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Filtered Search Results
Medchemexpress LLC Guanfacine (hydrochloride) | 29110-48-3 | 99.98% | 282.55 | 25 MG
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Guanfacine hydrochloride is an orally active and blood-brain barrier permeable noradrenergic α2A agonist, highly selective for the α2A receptor subtype. It has effects in producing hypotension and sedation, and can be used for research on various prefrontal cortex (PFC) cognitive disorders, including Tourette's syndrome and attention deficit hyperactivity disorder (ADHD).
- Orally active and blood-brain barrier permeable noradrenergic α2A agonist.
- High selectivity for the α2A receptor subtype.
- Increases delay-related neuronal firing needed for working memory on dIPFC neurons.
- Improves PFC cognitive function by inhibiting CAMP production, closing HCN channels, and strengthening PFC networks.
- Enhances PFC working memory function and improves impulse control in aged monkeys.
- Improves cognitive performance when infused directly into the rat or monkey PFC.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000656222 DFHBI-BI 10MG
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eMolecules 771-84-6 | 2-CYANO-2-PHENYLACETAMIDE | AstaTech | MFCD17240132 | 160.176 | C9H8N2O | 95.000 | NC(=O)C(C#N)c1ccccc1 | 0.25g | 323612008
2-CYANO-2-PHENYLACETAMIDE | AstaTech | 771-84-6 | MFCD17240132 | 160.176 | C9H8N2O | 95.000 | NC(=O)C(C#N)c1ccccc1 | 0.25g | 323612008
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![eMolecules 869901-24-6 | 4-[6-(Tributylstannyl)pyridin-2-yl]morpholine | Synthonix - Stock | MFCD08271894 | 453.258 | C21H38N2OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cccc(n1)N1CCOCC1 | 500mg | 525924523](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502454908.PNG-250.jpg)
eMolecules 869901-24-6 | 4-[6-(Tributylstannyl)pyridin-2-yl]morpholine | Synthonix - Stock | MFCD08271894 | 453.258 | C21H38N2OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cccc(n1)N1CCOCC1 | 500mg | 525924523
4-[6-(Tributylstannyl)pyridin-2-yl]morpholine | Synthonix - Stock | 869901-24-6 | MFCD08271894 | 453.258 | C21H38N2OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1cccc(n1)N1CCOCC1 | 500mg | 525924523
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![Medchemexpress LLC 3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-alpha-(1,1-dimethylethoxy)- | 1155419-89-8 | 99.7% | 442.51 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000387935-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-alpha-(1,1-dimethylethoxy)- | 1155419-89-8 | 99.7% | 442.51 | 100 MG
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3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-alpha-(1,1-dimethylethoxy)- | 1155419-89-8 | 99.7% | 442.51 | 100 MG
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Medchemexpress LLC PNU112455A hydrochloride | 21886-12-4 | 99.6% | 301.75 | 1 ML
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PNU112455A hydrochloride is an ATP-competitive inhibitor of CDK2 and CDK5. It binds to the ATP site of CDK2 and CDK5 with Km values of 3.6 μM and 3.2 μM, respectively. This product is intended for research use only and is not sold to patients.
- ATP-competitive CDK2 and CDK5 inhibitor.
- Binds to the ATP site of CDK2 and CDK5.
- Km for CDK2: 3.6 μM.
- Km for CDK5: 3.2 μM.
- Purity: 99.56%.
- Appearance: Solid, Light yellow to yellow.
- Shipping: Room temperature in continental US.
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month.
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Selleck Chemical LLC TA-02
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TA-02 is a p38 MAPK inhibitor with IC50 of 20 nM TA-02 especially inhibits TGFBR-2
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eMolecules 29671-92-9 | Chloroformamidine Hydrochloride | Accela ChemBio (ASD) | MFCD00035527 | 114.960 | CH4Cl2N2 | 95.000 | Cl.NC(Cl)=N | 25g | 490829087
Chloroformamidine Hydrochloride | Accela ChemBio (ASD) | 29671-92-9 | MFCD00035527 | 114.960 | CH4Cl2N2 | 95.000 | Cl.NC(Cl)=N | 25g | 490829087
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eMolecules 1186660-06-9 | Medchem Express | PKM2 activator 2 | 5mg | 779715147 | HY-147368 | 452.49 | C20H18F2N2O4S2
Ambeed | 5-(4-Carboxyphenyl)-246-trimethyl-[1131-terphenyl]-44-dicarboxylic acid | 250mg | 586453160 | A1188287 | 1246562-60-6 | 480.516 | C30H24O6
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Medchemexpress LLC Carmoxirole hydrochloride | 115092-85-8
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Carmoxirole hydrochloride | 115092-85-8
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Medchemexpress LLC Bi-78d3 | 883065-90-5 | MFCD12912396 | 99.9% | 379.37 g/mol | C13H9N5O5S2 | 10 MG
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BI-78D3 is a substrate-competitive inhibitor of c-Jun N-terminal kinase (JNK) used as a research tool to probe JNK-mediated signaling. It inhibits JNK kinase activity with an IC50 of approximately 280 nM and is supplied in solid and solution formats for in vitro and cell-based studies. For research use only.
- Substrate-competitive inhibitor of JNK.
- Reported IC50 of 280 nM against JNK.
- High purity (99.85%).
- Available as solid (10 mg) and as 10 mM solution in DMSO.
- Powder storage: -20°C for long-term stability.
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![eMolecules 13291-18-4 | Isopropenylmagnesium bromide, 0.50 M in THF | Synthonix | MFCD00192240 | 145.282 | C3H5BrMg | 0.000 | [Br-].CC([Mg+])=C | 100ml | 649431320](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695133.jpg-250.jpg)
eMolecules 13291-18-4 | Isopropenylmagnesium bromide, 0.50 M in THF | Synthonix | MFCD00192240 | 145.282 | C3H5BrMg | 0.000 | [Br-].CC([Mg+])=C | 100ml | 649431320
Isopropenylmagnesium bromide, 0.50 M in THF | Synthonix | 13291-18-4 | MFCD00192240 | 145.282 | C3H5BrMg | 0.000 | [Br-].CC([Mg+])=C | 100ml | 649431320
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Medchemexpress LLC Jnj28871063 hydrochloride | 944342-90-9 | 98.4% | 519.42 | C24H28Cl2N6O3 | 100 MG
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JNJ28871063 hydrochloride is an ATP-competitive pan-ErbB (EGFR/ErbB) kinase inhibitor used for research. It is orally active, shows potent inhibition of ErbB family kinases, crosses the blood-brain barrier, and has demonstrated antitumor activity in xenograft models.
- Orally active, ATP-competitive pan-ErbB kinase inhibitor.
- Potent inhibition of EGFR (ErbB1), ErbB2, and ErbB4 (IC50 ≈ 21-38 nM).
- Crosses the blood-brain barrier.
- Demonstrated antitumor activity in EGFR/ErbB2-overexpressing xenograft models.
- Supplied as the hydrochloride salt.
- Intended for in vitro and in vivo research use only.
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![eMolecules 92273-73-9 | Butylzinc bromide, 0.50 M in THF | Synthonix | MFCD00671997 | 202.400 | C4H9BrZn | 0.000 | [Br-].CCCC[Zn+] | 100ml | 627353799](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695217.jpg-250.jpg)
eMolecules 92273-73-9 | Butylzinc bromide, 0.50 M in THF | Synthonix | MFCD00671997 | 202.400 | C4H9BrZn | 0.000 | [Br-].CCCC[Zn+] | 100ml | 627353799
Butylzinc bromide, 0.50 M in THF | Synthonix | 92273-73-9 | MFCD00671997 | 202.400 | C4H9BrZn | 0.000 | [Br-].CCCC[Zn+] | 100ml | 627353799
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eMolecules 1678-25-7 | Benzenesulfonanilide | Ambeed | MFCD00035919 | 233.290 | C12H11NO2S | 98.000 | O=S(=O)(Nc1ccccc1)c1ccccc1 | 10g | 650568241
Benzenesulfonanilide | Ambeed | 1678-25-7 | MFCD00035919 | 233.290 | C12H11NO2S | 98.000 | O=S(=O)(Nc1ccccc1)c1ccccc1 | 10g | 650568241
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