Piperidines
Medchemexpress LLC HY-12882A 50mg Medchemexpress, Ifenprodil (tartrate) CAS:23210-58-4 Purity:>98%
Medchemexpress, HY-12882A 50mg Ifenprodil (tartrate) CAS:23210-58-4 Ifenprodil tartrate is a typical noncompetitive NMDA receptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors (IC50=0.34 μM) over 400-fold than at NR1A/NR2A receptors (IC50=146 μM). Ifenprodil tartrate inhibits GIRK (Kir3), reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has the potential to be a cerebral vasodilator. 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.
Accela Chembio Inc 3-quinuclidinone Hydrochloride | 100g | 1193-65-3 | MFCD00137391 | 95+% | Shelf Life: 1800 Days | Light Sensitive/moisture Sensitive
3-quinuclidinone Hydrochloride | 100g | 1193-65-3 | MFCD00137391 | 95+% | Shelf Life: 1800 Days | Light Sensitive/moisture Sensitive
eMolecules N-Cbz-2-piperidinecarboxylic acid t-butyl ester | 71170-89-3 | MFCD04038573 | 1g
Combi-Blocks, Inc. | N-Cbz-2-piperidinecarboxylic acid t-butyl ester | 1g | 586079299 | OR-6106 | 98.000 | 71170-89-3 | MFCD04038573 | 319.401 | C18H25NO4
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eMolecules Medchem Express / Quinagolide (hydrochloride) / 5mg / 446263406 / HY-13736A / / 94424-50-7 / MFCD00893553 / 432.020 / C20H34ClN3O3S
Medchem Express / Quinagolide (hydrochloride) / 5mg / 446263406 / HY-13736A / / 94424-50-7 / MFCD00893553 / 432.020 / C20H34ClN3O3S
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.
eMolecules CERITINIB | 1032900-25-6 | MFCD26142648 | 1g
AstaTech | CERITINIB | 1g | 411869845 | 43024 | 95.000 | 1032900-25-6 | MFCD26142648 | 558.140 | C28H36ClN5O3S
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Apexbio Technology LLC Mepivacaine HCl 1722-62-9 50mg
Mepivacaine hydrochloride (CAS 1722-62-9) is a synthetic tertiary amine local anesthetic It exerts its effect by reversibly inhibiting voltage-gated sodium channels on neuronal cell membranes thereby blocking nerve impulse conduction This action results in loss of sensation in targeted tissues without affecting consciousness Mepivacaine is frequently utilized in research settings to investigate mechanisms of nerve blockade neuronal excitability and pain signal transmission and serves as a standard control in studies comparing the pharmacological profiles of local anesthetic agents
STA PHARMACEUTICAL US LLC 3-(N-Fmoc-amino)piperidine-3-carboxylic acid HCl | 25 g | CAS 368866-20-0 | MDL MFCD04113564
3-(N-Fmoc-amino)piperidine-3-carboxylic acid HCl is a Amino Acid reagent (Subcategory: Unusual AA) sold by WuXi TIDES. Offered in 25 g. Store at 4 °C. SDS available for reference.
Specifications
- CAS: 368866-20-0
- MDL: MFCD04113564
- InChIKey: GZXZDFOJUNNXPX-UHFFFAOYSA-N
- Molecular Weight: 402.875
- Molecular Formula: C21H23ClN2O4
- Purity: ≥95%
- Container Type: 125 mL HDPE
- Pack Size: 25 g
- Net Weight: 25 g
- Gross Weight: 54.3 g
- Commodity Code: 29333999
- Country Of Origin: China
- IUPAC: 3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)piperidine-3-carboxylic acid hydrochloride
- SMILES: O=C(OCC1C2=CC=CC=C2C3=C1C=CC=C3)NC4(CCCNC4)C(O)=O.Cl
Medchemexpress LLC HY-100270 10mg Medchemexpress, Rho-Kinase-IN-1 CAS:1035094-83-7 Purity:>98%
Medchemexpress, HY-100270 10mg 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.
Apexbio Technology LLC Lenalidomide hemihydrate 847871-99-2 50mg
Lenalidomide hemihydrate (CAS 847871-99-2) is a small-molecule immunomodulator targeting the E3 ubiquitin ligase CRBN It is designed to induce selective ubiquitination and degradation of the lymphoid transcription factors IKZF1 and IKZF3 thereby modulating immune cell signaling pathways Lenalidomide hemihydrate exerts its biological activity primarily by inhibiting TNF- secretion with an IC50 value of approximately 13 nM Its mechanism of action also includes altering cytokine production and cellular interactions within the tumor microenvironment Based on these pharmacological properties Lenalidomide hemihydrate holds research potential in the investigation of inflammatory pathways immune response modulation and antitumor mechanisms particularly in hematological malignancies and inflammatory diseases
Medchemexpress LLC HY-103636 10mg Medchemexpress, PROTAC Sirt2 Degrader-1 CAS:2098487-75-1 Purity:>98%
Medchemexpress, HY-103636 10mg PROTAC Sirt2 Degrader-1 CAS:2098487-75-1 PROTAC Sirt2 Degrader-1 is a SirReal-based PROTAC, acts as a Sirt2 degrader, composed of a highly potent and isotype-selective Sirt2 inhibitor, a linker, and a bona fide cereblon ligand for E3 ubiquitin ligase. PROTAC Sirt2 Degrader-1 shows an IC50 of 0.25 μM for Sirt2, with no effect on Sirt1/Sirt3 (IC50s > 100 μM). 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.