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)
- (221)
- (6)
- (1)
- (1)
- (40)
- (2)
- (12)
- (48)
- (1)
- (37)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (8)
- (135)
- (1)
- (9)
- (16)
- (1)
- (36)
- (1)
- (1)
- (1)
- (1)
- (1)
- (189)
- (1)
- (1)
- (17)
- (1)
- (17)
- (17)
- (6)
- (1)
Molecular Weight (g/mol)
- (1)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (7)
- (21)
- (26)
- (2)
- (30)
- (4)
- (6)
- (1)
- (4)
- (1)
- (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)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (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)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (3)
- (1)
- (1)
- (1)
- (4)
- (2)
- (2)
- (1)
- (1)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (5)
- (1)
- (1)
- (2)
- (5)
- (2)
- (4)
- (2)
- (3)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (4)
- (1)
- (2)
- (4)
- (1)
- (1)
- (3)
- (3)
- (1)
- (7)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (2)
- (3)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (1)
- (2)
- (3)
- (1)
- (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)
- (2)
- (4)
- (3)
- (2)
- (1)
- (9)
- (5)
- (2)
- (3)
- (3)
- (2)
- (5)
- (6)
- (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)
- (1)
- (4)
- (5)
- (4)
- (3)
- (3)
- (7)
- (1)
- (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)
- (25)
- (19)
- (71)
- (1)
- (109)
- (3)
- (1)
- (2)
- (61)
- (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
- (2)
- (1)
- (1)
- (1)
- (3)
- (3)
- (2)
- (1)
- (1)
- (2)
- (1)
- (5)
- (4)
- (2)
- (1)
- (3)
- (1)
- (2)
- (2)
- (5)
- (3)
- (2)
- (3)
- (1)
- (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)
- (1)
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481
Ambeed 2Chloro9Hpurine
2-Chloro-9H-purine, 1681-15-8, 97%
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482
Ambeed 4Aminoisophthalic acid
4-Aminoisophthalic acid, 33890-03-8, 98%
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483
Ambeed 2Chloro9Hpurine
2-Chloro-9H-purine, 1681-15-8, 97%
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484
Ambeed 4Aminoisophthalic acid
4-Aminoisophthalic acid, 33890-03-8, 98%
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485
Ambeed Dicyclohexyl 3isopropoxy2 4
Dicyclohexyl(3-isopropoxy-2',4',6'-triisopropyl-[1,1'-biphenyl]-2-yl)phosphine, 2118959-55-8, 97%
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486
Ambeed Ferrocenemethanol
Ferrocenemethanol, 1273-86-5, 98%
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487
Ambeed Mono 6amino6deoxy cyclodextri
Mono-(6-amino-6-deoxy)-β-cyclodextrin, 29390-67-8, 95%
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488
Aobchem AOBCHEM
5001089658 1 3-DIMETHOXY-5- METHOXYMETHOX
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489
Aobchem AOBCHEM
5001088222 1 4-DIMETHOXY-2- METHOXYMETHOX
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490
Aobchem AOBCHEM
5001088502 1 4-DIMETHOXY-2- METHOXYMETHOX
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491
Medchemexpress LLC Sulfo-Cy5 amine | 2183440-44-8 | 98.0% | 740.97 | C38H52N4O7S2 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Sulfo-Cy5 amine is a water-soluble, near-infrared fluorescent dye containing a primary amine for covalent conjugation to electrophilic targets. Sulfonate groups increase aqueous solubility, making the dye suitable for labeling biomolecules in biological buffers and imaging applications.
- Water-soluble cyanine dye suitable for near-infrared imaging.
- Primary amine functional group enables amine-reactive conjugation.
- High purity (98.0%) supports reproducible labeling results.
- Sulfonate groups enhance solubility in aqueous media and biological buffers.
- Available in small milligram pack sizes for research-scale use.
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492
Aobchem AOBCHEM
5001093398 2 3-DIMETHOXY-6-FLUOROBENZALDE
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493
Aobchem AOBCHEM
5001093008 2 3-DIMETHOXY-6-FLUOROBENZALDE
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494
Medchemexpress LLC Propidium Iodide | 25535-16-4 | 99.69% | 100 MG
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Propidium Iodide (PI) is a nuclear staining agent that stains DNA. It is an analogue of ethidine bromide that emits red fluorescence when embedded in double-stranded DNA. PI cannot pass through living cell membranes, but it can pass through damaged cell membranes to stain the nucleus. It has a fluorescence wavelength of 493/617 nm and 536/635 nm after Mosaic with DNA. Propidium Iodide is commonly used in the detection of apoptosis or necrosis, and is often used in flow cytometry analysis.
- Nuclear staining agent for DNA.
- Emits red fluorescence upon embedding in double-stranded DNA.
- Passes through damaged cell membranes to stain the nucleus.
- Fluorescence wavelength: 493/617 nm and 536/635 nm (after Mosaic with DNA).
- Commonly used in the detection of apoptosis or necrosis.
- Often used in flow cytometry analysis.
- Used in cell cycle and cell viability assays.
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495
Medchemexpress LLC Quinine hemisulfate hydrate | 207671-44-1 | 99.4% | 1 G
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Quinine hemisulfate hydrate is an alkaloid derived from the bark of the cinchona tree, acting as an anti-malaria agent. It is a potassium channel inhibitor that inhibits WT mouse Slo3 (KCa5.1) channel currents evoked by voltage pulses to +100 mV, with an IC50 of 169 μM.
- Alkaloid derived from the bark of the cinchona tree.
- Acts as an anti-malaria agent.
- Potassium channel inhibitor.
- Inhibits WT mouse Slo3 (KCa5.1) channel currents with an IC50 of 169 μM.
- For research use only.
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