Piperidines
Medchemexpress LLC Piperidine-4-sulfonic acid | 72450-62-5 | MFCD00055097 | 100.0% | 165.21 | C5H11NO3S | 5 MG
Piperidine-4-sulfonic acid is a small-molecule research reagent and a potent GABA receptor agonist that inhibits H-GABA binding with a reported IC50 of 0.034 μM. The compound has molecular formula C5H11NO3S, molecular weight 165.21 g/mol, and is supplied at high purity for laboratory research use.
- Potent GABA receptor agonist with an IC50 of 0.034 μM for inhibition of H-GABA binding.
- High purity (99.95%).
- Supplied in small milligram pack sizes for research use.
- Includes product datasheet, certificate of analysis, and safety data sheet.
- Suitable for neuroscience and GABAergic studies.
![eMolecules 259110-61-7 | trans-3,5-Difluoro-piperidine hydrochloride | J&W PharmLab LLC157.590 | C5H10ClF2N | 96.000 | Cl.F[C@H]1CNC[C@H](F)C1 | 1g | 916356619](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC3843913.JPG-250.jpg)
eMolecules 259110-61-7 | trans-3,5-Difluoro-piperidine hydrochloride | J&W PharmLab LLC157.590 | C5H10ClF2N | 96.000 | Cl.F[C@H]1CNC[C@H](F)C1 | 1g | 916356619
trans-3,5-Difluoro-piperidine hydrochloride | J&W PharmLab LLC | 259110-61-7157.590 | C5H10ClF2N | 96.000 | Cl.F[C@H]1CNC[C@H](F)C1 | 1g | 916356619
eMolecules 4045-24-3 | 4-Methoxy-piperidine | Oakwood Chemicals | MFCD04115010 | 115.176 | C6H13NO | 98.000 | COC1CCNCC1 | 25g | 480121259
4-Methoxy-piperidine | Oakwood Chemicals | 4045-24-3 | MFCD04115010 | 115.176 | C6H13NO | 98.000 | COC1CCNCC1 | 25g | 480121259
Aobchem 5-Bromo-3-(piperidine-1-carbonyl)phenylboronic acid | ≥97% | CAS 2121514-06-3 | C12H15BBrNO3 | 250mg
5-Bromo-3-(piperidine-1-carbonyl)phenylboronic acid | ≥97% | CAS 2121514-06-3 | C12H15BBrNO3 | 250mg
Aobchem Tert-butyl 4-(p-tolyl)piperidine-1-carboxylate | ≥95% | CAS 732275-92-2 | C17H25NO2 | 250mg
Tert-butyl 4-(p-tolyl)piperidine-1-carboxylate | ≥95% | CAS 732275-92-2 | C17H25NO2 | 250mg
eMolecules 861998-00-7 | Medchem Express | Anamorelin (hydrochloride) | 5mg | 446264500 | HY-14734A | 1166.35 | C62H86Cl2N12O6
Medchem Express | Anamorelin (hydrochloride) | 5mg | 446264500 | HY-14734A | 861998-00-7 | 1166.350 | C62H86Cl2N12O6
Medchemexpress LLC Donepezil-d4 hydrochloride (E2020-d4) | 1219798-88-5 | 99.96% | C24H26D4ClNO3 | 1 MG
Donepezil-d4 (hydrochloride) is the deuterium labeled Donepezil hydrochloride. Donepezil Hydrochloride (E2020) is a reversible, selective AChE inhibitor with an IC50 of 6.7 nM for AChE activity. Donepezil shows high selectivity for AChE over BuChE and exhibits neuroprotective effect on Aβ42 neurotoxicity.
- Acts as a reversible, selective AChE inhibitor.
- Demonstrates high selectivity for AChE over BuChE.
- Shows neuroprotective effects against Aβ42 neurotoxicity.
- Can be utilized as a tracer in research.
- Serves as an internal standard for quantitative analysis using techniques such as NMR, GC-MS, or LC-MS.
- Stable heavy isotopes can influence pharmacokinetic and metabolic profiles of drugs.
Medchemexpress LLC (R,R)-GSK321 | 1816272-19-1 | 99.4% | 10 MG
(R,R)-GSK321 is an inhibitor of wild-type isocitrate dehydrogenase 1 (WT IDH1) with an IC50 value of 120 nM. This compound also acts as a mutant R132H IDH1 inhibitor and is an isomer of GSK321 with some wild-type cross-reactivity. It has a molecular weight of 501.55 and a chemical formula of C28H28FN5O3. This product appears as a white to off-white solid.
- Inhibits wild-type isocitrate dehydrogenase 1 (WT IDH1)
- IC50 value of 120 nM for WT IDH1
- Acts as a mutant R132H IDH1 inhibitor
- Isomer of GSK321 with some wild-type cross-reactivity
- Dose-dependently decreases reductive glutaminolysis in A-498 cells (0.1-3 μM for 5 hours)
- For research use only, not for patient use
Medchemexpress LLC (R,R)-GSK321 | 1816272-19-1 | 99.4% | 50 MG
(R,R)-GSK321 is a potent inhibitor of wild-type isocitrate dehydrogenase 1 (WT IDH1) with an IC50 value of 120 nM. This compound also acts as a mutant R132H IDH1 inhibitor, being an isomer of GSK321 with some wild-type cross-reactivity.
- Potent WT IDH1 inhibitor
- IC50 value of 120 nM for WT IDH1
- Mutant R132H IDH1 inhibitor
- Decreases reductive glutaminolysis in A-498 cells
- For research use only
- Associated with cancer, cancer targeted therapy, and cancer metabolism research
- Classified as a metabolic enzyme/protease and isocitrate dehydrogenase (IDH) inhibitor
eMolecules 1628317-18-9 | Medchem Express | MI-463 | 1mg | 446270394 | HY-19809 | MFCD28506301 | 484.55 | C24H23F3N6S
Ambeed | (3aR3aR8aS8aS)-22-(Cyclopropane-11-diyl)bis(88a-dihydro-3aH-indeno[12-d]oxazole) | 100mg | 539141856 | A1165102 | 229184-98-9 | 356.425 | C23H20N2O2
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<|a>
Medchemexpress LLC HY-10017 10mg Medchemexpress, SCH 546738 CAS:906805-42-3 Purity:>98%
Medchemexpress, HY-10017 10mg SCH 546738 CAS:906805-42-3 SCH 546738 is a potent, orally active and non-competitive CXCR3 antagonist, the affinity constant (Ki) of SCH 546738 binding to human CXCR3 receptor is determined to be 0.4 nM in multiple experiments. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC Anamorelin | 249921-19-5 | 546.70 | 5 MG
Anamorelin (RC-1291) is an orally active Ghrelin receptor agonist. It promotes appetite, increases body weight, and stimulates the secretion of growth hormone and insulin-like growth factor-1. Anamorelin can be used in the research of anorexia and cancer cachexia.
- Orally active Ghrelin receptor agonist
- Promotes appetite
- Increases body weight
- Stimulates growth hormone secretion
- Stimulates insulin-like growth factor-1 secretion
- Used in anorexia research
- Used in cancer cachexia research
eMolecules 138007-24-6 | tert-Butyl piperidine-4-carboxylate | Combi-Blocks | MFCD02684429 | 185.267 | C10H19NO2 | 98.000 | CC(C)(C)OC(=O)C1CCNCC1 | 1g | 303354730
tert-Butyl piperidine-4-carboxylate | Combi-Blocks | 138007-24-6 | MFCD02684429 | 185.267 | C10H19NO2 | 98.000 | CC(C)(C)OC(=O)C1CCNCC1 | 1g | 303354730
Aobchem 1-(3-Bromobenzyl)piperidine | ≥97% | CAS 59507-40-3 | C12H16BrN | 1g
1-(3-Bromobenzyl)piperidine | ≥97% | CAS 59507-40-3 | C12H16BrN | 1g