Piperidines
Aobchem Methanone (2 4-dimethoxyphenyl)-2-pyridinyl- | ≥95% | CAS 898780-42-2 | C14H13NO3 | 500mg
Methanone (2 4-dimethoxyphenyl)-2-pyridinyl- | ≥95% | CAS 898780-42-2 | C14H13NO3 | 500mg
eMolecules 13603-25-3 | 3-Benzylpiperidine | Oakwood Chemicals | MFCD03426127 | 175.275 | C12H17N | 97.000 | C(C1CCCNC1)c1ccccc1 | 1g | 480137519
3-Benzylpiperidine | Oakwood Chemicals | 13603-25-3 | MFCD03426127 | 175.275 | C12H17N | 97.000 | C(C1CCCNC1)c1ccccc1 | 1g | 480137519
Medchemexpress LLC Valopicitabine dihydrochloride | 640725-71-9 | MFCD34589916 | 99.8% | 429.30 g·mol⁻¹ | C15H26Cl2N4O6 | 25 MG
Valopicitabine dihydrochloride is the 3-O-valine ester prodrug of the nucleoside analog 2′-C-methylcytidine with antiviral activity against hepatitis C virus (HCV). Supplied as the dihydrochloride salt for research use, it is used in mechanism-of-action studies, preclinical pharmacology, and formulation development.
- High purity (99.8%) suitable for analytical and preclinical studies.
- Dihydrochloride salt form improves aqueous solubility for formulation work.
- Prodrug of 2′-C-methylcytidine enabling studies of prodrug activation.
- Available in small research quantities for assay development and screening.
- Characterized by CAS 640725-71-9 and molecular weight 429.30 g·mol⁻¹.
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 634616-95-8 | Medchem Express | TBPB | 10mg | 446264318 | HY-14562 | MFCD22666590 | 404.558 | C25H32N4O
Medchem Express | TBPB | 10mg | 446264318 | HY-14562 | 634616-95-8 | MFCD22666590 | 404.558 | C25H32N4O
eMolecules 5382-16-1 | 4-Piperidinol | J & W PharmLab, LLC | MFCD00005999 | 101.149 | C5H11NO | 96.000 | OC1CCNCC1 | 100g | 250013253
4-Piperidinol | J & W PharmLab, LLC | 5382-16-1 | MFCD00005999 | 101.149 | C5H11NO | 96.000 | OC1CCNCC1 | 100g | 250013253
eMolecules 133696-21-6 | (2R,4R)-4-Hydroxypiperidine-2-carboxylic acid hydrochloride | 250mg
Ambeed | H-Asp(Oet)-OEt.HCl | 25g | 490524090 | A176340 | 16115-68-7 | MFCD00038910 | 225.670 | C8H16ClNO4
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Medchemexpress LLC HY-100270 5mg Medchemexpress, Rho-Kinase-IN-1 CAS:1035094-83-7 Purity:>98%
Medchemexpress, HY-100270 5mg Rho-Kinase-IN-1 CAS:1035094-83-7 Rho-Kinase-IN-1 is a Rho kinase (ROCK) inhibitor (Ki values of 30.5 and 3.9 nM for ROCK1 and ROCK2, respectively) extracted from US20090325960A1, compound 1.008. 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 JNJ-1013 | 2597343-08-1 | C46H55N9O7S | 100 MG
JNJ-1013 is a potent and selective IRAK1 PROTAC degrader. It functions by inducing apoptosis and increasing the expression of cleaved PARP. This compound also plays a role in decreasing the expression of IRAK1, p-IKBα, and pSTAT3(Tyr705).
- Potent and selective IRAK1 PROTAC degrader
- Induces apoptosis
- Increases the expression of cleaved PARP
- Decreases the expression of IRAK1, p-IKBα, and pSTAT3(Tyr705)
Apexbio Technology LLC DIETHYL-FUMARATE-500MG
Diethyl fumarate (CAS No 623-91-6) is prominently used in biomedical research particularly in studies focusing on its chemical properties and biological activities Originating as an ester of fumaric acid it is known for modulating cellular pathways often targeting oxidative stress and inflammation-related mechanisms Its in vitro activity is observed in the nanomolar to low micromolar range making it a valuable compound in assays evaluating cellular responses Typical applications include its use in various cell models to study antioxidant effects and in animal studies to explore therapeutic potential against inflammatory conditions Diethyl fumarate is also employed in drug screening processes where its ability to influence specific biochemical pathways is of interest Experimental concentrations typically depend on the specific research design allowing for flexibility in its application across numerous study types
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
Medchemexpress LLC Anamorelin hydrochloride | 861998-00-7 | 99.6% | 583.16 | 50 MG
Anamorelin hydrochloride is an orally active Ghrelin receptor agonist with an EC50 of 0.74 nM. This compound can promote appetite, increase body weight, and stimulate the secretion of growth hormone and insulin-like growth factor-1. It is suitable for research into anorexia and cancer cachexia.
Solid: 4°C, sealed storage, away from moisture.
In solvent: -80°C for 6 months; -20°C for 1 month (sealed storage, away from moisture).
- Orally active Ghrelin receptor agonist.
- EC50 of 0.74 nM for the Ghrelin receptor.
- Promotes appetite and increases body weight.
- Stimulates growth hormone and insulin-like growth factor-1 secretion.