554 | 5 MG
α-Spinasterol is an orally taken antagonist of transient receptor potential vanilloid 1 (TRPV1), and it is also an inhibitor of COX-1 and COX-2, with IC50 values of 16.17 μM and 7.76 μM, respectively. It exhibits antibacterial, anti-inflammatory, antidepressant, and antioxidant effects, has the ability to cross the blood-brain barrier, and can improve diabetes in mice.
- Antagonist of transient receptor potential vanilloid 1 (TRPV1)
- Inhibitor of COX-1 and COX-2
- Exhibits antibacterial, anti-inflammatory, antidepressant, and antioxidant effects
- Ability to cross the blood-brain barrier
- Can improve diabetes in mice