Quinolines and derivatives
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Filtered Search Results
Ambeed 1R 2S 1Amino2 3dihydro1Hinden
(1R,2S)-1-Amino-2,3-dihydro-1H-inden-2-ol, 136030-00-7, 98%
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Ambeed Methyl pyrimidine2carboxylate
Methyl pyrimidine-2-carboxylate, 34253-03-7, 97%
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Ambeed 7Bromo1 2dihydroisoquinolin3 4
7-Bromo-1,2-dihydroisoquinolin-3(4H)-one, 943751-93-7, 95%
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Medchemexpress LLC Pyrroloquinoline quinone disodium salt | 122628-50-6 | 98.0% | 374.17 g/mol | C14H4N2Na2O8 | 100 MG
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Pyrroloquinoline quinone disodium salt is the sodium salt form of PQQ, a redox cofactor used as a research reagent for studies of redox biology and immune function. It is supplied as a pink to red solid with high reported purity and defined storage recommendations.
- High purity: 98.0%.
- Molecular weight: 374.17 g/mol.
- Chemical formula: C14H4N2Na2O8.
- Appearance: pink to red solid.
- Storage: store sealed at 4°C, away from moisture.
- Applications: suitable for redox and immune function research.
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Sigma Aldrich Fine Chemicals Biosciences Acriflavine hydrochloride | 8063-24-9 | MFCD00069039 | 25G
Acriflavine hydrochloride | 8063-24-9 | MFCD00069039 | 25G
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Ambeed Methyl pyrimidine2carboxylate
Methyl pyrimidine-2-carboxylate, 34253-03-7, 97%
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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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Medchemexpress LLC HSGN-94 | 2570797-85-0 | 98.8% | 508.51 | 1 ML
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HSGN-94 is a potent antimicrobial agent that inhibits lipoteichoic acid (LTA) biosynthesis. It is effective against drug-resistant Gram-positive bacteria, including MRSA and Vancomycin-resistant Enterococci, also inhibiting their biofilm formation. It reduces pro-inflammatory cytokines and shows in vivo efficacy in an MRSA murine wound infection model.
- Potent antimicrobial agent targeting lipoteichoic acid (LTA) biosynthesis.
- Effective against drug-resistant Gram-positive bacteria (MIC values: 0.25-2 μg/mL).
- Inhibits biofilm formation in MRSA and Vancomycin-resistant Enterococci.
- Reduces pro-inflammatory cytokines.
- Demonstrates in vivo efficacy in a murine wound infection model.
- Directly binds to CDP-diacylglycerol-glycerol-3-phosphate 3-phosphatidyltransferase (PgsA).
- Downregulates PgsA expression in *S. aureus*.
- Non-toxic to HaCat cells up to 64 μg/mL.
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Medchemexpress LLC Glucagon-like peptide-1 (GLP-1)(7-36), amide acetate | 1119517-19-9 | 99.0% | 3297.64 (free base) | 1 MG
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GLP-1(7-36), amide acetate is a major intestinal hormone that stimulates glucose-induced insulin secretion from β cells. It is for research use only.
- Stimulates glucose-induced insulin secretion from β cells.
- Active GLP-1 secretion is stimulated by fatty acids such as palmitic, oleic, linoleic, or linolenic acid.
- Increases active GLP-1 concentrations in vitro.
- Increases active GLP-1(7-36) amide levels in portal blood in vivo.
- Co-administration of glucose and tea oil additively increases peak GLP-1 levels.
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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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Medchemexpress LLC IL-31 Cynomolgus H 10ug | 10ug
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IL-31 is a multifunctional cytokine that activates STAT3 through IL-31 heterodimeric receptors (IL31RA and OSMR) and may activate STAT1 and STAT5 IL-31 is known for its involvement in skin immunity where it regulates immune responses IL-31 Protein Cynomolgus (HEK293 His) is the recombinant cynomolgus-derived IL-31 protein expressed by HEK293 with C-His labeled tag
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Medchemexpress LLC TL02-59 | 1315330-17-6 | 99.9% | 609.64 | 50 MG
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TL02-59 is an orally active, selective Src-family kinase Fgr inhibitor with an IC50 of 0.03 nM. It also inhibits Lyn and Hck with IC50s of 0.1 nM and 160 nM, respectively. This compound potently suppresses acute myelogenous leukemia (AML) cell growth.
- Selective Src-family kinase Fgr inhibitor with high potency.
- Inhibits Lyn and Hck.
- Potently suppresses acute myelogenous leukemia (AML) cell growth.
- Induces growth arrest and apoptosis in AML cell lines.
- Eliminates AML cells from spleen and peripheral blood in mouse models.
- Significantly suppresses bone marrow involvement in mouse models.
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Ambeed Methyl 4bromo3methylbenzoate
Methyl 4-bromo-3-methylbenzoate, 148547-19-7, 98%
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Medchemexpress LLC 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyluridine | 103285-22-9 | MFCD00274123 | 98.0% | 560.59 g/mol | C31H32N2O8 | 10 G
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5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyluridine is a DMT-protected 2'-O-methyl uridine nucleoside used as a building block and intermediate for solid-phase oligonucleotide synthesis and for research on modified RNA. It is supplied as a high-purity solid or as a DMSO solution to facilitate incorporation into synthesis workflows.
- DMT-protected 2'-O-methyl uridine suitable for oligonucleotide synthesis.
- High purity (98.03%) for reliable reactions.
- Available as powder and 10 mM solution in DMSO for flexibility.
- Long-term storage stability when kept at recommended temperatures.
- Datasheet, COA, and SDS available to support quality control.
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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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