Aralkylamines
Accela Chembio Inc 3-(dimethylamino)-1-(2-thienyl)-1-propanol | 5g | 13636-02-7 | MFCD09701963 | 97+% | Shelf Life: 1260 Days | Light Sensitive
3-(dimethylamino)-1-(2-thienyl)-1-propanol | 5g | 13636-02-7 | MFCD09701963 | 97+% | Shelf Life: 1260 Days | Light Sensitive
Accela Chembio Inc (s)-(-)-3-(n-methylamino)-1-(2-thienyl)-1-propanol | 5g | 116539-55-0 | MFCD07357308 | 97+% | Shelf Life: 1620 Days | Light Sensitive/n2/+4
(s)-(-)-3-(n-methylamino)-1-(2-thienyl)-1-propanol | 5g | 116539-55-0 | MFCD07357308 | 97+% | Shelf Life: 1620 Days | Light Sensitive/n2/+4
Accela Chembio Inc (1s | 2s)-(-)-1 | 2-diphenylethylenediamine | 25g | 29841-69-8 | MFCD00082751 | 97+% | Shelf Life: 540 Days | Air Sensitive/+4
(1s | 2s)-(-)-1 | 2-diphenylethylenediamine | 25g | 29841-69-8 | MFCD00082751 | 97+% | Shelf Life: 540 Days | Air Sensitive/+4
eMolecules 387350-88-1 | N-(Piperid-4-yl)-3-(trifluoromethylsulphonyl)aniline | Apollo Scientific | MFCD01319328 | 308.320 | C12H15F3N2O2S | 97.000 | FC(F)(F)S(=O)(=O)c1cccc(NC2CCNCC2)c1 | 1g | 562445153
N-(Piperid-4-yl)-3-(trifluoromethylsulphonyl)aniline | Apollo Scientific | 387350-88-1 | MFCD01319328 | 308.320 | C12H15F3N2O2S | 97.000 | FC(F)(F)S(=O)(=O)c1cccc(NC2CCNCC2)c1 | 1g | 562445153
STA PHARMACEUTICAL US LLC 2-(Fmoc-amino)-3-(1-Boc-3-piperidyl)propanoic Acid | 50 g | CAS 457060-97-8 | MDL MFCD02683129
2-(Fmoc-amino)-3-(1-Boc-3-piperidyl)propanoic Acid is a Amino Acid reagent (Subcategory: Unusual AA) sold by WuXi TIDES. Offered in 50 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 457060-97-8
- MDL: MFCD02683129
- InChIKey: WPCUPMFUJBWUFE-UHFFFAOYSA-N
- Molecular Weight: 494.588
- Molecular Formula: C28H34N2O6
- Purity: ≥95%
- Container Type: 250 mL HDPE
- Pack Size: 50 g
- Net Weight: 50 g
- Gross Weight: 89.8 g
- Commodity Code: 29333999
- Country Of Origin: China
- IUPAC: 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid
- SMILES: CC(OC(N1CCCC(CC(C(O)=O)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O)C1)=O)(C)C
Medchemexpress LLC Theodrenaline (hydrochloride) | 2572-61-4 | 411.84 | 25 MG
Theodrenaline hydrochloride is a cardiac stimulant that acts as an anti-hypotensive agent when combined with Cafedrine. It induces a positive inotropic effect in human atrial trabeculae by stimulating β-adrenoceptors and can enhance FSK effects, possibly due to PDE-inhibition.
- Cardiac stimulant
- Acts as an anti-hypotensive agent when combined with Cafedrine
- Induces a positive inotropic effect
- Stimulates β-adrenoceptors
- Enhances FSK effects, possibly due to PDE-inhibition
- Appears as a solid
- For research use only
- Store at 4°C, protected from light, under nitrogen
eMolecules 3-(2,6-Dimethyl-piperidin-1-yl)-propylamine | 85723-72-4 | MFCD03445119 | 500mg
Matrix Scientific | 3-(2,6-Dimethyl-piperidin-1-yl)-propylamine | 500mg | 389716615 | 8506 | | 85723-72-4 | MFCD03445119 | 170.300 | C10H22N2
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eMolecules Building Block Tool
eMolecules 586-70-9 | 1-(4-Methylphenyl)ethylamine | Chem-Impex | MFCD02177111 | 135.210 | C9H13N | 99.000 | CC(N)c1ccc(C)cc1 | 25g | 112761078
1-(4-Methylphenyl)ethylamine | Chem-Impex | 586-70-9 | MFCD02177111 | 135.210 | C9H13N | 99.000 | CC(N)c1ccc(C)cc1 | 25g | 112761078
Medchemexpress LLC Norfluoxetine hydrochloride | 57226-68-3 | MFCD00078972 | 99.6% | 331.76 | 50 MG
Norfluoxetine hydrochloride is an active N-demethylated metabolite of Fluoxetine. Fluoxetine is a selective serotonin (5-HT) reuptake inhibitor that is metabolized to Norfluoxetine hydrochloride by cytochrome P450 (CYP) 2D6, CYP2C19, and CYP3A4. Norfluoxetine hydrochloride inhibits 5-HT uptake and inhibits CaV3.3 T current (IC50 = 5 μM). It also has anticonvulsant activity.
- Inhibits 5-HT uptake.
- Inhibits CaV3.3 T current (IC50 = 5 μM).
- Exhibits anticonvulsant activity.
- Pretreatment with Norfluoxetine hydrochloride (20 mg/kg s.c.) significantly increases both the rate and duration of survival, demonstrating a significant protective effect against Pentylenetetrazol-induced epilepsy.
Sigma Aldrich Fine Chemicals Biosciences Muscimol phyproof(R) Reference Substance | 2763-96-4 | MFCD00057894 | 10MG
Muscimol phyproof(R) Reference Substance | Purity: >=98.0% (HPLC) | Mol Wt: 114.1 | 2763-96-4 | MFCD00057894 | 10MG
Medchemexpress LLC Grepafloxacin hydrochloride | 161967-81-3 | 99.6% | 395.86 g·mol⁻1 | C19H23ClFN3O3 | 10 MG
Grepafloxacin hydrochloride is the hydrochloride salt of a fluoroquinolone antibiotic used for antibacterial research. Supplied as a high-purity powder, it is suitable for in vitro and in vivo studies and analytical applications.
- Fluoroquinolone antibiotic hydrochloride salt.
- Suitable for in vitro and in vivo antibacterial research.
- High purity appropriate for analytical and biological assays.
- White to off-white powder, soluble in appropriate organic solvents.
eMolecules 93319-65-4 | Ambeed | Pyridazin-3-ylmethanamine | 50mg | 600835260 | A248559 | MFCD05664656 | 109.132 | C5H7N3
Ambeed | Pyridazin-3-ylmethanamine | 50mg | 600835260 | A248559 | 93319-65-4 | MFCD05664656 | 109.132 | C5H7N3
Medchemexpress LLC Grepafloxacin hydrochloride | 161967-81-3 | 99.55% | C19H23ClFN3O3 | 50 MG
Grepafloxacin hydrochloride, also known as OPC-17116 hydrochloride, is an orally active fluoroquinolone antibiotic. It demonstrates potent activity against common community-acquired respiratory pathogens, including *Streptococcus pneumoniae*. This compound is characterized by its high tissue penetration and a favorable pharmacodynamic profile, making it a promising agent for research into antibiotic treatments.
- Potent activity against community-acquired respiratory pathogens.
- Effective against *Streptococcus pneumoniae*.
- Exhibits high tissue penetration.
- Possesses a promising pharmacodynamic profile.
- Demonstrates in vitro antibacterial activity against Gram-positive bacteria.
- Shows in vivo efficacy in experimental systemic infections caused by Gram-positive and Gram-negative bacteria.
Medchemexpress LLC Mindeudesivir hydrobromide | 2779498-79-0 | 98.2% | C24H31DBrN5O7 | 25 MG
Mindeudesivir hydrobromide (VV116) is a deuterated version of Remdesivir, a highly orally active nucleoside antiviral agent against SARS-CoV-2 and respiratory syncytial virus (RSV). It maintains the antiviral activity of Remdesivir against COVID-19 and is noted as the first domestically produced deuterium targeting COVID-19. Deuteration can affect the pharmacokinetic and metabolic profiles of drugs, potentially offering several advantages.
- Used as a tracer or internal standard for quantitative analysis.
- Extends in vivo half-life and improves oral bioavailability.
- Improves metabolic characteristics and drug safety.
- Preserves therapeutic properties.
- Inhibits RSV replication in A549 cells.
- Shows strong antiviral activity against RSV in mice.
- Exhibits favorable pharmacokinetic properties and good safety profile.