Pyrazines
Sigma Aldrich Fine Chemicals Biosciences 2-Isobutyl-3-methoxypyrazine >=99%, FG | 24683-00-9 | MFCD00006128 |
2-Isobutyl-3-methoxypyrazine >=99%, FG | Purity: >=99% | Mol Wt: 166.22 | 24683-00-9 | MFCD00006128 |
Medchemexpress LLC 2-Methoxypyrazine | 3149-28-8 | 100.0% | 110.12 | 25 G
2-Methoxypyrazine is an active compound utilized for research in various biochemical studies. This compound is available as a colorless to light yellow liquid and is suitable for both in vitro and in vivo applications, offering reliable performance for scientific investigations.
- Appearance: liquid
- Color: colorless to light yellow
- Molecular formula: C5H6N2O
- Shipping: room temperature in continental US (may vary elsewhere)
- Storage for pure form: -20°C for 3 years, 4°C for 2 years
- Storage for in solvent form: -80°C for 6 months, -20°C for 1 month
- In vitro solubility: 100 mg/mL in DMSO (908.13 mM), requires sonication
Aobchem 4-Phenyltetrahydro-2H-pyran-4-ol | ≥95% | CAS 81462-07-9 | C11H14O2 | 25g
4-Phenyltetrahydro-2H-pyran-4-ol | ≥95% | CAS 81462-07-9 | C11H14O2 | 25g
Aobchem 4-Phenyltetrahydro-2H-pyran-4-ol | ≥95% | CAS 81462-07-9 | C11H14O2 | 5g
4-Phenyltetrahydro-2H-pyran-4-ol | ≥95% | CAS 81462-07-9 | C11H14O2 | 5g
Medchemexpress LLC N-(1-adamantyl)quinoxaline-2-carboxamide | 226878-01-9 | MFCD05865239 | 99.9% | 307.39 g·mol⁻¹ | C19H21N3O | 5 MG
NPS 2390 is a small-molecule research compound described as a noncompetitive antagonist of metabotropic glutamate receptors mGluR1 and mGluR5 and as an inhibitor of the calcium-sensing receptor (CaSR). It is supplied for laboratory research use only and is accompanied by technical documentation including a datasheet, COA, and SDS.
- Noncompetitive antagonist of mGluR1 and mGluR5.
- Inhibitor of the calcium-sensing receptor (CaSR).
- Molecular formula C19H21N3O; molecular weight 307.39 g·mol⁻¹.
- High purity (~99.9%) suitable for biochemical and cellular assays.
- Available as solid quantities and as a 10 mM solution in DMSO.
- Supplied for research use only with supporting COA, SDS, and handling instructions.
Medchemexpress LLC NPS 2390 | 226878-01-9 | 99.9% | 307.39 | 10 MG
NPS 2390 is a noncompetitive antagonist of mGluR1 and mGluR5. It is also a potent CaSR (calcium-sensing receptor) inhibitor.
- Noncompetitive antagonist of mGluR1 and mGluR5.
- Potent CaSR (calcium-sensing receptor) inhibitor.
- For research use only.
Medchemexpress LLC HY-10227 10mg Medchemexpress, Bortezomib CAS:179324-69-7 Purity:>98%
Medchemexpress, HY-10227 10mg Bortezomib CAS:179324-69-7 Bortezomib (PS-341) is a reversible and selective proteasome inhibitor, and potently inhibits 20S proteasome (Ki=0.6 nM) by targeting a threonine residue. Bortezomib disrupts the cell cycle, induces apoptosis, and inhibits NF-κB. Bortezomib is the first proteasome inhibitor anticancer agent. Anti-cancer activity[2]. 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 HY-101840 10mg Medchemexpress, EIPA CAS:1154-25-2 Purity:>98%
Medchemexpress, HY-101840 10mg EIPA CAS:1154-25-2 EIPA (L593754; MH 12-43) is a TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA (L593754; MH 12-43) also inhibits Na+/H+-exchanger (NHE) and macropinocytosis. 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 HY-101840A 5mg Medchemexpress, EIPA (hydrochloride) CAS:1345839-28-2 Purity:>98%
Medchemexpress, HY-101840A 5mg EIPA (hydrochloride) CAS:1345839-28-2 EIPA hydrochloride (L593754 hydrochloride) is a TRPP3 channel inhibitor with an IC 50 of 10.5 μM [1] . EIPA also inhibits Na + /H + -exchanger ( NHE ) [2] and macropinocytosis [3] . 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.
Aobchem 4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 1g
4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 1g
Aobchem 4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 250mg
4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 250mg
Aobchem 4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 500mg
4-Phenyltetrahydro-2H-thiopyran-4-ol | ≥97% | CAS 22397-92-8 | C11H14OS | 500mg
Medchemexpress LLC GSK-1520489A | 1042433-41-9 | 99.8% | 425.50 | 5 MG
GSK-1520489A is an inhibitor of PKMYT1 (active protein kinase) with an IC50 of 115 nM and a Ki of 10.94 nM. It is intended for research use only.
- Inhibits phosphorylation of Tyr15 in Cdk1 at a concentration of 4 μM after 24 hours of treatment.
- Reduces Cdk1-phosphorylation at tyrosine in HT29 cells when treated with 4 μM for 24 hours.
Medchemexpress LLC HY-12432 10mg Medchemexpress, Gilteritinib CAS:1254053-43-4 Purity:>98%
Medchemexpress, HY-12432 10mg Gilteritinib CAS:1254053-43-4 Gilteritinib is a potent FLT3/AXL inhibitor with IC50s of 0.29 nM/0.73 nM, respectively. 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.
Aobchem 4-(Cyclopropylmethoxy)-3-fluorobenzoic acid | ≥97% | CAS 1021144-38-6 | C11H11FO3 | 1g
4-(Cyclopropylmethoxy)-3-fluorobenzoic acid | ≥97% | CAS 1021144-38-6 | C11H11FO3 | 1g