Aralkylamines
eMolecules 18110-40-2 | 2-AMINO-2-PHENYLPROPAN-1-OL HCL | AstaTech | MFCD27980708 | 187.670 | C9H14ClNO | 95.000 | Cl.CC(N)(CO)c1ccccc1 | 1g | 164728233
2-AMINO-2-PHENYLPROPAN-1-OL HCL | AstaTech | 18110-40-2 | MFCD27980708 | 187.670 | C9H14ClNO | 95.000 | Cl.CC(N)(CO)c1ccccc1 | 1g | 164728233
eMolecules 39110-74-2 | Naphthalen-1-ylmethanamine hydrochloride | Combi-Blocks | MFCD15147375 | 193.670 | C11H12ClN | 96.000 | Cl.NCc1cccc2ccccc12 | 1g | 537620630
Naphthalen-1-ylmethanamine hydrochloride | Combi-Blocks | 39110-74-2 | MFCD15147375 | 193.670 | C11H12ClN | 96.000 | Cl.NCc1cccc2ccccc12 | 1g | 537620630
eMolecules 19725-18-9 | 3-(3-METHOXYPHENYL)PIPERIDINE HCL | AstaTech | MFCD05864427 | 227.730 | C12H18ClNO | 95.000 | Cl.COc1cccc(c1)C1CCCNC1 | 1g | 451913383
3-(3-METHOXYPHENYL)PIPERIDINE HCL | AstaTech | 19725-18-9 | MFCD05864427 | 227.730 | C12H18ClNO | 95.000 | Cl.COc1cccc(c1)C1CCCNC1 | 1g | 451913383
![eMolecules 1212115-75-7 | TRANS (+/-) 4-(TRIFLUOROMETHYL)PYRROLIDINE-3-CARBOXYLIC ACID METHYL ESTER HCL | AstaTech467.230 | C14H22Cl2F6N2O4 | 95.000 | Cl.Cl.COC(=O)[C@H]1CNC[C@@H]1C(F)(F)F.COC(=O)[C@@H]1CNC[C@H]1C(F)(F)F | 1g | 112530949](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502171607.JPG-250.jpg)
eMolecules 1212115-75-7 | TRANS (+/-) 4-(TRIFLUOROMETHYL)PYRROLIDINE-3-CARBOXYLIC ACID METHYL ESTER HCL | AstaTech467.230 | C14H22Cl2F6N2O4 | 95.000 | Cl.Cl.COC(=O)[C@H]1CNC[C@@H]1C(F)(F)F.COC(=O)[C@@H]1CNC[C@H]1C(F)(F)F | 1g | 112530949
TRANS (+/-) 4-(TRIFLUOROMETHYL)PYRROLIDINE-3-CARBOXYLIC ACID METHYL ESTER HCL | AstaTech | 1212115-75-7467.230 | C14H22Cl2F6N2O4 | 95.000 | Cl.Cl.COC(=O)[C@H]1CNC[C@@H]1C(F)(F)F.COC(=O)[C@@H]1CNC[C@H]1C(F)(F)F | 1g | 112530949
Medchemexpress LLC Vocacapsaicin hydrochloride | 1931116-92-5 | 95.7% | 496.08 | 1 ML
Vocacapsaicin hydrochloride (CA-008) is a proagent of Capsaicin and a first-in-class non-opioid TRPV1 agonist. Designed to provide meaningful and long-lasting pain relief, this product is intended for research use only.
- Proagent of capsaicin
- First-in-class non-opioid TRPV1 agonist
- Provides meaningful and long-lasting pain relief
- Involved in clinical trials for postsurgical pain
- Acts as a TRP channel inhibitor
Medchemexpress LLC Pivmecillinam (hydrochloride) | 32887-03-9 | 99.2% | 25 MG
Pivmecillinam hydrochloride is an orally active proagent of mecillinam, an extended-spectrum penicillin antibiotic. It is intended for research use only as a laboratory chemical for the manufacture of substances.
- Orally active proagent of mecillinam.
- Extended-spectrum penicillin antibiotic.
- Inhibits urinary tract infections caused by multidrug-resistant E. coli in mouse models.
- Significantly reduces E. coli strains in urine, bladder, and kidneys.
- Recommended storage at 4°C, sealed, away from moisture and light.
- In solvent, stores at -80°C for 6 months or -20°C for 1 month.
Medchemexpress LLC Clinafloxacin (hydrochloride) | 105956-99-8 | 99.6% | 25 MG
Clinafloxacin hydrochloride is a potent and broad-spectrum fluoroquinolone antibiotic. It exhibits inhibitory activity against gram-positive, gram-negative bacteria, and anaerobic pathogens in vitro, acting against DNA gyrase and topoisomerase IV of *S. aureus*.
- Potent and broad-spectrum fluoroquinolone antibiotic
- Inhibits gram-positive, gram-negative bacteria, and anaerobic pathogens
- Active against DNA gyrase and topoisomerase IV of *S. aureus*
- Effective against penicillin-resistant, ciprofloxacin-susceptible pneumococcal meningitis
- Exhibits activity against *S. pneumonia*
Medchemexpress LLC Taniborbactam hydrochloride | 2244235-49-0 | 99.97% | 462.18 | 10 MG
Taniborbactam hydrochloride (VNRX-5133 hydrochloride) is a reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor with IC50s of 8-530 nM. It has IC50s of 30 nM, 32 nM, 42 nM, and 20 nM for KPC-2, AmpC, OXA-48, and VIM-2, respectively, and is active against Gram-negative bacteria.
- Reversible and selective boronic acid-containing pan-spectrum β-lactamase inhibitor.
- Effective against KPC-2, AmpC, OXA-48, and VIM-2.
- Active against Gram-negative bacteria.
Accela Chembio Inc (s)-(-)-3-(n-methylamino)-1-(2-thienyl)-1-propanol | 25g | 116539-55-0 | MFCD07357308 | 97+% | Shelf Life: 1620 Days | Light Sensitive/n2/+4
(s)-(-)-3-(n-methylamino)-1-(2-thienyl)-1-propanol | 25g | 116539-55-0 | MFCD07357308 | 97+% | Shelf Life: 1620 Days | Light Sensitive/n2/+4
eMolecules 71766-76-2 | piperidin-3-ylmethanamine dihydrochloride | Combi-Blocks | MFCD04039795 | 187.110 | C6H16Cl2N2 | 95.000 | Cl.Cl.NCC1CCCNC1 | 1g | 537620775
piperidin-3-ylmethanamine dihydrochloride | Combi-Blocks | 71766-76-2 | MFCD04039795 | 187.110 | C6H16Cl2N2 | 95.000 | Cl.Cl.NCC1CCCNC1 | 1g | 537620775
Medchemexpress LLC Theodrenaline hydrochloride | 2572-61-4 | 411.84 | 5 MG
Theodrenaline hydrochloride is a cardiac stimulant that also functions as an anti-hypotensive agent when used in conjunction with Cafedrine. It has been shown to evoke a positive inotropic effect in human atrial trabeculae through the stimulation of β-adrenoceptors (AR).
- Cardiac stimulant
- Acts as an anti-hypotensive agent when combined with Cafedrine
- Evokes a positive inotropic effect in human atrial trabeculae by stimulating β-adrenoceptors
- May potentiate certain effects through phosphodiesterase (PDE) inhibition
- Targets phosphodiesterase (PDE)
- Part of the metabolic enzyme/protease pathway
eMolecules 67967-19-5 | 5,8-DIBROMO-1,7-NAPHTHYRIDINE | MFCD12404065 | 0.25g
AstaTech | 5,8-DIBROMO-1,7-NAPHTHYRIDINE | 0.25g | 490590946 | 95145 | 95.000 | 67967-19-5 | MFCD12404065 | 287.942 | C8H4Br2N2
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eMolecules 43148-65-8 | Ambeed | (1R2R)-rel-N1N1N2N2-Tetramethylcyclohexane-12-diamine | 5g | 626256571 | A1471253 | 340.6 | C20H44N4
Medchem Express | Ruxolitinib (S enantiomer) | 5mg | 446271138 | HY-50856A | 941685-37-6 | MFCD13184797 | 306.373 | C17H18N6
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eMolecules 161805-76-1 | Thiazol-5-yl-methylamine | Combi-Blocks | MFCD02853613 | 114.170 | C4H6N2S | 96.000 | NCc1cncs1 | 1g | 205411327
Thiazol-5-yl-methylamine | Combi-Blocks | 161805-76-1 | MFCD02853613 | 114.170 | C4H6N2S | 96.000 | NCc1cncs1 | 1g | 205411327
Medchemexpress LLC Jatrorrhizine hydroxide | 483-43-2 | 355.38 | 50 MG
Jatrorrhizine hydroxide is an alkaloid isolated from *Coptis chinensis* with neuroprotective, antimicrobial, antiplasmodial, and antioxidant activities. It is a potent and orally active inhibitor of AChE (IC50=872 nM) with >115-fold selectivity for BuChE. Jatrorrhizine hydroxide reduces the uptake of serotonin (5-HT) and norepinephrine (NE) through the inhibition of uptake-2 transporters.
- Neuroprotective activity
- Antimicrobial activity
- Antiplasmodial activity
- Antioxidant activity
- Potent and orally active inhibitor of AChE (IC50=872 nM) with high selectivity over BuChE (>115-fold)
- Reduces uptake of serotonin (5-HT) and norepinephrine (NE) via inhibition of uptake-2 transporters