Quinolines and derivatives
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences 8-Hydroxyquinoline crystalline | 148-24-3 | MFCD00006807 | 100G
8-Hydroxyquinoline crystalline | Purity: 98.5-101.5% | Mol Wt: 145.16 | 148-24-3 | MFCD00006807 | 100G
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Sigma Aldrich Fine Chemicals Biosciences Mefloquine hydrochloride United States Pharmacopeia (USP) Reference Standard | 51773-92-3 | MFCD00797519 | 100MG
Mefloquine hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 414.77 | 51773-92-3 | MFCD00797519 | 100MG
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Chemscene ChemScene | 2-Oxo-1,2-dihydroquinoline-6-carboxylic acid | 250MG | CS-0135806 | 0.95 | 70639-78-0| MFCD03840853 | 189.17
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ChemScene | 2-Oxo-1,2-dihydroquinoline-6-carboxylic acid | 250MG | CS-0135806 | 0.95 | 70639-78-0| MFCD03840853 | 189.17
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Medchemexpress LLC Guanidinoethyl sulfonate | 543-18-0 | MFCD00084865 | 99.9% | 167.19 g/mol | C3H9N3O3S | 5 MG
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Guanidinoethyl sulfonate (taurocyamine) is a small-molecule research reagent that inhibits taurine transport and antagonizes glycine receptors in the central nervous system. It is blood-brain barrier permeable and has been used in neuroprotection studies of ischemic brain injury; it also exhibits weak modulatory effects on GABAA receptors.
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Medchemexpress LLC Regorafenib monohydrate | 1019206-88-2 | MFCD17170366 | 99.9% | 500.8 g/mol | C21H17ClF4N4O4 | 50 MG
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Regorafenib monohydrate is the monohydrate form of regorafenib, a multi-targeted receptor tyrosine kinase inhibitor used as a research reagent and analytical standard. It exhibits potent inhibition of VEGFR, PDGFR, KIT, RET, and RAF kinases and is used in preclinical assays to study antitumor and antiangiogenic activity.
- High purity (≈99.9%) suitable for analytical work.
- Monohydrate form with molecular weight 500.8 g/mol.
- Useful as an analytical standard and research reagent in kinase assays.
- Available in small, quantified laboratory packages for preclinical studies.
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5000353509 AZIDO-PEG8-AMINE 100MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000353500 ISAVUCONAZOLE 200MG
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Apexbio Technology LLC Tasquinimod 254964-60-8 200mg
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Tasquinimod (CAS 254964-60-8) is an orally bioavailable quinoline-3-carboxamide compound with antiangiogenic and antitumor properties It modulates angiogenesis primarily through dual inhibition of S100A9/TLR4 signaling in myeloid-derived suppressor cells (MDSCs) and downregulation of HIF-1 and VEGF expression in tumor and endothelial cells It also enhances thrombospondin-1 (TSP-1) expression further suppressing neovascularization Preclinical studies in human prostate cancer xenograft models indicate significant antineoplastic activity particularly in combination with docetaxel radiation therapy or androgen-depletion strategies suggesting its therapeutic potential for castration-resistant prostate cancer (CRPC)
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Ambeed 3 2 9HFluoren9yl methoxy ca
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3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)propanoic acid, 1654740-73-4, 97%
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eMolecules EMOLECULES INC
5000471486 7-BROMOQUINOLINE 1G
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Ambeed 4Nitroisophthalic acid
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4-Nitroisophthalic acid, 4315-09-7, 98%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000402376 7-HYDROXYCARBOSTYRIL 25G
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eMolecules 7-Hydroxyquinoline-8-carboxylic acid | 1146298-53-4 | MFCD11869106 | 100mg
Ambeed | 7-Hydroxyquinoline-8-carboxylic acid | 100mg | 602850335 | A549352 | | 1146298-53-4 | MFCD11869106 | 189.170 | C10H7NO3
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5000406778 NITRENDIPINE 200MG
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Apexbio Technology LLC DGAT-1 inhibitor 701232-20-4 200mg
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DGAT-1 inhibitor (CAS 701232-20-4) also known as T863 is an orally active small molecule that selectively inhibits diacylglycerol acyltransferase 1 (DGAT1) DGAT1 is responsible for catalyzing the final step in triglyceride biosynthesis T863 suppresses enzyme activity by specifically binding to the acyl-CoA binding site of DGAT1 exhibiting an IC50 of 15 nM without affecting enzymatic activities of human DGAT2 MGAT2 or MGAT3 This compound serves as a research tool for investigating DGAT1-mediated lipid synthesis and exploring lipid metabolic disorders using cellular and animal models
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