Aralkylamines
![eMolecules ChemScene / 1-((1R2R)-2-Amino-12-diphenylethyl)-3-(35-bis(trifluoromethyl)phenyl)thiourea / 50mg / 801475922 / CS-0092890 / 0.000 / 1088705-53-6 / [null] / 483.480 / C23H19F6N3S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502445736.PNG-250.jpg)
eMolecules ChemScene / 1-((1R2R)-2-Amino-12-diphenylethyl)-3-(35-bis(trifluoromethyl)phenyl)thiourea / 50mg / 801475922 / CS-0092890 / 0.000 / 1088705-53-6 / [null] / 483.480 / C23H19F6N3S
ChemScene / 1-((1R2R)-2-Amino-12-diphenylethyl)-3-(35-bis(trifluoromethyl)phenyl)thiourea / 50mg / 801475922 / CS-0092890 / 0.000 / 1088705-53-6 / [null] / 483.480 / C23H19F6N3S
Medchemexpress LLC (±)-Stylopine hydrochloride | 96087-21-7 | 359.8 | 1 MG
(±)-Stylopine (Tetrahydrocoptisine) hydrochloride is an alkaloid compound originally isolated from Corydalis tubers that exhibits anti-inflammatory and anti-parasitic activities.
- Alkaloid compound isolated from Corydalis tubers
- Exhibits anti-inflammatory activity
- Exhibits anti-parasitic activity
- Possible inhibition of TNF-α, IL-6, and NO production in lipopolysaccharide-stimulated peritoneal macrophages
- Inhibition of NF-κB activation and MAP
- Protective effect against ethanol-induced gastric ulcer in mice
Chemscene ChemScene | Thiazol-5-ylmethanamine | 250MG | CS-W008986 | 0.96 | 161805-76-1| MFCD02853613 | 114.17
ChemScene | Thiazol-5-ylmethanamine | 250MG | CS-W008986 | 0.96 | 161805-76-1| MFCD02853613 | 114.17
Medchemexpress LLC Levocabastine hydrochloride | 79547-78-7 | 99.4% | C26H30ClFN2O2 | 1 MG
Levocabastine hydrochloride is a potent and selective histamine H1-receptor antagonist. It also acts as a selective, high-affinity neurotensin receptor subtype 2 (NTR2) antagonist and functions as a VLA-4 antagonist, interfering with conjunctival eosinophil infiltration in allergic conjunctivitis (AC). It is a white to off-white solid with a molecular weight of 456.98.
- Potent and selective histamine H1-receptor antagonist.
- Selective, high-affinity neurotensin receptor subtype 2 (NTR2) antagonist.
- Functions as a VLA-4 antagonist.
- Interferes with conjunctival eosinophil infiltration in allergic conjunctivitis.
- Inhibits α4β1 integrin/VCAM-1-mediated cell adhesion.
- Inhibits virus-induced airway hyperresponsiveness in guinea pigs.
- Prevents conjunctival elevation of VLA-4 and eosinophil infiltration.
- Appears as a white to off-white solid.
Aurora Fine Chemicals 4-(AMINOMETHYL)-N-BENZYLPY50MG
4-(aminomethyl)-N-benzylpyridine-2-carboxamide | 1903199-81-4 | 50MG
Medchemexpress LLC Norvancomycin hydrochloride | 198774-23-1 | 1435.23 (free base) | 5 MG
Norvancomycin hydrochloride is a glycopeptide antibiotic found in Nocardia orientalis. It is active against several strains of S. aureus and S. epidermidis.
- Used for infection research.
eMolecules trans-2,6-Dimethyl-piperidine hydrochloride | 32166-04-4 | | 1g
J&W PharmLab LLC | trans-2,6-Dimethyl-piperidine hydrochloride | 1g | 592897674 | 60R1764S | 96.000 | 32166-04-4 | | 149.660 | C7H16ClN
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
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.
Medchemexpress LLC Nls (pkkkrkv) (hydrochloride) | 99.0% | 919.60 | 50 MG
NLS (PKKKRKV) hydrochloride is the hydrochloride form of NLS (PKKKRKV). It is a nuclear localization signal (NLS) derived from the simian virus 40 large tumor antigen (SV40 large T antigen). This NLS mediates the binding of karyophilic protein to importin α and can enhance nuclear entry in gene transfer research.
- Solid appearance.
- White to off-white color.
- Sequence: Pro-Lys-Lys-Lys-Arg-Lys-Val.
- Enhances nuclear entry in gene transfer research.
- Mediates binding of karyophilic protein to importin α.
- Recommended storage: powder at -80°c for 2 years or -20°c for 1 year; in solvent at -80°c for 6 months or -20°c for 1 month. Keep sealed, away from moisture and light.
eMolecules (R)-1-Methyl-2-trifluoromethoxy-ethylamine hydrochloride | 2718120-88-6 | | 1g
J & W PharmLab LLC | (R)-1-Methyl-2-trifluoromethoxy-ethylamine hydrochloride | 1g | 482942754 | 60R1418S | 97.000 | 2718120-88-6 | | 179.570 | C4H9ClF3NO
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
eMolecules N-(4-(2-HYDROXYETHYL)PHENYL)ACETAMIDE | 83345-11-3 | MFCD01536093 | 5g
AstaTech | N-(4-(2-HYDROXYETHYL)PHENYL)ACETAMIDE | 5g | 449752098 | AB11504 | 95.000 | 83345-11-3 | MFCD01536093 | 179.219 | C10H13NO2
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
eMolecules Methyl 7-bromo-1,5-naphthyridine-3-carboxylate | 958334-24-2 | MFCD11518964 | 1g
Ambeed | Methyl 7-bromo-1,5-naphthyridine-3-carboxylate | 1g | 600847140 | A754093 | | 958334-24-2 | MFCD11518964 | 267.082 | C10H7BrN2O2
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link:
eMolecules Building Block Tool
Medchemexpress LLC Navlimetostat hydrochloride | 2630904-45-7 | MFCD34604075 | 99.61% | 501.34 | 50 MG
Navlimetostat hydrochloride, also known as MRTX-1719 hydrochloride, is a potent, orally active, selective PRMT5-MTA complex inhibitor (IC50 values of 3.6 nM for PRMT5-MTA and 20.5 nM for PRMT5). It binds strongly to the PRMT5-MTA complex (KD of 0.14 pM) and demonstrates antineoplastic activity in vitro and in vivo, making it suitable for cancer research.
- In vitro activity: Inhibits PRMT5 activity (IC50 8 nM) and viability (IC50 12 nM) in MTAP-deleted HCT116 cells.
- In vivo activity: Significantly reduces tumor growth in Lu-99 orthotopic xenograft models (12.5-100 mg/kg/day, oral, 21 days).
- Pharmacokinetics: High bioavailability in CD-1 mice (80% at 30 mg/kg p.o.) and Beagle dogs (59% at 10 mg/kg p.o.).
Chem-Impex International, Inc. (R)-(+)-alpha-Methylbenzylamine | 3886-69-9 | MFCD00064405 | 100G
(R)-(+)-alpha-Methylbenzylamine, 3886-69-9, MFCD00064405, 100G