Quinolines and derivatives
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Filtered Search Results
Apexbio Technology LLC SKF38393 HCl 62717-42-4 200mg
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SKF38393 HCl is a selective dopamine D1 receptor agonist exhibiting activity through direct binding and stimulation of D1 receptors Activation of D1 receptors primarily induces adenylyl cyclase stimulation and increases cAMP-dependent protein kinase signaling subsequently modulating neuronal differentiation growth and dopamine-mediated functional responses Experimental evidence indicates that SKF38393 administration impacts gene expression patterns related to dopamine receptor-sensitive neuronal pathways and neuropeptides Additionally in vitro studies report SKF38393 to inhibit proliferation of certain tumor cell lines exemplified by decreased cell growth in breast carcinoma-derived MCF-7 cells at submicromolar concentrations It is widely utilized as a pharmacological tool in neuroscience and oncology research
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Apexbio Technology LLC CUDC-907 1339928-25-4 200mg
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CUDC-907 (CAS 1339928-25-4) is a dual inhibitor targeting histone deacetylases (HDACs 1 2 3 10) and class I phosphatidylinositol 3-kinases (PI3K) It exhibits nanomolar inhibitory activity against these enzymes blocking PI3K-mediated Akt signaling and increasing acetylation of histones and non-histone substrates (e g tubulin p53) In cancer cell models CUDC-907 induces G2-M phase arrest and reduces phosphorylation of downstream proteins such as p70S6 4EBP-1 MEK STAT3 and SRC Preclinical studies demonstrate its anti-tumor activity in lymphoma and NSCLC xenografts making it relevant for oncology research
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Medchemexpress LLC ACT-1004-1239 | 2178049-58-4 | 98.8% | C27H28F2N6O3 | 1 MG
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ACT-1004-1239 is a potent, selective, orally active CXCR7 antagonist with an IC50 value of 3.2 nM. It is intended for research use only.
- Inhibits human, dog, rat, mouse, guinea pig, macaque CXCR7 with IC50s of 3.2, 2.3, 3.1, 2.3, 0.6, 1.5 nM respectively.
- Promotes oligodendrocyte precursor cell (OPC) differentiation by increasing CXCL12 levels.
- Increases plasma CXCL12 concentration in naive male DBA/1 mice.
- Reduces disease severity in MOG-induced experimental autoimmune encephalomyelitis (EAE) model.
- Increases myelination in the Cuprizone-induced demyelination model mice.
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Medchemexpress LLC MPEG-amine (MW 20000) | 80506-64-5 | 98.0% | (C2H4O)nC3H9NO | 100 MG
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m-PEG-NH2 (MW 20000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
- Peg-based PROTAC linker
- Used in the synthesis of PROTACs
- Purity: 98.0%
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Ambeed S 2 9HFluoren9yl methoxy c
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,3-dimethylbutanoic acid, 169566-81-8, 95%
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Ambeed Methyl 5bromo6oxo1 6dihydropyr
Methyl 5-bromo-6-oxo-1,6-dihydropyridine-2-carboxylate, 178876-86-3, 98%
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Ambeed 3Aminopiperidine2 6dione
3-Aminopiperidine-2,6-dione, 2353-44-8, 98%
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Ambeed 4Bromobenzylamine
4-Bromobenzylamine, 3959-07-7, 98% GC
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Ambeed tertButyl 1 8diazaspiro 4.5 de
tert-Butyl 1,8-diazaspiro[4.5]decane-8-carboxylate, 937729-06-1, 95%
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Ambeed 3 4Chlorophenyl N pyridin4ylme
3-(4-Chlorophenyl)-N-(pyridin-4-ylmethyl)adamantane-1-carboxamide, 915385-81-8, 98%
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Ambeed tertButyl 1S 3S 3aminocyclop
tert-Butyl ((1S,3S)-3-aminocyclopentyl)carbamate, 645400-44-8, 95%
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Ambeed 3 Bromomethyl oxetane
3-(Bromomethyl)oxetane, 1374014-30-8, 95%
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Ambeed 4 Ethoxycarbonyl N N Ntrimethy
4-(Ethoxycarbonyl)-N,N,N-trimethylbenzenaminium trifluoromethanesulfonate, 124915-06-6, 95%
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Ambeed Anthracen9ylmethanamine
Anthracen-9-ylmethanamine, 2476-68-8, 97%
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Ambeed 11bR 2R 5R 1 Dinaphtho 2 1d
(11bR)-(2R,5R)-1-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2,5-diphenylpyrrolidine, 444667-33-8, 98%
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