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Filtered Search Results
Ambeed AMBEED
5000870148 ETHYL 5-PHENYLTHIAZOLE-2 100MG
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![Medchemexpress LLC [Sar9,Met(O2)11]-Substance P | 110880-55-2 | 99.6% | 1393.66 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000424719.png-250.jpg)
Medchemexpress LLC [Sar9,Met(O2)11]-Substance P | 110880-55-2 | 99.6% | 1393.66 | 5 MG
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[Sar9,Met(O2)11]-Substance P is a tachykinin NK1 receptor selective agonist.
- High purity: 99.6%
- Appearance: White to off-white solid
- Molecular weight: 1393.66
- Soluble in H2O and PBS at 100 mg/mL with sonication
- Powder stability: 2 years at -80°C, 1 year at -20°C (sealed, away from moisture)
- In-solvent stability: 6 months at -80°C, 1 month at -20°C (sealed, away from moisture)
- Targets NK1 receptor with an IC50 of 1.1 x 10-10 M in human U373MG cells
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Medchemexpress LLC Cis VH-298 | 2097381-86-5 | 100.0% | 523.65 g/mol | C27H33N5O4S | 10 MG
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cis VH-298 is the cis stereoisomer of VH-298 that acts as a VHL:HIF-α interaction inhibitor. Compared with the trans isomer, the cis form shows a significant loss of binding specificity of hydroxylated HIF-1α peptides to the VHL protein in vitro. The compound is supplied as a white to off-white solid with high purity for research use and should be stored protected from light.
- Cis stereochemistry reduces binding specificity to VHL.
- Useful as a comparator in VHL-HIF biological studies.
- High purity (approximately 99.96%) suitable for biochemical assays.
- Molecular weight 523.65 g/mol; formula C27H33N5O4S.
- Solid, white to off-white appearance; store protected from light.
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eMolecules 3008-39-7 | 1,2-Cycloheptanedione | Accela ChemBio (ASD) | MFCD00046507 | 126.155 | C7H10O2 | 95.000 | O=C1CCCCCC1=O | 0.25g | 528278104
1,2-Cycloheptanedione | Accela ChemBio (ASD) | 3008-39-7 | MFCD00046507 | 126.155 | C7H10O2 | 95.000 | O=C1CCCCCC1=O | 0.25g | 528278104
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BIOHIPPO
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5000856598 HUMAN MET/C-MET/HGFR PE
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Aobchem AOBCHEM
5000863096 2 2-DIBROMO-1- 2-CHLOROPHENYL
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000369518 C-MET INHIBITOR 1 50MG
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eMolecules THIAZOL-5-YLMETHYL 2S 3S 10G
5000160532 THIAZOL-5-YLMETHYL 2S 3S 10G
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![Medchemexpress LLC 4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide | 2097381-85-4 | MFCD30742947 | >=98.0% | 523.6 g/mol | C27H33N5O4S | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000212364.png-250.jpg)
Medchemexpress LLC 4-hydroxy-N-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide | 2097381-85-4 | MFCD30742947 | >=98.0% | 523.6 g/mol | C27H33N5O4S | 25 MG
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VH-298 is a cell-active small-molecule inhibitor of the VHL:HIF-α interaction used as a research tool to stabilize HIF-α and investigate hypoxia signaling and targeted protein degradation. It is applicable to biochemical and cellular assays and is commonly used in PROTAC development.
- Potent inhibitor of VHL:HIF-α interaction.
- Cell-active; promotes HIF-α accumulation in cells.
- Useful as a tool compound in hypoxia signaling studies and PROTAC research.
- High purity suitable for biochemical and cellular assays.
- Well-characterized chemical identifiers for compound tracking.
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![Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 5mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000096433.png-250.jpg)
Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 5mg
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Cytochrome P450 CYP1B1 190-198 is a tumor-associated antigen peptide derived from CYP1B1 It is designed to induce HLA-A2-restricted T-cell responses against the CYP1B1(190-198) epitope thereby promoting tumor-specific cytotoxic immune responses Cytochrome P450 CYP1B1 190-198 exerts its biological activity primarily through antigen-specific activation of CD8 T cells In HLA-A2 transgenic mouse models this peptide delivered via plasmid DNA and poly(lactide-co-glycolide) microparticles demonstrates the ability to elicit CYP1B1 peptide-specific T-cell immunity Based on these pharmacological properties Cytochrome P450 CYP1B1 190-198 holds research potential in cancer immunotherapy and studies of tumor-specific cytotoxic T-cell responses
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Aobchem AOBCHEM
5000863517 1- 2 3-DIFLUOROPHENYL -2 2 2-T
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eMolecules 59020-44-9 | Ambeed | 4-Phenylthiazole-2-carboxylic acid | 250mg | 513350042 | A444619 | MFCD00990415 | 205.23 | C10H7NO2S
Ambeed | 4-Phenylthiazole-2-carboxylic acid | 250mg | 513350042 | A444619 | 59020-44-9 | MFCD00990415 | 205.230 | C10H7NO2S
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Aobchem AOBCHEM
5000863129 1- 6-CHLORO-2 3-DIFLUOROPHENYL
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Medchemexpress LLC Coblopasvir dihydrochloride | 1966138-53-3 | 99.2% | 855.81 | C41H52Cl2N8O8 | 50 MG
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Coblopasvir dihydrochloride is a pangenotypic non-structural protein 5A (NS5A) inhibitor provided for research use in studies of chronic hepatitis C virus (HCV) infection. The dihydrochloride salt is supplied with high purity and is available as a solid and as ready-to-use DMSO solutions for in vitro and preclinical research.
- High purity (99.2%).
- Molecular weight 855.81 g/mol.
- Empirical formula C41H52Cl2N8O8.
- Available in solid (mg quantities) and 10 mM DMSO solution formats.
- CAS number 1966138-53-3 for unambiguous identification.
- Store sealed, away from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
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eMolecules 937369-77-2 | AstaTech | 5-PHENYLTHIAZOLE-2-CARBOXYLIC ACID | 0.25g | 448262900 | O11490 | 95 | MFCD11846699 | 205.23 | C10H7NO2S
AstaTech | 5-PHENYLTHIAZOLE-2-CARBOXYLIC ACID | 0.25g | 448262900 | O11490 | 95.000 | 937369-77-2 | MFCD11846699 | 205.230 | C10H7NO2S
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