Quinolines and derivatives
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Filtered Search Results
Medchemexpress LLC 4-quinolinecarboxylic acid, 7-bromo- | 31009-04-8 | MFCD11108751 | 96.1% | 252.06 | C10H6BrNO2 | 250 MG
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7-Bromoquinoline-4-carboxylic acid is an aromatic heterocyclic carboxylic acid used as an intermediate and building block in organic synthesis, particularly in medicinal chemistry and materials research. It is typically handled as a solid reagent and supplied with batch documentation for quality control.
- Used as an intermediate in organic and medicinal chemistry.
- HPLC purity 96.1%.
- Molecular formula C10H6BrNO2; molecular weight 252.06.
- Appearance: gray to brown solid.
- Storage: powder -20°C (stable 3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Batch certificate of analysis and safety data sheet available.
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eMolecules 1447607-02-4 | ChemScene | Ethyl 7-aminoquinoline-2-carboxylate | 100mg | 711937895 | CS-0149239 | MFCD25542354 | 216.24 | C12H12N2O2
Ambeed | Fmoc-D-Tle-OH | 5g | 572840678 | A547654 | 198543-64-5 | MFCD00065650 | 353.418 | C21H23NO4
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Medchemexpress LLC (2R)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N'-hydroxy-2-(2-methylpropyl)butamid | 145337-55-9 | 99.4% | 315.41 g/mol | C15H29N3O4 | 100 MG
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Ro 31-9790 is a synthetic matrix metalloproteinase (MMP) inhibitor provided for research use. It serves as a biochemical probe to study MMP-related activity in vitro and in cell-based assays. The compound is identified by CAS 145337-55-9 and is characterized by a defined molecular formula and high reported purity.
- Acts as a matrix metalloproteinase inhibitor for research applications.
- High purity, approximately 99.4%.
- Molecular weight 315.41 g/mol; formula C15H29N3O4.
- Suitable as a research-grade chemical for biochemical and cell biology studies.
- Synonyms and systematic names are available in chemical databases for cross-referencing.
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Ambeed AMBEED
5000885102 4-BROMOPYRIDINE-2-CARBAL 10G
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Ambeed AMBEED
5000886094 4-CHLORO-7-METHOXYQUINOL 10G
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eMolecules 885276-33-5 | Methyl 2,3-dibromo-3,3-difluoropropionate | Combi-Blocks | MFCD07784249 | 281.879 | C4H4Br2F2O2 | 95.000 | COC(=O)C(Br)C(F)(F)Br | 1g | 401041469
Methyl 2,3-dibromo-3,3-difluoropropionate | Combi-Blocks | 885276-33-5 | MFCD07784249 | 281.879 | C4H4Br2F2O2 | 95.000 | COC(=O)C(Br)C(F)(F)Br | 1g | 401041469
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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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Selleck Chemical LLC JNK-IN-8 S4901-1g
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JNK-IN-8 (JNK Inhibitor XVI) is the first irreversible JNK inhibitor for JNK1 JNK2 and JNK3 with IC50 of 4 7 nM 18 7 nM and 1 nM 10-fold selectivity against MNK2 Fms and no inhibition to c-Kit Met PDGFR in A375 cell line
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Medchemexpress LLC MI-773 | 1303607-07-9 | 96.3% | 562.50 | 100 MG
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MI-773 is a potent MDM2-p53 protein-protein interaction (PPI) inhibitor. It demonstrates high binding affinity against MDM2 and exhibits antitumor activity. An analog, MI-77301, shows even higher binding affinity and more pronounced antitumor activity in various p53 xenograft models.
- Potent MDM2-p53 protein-protein interaction (PPI) inhibitor.
- High binding affinity against MDM2 (Kd=8.2 nM).
- Exhibits antitumor activity.
- Analog shows enhanced binding affinity and antitumor activity.
- Effective in various p53 xenograft models including osteosarcoma, human prostate, melanoma, colorectal tumor, and human acute lymphoblastic leukemia.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000746657 ALPELISIB 200MG
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Medchemexpress LLC AM095 | 1345614-59-6 | 99.7% | 478.47 | 200 MG
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AM095 is a selective LPA1 receptor antagonist known for its potent inhibition of LPA-induced calcium flux in human and mouse LPA1-transfected CHO cells. It demonstrates an exceedingly low IC50 for human (0.025 μM) and mouse (0.023 μM) cells, positioning it as a valuable tool for research involving LPA1 receptor pathways.
- Selective LPA1 receptor antagonist.
- Potently inhibits LPA-induced calcium flux.
- Applicable in studies involving human or mouse LPA1-transfected CHO cells.
- Useful for researching LPA1 receptor pathways.
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Selleck Chemical LLC Chelerythrine Chloride (NSC 646662) S1292-5mg
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Chelerythrine Chloride (NSC 646662 Broussonpapyrine) is a potent selective antagonist of PKC with IC50 of 0 66 M
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Medchemexpress LLC Amifostine thiol dihydrochloride | 14653-77-1 | MFCD00460339 | ≥98.0% | 207.16 g/mol | C5H16Cl2N2S | 1 MG
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Amifostine thiol dihydrochloride is the dihydrochloride salt of WR-1065, the active thiol metabolite of amifostine. It is supplied as a research reagent and analytical standard for studies of radioprotection, cytoprotection from chemotherapeutic agents, and p53/JNK-dependent signaling.
- Protects normal tissues from toxic effects of certain cancer agents.
- Activates p53 through a JNK-dependent signaling pathway.
- Supplied as a dihydrochloride salt for improved handling and stability.
- Provided in small research quantities suitable for analytical and biological studies.
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Medchemexpress LLC Bosutinib hydrate | 918639-08-4 | MFCD29920031 | 100.0% | 548.46 g/mol | C26H31Cl2N5O4 | 200 MG
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Bosutinib hydrate is a small-molecule dual Src/Abl tyrosine kinase inhibitor supplied as a white to off-white solid for research use. It exhibits low-nanomolar potency against Src and Abl kinases and is intended for biochemical and cell-based studies; supporting documents such as SDS and COA are provided for analytical verification and safe handling.
- Dual Src and Abl kinase inhibition at low-nanomolar concentrations.
- High reported purity suitable for research applications.
- Available in multiple packaging sizes, including 200 MG.
- White to off-white solid appearance for easy handling.
- Storage and stability guidance provided for solid and solution forms.
- COA and SDS available to support quality and safety use.
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Medchemexpress LLC Sevabertinib (BAY 2927088) | 2521285-05-0 | 99.9% | 484.93 | 200 MG
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Sevabertinib (BAY 2927088) is an orally active and reversible dual EGFR-HER2 inhibitor with potent anticancer activity against lung cancer. It shows significantly reduced activity against HER4.
- Orally active and reversible dual EGFR-HER2 inhibitor
- Exhibits anticancer activity against lung cancer
- Potently inhibits proliferation of isogenic Ba/F3 cells ectopically expressing HER2 exon 20 insertions
- Potently inhibits proliferation of isogenic Ba/F3 cells activating HER2 point mutations or putative secondary acquired resistance mutations
- Inhibits proliferation of lung cancer cell lines NCI-H1781 and NCI-H2170
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