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Filtered Search Results
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 |
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 |
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 |
Pifithrin-μ, MedChemExpress
MedChemExpress Pifithrin-μ is an inhibitor of p53 and HSP70, with antitumor and neuroprotective activity.
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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 |
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 |
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 |
FGH10019, MedChemExpress
MedChemExpress FGH10019 is a novel sterol regulatory element-binding protein (SREBP) inhibitor with IC50 of 1 μM.
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| Molecular Weight (g/mol) | 373.49 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | FGH10019 |
| Grade | Research |
| SMILES | CS(=O)(NC1=CC=C(C2=CSC(C3=CC(CCC)=NC=C3)=N2)C=C1)=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 99.43% |
| CAS | 1046045-61-7 |
| Solubility Information | DMSO : ≥ 38 mg/mL (101.74 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 | C18H19N3O2S2 |
| Formula Weight | 373.49 |
Reparixin, MedChemExpress
MedChemExpress Reparixin is a non-competitive allosteric inhibitor of the chemokine receptors CXCR1 and CXCR2 activation with IC50s of 1 and 100 nM, respectively.
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| Molecular Weight (g/mol) | 283.39 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Reparixin |
| Grade | Research |
| SMILES | CS(=O)(NC([C@@H](C1=CC=C(CC(C)C)C=C1)C)=O)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 95.05% |
| CAS | 266359-83-5 |
| Solubility Information | DMSO : ≥ 100 mg/mL (352.87 mM) ∣H2O : < 0.1 mg/mL (insoluble) |
| Health Hazard 1 | H302 |
| Synonym | Repertaxin DF 1681Y |
| 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 | C14H21NO3S |
| Formula Weight | 283.39 |
CMPDA, MedChemExpress
MedChemExpress CMPDA is a positive allosteric modulator of AMPA receptors with EC50s of 45.4 (plusmn) 4.2 nM/63.4 (plusmn) 5.6 nM for GluA2i/GluA2o receptor.
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Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 376.53 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | CMPDA |
| Grade | Research |
| SMILES | O=S(NCCC1=CC=C(CCNS(=O)(C(C)C)=O)C=C1)(C(C)C)=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 97.19% |
| CAS | 380607-77-2 |
| Solubility Information | DMSO : ≥ 100 mg/mL (265.58 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 | C16H28N2O4S2 |
| Formula Weight | 376.53 |
ML335, MedChemExpress
MedChemExpress ML335 is a selective activator of both TREK-1 and TREK-2.
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| Molecular Weight (g/mol) | 373.25 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | ML335 |
| Grade | Research |
| SMILES | O=C(NCC1=CC=C(Cl)C=C1Cl)C2=CC=C(NS(=O)(C)=O)C=C2 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.93% |
| CAS | 825658-06-8 |
| Solubility Information | DMSO : 155 mg/mL (415.27 mM; Need ultrasonic and warming) |
| 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 | C15H14Cl2N2O3S |
| Formula Weight | 373.25 |
Litronesib, MedChemExpress
MedChemExpress Litronesib (LY2523355) is a selective mitosis-specific kinesin Eg5 inhibitor, with antitumor activity.
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| Molecular Weight (g/mol) | 511.7 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Litronesib |
| Grade | Research |
| SMILES | CC(C)(C)C(N1[C@@](C2=CC=CC=C2)(CNS(CCNCC)(=O)=O)SC(NC(C(C)(C)C)=O)=N1)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.48% |
| CAS | 910634-41-2 |
| Solubility Information | DMSO : ≥ 50 mg/mL (97.71 mM) |
| Synonym | LY2523355 |
| 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 | C23H37N5O4S2 |
| Formula Weight | 511.7 |
Mibampator, MedChemExpress
MedChemExpress Mibampator (LY451395) is a potent and highly selective potentiator of the AMPA receptors.
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| Molecular Weight (g/mol) | 438.6 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Mibampator |
| Grade | Research |
| SMILES | C[C@@H](CNS(C(C)C)(=O)=O)C1=CC=C(C2=CC=C(CCNS(C)(=O)=O)C=C2)C=C1 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.03% |
| CAS | 375345-95-2 |
| Solubility Information | DMSO : ≥ 25 mg/mL (57.00 mM) |
| Synonym | LY451395 |
| 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 | C21H30N2O4S2 |
| Formula Weight | 438.6 |
GNE-477, MedChemExpress
MedChemExpress GNE-477 is a potent and efficacious dual PI3K (IC50=4 nM)/mTOR(Ki=21 nM) inhibitor.
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| Molecular Weight (g/mol) | 504.63 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GNE-477 |
| Grade | Research |
| SMILES | NC1=NC=C(C2=NC(N3CCOCC3)=C4C(C(C)=C(CN5CCN(S(=O)(C)=O)CC5)S4)=N2)C=N1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.7% |
| CAS | 1032754-81-6 |
| Solubility Information | DMSO : 16.67 mg/mL (33.03 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 | C21H28N8O3S2 |
| Formula Weight | 504.63 |