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Filtered Search Results
ITX3, MedChemExpress
MedChemExpress ITX3 is a specific and nontoxic inhibitor of the TrioN (N-terminal GEF domain of the multidomain Trio protein) with IC50 of 76 uM; inhibits TrioN-stimulated RhoG exchange in vitro.
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| Molecular Weight (g/mol) | 371.45 |
|---|---|
| Color | Light Green |
| Physical Form | Solid |
| Chemical Name or Material | ITX3 |
| Grade | Research |
| SMILES | O=C(/C1=C\C2=C(C)N(C(C)=C2)C3=CC=CC=C3)N4C(S1)=NC5=CC=CC=C45 |
| Percent Purity | 98.01% |
| CAS | 347323-96-0 |
| Solubility Information | DMSO : 2 mg/mL (5.38 mM; ultrasonic and warming and heat to 80°C) |
| 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 | C22H17N3OS |
| Formula Weight | 371.45 |
Mebhydrolin, MedChemExpress
MedChemExpress Mebhydrolin is a specific histamine H1 receptor antagonist.
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BQ-788, MedChemExpress
MedChemExpress BQ-788 is a potent, selective ETB receptor antagonist with IC50 of 1.2 nM for inhibition of ET-1 binding to human Girardi heart cells, poorly inhibiting the binding to ETA receptors in human neuroblastoma cell line SK-N-MC cells with IC50 of 1300 nM.
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| Molecular Weight (g/mol) | 641.8 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | BQ-788 |
| Grade | Research |
| SMILES | CCCC[C@H](C(O)=O)NC([C@@H](CC1=CN(C(OC)=O)C2=CC=CC=C12)NC([C@H](CC(C)(C)C)NC(N3[C@H](C)CCC[C@@H]3C)=O)=O)=O |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 98.28% |
| CAS | 173326-37-9 |
| Solubility Information | DMSO : 170 mg/mL (264.88 mM; ultrasonic and warming and heat to 60°C) |
| 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 | C34H51N5O7 |
| Formula Weight | 641.8 |
BMS-986158, MedChemExpress
MedChemExpress BMS-986158 is a potent BET inhibitor with IC50s of 6.6 and 5 nM in NCI-H211 small cell lung cancer (SCLC) cells and MDA-MB231 triple negative breast cancer (TNBC) cells, respectively.
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| Molecular Weight (g/mol) | 495.62 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | BMS-986158 |
| Grade | Research |
| SMILES | OC(C)(C)C1=CC=C2C(N([C@H](C3=CC=CC=C3)C4CCOCC4)C5=C2N=CC(C6=C(C)N=NN6C)=C5)=C1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.22% |
| CAS | 1800340-40-2 |
| Solubility Information | DMSO : 50 mg/mL (100.88 mM; Need ultrasonic) ∣H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| 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 | C30H33N5O2 |
| Formula Weight | 495.62 |
Mebhydrolin napadisylate, MedChemExpress
MedChemExpress Mebhydrolin napadisylate is a specific histamine H1 receptor antagonist.
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Eniporide hydrochloride, MedChemExpress
MedChemExpress Eniporide hydrochloride (EMD-96785 hydrochloride) is a potent Na+/H+ exchange inhibitor.
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| Molecular Weight (g/mol) | 356.83 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Eniporide hydrochloride |
| Grade | Research |
| SMILES | CS(=O)(C1=C(N2C=CC=C2)C=C(C)C(C(NC(N)=N)=O)=C1)=O.[H]Cl |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.05% |
| CAS | 211813-86-4 |
| Solubility Information | DMSO : 55 mg/mL (154.14 mM; Need ultrasonic) ∣H2O : 4.17 mg/mL (11.69 mM; ultrasonic and warming and heat to 60°C) |
| Synonym | EMD-96785 hydrochloride |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C14H17ClN4O3S |
| Formula Weight | 356.83 |
PhiKan 083 hydrochloride, MedChemExpress
MedChemExpress PhiKan 083 hydrochloride is a carbazole derivative, which binds to the surface cavity and stabilizes Y220C (a p53 mutant), with a Kd of 167 μM, and a relative binding affinity (Kd) of 150 μM in Ln229 cells.
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Osimertinib mesylate, MedChemExpress
MedChemExpress Osimertinib mesylate (AZD9291 mesylate) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. Osimertinib overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
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| Molecular Weight (g/mol) | 595.71 |
|---|---|
| Color | Yellow |
| Physical Form | Powder |
| Chemical Name or Material | Osimertinib mesylate |
| Grade | Research |
| SMILES | C=CC(NC1=CC(NC2=NC=CC(C3=CN(C)C4=C3C=CC=C4)=N2)=C(OC)C=C1N(CCN(C)C)C)=O.CS(=O)(O)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.74% |
| CAS | 1421373-66-1 |
| Solubility Information | DMSO : 13.89 mg/mL (23.32 mM; ultrasonic and warming and heat to 80°C) |
| Health Hazard 1 | H315∣H319∣H335 |
| Synonym | AZD-9291 mesylate Mereletinib mesylate |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C29H37N7O5S |
| Formula Weight | 595.71 |
Ribociclib succinate, MedChemExpress
MedChemExpress Ribociclib succinate (LEE011 succinate) is a highly specific CDK4/6 inhibitor with IC50 values of 10 nM and 39 nM, respectively, and is over 1,000-fold less potent against the cyclin B/CDK1 complex.
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| Molecular Weight (g/mol) | 552.63 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Ribociclib succinate |
| Grade | Research |
| SMILES | O=C(N(C)C)C(N1C2CCCC2)=CC(C1=N3)=CN=C3NC(N=C4)=CC=C4N5CCNCC5.OC(CCC(O)=O)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.01% |
| CAS | 1374639-75-4 |
| Solubility Information | DMSO : 41.67 mg/mL (75.40 mM; Need ultrasonic) ∣H2O : 4.17 mg/mL (7.55 mM; ultrasonic and warming and heat to 60°C) |
| Synonym | LEE011 succinate |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C27H36N8O5 |
| Formula Weight | 552.63 |
HLCL-61 hydrochloride, MedChemExpress
MedChemExpress HLCL-61 hydrochloride is a first-in-class inhibitor of protein arginine methyltransferase 5 (PRMT5).
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| Molecular Weight (g/mol) | 380.91 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | HLCL-61 hydrochloride |
| Grade | Research |
| SMILES | [H]Cl.COC1=CC=CC=C1CNCC2=CC3=C(C=C2)N(CC)C4=C3C=CC=C4 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.95% |
| CAS | 1158279-20-9 |
| Solubility Information | DMSO : 50 mg/mL (131.26 mM; Need ultrasonic) ∣H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C23H25ClN2O |
| Formula Weight | 380.91 |
(E)-SIS3, MedChemExpress
MedChemExpress (E)-SIS3 is a potent and selective inhibitor of Smad3 with an IC50 of 3 μM for Smad3 phosphorylation. (E)-SIS3 inhibits the myofibroblast differentiation of fibroblasts by TGF-β1.
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| Molecular Weight (g/mol) | 489.99 |
|---|---|
| Color | Deep Yellow |
| Physical Form | Solid |
| Chemical Name or Material | (E)-SIS3 |
| Grade | Research |
| SMILES | [H]Cl.O=C(/C=C/C1=C(N(C2=NC=CC=C21)C)C3=CC=CC=C3)N4CC5=C(CC4)C=C(C(OC)=C5)OC.[E] |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.0% |
| CAS | 521984-48-5 |
| Solubility Information | DMSO : 125 mg/mL (255.11 mM; Need ultrasonic) ∣H2O : < 0.1 mg/mL (ultrasonic;warming;heat to 60°C) (insoluble) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C28H28ClN3O3 |
| Formula Weight | 489.99 |
Ulixertinib hydrochloride, MedChemExpress
MedChemExpress Ulixertinib hydrochloride (BVD-523 hydrochloride) is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC50 of <0.3 nM against ERK2. Ulixertinib hydrochloride inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line.
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| Molecular Weight (g/mol) | 469.79 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Ulixertinib hydrochloride |
| Grade | Research |
| SMILES | O=C(C1=CC(C2=CC(NC(C)C)=NC=C2Cl)=CN1)N[C@@H](C3=CC=CC(Cl)=C3)CO.[H]Cl |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.81% |
| CAS | 1956366-10-1 |
| Solubility Information | DMSO : 100 mg/mL (212.86 mM; Need ultrasonic) ∣H2O : 0.1 mg/mL (0.21 mM; ultrasonic and warming and heat to 80°C) |
| Synonym | BVD-523 hydrochlorideVRT752271 hydrochloride |
| Purity Grade Notes | Research |
| Recommended Storage | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Shelf Life | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molecular Formula | C21H23Cl3N4O2 |
| Formula Weight | 469.79 |