Dimethyl Sulfoxide
Dimethyl sulfoxide, ACS, 99.9% min
CAS: 67-68-5 Molecular Formula: C2H6OS Molecular Weight (g/mol): 78.13 MDL Number: MFCD00002089 InChI Key: IAZDPXIOMUYVGZ-UHFFFAOYSA-N Synonym: dimethyl sulfoxide,dmso,methyl sulfoxide,dimethylsulfoxide,dimethyl sulphoxide,methane, sulfinylbis,demsodrox,demasorb,demavet,dimexide PubChem CID: 679 ChEBI: CHEBI:28262 IUPAC Name: methylsulfinylmethane SMILES: CS(C)=O
Dimethyl Sulfoxide, for HPLC, GC and spectrophotometry, >99.5%, Solstice
CAS: 67-68-5 Molecular Formula: C2H6OS Molecular Weight (g/mol): 78.13 MDL Number: MFCD00002089 InChI Key: IAZDPXIOMUYVGZ-UHFFFAOYSA-N Synonym: dimethyl sulfoxide,dmso,methyl sulfoxide,dimethylsulfoxide,dimethyl sulphoxide,methane, sulfinylbis,demsodrox,demasorb,demavet,dimexide PubChem CID: 679 ChEBI: CHEBI:28262 IUPAC Name: methanesulfinylmethane SMILES: CS(C)=O
Gaylord Chemical Company, LLC PROCIPIENT™ (Dimethyl Sulfoxide USP, PhEur)
CAS: 67-68-5 Molecular Formula: C2H6OS Molecular Weight (g/mol): 78.13 InChI Key: IAZDPXIOMUYVGZ-UHFFFAOYSA-N IUPAC Name: methanesulfinylmethane SMILES: CS(C)=O
Dimethyl sulfoxide, Solstice™
CAS: 67-68-5 PubChem CID: 679 ChEBI: CHEBI:28262
Dimethyl Sulfoxide, ≥99.9%, Solstice
CAS: 67-68-5 Molecular Formula: C2H6OS Molecular Weight (g/mol): 78.13 MDL Number: MFCD00002089 InChI Key: IAZDPXIOMUYVGZ-UHFFFAOYSA-N Synonym: dimethyl sulfoxide,dmso,methyl sulfoxide,dimethylsulfoxide,dimethyl sulphoxide,methane, sulfinylbis,demsodrox,demasorb,demavet,dimexide PubChem CID: 679 ChEBI: CHEBI:28262 SMILES: CS(C)=O
Dimethyl sulfoxide, CHROMASOLV™ Plus, for HPLC, ≥99.7%, Solstice
CAS: 67-68-5 Molecular Formula: C2H6OS Molecular Weight (g/mol): 78.13 MDL Number: MFCD00002089 InChI Key: IAZDPXIOMUYVGZ-UHFFFAOYSA-N Synonym: dimethyl sulfoxide,dmso,methyl sulfoxide,dimethylsulfoxide,dimethyl sulphoxide,methane, sulfinylbis,demsodrox,demasorb,demavet,dimexide PubChem CID: 679 ChEBI: CHEBI:28262 SMILES: CS(C)=O
N,N-Dimethylformamide (Spectranalyzed™), Fisher Chemical™
CAS: 68-12-2 Molecular Formula: C3H7NO Molecular Weight (g/mol): 73.10 MDL Number: MFCD00003284 InChI Key: ZMXDDKWLCZADIW-UHFFFAOYSA-N Synonym: dimethylformamide,dimethyl formamide,n,n-dimethylmethanamide,n-formyldimethylamine,formamide, n,n-dimethyl,dmf,dimethylformamid,dimetilformamide,dwumetyloformamid,dmfa PubChem CID: 6228 ChEBI: CHEBI:17741 IUPAC Name: N,N-dimethylformamide SMILES: CN(C)C=O
Apexbio Technology LLC Triapine 236392-56-6; 200933-27-3; 143621-35-6 10mM (in 1mL DMSO)
Triapine is a small molecule thiosemicarbazone derivative known to inhibit ribonucleotide reductase an enzyme essential for the conversion of ribonucleotides to deoxyribonucleotides thereby interfering with DNA synthesis and repair pathways Through this inhibition mechanism Triapine exhibits antitumor activity in a range of experimental cancer models including human ovarian carcinoma xenografts and murine leukemia models and inhibits proliferation across multiple tumor cell lines Due to its mechanistic specificity Triapine serves as a useful chemical tool for biomedical research into nucleic acid metabolism cancer cell replication and therapeutic resistance mechanisms
Medchemexpress LLC Pemigatinib | 1513857-77-6 | 487.5 g/mol | 1ML
Pemigatinib | 1513857-77-6 | 487.5 g/mol | 1ML
Apexbio Technology LLC Prilocaine 721-50-6 10mM (in 1mL DMSO)
Prilocaine (CAS 721-50-6) is a local anesthetic molecule categorized within the amino amide class Its primary pharmacological mechanism involves reversible blockade of voltage-gated sodium channels in neuronal membranes thereby inhibiting action potential propagation and sensory nerve impulse conduction Due to its sodium channel-blocking profile prilocaine is commonly investigated in biomedical research examining reversible neural inhibition pain modulation pathways and sensory signal transmission mechanisms
Apexbio Technology LLC GSK2334470 1227911-45-6 10mM (in 1mL DMSO)
GSK2334470 (CAS 1227911-45-6) is a highly selective inhibitor of 3-phosphoinositide-dependent protein kinase-1 (PDK1) demonstrating an IC50 of approximately 10 nM It specifically blocks PDK1-mediated phosphorylation of substrate proteins including Akt1 S6K1 and SGK isoforms inhibiting their T-loop phosphorylation sites GSK2334470 does not significantly inhibit other tested protein or lipid kinases This compound facilitates mechanistic research into signaling pathways regulated by PDK1 particularly those involving Akt and downstream effectors in cellular contexts
Apexbio Technology LLC Dofetilide 115256-11-6 10mM (in 1mL DMSO)
Dofetilide (CAS 115256-11-6) chemically designated as UK 68789 is a class III antiarrhythmic small molecule that selectively inhibits the rapid delayed rectifier potassium channel (IKr) This inhibition leads to prolonged ventricular action potential duration and extended effective refractory periods in cardiac cells Noted for favorable oral bioavailability Dofetilide is extensively utilized in cardiac electrophysiological research including studies aimed at elucidating arrhythmogenic mechanisms linked to IKr channel function assessing novel antiarrhythmic candidates and exploring physiological and pathological aspects of cardiac rhythm regulation
Apexbio Technology LLC A939572 1032229-33-6 10mM (in 1mL DMSO)
A939572 (CAS 1032229-33-6) is an orally bioavailable small-molecule inhibitor targeting stearoyl-CoA desaturase 1 (SCD1) an enzyme that catalyzes the formation of monounsaturated fatty acids involved in lipid metabolism and body weight regulation A939572 selectively inhibits human and mouse SCD1 with IC50 values of 37 nM and 4 nM respectively exhibiting no inhibitory effect on associated cofactors cytochrome b5 or cytochrome b5 reductase By specifically interacting with SCD1 A939572 serves as a pharmacological tool in metabolic research particularly in studies focused on obesity and diabetes
Apexbio Technology LLC Polydatin 27208-80-6 10mM (in 1mL DMSO)
Polydatin (CAS 27208-80-6) is a naturally occurring stilbenoid isolated primarily from the roots of Polygonum cuspidatum Structurally it represents the glucoside derivative of resveratrol exerting antioxidant and anti-inflammatory effects through modulation of oxidative stress-related pathways Research indicates that polydatin influences signaling cascades such as NF- B MAPK and Nrf2 contributing to its protective roles in cellular injury models including cardiovascular dysfunction neurodegeneration and inflammatory conditions Polydatin is soluble in methanol ethanol and acetone and stability is maintained by storage under sealed cool dry conditions