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Filtered Search Results
Medchemexpress LLC Emvododstat (PTC299) | 1256565-36-2 | 99.9% | 467.34 g/mol | C25H20Cl2N2O3 | 50MG
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PTC299 (emvododstat) is an orally active small-molecule inhibitor that selectively suppresses VEGFA mRNA translation and inhibits dihydroorotate dehydrogenase (DHODH). Provided for research use, it is supplied as solid samples and DMSO solutions and is used in studies of VEGF regulation, pyrimidine biosynthesis, and oncology and immunology research.
- High purity: 99.9% by assay.
- Molecular weight: 467.34 g/mol.
- Chemical formula: C25H20Cl2N2O3.
- Physical appearance: white to light yellow solid.
- Available as solid and as 10 mM solution in DMSO.
- Suitable for studies of VEGF regulation and DHODH-related pathways.
- Offered in multiple package sizes including 50 mg.
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![eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502148824.JPG-250.jpg)
eMolecules 58879-34-8 | (S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
(S)-(5-Oxotetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate | Oakwood Chemical | 58879-34-8 | MFCD00082548 | 270.300 | C12H14O5S | 98.000 | Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1CCC(=O)O1 | 100mg | 537714944
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Medchemexpress LLC SRC INHIBITOR 1 5MG
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Src Inhibitor 1 is a potent, ATP-competitive and selective dual site Src tyrosine kinase inhibitor with IC50 values of 44 nM for Src and 88nM for Lck.CAS No. : 179248-59-0
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Apexbio Technology LLC Ipriflavone (Osteofix) 35212-22-7 500mg
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Ipriflavone Osteofix is a small-molecule inhibitor targeting bone resorption It is designed to modulate osteoclast-related signaling pathways thereby reducing bone resorptive activity Ipriflavone Osteofix exerts its biological activity primarily through inhibition of osteoclast-mediated bone remodeling In in vitro studies Ipriflavone Osteofix demonstrates inhibition of cellular signaling processes involved in bone mineral loss Based on these pharmacological properties Ipriflavone Osteofix holds research potential in experimental studies of osteoporosis and related bone disorders
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Medchemexpress LLC HY-19477 5mg Medchemexpress, SB-616234-A CAS:908601-49-0 Purity:>98%
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Medchemexpress, HY-19477 5mg SB-616234-A CAS:908601-49-0 SB-616234-A is a selective and orally bioavailable 5-HT1B receptor antagonist, with anxiolytic and antidepressant activity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1187187-10-5 | Medchem Express | AN3199 | 5mg | 446270438 | HY-19830 | MFCD29924720 | 327.14 | C17H18BNO5
Ambeed | (transtrans)-4-(4-Ethoxy-23-difluorophenyl)-4-pentyl-11-bi(cyclohexane) | 1g | 525163281 | A267675 | 124728-81-0 | MFCD27978437 | 392.575 | C25H38F2O
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Medchemexpress LLC Phenothrin | 26002-80-2 | 97.7% | 5 MG
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Phenothrin is a Type I pyrethroid insecticide that induces dose-dependent DNA damage in human peripheral blood lymphocytes and hepatocytes. It exhibits genotoxic potential and is used for pest control in agriculture, households, public health, and for eliminating human head lice infestations.
- Induces dose-dependent DNA damage
- Exhibits genotoxic potential
- Used for pest control in agriculture, households, and public health
- Effective for eliminating human head lice infestations
- Available in liquid form
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Medchemexpress LLC Redafamdastat | 1020315-31-4 | 98.86% | C23H20F3N5O2 | 100 MG
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Redafamdastat (PF-04457845) is a highly efficacious and selective FAAH inhibitor, functioning through a covalent, irreversible mechanism by carbamylating the active-site serine nucleophile of FAAH. It demonstrates exquisite selectivity for FAAH over other members of the serine hydrolase superfamily, completely inhibiting FAAH in human and mouse membrane proteomes without affecting off-targets even at high concentrations. Oral administration has shown efficacy comparable to naproxen in a rat model of inflammatory pain, significantly inhibiting mechanical allodynia.
- Highly efficacious and selective FAAH inhibitor
- Inhibits FAAH through a covalent, irreversible mechanism
- Shows exquisite selectivity for FAAH over other serine hydrolases
- Completely inhibits FAAH in human and mouse membrane proteomes
- Effective in reducing inflammatory pain in vivo
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Medchemexpress LLC 1,3-Dimethoxybenzene | 151-10-0 | 99.99% | 138.17 | 1 ML
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1,3-Dimethoxybenzene is a volatile compound characterized by a sweet medicinal odor, featuring hazelnut, resinous, and woody notes. It has been identified as a new volatile component in Douro region grape musts and port wines.
- Possesses a distinct sweet medicinal odor with notes of hazelnut, resin, and wood.
- Identified as a new volatile component of Douro region grape musts and port wines.
- Can be isolated from port wine extracts using flash chromatography.
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Medchemexpress LLC HY-15729A 5mg Medchemexpress, Rociletinib hydrobromide CAS:1446700-26-0 Purity:>98%
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Medchemexpress, HY-15729A 5mg Rociletinib hydrobromide CAS:1446700-26-0 Rociletinib hydrobromide (CO-1686 hydrobromide) is an orally delivered kinase inhibitor that specifically targets the mutant forms of EGFR including T790M, and the Ki values for EGFRL858R/T790M and EGFRWT are 21.5 nM and 303.3 nM, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1260672-37-4 | 2,5-dibromo-3-methylpyrazine | MFCD18250173 | 1g
Ambeed | 45-Dichloro-13-bis(26-di(pentan-3-yl)phenyl)-1H-imidazol-3-ium chloride | 50mg | 666597984 | A1483524 | 1435347-23-1 | 606.160 | C35H51Cl3N2
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eMolecules 2139330-34-8 | Medchem Express | SERCA2a activator 1 | 5mg | 713705957 | HY-124873 | 551.66 | C32H29N3O4S
Ambeed | Bis(2-Bromoethyl)amine hydrobromide | 250mg | 506387351 | A100034 | 43204-63-3 | MFCD11044002 | 311.843 | C4H10Br3N
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Medchemexpress LLC AMG 837 calcium hydrate | 1259389-38-2 | 99.0% | 455.45 | 100 MG
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AMG 837 calcium hydrate is a potent, orally bioavailable, and partial agonist of GPR40/FFA1. It inhibits specific [3H]AMG 837 binding at the human FFA1 receptor with a pIC50 of 8.13. AMG 837 calcium hydrate can enhance insulin secretion and lower glucose levels in rodents. It is also a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent, orally bioavailable, and partial agonist of GPR40/FFA1.
- Inhibits specific [3H]AMG 837 binding at the human FFA1 receptor with a pIC50 of 8.13.
- Enhances insulin secretion and lowers glucose levels in rodents.
- Click chemistry reagent with an Alkyne group for CuAAc reactions.
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Medchemexpress LLC Epertinib hydrochloride | 2071195-74-7 | 98.2% | 596.48 g/mol | C30H28Cl2FN5O3 | 100 MG
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Epertinib hydrochloride is the hydrochloride salt of epertinib, a potent, orally active, reversible, and selective inhibitor of EGFR, HER2, and HER4. It is provided for preclinical research to evaluate signaling pathways and antitumor efficacy and is compatible with click-chemistry applications because of an alkyne functional group.
- Potent, selective tyrosine kinase inhibitor of EGFR, HER2, and HER4.
- Used in preclinical antitumor and signaling research.
- Contains an alkyne moiety compatible with copper-catalyzed azide-alkyne cycloaddition (CuAAC).
- Supplied as a light yellow to yellow solid with high purity.
- Stable under recommended storage: 4°C sealed; in solvent -80°C (6 months), -20°C (1 month).
- Molecular weight 596.48 g/mol; molecular formula C30H28Cl2FN5O3.
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MEDCHEMEXPRESS LLC TAK-593 5MG
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501873261 TAK-593 5MG
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