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Filtered Search Results
eMolecules 72716-87-1 | 2-methoxypyridine-4-carbaldehyde | Pharmablock | MFCD06410680 | 137.138 | C7H7NO2 | 97.000 | COc1cc(C=O)ccn1 | 50mg | 551201751
2-methoxypyridine-4-carbaldehyde | Pharmablock | 72716-87-1 | MFCD06410680 | 137.138 | C7H7NO2 | 97.000 | COc1cc(C=O)ccn1 | 50mg | 551201751
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Aobchem 2-Fluoro-5-(morpholine-4-carbonyl)phenylboronic acid | ≥97% | CAS 1072951-41-7 | C11H13BFNO4 | 5g
2-Fluoro-5-(morpholine-4-carbonyl)phenylboronic acid | ≥97% | CAS 1072951-41-7 | C11H13BFNO4 | 5g
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Medchemexpress LLC Z-LYS-SBZL monohydrochloride | 69861-89-8 | 99.7% | C21H27ClN2O3S | 25 MG
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Z-LYS-SBZL monohydrochloride (α-N-Carbobenzoxy-L-lysine thiobenzyl ester monohydrochloride) is a lysine derivative primarily intended for research use. Amino acids and their derivatives, like this product, are recognized as beneficial ergogenic dietary substances. It is designed to support various biological activities related to physical and mental performance.
- Influences anabolic hormone secretion
- Supplies fuel during exercise
- Enhances mental performance during stress-related tasks
- Prevents exercise-induced muscle damage
- For research use only
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Aobchem 2 4-Dimethylthiophene-3-carbaldehyde | ≥97% | CAS 63826-85-7 | C7H8OS | 250mg
2 4-Dimethylthiophene-3-carbaldehyde | ≥97% | CAS 63826-85-7 | C7H8OS | 250mg
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Apexbio Technology LLC SR-9243 1613028-81-1 200mg
SR-9243 (CAS 1613028-81-1) is a small-molecule inverse agonist targeting liver X receptors (LXRs) nuclear transcription factors involved in metabolic regulation It is designed to induce LXR corepressor interactions thereby suppressing transcriptional activation of glycolytic and lipogenic enzyme genes SR-9243 exerts its biological activity primarily through inhibition of glycolysis- and lipid biosynthesis-associated gene expression In in vitro assays SR-9243 reduces cancer cell viability and induces apoptosis through caspase 3/7 activation in colorectal cancer cell lines Based on these pharmacological properties SR-9243 holds research potential in investigating metabolic reprogramming in cancer particularly in prostate colon and lung cancer models
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Apexbio Technology LLC Amadacycline 389139-89-3 200mg
Amadacycline (CAS 389139-89-3) is a tetracycline-class antibiotic targeting the bacterial ribosomal 30S subunit It is designed to inhibit bacterial protein synthesis thereby preventing microbial proliferation Amadacycline exerts its biological activity primarily through interference with bacterial translation by inhibiting the 30S ribosomal subunit The exact IC50 value for Amadacycline has not been established Based on these pharmacological properties Amadacycline holds research potential in investigating antibiotic resistance mechanisms bacterial ribosome-targeting strategies and as a candidate in studies evaluating therapeutic agents for complicated skin and skin structure infections
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Aobchem 3 4-Dimethoxythiophene-2-carboxylic acid | ≥97% | CAS 113589-62-1 | C7H8O4S | 250mg
3 4-Dimethoxythiophene-2-carboxylic acid | ≥97% | CAS 113589-62-1 | C7H8O4S | 250mg
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eMolecules 36404-88-3 | 2-CHLORO-PYRIDINE-3-CARBALDEHYDE | AstaTech | MFCD01315308 | 141.550 | C6H4ClNO | 97.000 | Clc1ncccc1C=O | 100g | 206680064
2-CHLORO-PYRIDINE-3-CARBALDEHYDE | AstaTech | 36404-88-3 | MFCD01315308 | 141.550 | C6H4ClNO | 97.000 | Clc1ncccc1C=O | 100g | 206680064
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Medchemexpress LLC Ipatasertib | 1001264-89-6 | 458.00 | 200 MG
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Ipatasertib (GDC-0068) is an orally active, highly selective, and ATP-competitive pan-Akt inhibitor. It activates FoxO3a and NF-κB through Akt inhibition, leading to p53-independent activation of PUMA, and induces apoptosis in cancer cells and inhibits tumor growth in xenograft mouse models.
- Orally active and highly selective pan-Akt inhibitor
- ATP-competitive inhibition of Akt1, Akt2, and Akt3
- Synchronously activates FoxO3a and NF-κB
- Leads to p53-independent activation of PUMA
- Induces apoptosis in cancer cells
- Inhibits tumor growth in xenograft mouse models
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Medchemexpress LLC Carboplatin | 41575-94-4 | 99.9% | 371.25 | 200 MG
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Carboplatin (NSC 241240) is a DNA synthesis inhibitor that works by binding to DNA, which in turn inhibits replication and transcription, ultimately inducing cell death. It is a derivative of CDDP and is considered a potent anti-cancer agent.
- DNA synthesis inhibitor
- Binds to DNA
- Inhibits replication and transcription
- Induces cell death
- Derivative of CDDP
- Potent anti-cancer agent
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Medchemexpress LLC Piperidolate | 82-98-4 | 99.3% | 200 MG
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Piperidolate is an antimuscarinic that inhibits intestinal cramps induced by acetylcholine in rats and dogs. It is intended for research and analytical applications.
- Inhibits intestinal cramps
- Targets muscarinic acetylcholine receptors (mAChR)
- Relevant for neurological and neurodegenerative diseases
- Useful for GPCR/G protein and neuronal signaling research
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TARGETMOL CHEMICALS INC BAY-2402234 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BAY-2402234 is an inhibitor of dihydroorotate dehydrogenase (DHODH) for the treatment of myeloid malignancies.BAY 2402234 is a selective low-nanomolar inhibitor of human DHODH enzymatic activity. purity: 99%
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Apexbio Technology LLC Taurochenodeoxycholic acid sodium salt 6009-98-9 200mg
Taurochenodeoxycholic acid sodium salt (CAS 6009-98-9) is an animal-derived bile acid derivative that modulates cell signaling pathways involved in apoptosis thereby influencing cellular growth and survival Research indicates that it also participates in the regulation of inflammatory responses and immune-related signaling mechanisms This compound is frequently utilized in cellular and animal models to investigate bile acid receptor-mediated physiological and pathological processes including its roles in metabolic disorders inflammatory diseases and immune-mediated conditions
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Apexbio Technology LLC Panobinostat (LBH589) 404950-80-7 200mg
Panobinostat (LBH589) is a histone deacetylase (HDAC) inhibitor targeting class I II and IV HDAC enzymes regulating gene expression through histone hyperacetylation In vitro studies indicate panobinostat induces apoptosis and growth arrest in Ph-negative acute lymphoblastic leukemia (ALL) cell lines T-cell (MOLT-4) and pre-B cell (Reh) via caspase activation PARP cleavage and downregulation of c-Myc accompanied by H3K9 and H4K8 hyperacetylation and elevation of cell-cycle regulators (p21 p27) Panobinostat has shown anti-proliferative effects in various cancer models including cutaneous T-cell lymphoma and multiple myeloma (IC50 5-30 nM) and serves as a research tool in studies assessing epigenetic regulation and tumor biology
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Apexbio Technology LLC KNK437 218924-25-5 200mg
KNK437 (CAS 218924-25-5) is a benzylidene lactam small molecule that inhibits stress-induced synthesis of heat shock proteins (HSPs) HSPs function as molecular chaperones with increased expression under cellular stress and involvement in protein folding cancer and cardiovascular disease KNK437 suppresses the induction of various HSPs in human colon carcinoma cells (COLO 320DM) including after heat stress and arsenite exposure thereby preventing the development of thermotolerance in a dose-dependent manner In murine tumor models KNK437 reduces Hsp72 synthesis when administered prior to hyperthermia This compound is widely used to investigate HSP-mediated stress responses and mechanisms of thermotolerance in cancer research
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