Oxazinanes
Medchemexpress LLC 1-methyl-1,4-dihydronicotinamide | 17750-23-1 | MFCD006277282 | >98.0% | 138.17 g/mol | C7H10N2O | 5MG
1-Methyl-1,4-dihydronicotinamide (CAS 17750-23-1) is a reduced nicotinamide derivative used in biochemical research as a radical scavenger and an NADH model compound. It is typically supplied as a crystalline solid of high purity and is used as a substrate or inhibitor in studies of NADH-dependent enzymes and serine racemase activity.
- Used as a radical scavenger in redox and oxidative stress studies.
- Serves as an NADH model and substrate for enzyme assays.
- High reported purity suitable for research applications.
- Supplied as a crystalline solid with typical cold-storage recommendations.
- Available in small-mass vials for laboratory assays and screening.
eMolecules 16681-67-7 | 4-Bromo-2-methyl-2H-1,2,3-triazole | Ambeed | MFCD23378485 | 161.990 | C3H4BrN3 | 95.000 | Cn1ncc(Br)n1 | 5g | 525043186
4-Bromo-2-methyl-2H-1,2,3-triazole | Ambeed | 16681-67-7 | MFCD23378485 | 161.990 | C3H4BrN3 | 95.000 | Cn1ncc(Br)n1 | 5g | 525043186
TARGETMOL CHEMICALS INC GPNA HYDROCHLORIDE 50MG
Also available in 10 mg 25 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. GPNA hydrochloride is specific glutamine (Gln) transporter ASCT2(SLC1A5) inhibitor. GPNA reversibly induces apoptosis in A549 cells. GPNA hydrochloride is a well-known substrate of the enzyme (gamma)-glutamyltransferase (GGT). GPNA hydrochloride also inhibits Na+-dependent carriers such as SNAT family (SNAT1/2/4/5) and the Na+-independent leucine transporters LAT1/2. purity: 99%
TARGETMOL CHEMICALS INC Dihydro-N-Caffeoyltyramine 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Dihydro-N-Caffeoyltyramine is a compound extracted from Lycii Cortex that has antioxidant and antifungal activities and can be used to study fungal infections. Purity 100%
Medchemexpress LLC ML133 hydrochloride | 1222781-70-5 | 313.82 g/mol | C19H20ClNO | 1 ML
ML133 hydrochloride is a selective inhibitor of Kir2 family inward-rectifier potassium channels used in ion channel research and electrophysiology. It displays pH-dependent potency with reported IC50 values of 1.8 μM at pH 7.4 and 290 nM at pH 8.5. Supplied as a hydrochloride salt and commonly provided as a 10 mM solution in DMSO for laboratory research use only.
- Selective Kir2 family inhibitor suitable for electrophysiology studies.
- pH-dependent potency with IC50 values at physiological and alkaline pH.
- Convenient 10 mM solution in DMSO for immediate experimental use.
- Hydrochloride salt form for improved solubility in polar solvents.
- Provided for research use only; not for human or veterinary use.
TARGETMOL CHEMICALS INC ALE-0540 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ALE-0540 is a nonpeptidic heterocyclic molecule that inhibits the binding of NGF to p75 and TrkA as well as signal transduction and biological responses mediated by TrkA receptors. purity: 97%
eMolecules 198959-37-4 | Methyl pyrrolidine-3-carboxylate hydrochloride | ChemScene | MFCD08436169 | 165.620 | C6H12ClNO2 | 95.000 | Cl.COC(=O)C1CCNC1 | 5g | 572228223
Methyl pyrrolidine-3-carboxylate hydrochloride | ChemScene | 198959-37-4 | MFCD08436169 | 165.620 | C6H12ClNO2 | 95.000 | Cl.COC(=O)C1CCNC1 | 5g | 572228223
TARGETMOL CHEMICALS INC Neboglamine hydrochloride 1MG
Also available in 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Neboglamine (CR-2249, XY-2401) hydrochloride, an orally active positive modulator of the NMDA receptor glycine site, can be used in schizophrenia research [1]. Purity 99.11%
Cayman Chemical Leelamine hydrochloride
The hydrochloride of leelamine, an inhibitor of pyruvate dehydrogenase kinase.
Apexbio Technology LLC Tiagabine hydrochloride 145821-59-6 10mM (in 1mL DMSO)
Tiagabine hydrochloride (CAS 145821-59-6) is a selective inhibitor of the GAT-1 subtype -aminobutyric acid (GABA) transporter By blocking GAT-1-mediated reuptake tiagabine hydrochloride elevates extracellular GABA concentrations and potentiates GABAergic inhibitory neurotransmission Experimental studies demonstrate its capacity to suppress GABA uptake in neuronal glial and synaptic models at varying levels This compound is widely utilized in research on epileptic seizure mechanisms and for investigating neuroprotective effects in models of neurodegenerative disorders associated with disrupted GABA metabolism
Selleck Chemical LLC Bobcat339 hydrochloride
Bobcat339 is a selective cytosine-based TET enzyme inhibitor with IC50 of 33 M and 73 M for TET1 and TET2 respectively Bobcat339 can reduce DNA 5-hydroxymethylcytosine abundance by inhibiting TET enzyme function in living cells and provide support for its utility as a viable pharmacological probe
Medchemexpress LLC Pirenzepine dihydrochloride | 29868-97-1 | 99.8% | 424.32 | 1 G
Pirenzepine dihydrochloride is a selective M1 muscarinic acetylcholine receptor antagonist that poorly penetrates the blood-brain barrier. It is used in peptic ulcer research due to its ability to reduce gastric acid secretion and muscle spasm. This compound also exhibits anti-proliferative activity against cancer cells.
- Selective M1 muscarinic acetylcholine receptor antagonist.
- Reduces gastric acid secretion.
- Reduces muscle spasm.
- Useful in peptic ulcer research.
- Exhibits anti-proliferative activity against cancer cells.
![eMolecules 152140-65-3 | Ambeed | NN-(11R12R)-(910-Dihydro-910-ethanoanthracene-1112-diyl)bis[2-(diphenylphosphino)benzamide] | 100mg | 595929513 | A790190 | 812.89 | C54H42N2O2P2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502452885.PNG-250.jpg)
eMolecules 152140-65-3 | Ambeed | NN-(11R12R)-(910-Dihydro-910-ethanoanthracene-1112-diyl)bis[2-(diphenylphosphino)benzamide] | 100mg | 595929513 | A790190 | 812.89 | C54H42N2O2P2
Ambeed | O-(4-Methoxybenzyl)hydroxylamine | 1g | 592393493 | A184536 | 21038-22-2 | MFCD01722038 | 153.181 | C8H11NO2
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![eMolecules 1086398-02-8 | 2-Boc-2,5-diaza-spiro[3.4]octane | Combi-Blocks, Inc. | MFCD11501185 | 212.293 | C11H20N2O2 | 95.000 | CC(C)(C)OC(=O)N1CC2(C1)CCCN2 | 5g | 837473149](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502694279.jpg-250.jpg)
eMolecules 1086398-02-8 | 2-Boc-2,5-diaza-spiro[3.4]octane | Combi-Blocks, Inc. | MFCD11501185 | 212.293 | C11H20N2O2 | 95.000 | CC(C)(C)OC(=O)N1CC2(C1)CCCN2 | 5g | 837473149
2-Boc-2,5-diaza-spiro[3.4]octane | Combi-Blocks, Inc. | 1086398-02-8 | MFCD11501185 | 212.293 | C11H20N2O2 | 95.000 | CC(C)(C)OC(=O)N1CC2(C1)CCCN2 | 5g | 837473149
TARGETMOL CHEMICALS INC OTS964 HYDROCHLORIDE 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. OTS964 hydrochloride (OTS964) is a potent and selective TOPK inhibitor with potential anticancer activity. purity: 98%