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Filtered Search Results
4,4'-Diaminodiphenyl sulfone, 98%
CAS: 80-08-0 Molecular Formula: C12H12N2O2S Molecular Weight (g/mol): 248.3 MDL Number: MFCD00007887 InChI Key: MQJKPEGWNLWLTK-UHFFFAOYSA-N Synonym: dapsone,diaphenylsulfone,4,4'-diaminodiphenyl sulfone,dapson,4,4'-sulfonyldianiline,diaphenylsulfon,sulfona,4-aminophenyl sulfone,avlosulfone,diphenasone PubChem CID: 2955 ChEBI: CHEBI:4325 IUPAC Name: 4-(4-aminophenyl)sulfonylaniline SMILES: C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N
| PubChem CID | 2955 |
|---|---|
| CAS | 80-08-0 |
| Molecular Weight (g/mol) | 248.3 |
| ChEBI | CHEBI:4325 |
| MDL Number | MFCD00007887 |
| SMILES | C1=CC(=CC=C1N)S(=O)(=O)C2=CC=C(C=C2)N |
| Synonym | dapsone,diaphenylsulfone,4,4'-diaminodiphenyl sulfone,dapson,4,4'-sulfonyldianiline,diaphenylsulfon,sulfona,4-aminophenyl sulfone,avlosulfone,diphenasone |
| IUPAC Name | 4-(4-aminophenyl)sulfonylaniline |
| InChI Key | MQJKPEGWNLWLTK-UHFFFAOYSA-N |
| Molecular Formula | C12H12N2O2S |
Stattic, MedChemExpress
MedChemExpress Stattic is a potent STAT3 inhibitor and inhibits STAT3 phosphorylation (at Y705 and S727). Stattic inhibits the binding of a high affinity phosphopeptide for the SH2 domain of STAT3. Stattic ameliorates the renal dysfunction in Alport syndrome (AS) mice.
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| Molecular Weight (g/mol) | 211.19 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Stattic |
| Grade | Research |
| SMILES | O=[N+](C1=CC=C(C=CS2(=O)=O)C2=C1)[O-] |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 97.0% |
| CAS | 19983-44-9 |
| Solubility Information | DMSO : 50 mg/mL (236.75 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C8H5NO4S |
| Formula Weight | 211.19 |
BAY 11-7082, MedChemExpress
MedChemExpress BAY 11-7082 is an IκBα phosphorylation and NF-κB inhibitor.
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| Molecular Weight (g/mol) | 207.25 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | BAY 11-7082 |
| Grade | Research |
| SMILES | N#C/C=C/S(=O)(C1=CC=C(C)C=C1)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.28% |
| CAS | 19542-67-7 |
| Solubility Information | DMSO : ≥ 100 mg/mL (482.51 mM) |
| Synonym | BAY 11-7821 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C10H9NO2S |
| Formula Weight | 207.25 |
Imrecoxib, MedChemExpress
MedChemExpress Imrecoxib (BAP-909) is a novel and selective cyclooxygenase 2 (COX-2) inhibitor with an IC50 value of 18 nM, it also inhibits COX1- activity with an IC50 value of 115 nM. Imrecoxib (BAP-909) has anti-inflammatory effect.
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| Molecular Weight (g/mol) | 369.48 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | Imrecoxib |
| Grade | Research |
| SMILES | O=C1N(CCC)CC(C2=CC=C(S(=O)(C)=O)C=C2)=C1C3=CC=C(C)C=C3 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.64% |
| CAS | 395683-14-4 |
| Solubility Information | DMSO : 100 mg/mL (270.65 mM; Need ultrasonic) |
| Synonym | BAP-909 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C21H23NO3S |
| Formula Weight | 369.48 |
BTB-1, MedChemExpress
MedChemExpress BTB-1 is a potent, selective and reversible mitotic motor protein Kif18A inhibitor with an IC50 of 1.69 μM.
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| Molecular Weight (g/mol) | 297.71 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | BTB-1 |
| Grade | Research |
| SMILES | O=S(C1=CC=C(Cl)C=C1[N+]([O-])=O)(C2=CC=CC=C2)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.69% |
| CAS | 86030-08-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (335.90 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C12H8ClNO4S |
| Formula Weight | 297.71 |
NNC-0640, MedChemExpress
MedChemExpress NNC-0640 is a potent human G-protein-coupled glucagon receptor (GCGR) negative allosteric modulator (NAM) with an IC50 of 69.2 nM.
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GSK2801, MedChemExpress
MedChemExpress GSK2801 is a potent, selective, orally active and cell active acetyl-lysine competitive BAZ2A and BAZ2B bromodomains inhibitor with Kd values of 136 nM and 257 nM, respectively. GSK2801 shows >50-fold selectivity for BAZ2A/B over BRD4.
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| Molecular Weight (g/mol) | 371.45 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GSK2801 |
| Grade | Research |
| SMILES | O=C(C)C1=CC(C2=C(S(=O)(C)=O)C=CC=C2)=C3N1C=CC(OCCC)=C3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 95.0% |
| CAS | 1619994-68-1 |
| Solubility Information | DMSO : 50 mg/mL (134.61 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C20H21NO4S |
| Formula Weight | 371.45 |
STF-118804, MedChemExpress
MedChemExpress STF-118804 is a highly specific NAMPT inhibitor; reduces the viability of most B-ALL cell lines with IC50 <10 nM.
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| Molecular Weight (g/mol) | 461.53 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | STF-118804 |
| Grade | Research |
| SMILES | O=C(NCC1=CC=CN=C1)C2=CC=C(C3=NC(CS(=O)(C4=CC=C(C)C=C4)=O)=C(C)O3)C=C2 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.03% |
| CAS | 894187-61-2 |
| Solubility Information | DMSO : ≥ 31 mg/mL (67.17 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C25H23N3O4S |
| Formula Weight | 461.53 |
AZD-0284, MedChemExpress
MedChemExpress AZD-0284 is a selective inverse agonist of the nuclear receptor RORγ. AZD-0284 has the potential for plaque psoriasis vulgaris and respiratory tract disorders treatment.
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| Molecular Weight (g/mol) | 524.43 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | AZD-0284 |
| Grade | Research |
| SMILES | O=C([C@@H]1N(C(C)=O)CC2=C1C=CC(S(=O)(C)=O)=C2)NC3=CC=C(C(C(F)(F)F)(O)C(F)(F)F)C=C3 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.84% |
| CAS | 2101291-07-8 |
| Solubility Information | DMSO : 100 mg/mL (190.68 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| Shelf Life | 4°C, stored under nitrogen∣In solvent : -80°C, 6 months∣-20°C, 1 month (stored under nitrogen) |
| Molecular Formula | C21H18F6N2O5S |
| Formula Weight | 524.43 |
Globalagliatin, MedChemExpress
MedChemExpress Globalagliatin (LY2608204) is a activator of glucokinase (GK) with EC50 of 42 nM.
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| Molecular Weight (g/mol) | 559.81 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Globalagliatin |
| Grade | Research |
| SMILES | O=C([C@@]1(C2=CC=C(S(=O)(C3CC3)=O)C=C2)[C@H](C4CCCCC4)C1)NC5=NC=C(SCCN6CCCC6)S5 |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 98.0% |
| CAS | 1234703-40-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (178.63 mM) |
| Synonym | LY2608204 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C28H37N3O3S3 |
| Formula Weight | 559.81 |
BAY-85-8501, MedChemExpress
MedChemExpress BAY-85-8501 is a selective, reversible and potent inhibitor of Human Neutrophil Elastase (HNE), with an IC50 of 65 pM.
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| Molecular Weight (g/mol) | 474.46 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | BAY-85-8501 |
| Grade | Research |
| SMILES | N#CC1=C(C)N(C2=CC=CC(C(F)(F)F)=C2)C(N(C)[C@@H]1C3=CC=C(C#N)C=C3S(=O)(C)=O)=O |
| For Use With (Application) | Metabolism-protein/nucleotide metabolism |
| Percent Purity | 99.24% |
| CAS | 1161921-82-9 |
| Solubility Information | DMSO : 200 mg/mL (421.53 mM; Need ultrasonic) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C22H17F3N4O3S |
| Formula Weight | 474.46 |
AZD7545, MedChemExpress
MedChemExpress AZD7545 is a potent, competitive, selective PDHK2 (pyruvate dehydrogenase kinase 2) inhibitor with IC50s of 36.8 nM, 6.4 nM for PDHK1 and PDHK2, respectively.
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| Molecular Weight (g/mol) | 478.87 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | AZD7545 |
| Grade | Research |
| SMILES | O=C(N(C)C)C1=CC=C(S(=O)(C2=CC=C(NC([C@@](C)(O)C(F)(F)F)=O)C(Cl)=C2)=O)C=C1 |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 99.91% |
| CAS | 252017-04-2 |
| Solubility Information | DMSO : ≥ 46 mg/mL (96.06 mM) |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C19H18ClF3N2O5S |
| Formula Weight | 478.87 |
Rimeporide, MedChemExpress
MedChemExpress Rimeporide (EMD-87580) is a potent and selective inhibitor of the Na+/H+ exchanger (NHE-1).
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| Molecular Weight (g/mol) | 333.38 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Rimeporide |
| Grade | Research |
| SMILES | O=C(NC(N)=N)C1=CC(S(=O)(C)=O)=C(S(=O)(C)=O)C=C1C |
| For Use With (Application) | Metabolism-protein/nucleotide metabolism |
| Percent Purity | 98.0% |
| CAS | 187870-78-6 |
| Solubility Information | DMSO : 20 mg/mL (59.99 mM; Need ultrasonic and warming) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | EMD-87580 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C11H15N3O5S2 |
| Formula Weight | 333.38 |
Intepirdine, MedChemExpress
MedChemExpress Intepirdine (SB742457) is a highly selective 5-HT6 receptor antagonist with pKi of 9.63; exhibits >100-fold selectivity over other receptors.
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| Molecular Weight (g/mol) | 353.44 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Intepirdine |
| Grade | Research |
| SMILES | O=S(C1=CC=CC=C1)(C2=CC(C=CC=C3N4CCNCC4)=C3N=C2)=O |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 98.06% |
| CAS | 607742-69-8 |
| Solubility Information | DMSO : 50 mg/mL (141.47 mM; Need ultrasonic) |
| Synonym | SB-742457 GSK-742457 RVT-101 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C19H19N3O2S |
| Formula Weight | 353.44 |
BAY-8002, MedChemExpress
MedChemExpress BAY-8002 is a potent, selective, orally active inhibitor of monocarboxylate transporter 1 (MCT1), with an IC50 of 85 nM in the MCT1-expressing DLD-1 cells, displays excellent selectivity against MCT4. Anti-tumor activity.
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| Molecular Weight (g/mol) | 415.85 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | BAY-8002 |
| Grade | Research |
| SMILES | O=C(O)C1=CC=CC=C1NC(C2=CC(S(=O)(C3=CC=CC=C3)=O)=CC=C2Cl)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.1% |
| CAS | 724440-27-1 |
| Solubility Information | DMSO : 125 mg/mL (300.59 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C20H14ClNO5S |
| Formula Weight | 415.85 |