Quinolines and derivatives
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Filtered Search Results
Ambeed 7Bromoindole
7-Bromoindole, 51417-51-7, 97%
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Chemscene CHEMSCENE
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5000576096 6 7-DIMETHOXYQUINAZOLIN-4 25G
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Ambeed 2 4DibromoN 4bromophenyl N 2 4
2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline, 73087-81-7, 95%
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Ambeed S 4 9HFluoren9yl methoxy c
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(tert-butoxy)-5-oxopentanoic acid, 84793-07-7, 98%
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Medchemexpress LLC Benzene, 1-(1,1-dimethylethyl)-3-ethoxy- | 133073-81-1 | 95.0% | C12H18O | 10 G
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1-tert-Butyl-3-ethoxybenzene is a drug intermediate used for the synthesis of various active compounds. It is for research use only and not intended for human use. The appearance is liquid, with a color ranging from light yellow to light brown.
- Used for synthesis of various active compounds
- For research use only
- Appearance: liquid, light yellow to light brown
- Pure form storage: -20°C for 3 years or 4°C for 2 years
- In solvent storage: -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Recombinant mouse interleukin-31 (IL-31) | >85.0% | 50 UG
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Recombinant mouse interleukin-31 (IL-31) produced in HEK293 cells with a C-terminal His tag, supplied as a 0.22 μm filtered solution in PBS (pH 7.4). The protein is designed for biochemical and cell-based assays, including receptor binding and signaling studies; manufacturer provides activity, purity, and storage data.
- Expressed in HEK293 mammalian cells.
- C-terminal His tag for detection and purification.
- Supplied in PBS (pH 7.4), 0.22 μm filtered.
- >85.0% purity by reducing SDS-PAGE.
- Approximate molecular weight 17.1 kDa (reducing SDS-PAGE).
- Bioactivity: ED50 ≈ 2.916 μg/mL in receptor-binding ELISA.
- Store long-term at -80°C; avoid repeated freeze-thaw.
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Selleck Chemical LLC STF-31
STF-31 is a selective glucose transporter GLUT1 inhibitor
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Selleck Chemical LLC SH-4-54
SH-4-54 is a potent STAT inhibitor with KD of 300 nM and 464 nM for STAT3 and STAT5 respectively
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Accela Chembio Inc Ethyl 4-hydroxyquinoline-3-carboxylate | 25g | 26892-90-0 | MFCD00173406 | 97+% | Shelf Life: 2520 Days | Regular
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Ethyl 4-hydroxyquinoline-3-carboxylate | 25g | 26892-90-0 | MFCD00173406 | 97+% | Shelf Life: 2520 Days | Regular
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Ambeed 3Chloro5nitrobenzoic acid
3-Chloro-5-nitrobenzoic acid, 34662-36-7, 98%
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Medchemexpress LLC (S,R,S)-AHPC-amido-C7-acid | 2172819-76-8 | 98.7% | 600.77 | 25 MG
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(S,R,S)-AHPC-amido-C7-acid incorporates a VHL ligand for the E3 ubiquitin ligase and a PROTAC linker, making it suitable for PROTAC development and research applications.
- Incorporates a VHL ligand and a PROTAC linker
- Suitable for research applications
- Designed for PROTAC development
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Medchemexpress LLC Endothelin-1 (1-31) (Human) | 133972-52-8 | 99.7% | 3628.16 | 1 MG
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Endothelin-1 (1-31) (Human) is a potent vasoconstrictor and hypertensive agent derived from the selective hydrolysis of big ET-1 by chymase. In vitro, it induces human mesangial cell proliferation and ERK activation. In vivo, it induces contraction in the mouse mesenteric artery, possibly mediated by the ETA receptor. This contraction can be increased by aging, and gender differences have been observed in chronic diabetic conditions.
- Potent vasoconstrictor.
- Hypertensive agent.
- Derived from selective hydrolysis of big ET-1 by chymase.
- Induces human mesangial cell proliferation and ERK activation in vitro.
- Induces contraction in mouse mesenteric artery in vivo.
- Possible ETA receptor mediation.
- Effects can be increased by aging.
- Gender differences observed in chronic diabetic conditions.
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Ambeed 3 2 9HFluoren9yl methoxy ca
3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)propanoic acid, 1654740-73-4, 97%
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Accela Chembio Inc 4-hydroxyquinoline | 100g | 611-36-9 | MFCD00006777 | 98% | Shelf Life: 1800 Days | Regular
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4-hydroxyquinoline | 100g | 611-36-9 | MFCD00006777 | 98% | Shelf Life: 1800 Days | Regular
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TARGETMOL CHEMICALS INC MK2-IN-1 HYDROCHLORIDE 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. MK2-IN-1 hydrochloride (MK 25) is a highly selective non-ATP competitive inhibitor of p38/mitogen-activated protein kinase-activated protein kinase 2 (MAPKAPK2 or MK2 IC50 0.11 uM) [1]. purity: 99%
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