Piperidines
eMolecules 612847-09-3 | Medchem Express | AKT inhibitor VIII | 5mg | 446258191 | HY-10355 | MFCD23843802 | 551.654 | C34H29N7O
Medchem Express | AKT inhibitor VIII | 5mg | 446258191 | HY-10355 | 612847-09-3 | MFCD23843802 | 551.654 | C34H29N7O
Medchemexpress LLC Valopicitabine (dihydrochloride) | 640725-71-9 | MFCD34589916 | 99.8% | 429.3 g/mol | C15H26Cl2N4O6 | 50 MG
Valopicitabine (dihydrochloride) is the dihydrochloride salt of valopicitabine (NM-283), a nucleoside-analog prodrug of 2'-C-methylcytidine with activity against hepatitis C virus through inhibition of the NS5B RNA polymerase. It is provided as a research reagent for biochemical and antiviral studies.
- High purity suitable for analytical and biological assays.
- Dihydrochloride salt form, improving aqueous solubility compared with the free base.
- Acts as an orally bioavailable prodrug of an HCV polymerase inhibitor.
- Molecular weight 429.3 g/mol; formula C15H26Cl2N4O6.
- Supplied in small research quantities (e.g., 50 MG) for laboratory use.
- Accompanied by analytical documentation such as COA, H NMR, and LC-MS.
Medchemexpress LLC JNJ-1013 | 2597343-08-1 | C46H55N9O7S | 50 MG
JNJ-1013 is a potent and selective IRAK1 PROTAC degrader. It induces apoptosis, increases the expression of cleaved PARP, and decreases the expression of IRAK1, p-IKBα, and pSTAT3(Tyr705).
- Potent and selective IRAK1 PROTAC degrader
- IC50s of 72 nM for IRAK1, 443 nM for IRAK4, and 1071 nM for VHL FP
- Induces apoptosis and increases cleaved PARP expression
- Decreases expression of IRAK1, p-IKBα, and pSTAT3(Tyr705)
TARGETMOL CHEMICALS INC KARTOGENIN 50MG
Also available in 2 mg 5 mg 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Kartogenin (KGN) is an activator of the smad4/smad5 pathway and promotes the selective differentiation of multipotent mesenchymal stem cells into chondrocytes. purity: 96%
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
Medchemexpress LLC Roxatidine | 78273-80-0 | 98.25% | 306.41 | 100 MG
Roxatidine is an active metabolite of Roxatidine acetate hydrochloride and an orally active histamine H2-receptor antagonist. As an anti-ulcer agent, it suppresses histamine release, inhibiting proton secretion, and inhibits the production of VEGF-1, which is a marker of inflammation and angiogenesis. It also has an anti-allergic inflammatory effect and is being researched for gastric and duodenal ulcers.
- Orally active histamine H2-receptor antagonist
- Suppresses histamine release (inhibiting proton secretion)
- Inhibits the production of VEGF-1
- Exhibits anti-allergic inflammatory effects
- Researched for gastric and duodenal ulcers
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 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
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
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
eMolecules 138007-24-6 | tert-Butyl 4-Piperidinecarboxylate | Accela ChemBio | MFCD02684429 | 185.267 | C10H19NO2 | 98.000 | CC(C)(C)OC(=O)C1CCNCC1 | 25g | 796984132
tert-Butyl 4-Piperidinecarboxylate | Accela ChemBio | 138007-24-6 | MFCD02684429 | 185.267 | C10H19NO2 | 98.000 | CC(C)(C)OC(=O)C1CCNCC1 | 25g | 796984132
Medchemexpress LLC Roxatidine | 78273-80-0 | MFCD00871807 | 98.3% | C17H26N2O3 | 10MG
Roxatidine is a histamine H2-receptor antagonist and the active metabolite of roxatidine acetate hydrochloride, supplied as a research standard for studies of gastric acid secretion, peptic ulcers, and inflammatory responses. The material is provided as a solid powder for in vitro and preclinical research.
- High purity (~98.3%) suitable for research applications
- Confirmed identity: CAS 78273-80-0
- Molecular formula C17H26N2O3; mol wt 306.41 g/mol
- Soluble in DMSO for assay preparation
- Available in small milligram quantities for screening and method development