Quinolines and derivatives
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Filtered Search Results
Ambeed Methyl 5bromo2fluorobenzoate
Methyl 5-bromo-2-fluorobenzoate, 57381-59-6, 98%
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Ambeed tertButyl 3 8diazabicyclo 3.2.
tert-Butyl 3,8-diazabicyclo[3.2.1]octane-8-carboxylate, 149771-44-8, 96%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000771082 2 4 6-TRIMETHYL-1 3 10G
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Ambeed 6Cyclopropylpyridin3amine
6-Cyclopropylpyridin-3-amine, 1159821-66-5, 95%
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Medchemexpress LLC Act-1004-1239 | 2178049-58-4 | 98.8% | C27H28F2N6O3 | 1 MG
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Act-1004-1239 | 2178049-58-4 | 98.8% | C27H28F2N6O3 | 1 MG
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Ambeed R tertButyl 3 hydroxymethyl p
(R)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate, 278788-66-2, 95%
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Medchemexpress LLC N2-ACETYLGUANINE 1G
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5000208514 N2-ACETYLGUANINE 1G
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Medchemexpress LLC MI-773 | 1303607-07-9 | MFCD28168022 | 96.3% | 562.50 | C29H34Cl2FN3O3 | 10 MG
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MI-773 is a small-molecule inhibitor of the MDM2-p53 protein-protein interaction with high binding affinity for MDM2 and reported antitumor activity in preclinical studies. It is provided as a research-grade compound for use in cancer biology and p53 pathway experiments.
- High-affinity MDM2 binding (reported Kd 8.2 nM).
- Reported antitumor activity in preclinical studies.
- Provided as a research-grade compound suitable for in vitro and in vivo studies.
- Available in small mg-scale quantities for research use.
- Molecular weight 562.50 and formula C29H34Cl2FN3O3 for reference.
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Ambeed 4 6 2 3Methylbenzylidene hydra
4-(6-(2-(3-Methylbenzylidene)hydrazinyl)-2-(2-(pyridin-2-yl)ethoxy)pyrimidin-4-yl)morpholine dimethanesulfonate, 870087-36-8, 98%
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5000697381 77PD-Q 500UG
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Medchemexpress LLC Benzyl-PEG2-amine | 1268135-96-1 | C11H17NO2 | 1 G
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Benzyl-PEG2-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Connects ligands for E3 ubiquitin ligase and target proteins
- Utilizes the ubiquitin-proteasome system
- Selectively degrades target proteins
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Ipragliflozin L-Proline | 951382-34-6 | 99.9% | 519.58 | 200 MG
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Ipragliflozin (L-Proline) is a highly potent and selective SGLT2 inhibitor with an IC50 of 2.8 nM, showing little to no potency for SGLT1/3/4/5/6. It is intended for research use only.
- Potently and selectively inhibits human, rat, and mouse SGLT2.
- Exhibits stability against intestinal glucosidases.
- Shows good pharmacokinetic properties following oral dosing.
- Dose-dependently increases urinary glucose excretion.
- Reduces blood glucose and plasma insulin levels.
- Improves glucose intolerance.
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Ambeed 4 6 2 3Methylbenzylidene hydra
4-(6-(2-(3-Methylbenzylidene)hydrazinyl)-2-(2-(pyridin-2-yl)ethoxy)pyrimidin-4-yl)morpholine dimethanesulfonate, 870087-36-8, 98%
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Medchemexpress LLC Mal-amido-PEG9-acid | 2112731-43-6 | 99.5% | 250 MG
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Mal-amido-PEG9-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. These PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. This product is for research use only and has not been fully validated for medical applications.
- PEG-based linker
- Used in synthesis of PROTACs
- Facilitates selective degradation of target proteins
- Utilizes ubiquitin-proteasome system
- Contains two ligands connected by a linker
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Cephradine monohydrate | 75975-70-1 | 91.0% | 100 MG
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Cephradine monohydrate is a broad-spectrum, orally active cephalosporin effective against both gram-positive and gram-negative pathogens. It eradicates most penicillinase-producing organisms resistant to penicillin G, penicillin V, and ampicillin. This compound has been utilized in research concerning genitourinary, gastrointestinal, and respiratory tract infections, as well as infections of the skin and soft tissues. It also blocks solar-ultraviolet induced skin inflammation.
- Active against gram-positive and gram-negative pathogens.
- Effective in eradicating most penicillinase-producing organisms resistant to penicillin G, penicillin V, and ampicillin.
- Used in research of genitourinary, gastrointestinal, and respiratory tract infections.
- Used in research of infections of the skin and soft tissues.
- Blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK.
- Targets β-lactam.
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