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Filtered Search Results
Medchemexpress LLC KSPWFTTL TFA | 99.3% | 1093.15 | 5 MG
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KSPWFTTL TFA is an immunodominant Kb-restricted epitope derived from the p15E transmembrane protein. This peptide can restore susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes. It is derived from the retroviral p15 TM envelope protein.
- Immunodominant Kb-restricted epitope.
- Derived from p15E transmembrane protein.
- Restores susceptibility of tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes.
- Makes cytolytic T-lymphocyte (CTL)-insusceptible clonal line susceptible to lysis by antiviral CTL when pulsed with the peptide.
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eMolecules 850568-27-3 | 4-(4-Fluorophenyl)aminocarbonylphenylboronic acid | Combi-Blocks | MFCD06659878 | 259.040 | C13H11BFNO3 | 97.000 | OB(O)c1ccc(cc1)C(=O)Nc1ccc(F)cc1 | 1g | 117522308
4-(4-Fluorophenyl)aminocarbonylphenylboronic acid | Combi-Blocks | 850568-27-3 | MFCD06659878 | 259.040 | C13H11BFNO3 | 97.000 | OB(O)c1ccc(cc1)C(=O)Nc1ccc(F)cc1 | 1g | 117522308
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eMolecules 58469-03-7 | Methyl 1-phenylcyclobutane-1-carboxylate | ChemScene | MFCD11035753 | 190.242 | C12H14O2 | 97.000 | COC(=O)C1(CCC1)c1ccccc1 | 100mg | 801476554
Methyl 1-phenylcyclobutane-1-carboxylate | ChemScene | 58469-03-7 | MFCD11035753 | 190.242 | C12H14O2 | 97.000 | COC(=O)C1(CCC1)c1ccccc1 | 100mg | 801476554
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Medchemexpress LLC Nav1.7-IN-3 | 1788872-06-9 | 98.2% | 430.95 g·mol⁻¹ | C17H20ClFN4O2S2 | 25 MG
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Nav1.7-IN-3 is a selective, orally bioavailable inhibitor of the voltage-gated sodium channel Nav1.7, showing potent activity (IC50 8 nM). The compound is reported to have limited central nervous system penetration and is supplied for research use only.
- Potent Nav1.7 inhibition (IC50 8 nM).
- Orally bioavailable profile suitable for in vivo studies.
- Limited CNS penetration, supporting peripheral pain models.
- High analytical purity (98.21%).
- Well-characterized composition (MW 430.95 g·mol⁻¹; formula C17H20ClFN4O2S2).
- Provided for research use only.
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STA Pharmaceutical Fmoc-(R)-3-Amino-4-(pentafluoro-phenyl)-butyric acid | 1 g | CAS 269398-94-9 | MDL MFCD01860941
Fmoc-(R)-3-Amino-4-(pentafluoro-phenyl)-butyric acid is a Amino Acid reagent (Subcategory: Beta AA) sold by WuXi TIDES. Offered in 1 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 269398-94-9
- MDL: MFCD01860941
- InChIKey: HCBMYXPXBOUBBR-GFCCVEGCSA-N
- Molecular Weight: 491.414
- Molecular Formula: C25H18F5NO4
- Purity: ≥95%
- Container Type: 15 mL HDPE
- Pack Size: 1 g
- Net Weight: 1 g
- Gross Weight: 7.8 g
- Commodity Code: 29242970
- Country Of Origin: China
- IUPAC: (R)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(perfluorophenyl)butanoic acid
- SMILES: FC1=C(C(F)=C(C(F)=C1C[C@@H](NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)CC(O)=O)F)F
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STA Pharmaceutical 1-Fmoc-4-(4-fluorophenyl)-4-carboxypiperidine | 25 g | CAS 1076197-06-2 | MDL MFCD11226817
1-Fmoc-4-(4-fluorophenyl)-4-carboxypiperidine is a Amino Acid reagent (Subcategory: Unusual AA) sold by WuXi TIDES. Offered in 25 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 1076197-06-2
- MDL: MFCD11226817
- InChIKey: DPGFVVPTWGNEHH-UHFFFAOYSA-N
- Molecular Weight: 445.49
- Molecular Formula: C27H24FNO4
- Purity: ≥95%
- Container Type: 125 mL HDPE
- Pack Size: 25 g
- Net Weight: 25 g
- Gross Weight: 54.3 g
- Commodity Code: 29333999
- Country Of Origin: China
- IUPAC: 1-(((9H-fluoren-9-yl)methoxy)carbonyl)-4-(4-fluorophenyl)piperidine-4-carboxylic acid
- SMILES: O=C(N1CCC(C2=CC=C(C=C2)F)(CC1)C(O)=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
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Medchemexpress LLC HY-112269 5mg Medchemexpress, Glutaminyl Cyclase Inhibitor 1 CAS:2110449-60-8 Purity:>98%
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Medchemexpress, HY-112269 5mg Glutaminyl Cyclase Inhibitor 1 CAS:2110449-60-8 Glutaminyl Cyclase Inhibitor 1 is a glutaminyl cyclase inhibitor with an IC50 of 0.5 μM. 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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Medchemexpress LLC HY-107329 10mg Medchemexpress, Cefathiamidine CAS:33075-00-2 Purity:>98%
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Medchemexpress, HY-107329 10mg Cefathiamidine CAS:33075-00-2 Cefathiamidine is a first-generation cephalosporin antibacterial agent and is used to treat infections caused by susceptible bacteria. Cefathiamidine exhibits a wide spectrum of antimicrobial activity against bacteria. Cefathiamidine is used for the treatment of respiratory, liver, five senses, urinary tract infections, endocarditis and sepsis. 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 (4-Fluorophenyl)(4-methoxyphenyl)methanol | 1426-55-7 | MFCD06201347 | 1g
Combi-Blocks | (4-Fluorophenyl)(4-methoxyphenyl)methanol | 1g | 205410030 | SH-5363 | 97.000 | 1426-55-7 | MFCD06201347 | 232.254 | C14H13FO2
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eMolecules 308831-61-0 | Medchem Express | Sufugolix | 5mg | 446255107 | HY-100209 | MFCD09837896 | 667.73 | C36H31F2N5O4S
Ambeed | Methyl 1H-indazole-7-carboxylate | 1g | 552544854 | A119107 | 755752-82-0 | MFCD07371608 | 176.175 | C9H8N2O2
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Medchemexpress LLC HY-111386 5mg Medchemexpress, E-7386 CAS:1799824-08-0 Purity:>98%
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Medchemexpress, HY-111386 5mg E-7386 CAS:1799824-08-0 E-7386 is an orally active CBP/beta-catenin modulator. 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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Medchemexpress LLC QTX125 TFA | 2989537-78-0 | 99.9% | 10 MG
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QTX125 TFA is the trifluoroacetic acid salt of QTX125, a potent and highly selective histone deacetylase 6 (HDAC6) inhibitor with reported antitumor activity. It is supplied as a high-purity research compound for biochemical and in vivo studies.
- Potent, selective HDAC6 inhibitor.
- High purity: 99.9%.
- Molecular weight: 531.44 g/mol; formula: C25H20F3N3O7.
- Solubility: soluble in DMSO (125 mg/mL), insoluble in water.
- Storage: store sealed at 4°C; stock solutions -80°C (6 months), -20°C (1 month).
- Available in small research sizes including 10 MG.
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eMolecules 896720-20-0 | VX-11e | MFCD18433366 | 10mg
Ambeed | VX-11e | 10mg | 525159308 | A260385 | 896720-20-0 | MFCD18433366 | 500.360 | C24H20Cl2FN5O2
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Medchemexpress LLC N-((5-fluoro-2,3-dihydro-1-benzofuran-4-yl)methyl)-8-(2-methylpyridin-3-yl)triazolopyrimidin-5-amine | 1951408-58-4 | MFCD31630846 | 99.2% | 376.39 g/mol | C20H17FN6O | 100 MG
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MAK683 is a small-molecule embryonic ectoderm development (EED) inhibitor that binds the EED subunit of PRC2 and acts as an allosteric antagonist of PRC2 function. Supplied for research use, it supports biochemical and cellular studies of epigenetic regulation.
- Allosteric EED/PRC2 inhibitor for epigenetic research.
- Reported purity: 99.18% (manufacturer data).
- Chemical formula: C20H17FN6O; molecular weight: 376.39 g/mol.
- Soluble in DMSO; typical handling for small-molecule reagents.
- Available in multiple pack sizes for laboratory use.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC 5-chloro-2-fluoro-4-(hexahydropyrrolizin-8-ylmethylamino)-N-(thiazol-2-yl)benzenesulfonamide | 1788872-06-9 | 98.2% | 430.95 g/mol | C17H20ClFN4O2S2 | 10 MG
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Nav1.7-IN-3 is a selective, orally bioavailable small-molecule inhibitor of the voltage-gated sodium channel Nav1.7 with a reported IC50 of 8 nM. The compound shows limited central nervous system penetration and is supplied for laboratory research (CAS 1788872-06-9).
- Selective Nav1.7 inhibition (IC50 = 8 nM).
- Orally bioavailable.
- Limited CNS penetration.
- High purity (~98.2%).
- Molecular weight 430.95 g/mol; formula C17H20ClFN4O2S2.
- Provided in small research quantities (e.g., 10 MG).
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