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Filtered Search Results
Medchemexpress LLC PYRIMIDINE-4 6-DICAR 1G
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PYRIMIDINE-4 6-DICAR 1G
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Medchemexpress LLC N2-ACETYLGUANINE 100G
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N2-ACETYLGUANINE 100G
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Medchemexpress LLC 2 6-DIPYRIDIN-4-YL 250 mg
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2 6-DIPYRIDIN-4-YL 250MG
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Medchemexpress LLC Ethyl 2-(dimethylamino)acetate | 33229-89-9 | 99.7% | 131.18 | 25 G
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Ethyl 2-(dimethylamino)acetate is a Glycine derivative intended for research use only. Amino acids and amino acid derivatives are recognized as beneficial ergogenic dietary substances due to their influence on anabolic hormone secretion, fuel supply during exercise, mental performance during stress-related tasks, and prevention of exercise-induced muscle damage. It is a colorless to light yellow liquid.
- For research use only
- Beneficial as ergogenic dietary substances
- Influences anabolic hormone secretion
- Supplies fuel during exercise
- Enhances mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
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eMolecules 1878-69-9 | Ambeed | 2-(3-Iodophenyl)acetic acid | 100mg | 552527393 | A108605 | MFCD00046548 | 262.046 | C8H7IO2
Ambeed | N-(3-Amino-4-methylphenyl)-3-(trifluoromethyl)benzamide | 100mg | 672838858 | A684796 | 30069-31-9 | MFCD09930727 | 294.277 | C15H13F3N2O
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Medchemexpress LLC 1 3-DIMETHYLNAPHTHAL 250 mg
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1 3-DIMETHYLNAPHTHAL 250MG
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Medchemexpress LLC D-Allose | 2595-97-3 | 99.85% | 250 MG
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D-Allose is an endogenous metabolite that exhibits antitumor activity against various cancer cells. It scavenges reactive oxygen species (ROS) and reduces oxidative stress damage. D-Allose also shows anti-inflammatory and neuroprotective effects through the inhibition of the TLR4/PI3K/AKT signaling pathway. Additionally, it possesses antihypertensive, cryoprotective, and anti-osteoporotic activities.
- Exhibits antitumor activity
- Scavenges reactive oxygen species (ROS)
- Reduces oxidative stress damage
- Shows anti-inflammatory effects
- Provides neuroprotective effects
- Inhibits the TLR4/PI3K/AKT signaling pathway
- Possesses antihypertensive activity
- Possesses cryoprotective activity
- Possesses anti-osteoporotic activity
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eMolecules 1363381-59-2 | 1-(4-Chloro-7h-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone | Combi-Blocks, Inc. | MFCD22205848 | 195.610 | C8H6ClN3O | 98.000 | CC(=O)c1c[nH]c2ncnc(Cl)c12 | 25g | 837464375
1-(4-Chloro-7h-pyrrolo[2,3-d]pyrimidin-5-yl)ethanone | Combi-Blocks, Inc. | 1363381-59-2 | MFCD22205848 | 195.610 | C8H6ClN3O | 98.000 | CC(=O)c1c[nH]c2ncnc(Cl)c12 | 25g | 837464375
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Medchemexpress LLC 5 -GUANYLIC ACID 1G
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5 -GUANYLIC ACID 1G
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Medchemexpress LLC Melanin probe-2 | 1285446-04-9 | 99.4% | 300.19 | 250 MG
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Melanin probe-2 is a non-radioactive bromopicolinamide precursor. It is primarily used for the synthesis of 18F-Labeled Picolinamide PET probes.
- Non-radioactive bromopicolinamide precursor.
- Used for the synthesis of 18F-Labeled Picolinamide PET probes.
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Medchemexpress LLC METHYL 3-CYANOPROPAN 250 mg
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METHYL 3-CYANOPROPAN 250MG
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Medchemexpress LLC ETHYL 3-4-BROMOPHEN 25G
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ETHYL 3-4-BROMOPHEN 25G
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Medchemexpress LLC CGP 44 645 | 134521-16-7 | 234.25 | 100 MG
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CGP 44 645 is the methanol metabolite of Letrozole and serves as a molecular indicator for evaluating its metabolic kinetics in microsomes in vitro. Levels in rat liver microsomes may be sex-specific. This product is for research use only.
- Purity: 98.1%
- Molecular weight: 234.25
- Formula: C15H10N2O
- Appearance: Solid, white to off-white
- Solubility in DMSO: ≥ 200 mg/mL (853.79 mM)
- Recommended storage: Powder at -20°C for 3 years or 4°C for 2 years; in solvent at -80°C for 6 months or -20°C for 1 month.
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Medchemexpress LLC Ethyl 7-bromoheptanoate | 29823-18-5 | 237.13 | 25 G
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Ethyl 7-bromoheptanoate is a key intermediate and alkylating agent used in the synthesis of other active compounds. It can be utilized in the synthesis of prostaglandins and their analogues, and can react with quinazoline derivatives containing hydroxyl groups to introduce ester group-containing side chains.
- Key intermediate
- Alkylating agent
- Used in the synthesis of prostaglandins and their analogues
- Can introduce ester group-containing side chains to quinazoline derivatives
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Medchemexpress LLC PARP14 inhibitor H10 | 2084811-68-5 | 99.5% | 557.58 g/mol | C24H27N7O7S | 25 MG
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PARP14 inhibitor H10 is a research-grade small-molecule inhibitor selective for PARP14 (IC50 ≈ 490 nM) that demonstrates approximately 24-fold selectivity over PARP1. Supplied as a solid for laboratory research use, the compound is provided with analytical documentation and safety data for handling.
- Selective PARP14 inhibition (IC50 ≈ 490 nM).
- Approximately 24-fold selectivity over PARP1.
- Induces caspase-3/7-mediated cell apoptosis.
- High purity (~99.5%) with HNMR, LCMS, and RP-HPLC characterization.
- Available in mg pack sizes for research use only.
- Includes datasheet, certificate of analysis, and SDS for handling and safety.
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