Oxazoles
eMolecules Ambeed / N-(3-Ethynylphenyl)-67-bis(2-methoxyethoxy)quinazolin-4-amine hydrochloride / 1g / 525067752 / A154463 / / 183319-69-9 / MFCD07781272 / 429.900 / C22H24ClN3O4
Ambeed / N-(3-Ethynylphenyl)-67-bis(2-methoxyethoxy)quinazolin-4-amine hydrochloride / 1g / 525067752 / A154463 / / 183319-69-9 / MFCD07781272 / 429.900 / C22H24ClN3O4
Medchemexpress LLC Dimethyl octadecaned 5g
Dimethyl octadecanedioate (Octadecanedioic acid dimethyl ester) is an ester product
Sigma Aldrich Fine Chemicals Biosciences Neuropeptide Y human 95 HP1MG
Neuropeptide Y is a regulatory molecule encoded by a gene mapped to human chromosome 7p15. Neuropeptide Y is a 36 amino acid protein with C-terminal amide structure. It is ubiquitously distributed in heart and brain but at high levels in paraventricular hypothalamic nucleus hypothalamic arcuate nucleus suprachiasmatic nucleus median eminence dorsomedial hypothalamic nucleus paraventricular thalamic nuclei. NPY is a member of antimicrobial peptide family which also include dermaseptins cecropins or magainins.
Medchemexpress LLC (4S)-PROTAC SOS1 degrader-1 diTFA | 98.1% | C61H78ClF7N10O8S | 25 MG
(4S)-PROTAC SOS1 degrader-1 (diTFA) is a potent PROTAC SOS1 degrader that decreases the expression of pERK and RAS-GTP levels in a dose-dependent manner. It has been shown to significantly inhibit tumor growth in vivo.
- Potent PROTAC SOS1 degrader
- Decreases expression of pERK and RAS-GTP levels in a dose-dependent manner
- Significantly inhibits tumor growth in vivo
Medchemexpress LLC (4S)-PROTAC SOS1 degrader-1 | 2913176-81-3 | C57H76ClFN10O4S | 50 MG
(4S)-PROTAC SOS1 degrader-1 is a potent PROTAC SOS1 degrader. It decreases the expression of pERK and RAS-GTP levels in a dose-dependent manner. It also significantly inhibits tumor growth in vivo.
- Shows potent SOS1 degradation activity with 56.2% and 92.5% SOS1 protein degradation at 0.1 and 1 μM, respectively, in NCI-H358 cells.
- Degrades SOS1 in a dose- and time-dependent manner in NCI-H358 cells (24 h incubation).
- Does not induce SOS2 and KRAS degradation in NCI-H358 cells (9.8-2500 nM; 24 h).
- Decreases the expression of pERK and RAS-GTP levels in NCI-H358 cells in a dose-dependent manner (7.8-2000 nM; 24 h).
- Significantly inhibits tumor growth in vivo.
Medchemexpress LLC 4-(Chloromethyl)-7-hydroxycoumarin | 25392-41-0 | 98.0% | C10H7ClO3 | 250 MG
4-(Chloromethyl)-7-hydroxycoumarin is a hydroxycoumarin derivative exhibiting potent antioxidant effects and high hydroxyl radical-scavenging properties. It contains a methyl group and a chlorine group within its heterocyclic ring. This compound has been investigated for its ability to inhibit the zinc enzyme carbonic anhydrase, particularly tumor-associated isoforms CA IX and XII.
- Exhibits potent antioxidant effect
- Possesses high hydroxyl radical-scavenging property
- Contains methyl and chlorine groups in the heterocyclic ring
- Investigated as an inhibitor of zinc enzyme carbonic anhydrase
- Targets tumor-associated isoforms CA IX and XII
- For research use only
![Medchemexpress LLC 5-Amino-1,3-dimethyl-6-(3-propoxyphenoxy)-1H-benzo[d]imidazol-2(3H)-one | 1800477-35-3 | 96.9% | 327.38 | 250 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000402937-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 5-Amino-1,3-dimethyl-6-(3-propoxyphenoxy)-1H-benzo[d]imidazol-2(3H)-one | 1800477-35-3 | 96.9% | 327.38 | 250 MG
This chemical is 5-Amino-1,3-dimethyl-6-(3-propoxyphenoxy)-1H-benzo[d]imidazol-2(3H)-one, identified for use as a laboratory chemical and in the manufacture of substances.
- Used as a laboratory chemical.
- Used in the manufacture of substances.
- Off-white to light yellow solid.
- Recommended storage conditions for powder and in solvent.
- For research use only.
eMolecules 5006-57-5 | Ambeed | 36-Dibromo-24-dimethylpyridine | 100mg | 491649985 | A255928 | MFCD18800908 | 264.948 | C7H7Br2N
Ambeed | 36-Dibromo-24-dimethylpyridine | 100mg | 491649985 | A255928 | 5006-57-5 | MFCD18800908 | 264.948 | C7H7Br2N