Piperidines
Medchemexpress LLC (R,R)-GSK321 | 1816272-19-1 | 99.36% | 100 MG
(R,R)-GSK321 is a high-purity wild-type isocitrate dehydrogenase 1 (WT IDH1) inhibitor. This compound acts as an isomer of GSK321, exhibiting potent inhibition with an IC50 value of 120 nM. It also functions as a mutant R132H IDH1 inhibitor with some wild-type cross-reactivity, making it a valuable tool for relevant research.
- Inhibits wild-type isocitrate dehydrogenase 1 (WT IDH1)
- IC50 value of 120 nM
- Functions as a mutant R132H IDH1 inhibitor
- High purity of 99.36%
- Appearance as a white to off-white solid
- For research use only
Medchemexpress LLC Valopicitabine dihydrochloride | 640725-71-9 | MFCD34589916 | >99.0% | 429.3 g/mol | C15H26Cl2N4O6 | 10 MG
Valopicitabine dihydrochloride is the dihydrochloride salt of valopicitabine, an orally bioavailable nucleoside prodrug of 2'-C-methylcytidine (NM107) developed as an NS5B polymerase inhibitor for hepatitis C virus. It is provided as a purified powder for research and antiviral biochemical studies.
- Acts as a nucleoside prodrug of 2'-C-methylcytidine (NM107)
- Inhibits HCV NS5B polymerase activity in antiviral assays
- Supplied as a dihydrochloride salt with formula C15H26Cl2N4O6
- Molecular weight approximately 429.3 g/mol
- Typical analytical purity ≥99.0% for research use
- Provided as a powder suitable for biochemical and cellular studies
eMolecules 72518-41-3 | 2-METHYL-2-PIPERIDINECARBOXYLIC ACID | AstaTech | MFCD01318631 | 143.186 | C7H13NO2 | 98.000 | CC1(CCCCN1)C(O)=O | 0.25g | 491175833
2-METHYL-2-PIPERIDINECARBOXYLIC ACID | AstaTech | 72518-41-3 | MFCD01318631 | 143.186 | C7H13NO2 | 98.000 | CC1(CCCCN1)C(O)=O | 0.25g | 491175833
eMolecules 5382-16-1 | 4-Hydroxypiperidine | Oakwood Chemical | MFCD00005999 | 101.149 | C5H11NO | 98.000 | OC1CCNCC1 | 500g | 599423880
4-Hydroxypiperidine | Oakwood Chemical | 5382-16-1 | MFCD00005999 | 101.149 | C5H11NO | 98.000 | OC1CCNCC1 | 500g | 599423880
eMolecules 162686-54-6 | (4-(AMINOMETHYL)-1-BENZYLPIPERIDIN-4-YL)METHANOL | MFCD09999243 | 1g
Medchem Express | S-Allylmercaptocysteine | 5mg | 713706809 | HY-145532 | 2281-22-3 | 193.280 | C6H11NO2S2
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eMolecules 32838-55-4 | 2-Benzylpiperidine | Oakwood Chemical | MFCD01701452 | 175.275 | C12H17N | 97.000 | C(C1CCCCN1)c1ccccc1 | 1g | 537683684
2-Benzylpiperidine | Oakwood Chemical | 32838-55-4 | MFCD01701452 | 175.275 | C12H17N | 97.000 | C(C1CCCCN1)c1ccccc1 | 1g | 537683684
![eMolecules 88720-65-4 | [(Pyridin-4-ylmethyl)-amino]-acetic acid | Combi-Blocks, Inc. | MFCD08443132 | 166.180 | C8H10N2O2 | 98.000 | OC(=O)CNCc1ccncc1 | 1g | 603134372](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502187313.JPG-250.jpg)
eMolecules 88720-65-4 | [(Pyridin-4-ylmethyl)-amino]-acetic acid | Combi-Blocks, Inc. | MFCD08443132 | 166.180 | C8H10N2O2 | 98.000 | OC(=O)CNCc1ccncc1 | 1g | 603134372
[(Pyridin-4-ylmethyl)-amino]-acetic acid | Combi-Blocks, Inc. | 88720-65-4 | MFCD08443132 | 166.180 | C8H10N2O2 | 98.000 | OC(=O)CNCc1ccncc1 | 1g | 603134372
Accela Chembio Inc Ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate Hydrochloride | 5g | 52763-21-0 | MFCD00012792 | 95+% | Shelf Life: 1260 Days | Moisture Sensitive/+4
Ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate Hydrochloride | 5g | 52763-21-0 | MFCD00012792 | 95+% | Shelf Life: 1260 Days | Moisture Sensitive/+4
eMolecules 116140-16-0 | 6-METHYL-3-PIPERIDINECARBOXYLIC ACID | MFCD13179002 | 1g
Medchem Express | PF-04979064 | 5mg | 446255359 | HY-100398 | 1220699-06-8 | MFCD28155091 | 446.511 | C24H26N6O3
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Selleck Chemical LLC BIX-01294 trihydrochloride
BIX-01294 trihydrochloride is an inhibitor of G9a histone methyltransferase with IC50 of 2 7 M in a cell-free assay reduces H3K9me2 of bulk histones also weakly inhibits GLP (primarily H3K9me3) no significant activity observed at other histone methyltransferases BIX01294 induces autophagy BIX01294 also inhibits H3K36 methylation by oncoproteins NSD1 NSD2 and NSD3
Medchemexpress LLC GSK2879552 dihydrochloride | 1902123-72-1 | MFCD30481342 | 99.8% | 437.4 g·mol⁻1 | C23H30Cl2N2O2 | 10 MG
GSK2879552 dihydrochloride is the dihydrochloride salt of an orally bioavailable, selective, mechanism-based irreversible inhibitor of lysine-specific demethylase 1 (LSD1/KDM1A). It is used as a research reagent in epigenetic and oncology studies and has been evaluated in early clinical trials for hematologic and solid tumor indications.
- Dihydrochloride salt form for improved solubility.
- Irreversible LSD1 inhibitor (mechanism-based inactivator).
- Orally bioavailable scaffold used in preclinical and clinical research.
- High purity (≈99.8%) suitable for research applications.
- Available in multiple solid and solution formats and milligram quantities.
eMolecules 368429-78-1 | 1-Benzylpiperidin-3-amine hydrochloride | MFCD19980510 | 1g
Ambeed | 5-Iodo-2-(trifluoromethyl)pyridine | 250mg | 490538873 | A227888 | 873107-98-3 | MFCD11226772 | 272.997 | C6H3F3IN
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Selleck Chemical LLC Donepezil HCl S2462-200mg
Donepezil HCl is a specific and potent AChE inhibitor for bAChE and hAChE with IC50 of 8 12 nM and 11 6 nM respectively This product is not soluble in PBS solution Please do not dissolve it in PBS for administration
Medchemexpress LLC pJAK2(1001-1013) | 1259928-08-9 | 99.9% | 1716.82 | 10 MG
pJAK2(1001-1013) | 1259928-08-9 | 99.9% | 1716.82 | 10 MG
Medchemexpress LLC HY-114363A 5mg Medchemexpress, SRI 31215 (TFA) CAS:1832686-44-8 Purity:>98%
Medchemexpress, HY-114363A 5mg SRI 31215 (TFA) CAS:1832686-44-8 SRI 31215 (TFA), a triplex inhibitor of matriptase , hepsin and hepatocyte growth factor activator (HGFA) with IC 50 s of 0.69 μM, 0.65 μM, 0.3 μM, blocks pro-HGF activation and thus mimics the activity of HAI-1/2 [1] . 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.