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
- (1)
- (1)
- (1)
- (219)
- (6)
- (40)
- (2)
- (12)
- (47)
- (1)
- (37)
- (1)
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- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (7)
- (132)
- (1)
- (9)
- (16)
- (1)
- (35)
- (1)
- (1)
- (1)
- (1)
- (1)
- (189)
- (1)
- (1)
- (15)
- (1)
- (17)
- (17)
- (7)
- (1)
Molecular Weight (g/mol)
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- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (7)
- (22)
- (26)
- (30)
- (4)
- (6)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (5)
- (2)
- (6)
- (5)
- (2)
- (1)
- (11)
- (1)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (25)
- (16)
- (2)
- (3)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
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- (4)
- (4)
- (8)
- (2)
- (1)
- (2)
- (1)
- (1)
- (6)
- (2)
- (1)
- (1)
- (2)
- (1)
- (6)
- (1)
- (20)
- (1)
- (5)
- (1)
- (3)
- (5)
- (1)
- (2)
- (2)
- (2)
- (2)
- (8)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (2)
- (1)
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- (1)
- (4)
- (2)
- (2)
- (1)
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- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (5)
- (1)
- (2)
- (5)
- (2)
- (4)
- (2)
- (3)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (4)
- (2)
- (4)
- (1)
- (1)
- (3)
- (3)
- (1)
- (7)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (4)
- (1)
- (2)
- (1)
- (1)
- (2)
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- (2)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (1)
- (2)
- (3)
- (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)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (4)
- (5)
- (1)
- (2)
- (1)
- (1)
- (2)
- (4)
- (3)
- (2)
- (1)
- (9)
- (2)
- (3)
- (3)
- (2)
- (5)
- (3)
- (13)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (3)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (4)
- (5)
- (4)
- (3)
- (3)
- (7)
- (1)
- (2)
- (3)
- (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)
- (110)
- (3)
- (1)
- (2)
- (59)
- (5)
- (1)
- (1)
Physical Form
- (2)
- (299)
- (2)
- (2)
- (4)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (3)
- (9)
- (3)
- (2)
- (62)
- (2)
- (29)
- (3)
Boiling Point
- (1)
- (1)
- (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)
- (12)
- (4)
- (1)
- (5)
- (3)
- (5)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
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1,711
eMolecules 6-FLUORO-2-METHYL-QUINOL 500MG
5000191298 6-FLUORO-2-METHYL-QUINOL 500MG
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1,712
Medchemexpress LLC Pyrroloquinoline quinone-13C3 sodium | 72909-34-3 | 99.3% | 421.11 g·mol⁻¹ | C1113C3H2N2Na4O8 | 1 MG
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Pyrroloquinoline quinone-13C3 sodium is the 13C3 isotopically labeled sodium salt of pyrroloquinoline quinone, supplied as a high-purity tracer and internal standard for quantitative analytical methods. It is intended for research use in studies of redox chemistry and biological activity, and for method development and validation in mass spectrometry and NMR-based assays.
- Isotopically labeled sodium salt for tracer and internal standard use.
- High purity suitable for quantitative analytical methods.
- Compatible with NMR, GC-MS, and LC-MS workflows.
- Supports studies of redox activity and biological function.
- Supplied in small, weighed quantities for research applications.
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1,713
eMolecules 4-4 6-DIMETHOXY-1 3 5-TR 500G
5000224935 4-4 6-DIMETHOXY-1 3 5-TR 500G
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1,714
eMolecules 7-HYDROXYQUINOLINE-6-CAR 0.25G
5000225524 7-HYDROXYQUINOLINE-6-CAR 0.25G
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1,715
eMolecules 2-1 4-DIOXASPIRO 4.5 DEC- 10G
5000280460 2-1 4-DIOXASPIRO 4.5 DEC- 10G
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1,716
Medchemexpress LLC 5'-O-(4,4'-dimethoxytrityl)-2'-O-methyluridine | 103285-22-9 | 98.0% | 560.59 g/mol | C31H32N2O8 | 1 G
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5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyluridine is a DMT-protected uridine nucleoside analog with a 2'-O-methyl ribose modification, used as an intermediate in the chemical synthesis of modified oligonucleotides and nucleoside derivatives. Molecular formula C31H32N2O8; molecular weight 560.59 g/mol. Follow supplier storage recommendations for long-term stability.
- DMT-protected at the 5'-position for controlled deprotection.
- 2'-O-methyl modification enhances nuclease resistance.
- Designed for incorporation into synthetic oligonucleotides.
- High purity (98.0%) suitable for research applications.
- Stable as a powder under recommended storage conditions.
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1,717
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000370453 KRAS INHIBITOR-31 25MG
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1,718
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000370785 PRMT5-IN-31 5MG
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1,719
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000370934 PRMT5-IN-31 10MM 1ML
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1,720
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371112 CDK2-IN-31 25MG
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1,721
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000378146 ORN 06 SODIUM 1MG
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1,722
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382624 POMALIDOMIDE-AMIDO-C 25MG
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1,723
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000386072 STF-31 100MG
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1,724
Medchemexpress LLC 2-Octyl-4(1H)-quinolone | 80554-60-5 | >=98.0% | 257.37 | 50 MG
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2-Octyl-4(1H)-quinolone is a quinolinone alkaloid that can be isolated from *Ruta graveolens*. It is intended for research use only. It has shown antiproliferative activity against human A2780 cells with an IC50 of 12 μM after 2 days by Alamar blue assay. The compound is a solid, white to off-white in color, with the formula C17H23NO. It is classified under Alkaloids and Other Alkaloids, and its initial source is from the plants Rutaceae, specifically *Ruta graveolens Linn.*.
- Quinolone alkaloid.
- Isolated from *Ruta graveolens*.
- For research use only.
- Exhibits antiproliferative activity against human A2780 cells with an IC50 of 12 μM after 2 days by Alamar blue assay.
- Solid, white to off-white in color.
- Chemical formula C17H23NO.
- Classified under alkaloids.
- Sourced from Rutaceae, *Ruta graveolens Linn.*.
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1,725
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000403372 ENDO CNTINH-03 25MG
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