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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- (12)
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- (37)
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- (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)
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- (1)
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- (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)
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- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (4)
- (4)
- (8)
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- (1)
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- (1)
- (1)
- (6)
- (2)
- (1)
- (1)
- (2)
- (1)
- (6)
- (1)
- (20)
- (1)
- (5)
- (1)
- (3)
- (5)
- (1)
- (2)
- (2)
- (2)
- (2)
- (8)
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- (1)
- (1)
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- (1)
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- (2)
- (1)
- (1)
- (1)
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- (4)
- (1)
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- (3)
- (1)
- (7)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
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- (2)
- (4)
- (1)
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- (2)
- (1)
- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (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)
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- (2)
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- (1)
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- (2)
- (2)
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- (1)
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- (4)
- (3)
- (3)
- (7)
- (1)
- (1)
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- (7)
- (5)
- (2)
- (1)
- (10)
- (1)
- (1)
Percent Purity
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- (2)
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- (4)
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- (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)
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- (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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4,561
Aobchem 4-Fluoro-3-isopropoxy-5-methylbenzaldehyde | ≥97% | CAS 2484889-03-2 | C11H13FO2 | 250mg
4-Fluoro-3-isopropoxy-5-methylbenzaldehyde | ≥97% | CAS 2484889-03-2 | C11H13FO2 | 250mg
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4,562
Aobchem 4-Fluoro-2-isopropoxy-5-methylbenzaldehyde | 97% | CAS 2764731-88-4 | C11H13FO2 | 500mg
4-Fluoro-2-isopropoxy-5-methylbenzaldehyde | 97% | CAS 2764731-88-4 | C11H13FO2 | 500mg
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4,563
Aobchem 1-Fluoro-2-isopropoxy-4 5-dimethoxybenzene | 97% | CAS 2901103-45-3 | C11H15FO3 | 500mg
1-Fluoro-2-isopropoxy-4 5-dimethoxybenzene | 97% | CAS 2901103-45-3 | C11H15FO3 | 500mg
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4,564
Aobchem 3-Fluoro-2-isopropoxy-6-methylbenzaldehyde | 97% | CAS 2901096-31-7 | C11H13FO2 | 1g
3-Fluoro-2-isopropoxy-6-methylbenzaldehyde | 97% | CAS 2901096-31-7 | C11H13FO2 | 1g
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4,565
Aobchem Trimethyl(3-methylthiophen-2-yl)silane | ≥97% | CAS 143266-59-5 | C8H14SSi | 10g
Trimethyl(3-methylthiophen-2-yl)silane | ≥97% | CAS 143266-59-5 | C8H14SSi | 10g
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4,566
Aobchem 2-Trimethyl-6-quinolinemethanol | 97% | CAS 1515644-29-7 | C13H15NO | 1g
2-Trimethyl-6-quinolinemethanol | 97% | CAS 1515644-29-7 | C13H15NO | 1g
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4,567
Aobchem 1-Bromo-4-(tert-butyl)-2-ethoxybenzene | 97% | CAS 1418005-59-0 | C12H17BrO | 1g
1-Bromo-4-(tert-butyl)-2-ethoxybenzene | 97% | CAS 1418005-59-0 | C12H17BrO | 1g
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4,568
Aobchem 3 5-Trimethyl- -(1-methylethyl)benzenemethanol | 95% | CAS 1182749-71-8 | C13H20O | 1g
3 5-Trimethyl- -(1-methylethyl)benzenemethanol | 95% | CAS 1182749-71-8 | C13H20O | 1g
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4,569
Aobchem 1 2-Dimethoxy-4-(methoxymethoxy)benzene | 95% | CAS 133129-56-3 | C10H14O4 | 10g
1 2-Dimethoxy-4-(methoxymethoxy)benzene | 95% | CAS 133129-56-3 | C10H14O4 | 10g
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4,570
Aobchem 2 4-Dimethoxy-3-fluorophenylboronic acid | ≥97% | CAS 949146-39-8 | C8H10BFO4 | 5g
2 4-Dimethoxy-3-fluorophenylboronic acid | ≥97% | CAS 949146-39-8 | C8H10BFO4 | 5g
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4,571
Aobchem 2-Methoxyquinoline-3-boronic acid | 97% | CAS 886853-93-6 | C10H10BNO3 | 250mg
2-Methoxyquinoline-3-boronic acid | 97% | CAS 886853-93-6 | C10H10BNO3 | 250mg
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4,572
Aobchem Trimethyl((2 4 5-trifluorophenyl)ethynyl)silane | 95% | CAS 1097876-22-6 | C11H11F3Si | 5g
Trimethyl((2 4 5-trifluorophenyl)ethynyl)silane | 95% | CAS 1097876-22-6 | C11H11F3Si | 5g
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4,573
Medchemexpress LLC HCV-IN-31 | 1998705-62-6 | 99.7% | 312.30 | 25 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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HCV-IN-31 (compound 4) is a potent inhibitor of the Hepatitis C Virus (HCV) replicon, demonstrating an EC50/EC95 of 15.7 μM. This compound is provided as a white to off-white solid, suitable for various research applications.
- High purity of 99.7%
- Molecular weight: 312.30
- Molecular formula: C12H17FN6O3
- CAS number: 1998705-62-6
- Recommended storage: 4°C, protect from light
- In solvent storage: -80°C for 6 months, -20°C for 1 month (protect from light)
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4,574
Medchemexpress LLC 7-Deazahypoxanthine | 3680-71-5 | 99.9% | C6H5N3O | 25 G
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7-Deazahypoxanthine is a biochemical reagent designed for life science research. It can be used as a biological material or organic compound, and serves as a pharmaceutical intermediate. Its methylated forms are utilized as regiochemical probes of xanthine oxidase.
- Biochemical reagent for life science research
- Suitable as a biological material or organic compound
- Serves as a pharmaceutical intermediate
- Methylated forms act as regiochemical probes for xanthine oxidase
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4,575
Medchemexpress LLC BSJ-03-204 (triTFA) | 99.9% | 1174.97 | 25 MG
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BSJ-03-204 triTFA is a PROTAC connected by ligands for Cereblon and CDK. It is a potent and selective Palbociclib-based CDK4/6 dual degrader, with IC50s of 26.9 nM for CDK4/D1 and 10.4 nM for CDK6/D1. This compound does not induce IKZF1/3 degradation and demonstrates anti-cancer activity.
- PROTAC connected by ligands for Cereblon and CDK.
- Potent and selective Palbociclib-based CDK4/6 dual degrader.
- Demonstrates potent anti-proliferative effects on MCL cell lines.
- Induces a G1 arrest.
- Selectively degrades CDK4/6 in WT cells without affecting IKZF1/3 degradation.
- Exhibits anti-cancer activity.
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