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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 |
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 |
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 |
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 |
NU6300, MedChemExpress
MedChemExpress NU6300 is a covalent, irreversible and ATP-competitive CDK2 inhibitor with an IC50 value of 0.16 μM. NU6300 can be used for the research of eukaryotic cell cycle- and transcription-related.
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| Molecular Weight (g/mol) | 413.49 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | NU6300 |
| Grade | Research |
| SMILES | O=S(C(C=C1)=CC=C1NC2=NC(OCC3CCCCC3)=C4C(NC=N4)=N2)(C=C)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.34% |
| CAS | 2070015-09-5 |
| Solubility Information | DMSO : ≥ 32 mg/mL (77.39 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 | C20H23N5O3S |
| Formula Weight | 413.49 |
AVN-492, MedChemExpress
MedChemExpress AVN-492 is a very specific and highly-selective antagonist with picomolar affinity to 5-HT6R (Ki=91 pM).
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| Molecular Weight (g/mol) | 359.45 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | AVN-492 |
| Grade | Research |
| SMILES | O=S(C1=CC=CC=C1)(C2=C3N(C(C)=C(N(C)C)C(C)=N3)N=C2NC)=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.27% |
| CAS | 1220646-23-0 |
| Solubility Information | DMSO : ≥ 100 mg/mL (278.20 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 | C17H21N5O2S |
| Formula Weight | 359.45 |
Sulcotrione, MedChemExpress
MedChemExpress Sulcotrione is a β-triketone herbicide which can inhibit hydroxyphenylpyruvate dioxygenase (HPPD).
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| Molecular Weight (g/mol) | 328.77 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Sulcotrione |
| Grade | Research |
| SMILES | O=C(C1C(CCCC1=O)=O)C2=C(C=C(S(C)(=O)=O)C=C2)Cl |
| Percent Purity | 98.77% |
| CAS | 99105-77-8 |
| Solubility Information | DMSO : 100 mg/mL (304.16 mM; Need ultrasonic and warming) |
| Health Hazard 1 | H317∣H361 |
| 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 | C14H13ClO5S |
| Formula Weight | 328.77 |
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 |
RO-28-1675, MedChemExpress
MedChemExpress RO-28-1675 is a potent allosteric glucokinase (GK) activator with an EC50 of 54 nM. RO-28-1675 can be used for the research of type 2 diabetes.
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| Molecular Weight (g/mol) | 378.51 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | RO-28-1675 |
| Grade | Research |
| SMILES | O=C([C@@H](C1=CC=C(C=C1)S(=O)(C)=O)CC2CCCC2)NC3=NC=CS3 |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 99.62% |
| CAS | 300353-13-3 |
| Solubility Information | DMSO : 50 mg/mL (132.10 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 | C18H22N2O3S2 |
| Formula Weight | 378.51 |
BRD7116, MedChemExpress
MedChemExpress BRD7116 competitively binds to bacterial DNA gyrase, exhibits an EC50 of 200 nM for LSCe cells, with cell-non-autonomous anti-leukemia activity.
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| Molecular Weight (g/mol) | 496.66 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | BRD7116 |
| Grade | Research |
| SMILES | O=S(C1=CC=C(NC(C2C(C)(C)C2(C)C)=O)C=C1)(C3=CC=C(NC(C4C(C)(C)C4(C)C)=O)C=C3)=O |
| Percent Purity | 99.73% |
| CAS | 329059-55-4 |
| Solubility Information | DMSO : ≥ 48 mg/mL (96.65 mM) |
| 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 | C28H36N2O4S |
| Formula Weight | 496.66 |
Ezutromid, MedChemExpress
MedChemExpress Ezutromid (SMT C1100) is a first-in-class, orally active benzoxazole utrophin modulator with an EC50 of 0.91 μM. Ezutromid can be used for the research Duchenne muscular dystrophy (DMD). Ezutromid inhibits CYP1A2 enzymic activity in human liver microsomes (HLM) with an IC50 of 5.4 μM.
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| Molecular Weight (g/mol) | 337.39 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Ezutromid |
| Grade | Research |
| SMILES | O=S(C1=CC=C(OC(C2=CC=C3C=CC=CC3=C2)=N4)C4=C1)(CC)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.94% |
| CAS | 945531-77-1 |
| Solubility Information | DMSO : 10 mg/mL (29.64 mM; Need ultrasonic and warming) |
| Synonym | SMT C1100 BMN 195 VOX-C1100 |
| 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 | C19H15NO3S |
| Formula Weight | 337.39 |
(R)-BAY-85-8501, MedChemExpress
MedChemExpress (R)-BAY-85-8501 is the less active Enantiomer of BAY-85-8501. BAY-85-8501 is a selective 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 | (R)-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) | Neuroscience-Neuromodulation |
| Percent Purity | 98.57% |
| CAS | 2446175-39-7 |
| Solubility Information | DMSO : 100 mg/mL (210.77 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 |
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 |