Pyrazines
![Medchemexpress LLC Cellulose, methyl ether | 9004-67-5 | MFCD00081763 | 98.0% | Not specified (polymeric) | [C6H7O2(OH)x(OCH3)y]n | 100G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000235963.png-250.jpg)
Medchemexpress LLC Cellulose, methyl ether | 9004-67-5 | MFCD00081763 | 98.0% | Not specified (polymeric) | [C6H7O2(OH)x(OCH3)y]n | 100G
Methyl cellulose is a non-ionic cellulose ether powder specified at a viscosity of 40,000 mPa·s and a purity of 98.0%. It exhibits surface-active and thermogelation properties and is used as a thickener, stabilizer, emulsifier, and formulation excipient in pharmaceutical, food, cosmetic, and construction applications.
- High viscosity grade 40,000 mPa·s for strong thickening.
- Thermogelation behavior enables temperature-responsive gel formation.
- Non-ionic, water-soluble polymer compatible with many formulation types.
- Useful as a thickener, stabilizer, emulsifier, and drug-delivery excipient.
- Available in laboratory pack sizes including 100 g.
- Typical supplied purity 98.0% ensures consistent performance.
TARGETMOL CHEMICALS INC HTH-01-091 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50 10.5 nM).HTH-01-091 inhibits PIM1/2/3 RIPK2 DYRK3 smMLCK and CLK2. HTH-01-091 can be used to study breast cancer. purity: 98%
eMolecules 868594-52-9 | Fmoc-NH-PEG8-CH2COOH | Ambeed | MFCD27635163 | 649.734 | C33H47NO12 | 95.000 | OC(=O)COCCOCCOCCOCCOCCOCCOCCOCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 650570675
Fmoc-NH-PEG8-CH2COOH | Ambeed | 868594-52-9 | MFCD27635163 | 649.734 | C33H47NO12 | 95.000 | OC(=O)COCCOCCOCCOCCOCCOCCOCCOCCNC(=O)OCC1c2ccccc2-c2ccccc12 | 5g | 650570675
eMolecules 5961-85-3 | Tris(2-carboxyethyl)phosphine | Synthonix - Stock | MFCD12068446 | 250.187 | C9H15O6P | 98.000 | OC(=O)CCP(CCC(O)=O)CCC(O)=O | 1g | 525924600
Tris(2-carboxyethyl)phosphine | Synthonix - Stock | 5961-85-3 | MFCD12068446 | 250.187 | C9H15O6P | 98.000 | OC(=O)CCP(CCC(O)=O)CCC(O)=O | 1g | 525924600
TARGETMOL CHEMICALS INC SKF83959 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SKF83959 a benzazepine analog is a selective and potent partial agonist of the dopamine D1 receptor with Ki values of 1.18 7.56 920 and 399 nM for rat D1 D5 D2 and D3 receptors respectively.SKF83959 is a potent variant modulator of the sigma ((sigma))-1 receptor which ameliorates cognitive dysfunction for the study depression and Alzheimer's disease. purity: 98%
TARGETMOL CHEMICALS INC RU-TRAAK-2 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. RU-TRAAK-2 is a reversible inhibitor of TWIK-related arachidonic acid-stimulated K+ channel with no activity for non-K2P channels including Kv1.2 GIRK2 and Slo1. purity: 99%
TARGETMOL CHEMICALS INC IMDK 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. iMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice. purity: 99%
TARGETMOL CHEMICALS INC AM1241 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM exhibits 82-fold selectivity over CB1 receptor. purity: 98%
TARGETMOL CHEMICALS INC UVI 3003 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. UVI 3003 is a highly selective antagonist of the retinoid X receptor. UVI 3003 inhibits Xenopus and human RXR(alpha) in Cos7 cells (IC50s 0.22 and 0.24 uM respectively). purity: 99%
TARGETMOL CHEMICALS INC ODM-203 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ODM-203 a Selective Inhibitor of FGFR and VEGFR Shows Strong Antitumor Activity and Induces Antitumor Immunitypurity: 98%
TARGETMOL CHEMICALS INC BAFILOMYCIN A1 5MG
Also available in 1 mg 160 uL * 1 mM (in DMSO) and bulk. Please contact Fisher for quotes. Bafilomycin A1 induces caspase-independent cell death in hepatocellular carcinoma cells via targeting of autophagy and MAPK pathways. Bafilomycin A1 is a vacuolar H+-ATPase inhibitor (IC50 0.44 nM). It is also found to inhibit autophagy while induces apoptosis.Bafilomycin A1 triggers proliferative potential of senescent cancer cells in vitro and in NOD/SCID mice. purity: 98%
eMolecules 5780-66-5 | Pyrazine-2-carbaldehyde | ChemScene | MFCD02179278 | 108.100 | C5H4N2O | 95.000 | O=Cc1cnccn1 | 25g | 711936379
Pyrazine-2-carbaldehyde | ChemScene | 5780-66-5 | MFCD02179278 | 108.100 | C5H4N2O | 95.000 | O=Cc1cnccn1 | 25g | 711936379
TARGETMOL CHEMICALS INC GW788388 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. GW788388 is a potent and selective inhibitor of ALK5 also inhibits TGF-(beta) type II receptor and activin type II receptor activities. purity: 98%
TARGETMOL CHEMICALS INC REVERSINE 25MG
Also available in 1 mg 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Reversine a small synthetic purine analogue (2 6-disubstituted purine) is a potent inhibitior of Aurora A/B/C(IC50s=150-500 nM). purity: 99%
TARGETMOL CHEMICALS INC SR9009 25MG
Also available in 1 mg 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SR9009 (Stenabolic) a REV-ERB agonist increases the constitutive repression of genes regulated by REV-ERB(alpha)/ERB(beta) (IC50 670/800 nM). Through activation of REV-ERB SR9009 can decrease circadian locomotor activity during the dark phase and alter the expression pattern of core clock genes in the hypothalami of mice. The circadian pattern of expression of an array of metabolic genes in the liver skeletal muscle and adipose tissue was also altered in mice exposed to SR9009 resulting in increased energy expenditure. In Diet-induced obese mice SR9009 (100 mg/kg i.p. b.i.d. for 30 days) could decrease fat mass and markedly improve dyslipidemia and hyperglycemia. purity: 99%