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Filtered Search Results
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 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 |
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).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 |
GNE-131, MedChemExpress
MedChemExpress GNE-131 is a potent and selective inhibitor of human sodium channel NaV1.7, with an IC50 of 3 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 |
Selexipag, MedChemExpress
MedChemExpress Selexipag (NS-304) is an orally available and potent agonist for the Prostacyclin (PGI2) receptor (IP receptor).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 496.62 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Selexipag |
| Grade | Research |
| SMILES | O=C(NS(=O)(C)=O)COCCCCN(C1=NC(C2=CC=CC=C2)=C(C3=CC=CC=C3)N=C1)C(C)C |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.89% |
| CAS | 475086-01-2 |
| Solubility Information | DMSO : ≥ 50 mg/mL (100.68 mM) |
| Synonym | NS-304 ACT-293987 |
| 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 | C26H32N4O4S |
| Formula Weight | 496.62 |
ETP-46321, MedChemExpress
MedChemExpress ETP-46321 is a potent and orally bioavailable PI3Kα and PI3Kδ inhibitor with Kiapps of 2.3 and 14.2 nM, respectively.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 473.55 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | ETP-46321 |
| Grade | Research |
| SMILES | NC(N=C1)=NC=C1C2=CN3C=C(CN4CCN(S(=O)(C)=O)CC4)N=C3C(N5CCOCC5)=N2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.65% |
| CAS | 1252594-99-2 |
| Solubility Information | DMSO : ≥ 33 mg/mL (69.69 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 | C20H27N9O3S |
| Formula Weight | 473.55 |
BMS-214662, MedChemExpress
MedChemExpress BMS-214662 is a potent and selective farnesyl transferase inhibitor with potent antitumor activity with an IC50 of 1.35 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 489.61 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | BMS-214662 |
| Grade | Research |
| SMILES | N#CC1=CC=C(N(CC2=CN=CN2)C[C@@H](CC3=CC=CC=C3)N(S(=O)(C4=CC=CS4)=O)C5)C5=C1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.59% |
| CAS | 195987-41-8 |
| Solubility Information | DMSO : ≥ 100 mg/mL (204.24 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 | C25H23N5O2S2 |
| Formula Weight | 489.61 |
SR3335, MedChemExpress
MedChemExpress SR3335 (ML 176) is a selective RORα inverse agonist that directly binds to RORα with a Ki of 220 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 405.34 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | SR3335 |
| Grade | Research |
| SMILES | O=S(C1=CC=CS1)(NC2=CC=C(C(C(F)(F)F)(C(F)(F)F)O)C=C2)=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 99.43% |
| CAS | 293753-05-6 |
| Solubility Information | DMSO : ≥ 100 mg/mL (246.71 mM) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | ML 176 |
| 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 | C13H9F6NO3S2 |
| Formula Weight | 405.34 |
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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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CZC24832, MedChemExpress
MedChemExpress CZC24832 is a highly selective and potent PI3Kγ inhibitor (IC50=27 nM) with apparent dissociation constants (Kdapp) of 19 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 |
Litronesib Racemate, MedChemExpress
MedChemExpress Litronesib Racemate (LY2523355 Racemate) is the racemate of litronesib. Litronesib is a selective, allosteric inhibitor of kinesin Eg5.
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| Molecular Weight (g/mol) | 511.7 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Litronesib Racemate |
| Grade | Research |
| SMILES | CC(C)(C)C(N1C(C2=CC=CC=C2)(CNS(CCNCC)(=O)=O)SC(NC(C(C)(C)C)=O)=N1)=O |
| Percent Purity | 99.2% |
| CAS | 546111-97-1 |
| Solubility Information | DMSO : 100 mg/mL (195.43 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | LY2523355 Racemate |
| 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 |