Quinolines and derivatives
Aromatic organic heterocyclic compounds that contain a benzene ring fused with a six-membered ring that contains one nitrogen atom and five carbon atoms. Includes compounds that are derived from quinolines.
Quantity
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- (219)
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- (132)
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- (9)
- (16)
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- (34)
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- (1)
- (188)
- (1)
- (1)
- (15)
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- (17)
- (17)
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- (1)
Molecular Weight (g/mol)
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- (7)
- (21)
- (26)
- (2)
- (30)
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- (1)
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- (2)
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- (1)
- (11)
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- (25)
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- (1)
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- (1)
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- (1)
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- (1)
- (7)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
- (1)
- (1)
- (1)
- (13)
- (1)
- (2)
- (2)
- (4)
- (3)
- (4)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (19)
- (2)
- (1)
- (2)
- (4)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (4)
- (5)
- (1)
- (2)
- (1)
- (1)
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- (2)
- (1)
- (9)
- (5)
- (2)
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- (3)
- (2)
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- (6)
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- (13)
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- (1)
- (1)
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- (1)
- (1)
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- (2)
- (1)
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- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
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- (2)
- (2)
- (2)
- (2)
- (1)
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- (4)
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- (3)
- (7)
- (1)
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- (7)
- (5)
- (2)
- (1)
- (10)
- (1)
- (1)
Percent Purity
- (1)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (4)
- (2)
- (2)
- (6)
- (2)
- (7)
- (4)
- (3)
- (2)
- (2)
- (5)
- (2)
- (1)
- (14)
- (1)
- (1)
- (23)
- (42)
- (24)
- (18)
- (83)
- (3)
- (17)
- (3)
- (5)
- (8)
- (1)
- (6)
- (1)
- (5)
- (1)
- (6)
- (5)
- (2)
- (5)
- (2)
- (6)
- (2)
- (2)
- (4)
- (1)
- (26)
- (19)
- (70)
- (109)
- (3)
- (1)
- (2)
- (59)
- (5)
- (1)
- (1)
Physical Form
- (2)
- (299)
- (2)
- (2)
- (25)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (3)
- (9)
- (3)
- (2)
- (62)
- (2)
- (5)
- (29)
- (3)
Boiling Point
- (1)
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- (3)
- (3)
- (2)
- (1)
- (2)
- (1)
- (5)
- (4)
- (2)
- (1)
- (3)
- (1)
- (2)
- (2)
- (5)
- (3)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (12)
- (4)
- (1)
- (5)
- (3)
- (5)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (3)
- (5)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
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1,351
Medchemexpress LLC Aprepitant | 170729-80-3 | MFCD08277635 | 99.8% | 534.43 g/mol | C23H21F7N4O3 | 200 MG
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Aprepitant is a selective, high-affinity neurokinin 1 (NK1) receptor antagonist used in research to probe NK1-mediated signaling and substance P pathways. It is supplied as a white to off-white solid with high stated purity and is suitable for analytical, pharmacological, and GPCR studies.
- Selective neurokinin 1 receptor antagonist.
- High affinity with a reported Kd of ~86 pM.
- High purity suitable for analytical applications.
- White to off-white solid appearance.
- Available as powder and as DMSO solutions for convenience.
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1,352
eMolecules 4965-36-0 | 7-Bromoquinoline | Ambeed | MFCD03695823 | 208.058 | C9H6BrN | 98.000 | Brc1ccc2cccnc2c1 | 5g | 490534630
7-Bromoquinoline | Ambeed | 4965-36-0 | MFCD03695823 | 208.058 | C9H6BrN | 98.000 | Brc1ccc2cccnc2c1 | 5g | 490534630
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1,353
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371277 GSK269962A 200MG
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1,354
Aobchem AOBCHEM
5000864239 2-FLUORO-1- METHYLSULFANYL -3-
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1,355
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000427390 CINCHONIDINE 5G
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1,356
Cayman Chemical allcis4 7 10 13 16Docosapenta
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An ω-6 isomer of docosapentaenoic acid formed by the elongation and desaturation of arachidonic acid; diminished during fatty acid desaturase syndrome and increased in non-alcoholic steatohepatitis
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1,357
Medchemexpress LLC Mivavotinib monohydrochloride | 1312691-33-0 | 344.39 | C17H21FN6O | 25 MG
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Mivavotinib monohydrochloride is a research-grade small-molecule inhibitor of spleen tyrosine kinase (SYK) and fms-related tyrosine kinase 3 (FLT3), used to investigate kinase signaling and antitumor activity in preclinical studies. The compound is provided as a solid for formulation and assay use.
- Potent dual SYK and FLT3 inhibition with low-nanomolar activity.
- Suitable for biochemical and cell-based assays.
- Useful as a tool compound in oncology and signal-transduction research.
- Molecular formula C17H21FN6O and molecular weight 344.39 g/mol.
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1,358
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000656975 DIRECT YELLOW 86 50MG
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1,359
TARGETMOL CHEMICALS INC TAK-580 5MG
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Also available in 1 mL, 1 mg, 2 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. TAK-580 (MLN2480) is an oral, selective pan-Raf kinase inhibitor in Clinicalal trials. Purity 99.25%
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1,360
Medchemexpress LLC Mirin | 1198097-97-0 | MFCD05885480 | 99.6% | 220.25 | 200 MG
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Mirin | 1198097-97-0 | MFCD05885480 | 99.6% | 220.25 | 200 MG
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1,361
Medchemexpress LLC Infigratinib | 872511-34-7 | 99.8% | 560.48 | 200 MG
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Infigratinib, also known as BGJ-398 or NVP-BGJ398, is a potent inhibitor of the Fibroblast Growth Factor Receptor (FGFR) family. It targets FGFR1, FGFR2, FGFR3, and FGFR4 with high efficacy, making it suitable for various research applications.
- Potent inhibitor of FGFR1, FGFR2, FGFR3, and FGFR4
- Inhibits proliferation of FGFR-dependent BaF3 cells
- Effective against FGFR2-mutant endometrial cancer cells
- Extensively studied in clinical trials for multiple cancers and conditions
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1,362
Medchemexpress LLC Thiacetazone | 104-06-3 | MFCD00022157 | 99.7% | 236.29 | 200 MG
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Thiacetazone is a thiourea-containing antitubercular agent and an orally active antibiotic. It exhibits antibacterial action by inhibiting the growth of *Mycobacterium tuberculosis* H37Rv with a MIC value of 0.1 μg/mL. This prodrug is activated by the mycobacterial monooxygenase EthA.
- Thiourea-containing antitubercular agent
- Orally active antibiotic
- Inhibits growth of *Mycobacterium tuberculosis* H37Rv
- Exhibits antibacterial action with a MIC value of 0.1 μg/mL
- Activated by mycobacterial monooxygenase EthA
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1,363
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000370629 SCH900776 200MG
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1,364
Ambeed AMBEED
5000866764 5-BROMOISOQUINOLIN-6-AMINE 1GR
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1,365
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000428591 PARTHENOLIDE 200MG
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