Quinolines and derivatives
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Filtered Search Results
Gold Biotechnology Inc Leupeptin Hemisulfate 5 mg
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Leupeptin hemisulfate (Ac-Leu-Leu-argininal) is a reversible inhibitor of serine and cysteine endopeptidases Leupeptin hemisulfate is capable of inhibiting plasmin trypsin papain kallikrein calpain and cathepsin B Leupeptin is usually used in a concentration range of 10 to 100 M Leupeptin is widely used in many protease inhibitor cocktails due to its potency low toxicity and range of inhibition Leupeptin is also used in a quantitative assay to measure macroautophagic flux in mammals and is being investigated for its use in treating malaria
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MOLPORT INC 2 5-DIMETHOXY-N- QUINOLIN- 2UM
NC3232342 2 5-DIMETHOXY-N- QUINOLIN- 2UM
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000771962 MAL-C6-AMINE TFA 100MG
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eMolecules 39061-97-7 | 4-Chloro-3-nitroquinoline | Synthonix | MFCD07369246 | 208.600 | C9H5ClN2O2 | 95.000 | [O-][N+](=O)c1cnc2ccccc2c1Cl | 25g | 831794068
4-Chloro-3-nitroquinoline | Synthonix | 39061-97-7 | MFCD07369246 | 208.600 | C9H5ClN2O2 | 95.000 | [O-][N+](=O)c1cnc2ccccc2c1Cl | 25g | 831794068
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Medchemexpress LLC Branaplam | 1562338-42-4 | 98.90% | 393.48 | 200 MG
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Branaplam is a highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator with an EC50 of 20 nM for SMN. It inhibits human-ether-a-go-go-related gene (hERG) with an IC50 of 6.3 μM. Branaplam elevates full-length SMN protein and extends survival in a severe spinal muscular atrophy (SMA) mouse model.
- Highly potent, selective and orally active survival motor neuron-2 (SMN2) splicing modulator.
- Elevates full-length SMN protein.
- Extends survival in a severe spinal muscular atrophy (SMA) mouse model.
- EC50 of 20 nM for SMN.
- IC50 of 6.3 μM for hERG.
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Sigma Aldrich Fine Chemicals Biosciences Ciprofloxacin hydrochloride European Pharmacopoeia (EP) Reference Standard | 86393-32-0 | MFCD00242856 |
Ciprofloxacin hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 385.82 | 86393-32-0 | MFCD00242856 |
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Medchemexpress LLC Dihydroergotamine mesylate | 6190-39-2 | 99.9% | 100 MG
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Dihydroergotamine mesylate | 6190-39-2 | 99.9% | 100 MG
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Medchemexpress LLC Amino-PEG8-amine | 82209-36-7 | ≥98.0% | 1 G
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Amino-PEG8-amine is a PEG-based (8 units) PROTAC linker that can be used in the synthesis of PROTACs. PROTACs consist of two different ligands connected by a linker; one ligand is for an E3 ubiquitin ligase, and the other is for the target protein. PROTACs utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Utilizes the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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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 Nα-Boc-Nω-nitro-D-arginine | 50913-12-7 | MFCD00038091 | 25g
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Afatinib impurity 7 (Boc-D-Arg(NO2)-OH) is an impurity of Afatinib (HY-10261)
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Selleck Chemical LLC Resiquimod
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Resiquimod (R-848 S28463) is an immune response modifier that acts as a potent TLR 7/TLR 8 agonist that induces the upregulation of cytokines such as TNF- IL-6 and IFN- Resiquimod reduces hepatitis C virus (HCV) infection Phase 2
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Sigma Aldrich Fine Chemicals Biosciences 2-Hydroxyquinoline 98% | 59-31-4 | MFCD00006743 | 1G
2-Hydroxyquinoline 98% | Purity: 98% | Mol Wt: 145.16 | 59-31-4 | MFCD00006743 | 1G
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Medchemexpress LLC Trimethobenzamide hydrochloride | 554-92-7 | 99.9% | 200 MG
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Trimethobenzamide hydrochloride is a non-phenothiazine benzamide antiemetic that acts centrally to block D2 receptors. It inhibits the medullary chemoreceptor trigger zone, blocking emetic impulses to prevent nausea and vomiting.
- Acts as a blocker of the D2 receptor
- Used to prevent nausea and vomiting
- Exhibits 60% to 100% oral bioavailability
- Achieves peak effect approximately 45 minutes after oral administration
- Achieves peak effect approximately 30 minutes after intramuscular administration
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Medchemexpress LLC Pazufloxacin (mesylate) | 163680-77-1 | 100.0% | 1 ML
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Pazufloxacin mesylate is an orally active fluoroquinolone antimicrobial agent. It inhibits DNA gyrase with IC50 values of 0.88 μg/mL (E. coli) and 1.9 μg/mL (P. aeruginosa). This agent exhibits broad-spectrum antimicrobial activity with MIC90 values ranging from 0.025 to 100 μg/mL against Gram-positive and Gram-negative bacteria, non-fermenting bacteria, Legionella spp., and anaerobic bacteria. It is indicated for research on systemic infections, lung infections, urinary tract infections, and Legionella pneumonia.
- Orally active fluoroquinolone antimicrobial agent
- Inhibits DNA gyrase
- Exhibits broad-spectrum antimicrobial activity against a variety of bacteria, including gram-positive, gram-negative, non-fermenting, Legionella spp., and anaerobic bacteria
- Indicated for research on systemic infections, lung infections, urinary tract infections, and Legionella pneumonia
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TARGETMOL CHEMICALS INC ON-01910 25MG
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ON-01910 is a non-ATP-competitive PLK1 inhibitor(IC50 of 9 nM in a cell-free assay). It shows 30-fold greater selectivity against Plk2 and no activity to Plk3. Rigosertib inhibits PI3K/Akt pathway and activates oxidative stress signals. Rigosertib induces apoptosis in various cancer cells.It is a synthetic benzyl styryl sulfone analogue with potential antineoplastic activity. purity: 99%
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