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Filtered Search Results
Aobchem 4-(Ethoxycarbonyl)cyclohexene-1-boronic acid pinacol ester | ≥95% | CAS 1049004-32-1 | C15H25BO4 | 1g
4-(Ethoxycarbonyl)cyclohexene-1-boronic acid pinacol ester | ≥95% | CAS 1049004-32-1 | C15H25BO4 | 1g
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Medchemexpress LLC Α-D-Glucopyranose | 22415-91-4 | 98% | 700.69 | 25 G
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α-D-Glucopyranose, 98% (1,2,3,4,6-Pentabenzoate, 98%) can be used in glycobiology research. It is for research use only and not sold to patients. The appearance is a white to off-white solid.
- Can be used in glycobiology research.
- For research use only.
- Not sold to patients.
- White to off-white solid appearance.
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Medchemexpress LLC BMS-502 | 2407854-18-4 | 99.3% | 516.50 | 100 MG
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BMS-502 is a potent dual inhibitor of diacylglycerol kinase (DGK) α and ζ, with IC50 values of 4.6 nM and 2.1 nM, respectively. It has been shown to enhance T cell immune responses in mice and can be utilized in tumor immunity related research.
- Potent dual inhibitor of diacylglycerol kinase alpha and zeta.
- Enhances T cell immune responses.
- Useful in tumor immunity research.
- Has an EC50 of 340 nM in mouse cytotoxic T cell IFN-gamma assay.
- Demonstrates dose-dependent immune stimulation in mouse models.
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Medchemexpress LLC KCL-286 | 1952276-71-9 | 98.9% | 334.33 | 25 MG
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KCL-286 is an orally active and brain-penetrant retinoic acid receptor (RAR) β2 agonist. It targets RARβ2 with selectivity over RAR α and RAR γ, activating RARβ2 in injured neurons. This compound induces axonal regeneration of both spinal and sensory nerves through the inhibitory environment of the CNS, modulates neuroinflammation, and extracellular matrix molecules.
- Orally active and brain-penetrant RAR β2 agonist
- Selectivity for RARβ2 over RAR α and RAR γ
- Activates RARβ2 in injured neurons
- Induces axonal regeneration of spinal and sensory nerves
- Modulates neuroinflammation and extracellular matrix molecules
- Can modulate CSPG expression by neuronal secretion of decorin to promote myelination and axonal growth
- Potential for research in spinal cord injury and traumatic nerve injury
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Medchemexpress LLC PAP 248-286 (acetate) | 98.9% | 4551.39 (free acid) | 1 MG
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PAP 248-286 (Prostatic acid phosphatase (248-286)) acetate is a biologically active peptide that acts as a semen-derived enhancer of viral infection (SEVI) factor. This peptide significantly increases HIV infection by enhancing virion attachment to target cells.
- Biologically active peptide
- Semen-derived enhancer of viral infection (SEVI) factor
- Significantly increases HIV infection by enhancing virion attachment to target cells
- Applications in COVID-19 anti-virus research
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Medchemexpress LLC -D-GLUCOPYRANOSE 2- | 1G
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-D-GLUCOPYRANOSE 2- | 1G
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Medchemexpress LLC 2 5-ANHYDRO-D-GLUCIT 1 mg
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2 5-ANHYDRO-D-GLUCIT 1MG
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Medchemexpress LLC PAP 248-286 ACETATE 1 mg
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PAP 248-286 ACETATE 1MG
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Medchemexpress LLC A-D-GLUCOPYRANOSE 2 250 mg
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A-D-GLUCOPYRANOSE 2 250MG
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Medchemexpress LLC 2 5-ANHYDRO-D-MANNIT 100 mg
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2 5-ANHYDRO-D-MANNIT 100MG
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BIOHIPPO Research Grade Anti-Human CD340/ERBB2/HER2/NEU Biosimilar Antibody (ADCT-502), 100 µg
ADCT-502 is a research-grade biosimilar antibody targeting CD340/ERBB2/HER2/NEU. It reacts with Human. Suitable for ELISA, FACS, Functional assay, Research in vivo. This research-grade biosimilar supports comparability, functional, PK/PD and immunogenicity studies. Supplied as 100 ug.
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A2B CHEM LLC
NC3935814 D-RIBITOL 1 4 ANHYDRO 5 O 10G
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Selleck Chemical LLC FHD-286-E1178-1G
FHD-286 is a BRG1/BRM ATPase inhibitor for the treatment of BAF-related disorders such as acute myeloid leukemia
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Selleck Chemical LLC g-caprolactone
-caprolactone is well-known as a food flavor and is a biostimulant molecule promoting the growth of bacteria with biocontrol activity against soft-rot pathogens
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Medchemexpress LLC NCT-502 10mM 1mL | 1542213-00-2 | 1 ML
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NCT-502 is a research-grade small molecule inhibitor of phosphoglycerate dehydrogenase (PHGDH). It is cytotoxic to PHGDH-dependent cancer cells and reduces glucose-derived serine production; reported IC50 against PHGDH is 3.7 μM. The compound is supplied as a light yellow to yellow solid and is offered as a 10 mM solution in DMSO (1 mL) and multiple powder sizes for laboratory research.
- Mechanism: reversible PHGDH inhibitor with reported IC50 3.7 μM.
- Purity: ~98.6%.
- Appearance: light yellow to yellow solid.
- Solubility: highly soluble in DMSO (≈130 mg/mL).
- Storage: powder -20°C (long term) or 4°C; in solution -80°C or -20°C.
- Pack formats: 1 mL DMSO solution (10 mM) and multiple mg quantities available.
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