Sulfanilides
Filtered Search Results
Methazolamide, MedChemExpress
MedChemExpress Methazolamide (L584601) is a sulfonamide derivative used as a carbonic anhydrase inhibitor with a Ki of 14 nM for human carbonic anhydrase II. Methazolamide, an intraocular pressure-lowering agent, reduces intraocular pressure elevations associated with glaucoma and other ocular disorders.
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| Molecular Weight (g/mol) | 236.27 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Methazolamide |
| Grade | Research |
| SMILES | CC(/N=C1SC(S(=O)(N)=O)=NN/1C)=O |
| Percent Purity | 99.43% |
| CAS | 554-57-4 |
| Solubility Information | DMSO : ≥ 50 mg/mL (211.62 mM) |
| Health Hazard 1 | H302∣H312∣H332 |
| Synonym | L584601 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Shelf Life | 4°C, protect from light∣In solvent : -80°C, 6 months∣-20°C, 1 month (protect from light) |
| Molecular Formula | C5H8N4O3S2 |
| Formula Weight | 236.27 |
IBR2, MedChemExpress
MedChemExpress IBR2 is a potent and specific RAD51 inhibitor and inhibits RAD51-mediated DNA double-strand break repair. IBR2 disrupts RAD51 multimerization, accelerates proteasome-mediated RAD51 protein degradation, inhibits cancer cell growth and induces apoptosis.
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| Molecular Weight (g/mol) | 400.49 |
|---|---|
| Color | Pink |
| Physical Form | Solid |
| Chemical Name or Material | IBR2 |
| Grade | Research |
| SMILES | O=S(N1C(C2=CNC3=C2C=CC=C3)C4=C(C=CC=C4)C=C1)(CC5=CC=CC=C5)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.6% |
| CAS | 313526-24-8 |
| Solubility Information | DMSO : ≥ 100 mg/mL (249.69 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 | C24H20N2O2S |
| Formula Weight | 400.49 |
TC-G-1008, MedChemExpress
MedChemExpress TC-G-1008 (GPR39-C3) is a potent and orally available GPR39 agonist with EC50 values of 0.4 and 0.8 nM for rat and human receptors respectively.
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| Molecular Weight (g/mol) | 418.9 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | TC-G-1008 |
| Grade | Research |
| SMILES | CS(=O)(NC1=CC=C(CNC2=NC(NC)=NC(C3=NC=CC=C3)=C2)C(Cl)=C1)=O |
| For Use With (Application) | Metabolism-protein/nucleotide metabolism |
| Percent Purity | 99.03% |
| CAS | 1621175-65-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (238.72 mM) |
| Synonym | GPR39-C3 |
| 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 | C18H19ClN6O2S |
| Formula Weight | 418.9 |
CZC24832, MedChemExpress
MedChemExpress CZC24832 is a highly selective and potent PI3Kγ inhibitor (IC50=27 nM) with apparent dissociation constants (Kdapp) of 19 nM.
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| Molecular Weight (g/mol) | 364.4 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | CZC24832 |
| Grade | Research |
| SMILES | FC1=CC(C2=CC(S(=O)(NC(C)(C)C)=O)=CN=C2)=CN3C1=NC(N)=N3 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.35% |
| CAS | 1159824-67-5 |
| Solubility Information | DMSO : ≥ 53 mg/mL (145.44 mM) |
| Health Hazard 1 | 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 | C15H17FN6O2S |
| Formula Weight | 364.4 |
Begacestat, MedChemExpress
MedChemExpress Begacestat (GSI-953) is a selective thiophene sulfonamide inhibitor of amyloid precursor protein gamma-secretase (IC50Aβ40=15 nM) for the treatment of Alzheimer's disease.
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MK-8033, MedChemExpress
MedChemExpress MK-8033 is an orally active ATP competitive c-Met/Ron dual inhibitor (IC50s: 1 nM (c-Met),7 nM (Ron)), with preferential binding to the activated kinase conformation. MK-8033 can be used in the research of cancers, such as breast and bladder cancers, non-small cell lung cancers (NSCLCs).
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| Molecular Weight (g/mol) | 471.53 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | MK-8033 |
| Grade | Research |
| SMILES | O=S(NCC1=CC=CC=N1)(CC2=CC=C3C(C(C4=CC(C5=CN(N=C5)C)=CN=C4C=C3)=O)=C2)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| CAS | 1001917-37-8 |
| Solubility Information | DMSO : ≥ 46 mg/mL (97.55 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 | C25H21N5O3S |
| Formula Weight | 471.53 |
AZ876, MedChemExpress
MedChemExpress AZ876 is a potent and high-affinity LXR agonist. AZ876 displays 25-fold and 2.5-fold more potent than GW3965 (HY-10627) on human (h)LXRα and hLXRβ respectively.
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| Molecular Weight (g/mol) | 439.57 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | AZ876 |
| Grade | Research |
| SMILES | O=C(C(NC1=CC=C(N2CCCCC2)C=C1)=C3C4=CC=CC=C4)N(C(C)(C)C)S3(=O)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.26% |
| CAS | 898800-26-5 |
| Solubility Information | DMSO : 100 mg/mL (227.50 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 | C24H29N3O3S |
| Formula Weight | 439.57 |
CH5132799, MedChemExpress
MedChemExpress CH5132799 is a selective class I PI3K inhibitor. CH5132799 inhibits class I PI3Ks, particularly PI3Kα, with an IC50 of 14 nM.
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| Molecular Weight (g/mol) | 377.42 |
|---|---|
| Color | Gray |
| Physical Form | Solid |
| Chemical Name or Material | CH5132799 |
| Grade | Research |
| SMILES | NC1=NC=C(C2=C3C(N(S(=O)(C)=O)CC3)=NC(N4CCOCC4)=N2)C=N1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.81% |
| CAS | 1007207-67-1 |
| Solubility Information | DMSO : 4.55 mg/mL (12.06 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 | C15H19N7O3S |
| Formula Weight | 377.42 |
GNE-131, MedChemExpress
MedChemExpress GNE-131 is a potent and selective inhibitor of human sodium channel NaV1.7, with an IC50 of 3 nM.
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| Molecular Weight (g/mol) | 442.57 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GNE-131 |
| Grade | Research |
| SMILES | O=S(NC1=NN=C2N1C=C(C3CC3)C(OCC45C[C@@H](C6)C[C@@H](C[C@@H]6C5)C4)=C2)(C7CC7)=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.97% |
| CAS | 1629063-81-5 |
| Solubility Information | DMSO : 125 mg/mL (282.44 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 | C23H30N4O3S |
| Formula Weight | 442.57 |
Pifithrin-μ, MedChemExpress
MedChemExpress Pifithrin-μ is an inhibitor of p53 and HSP70, with antitumor and neuroprotective activity.
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SR1001, MedChemExpress
MedChemExpress SR1001 is a selective RORα and RORγt inverse agonist with Kis 172 and 111 nM, respectively.
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| Molecular Weight (g/mol) | 477.4 |
|---|---|
| Color | Off-White |
| Physical Form | Powder |
| Chemical Name or Material | SR1001 |
| Grade | Research |
| SMILES | CC(NC1=NC(C)=C(S(=O)(NC2=CC=C(C(C(F)(F)F)(O)C(F)(F)F)C=C2)=O)S1)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.0% |
| CAS | 1335106-03-0 |
| Solubility Information | DMSO : ≥ 39 mg/mL (81.69 mM) |
| Health Hazard 1 | H302∣H319 |
| 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 | C15H13F6N3O4S2 |
| Formula Weight | 477.4 |
Abrocitinib, MedChemExpress
MedChemExpress Abrocitinib (PF-04965842) is a potent, orally active and selective JAK1 inhibitor, with IC50s of 29 and 803 nM for JAK1 and JAK2, respectively. Abrocitinib (PF-04965842) exhibits less active effect on TYK2 (IC50, 1.253 μM), and inhibits phosphorylation of STAT1, STAT3 and STAT5 after stimulation. Effective in autoimmune disease.
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| Molecular Weight (g/mol) | 323.41 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Abrocitinib |
| Grade | Research |
| SMILES | CN([C@H]1C[C@@H](NS(CCC)(=O)=O)C1)C2=C3C(NC=C3)=NC=N2 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.04% |
| CAS | 1622902-68-4 |
| Solubility Information | DMSO : 125 mg/mL (386.51 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | PF-04965842 |
| 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 | C14H21N5O2S |
| Formula Weight | 323.41 |
S 3304, MedChemExpress
MedChemExpress S 3304 is a novel matrix metalloproteinases (MMP) inhibitor specific for MMP-2 and MMP-9.
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| Molecular Weight (g/mol) | 464.56 |
|---|---|
| Color | Brownish Yellow |
| Physical Form | Powder |
| Chemical Name or Material | S 3304 |
| Grade | Research |
| SMILES | O=S(N[C@@H](C(O)=O)CC1=CNC2=C1C=CC=C2)(C3=CC=C(C#CC4=CC=C(C)C=C4)S3)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.56% |
| CAS | 203640-27-1 |
| Solubility Information | DMSO : ≥ 83.3 mg/mL (179.31 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 | C24H20N2O4S2 |
| Formula Weight | 464.56 |
Brinzolamide, MedChemExpress
MedChemExpress Brinzolamide (AL-4862) is a selective carbonic anhydrase II inhibitor with anIC50 value of 3.2 nM. Brinzolamide hydrochloride reduces intraocular pressure (IOP) by inhibiting ciliary CA-II and decreasing atrial fluid secretion. Brinzolamide can be used in glaucoma disease research.
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| Molecular Weight (g/mol) | 383.51 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Brinzolamide |
| Grade | Research |
| SMILES | O=S(C(S1)=CC2=C1S(N(CCCOC)C[C@@H]2NCC)(=O)=O)(N)=O |
| Percent Purity | 99.33% |
| CAS | 138890-62-7 |
| Solubility Information | DMSO : 100 mg/mL (260.75 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | AL-4862 |
| 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 | C12H21N3O5S3 |
| Formula Weight | 383.51 |
Bromosporine, MedChemExpress
MedChemExpress Bromosporine is a broad spectrum inhibitor for bromodomains with IC50 of 0.41 (mu)M, 0.29 (mu)M, 0.122 (mu)M and 0.017 (mu)M for BRD2, BRD4, BRD9 and CECR2, respectively.
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| Molecular Weight (g/mol) | 404.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Bromosporine |
| Grade | Research |
| SMILES | O=C(OCC)NC1=CC(C2=CC=C(C)C(NS(=O)(C)=O)=C2)=NN3C1=NN=C3C |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.6% |
| CAS | 1619994-69-2 |
| Solubility Information | DMSO : ≥ 51.7 mg/mL (127.83 mM) |
| Health Hazard 1 | H315∣H317∣H318∣H334∣H335∣H341∣H361∣H370∣H413 |
| 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 | C17H20N6O4S |
| Formula Weight | 404.44 |