Pyrroles
Filtered Search Results
PCI-34051, MedChemExpress
MedChemExpress PCI-34051 is a potent and selective HDAC8 inhibitor with IC50 of 10 nM, with >200-fold selectivity over the other HDAC isoforms.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 296.32 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | PCI-34051 |
| Grade | Research |
| SMILES | COC(C=C1)=CC=C1CN2C3=CC(C(NO)=O)=CC=C3C=C2 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 97.28% |
| CAS | 950762-95-5 |
| Solubility Information | DMSO : ≥ 30 mg/mL (101.24 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 | C17H16N2O3 |
| Formula Weight | 296.32 |
Vinburnine, MedChemExpress
MedChemExpress Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
Oncrasin-1, MedChemExpress
MedChemExpress Oncrasin-1 is a potent and effective anticancer inhibitor that kills various human lung cancer cells with K-Ras mutations at low or submicromolar concentrations; also led to abnormal aggregation of PKCι in nucleus of sensitive cells but not in resistant cells.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 269.73 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Oncrasin-1 |
| Grade | Research |
| SMILES | O=CC1=CN(CC(C=C2)=CC=C2Cl)C3=CC=CC=C31 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.28% |
| CAS | 75629-57-1 |
| Solubility Information | DMSO : ≥ 43 mg/mL (159.42 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 | C16H12ClNO |
| Formula Weight | 269.73 |
Apyramide, MedChemExpress
MedChemExpress Apyramide is an anti-inflammatory agent (NSAID) and behaves as a prodrug of indomethacin (HY-14397). Indomethacin is a potent, blood-brain permeable and nonselective inhibitor of COX1 and COX2.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 490.93 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Apyramide |
| Grade | Research |
| SMILES | O=C(OC1=CC=C(NC(C)=O)C=C1)CC2=C(C)N(C(C3=CC=C(Cl)C=C3)=O)C4=C2C=C(OC)C=C4 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.06% |
| CAS | 68483-33-0 |
| 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 | C27H23ClN2O5 |
| Formula Weight | 490.93 |
Staurosporine, MedChemExpress
MedChemExpress Staurosporine is a potent, ATP-competitive and non-selective inhibitor of protein kinases with IC50s of 6 nM, 15 nM, 2 nM, and 3 nM for PKC, PKA, c-Fgr, and Phosphorylase kinase respectively. Staurosporine also inhibits TAOK2 with an IC50 of 3 μM. Staurosporine is an apoptosis inducer.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 466.53 |
|---|---|
| Color | Light Yellow |
| Physical Form | Powder |
| Chemical Name or Material | Staurosporine |
| Grade | Research |
| SMILES | O=C(NC1)C2=C1C3=C(C4=C2C5=C(C=CC=C5)N4[C@H]6C[C@@H](NC)[C@@H](OC)[C@]7(C)O6)N7C8=CC=CC=C83 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.0% |
| CAS | 62996-74-1 |
| Solubility Information | DMSO : 62.5 mg/mL (133.97 mM; Need ultrasonic) |
| Synonym | Antibiotic AM-2282 STS AM-2282 |
| 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 | C28H26N4O3 |
| Formula Weight | 466.53 |
Metergoline, MedChemExpress
MedChemExpress Metergoline is a serotonin (5-HT) receptor and dopamine receptors antagonist, with pKis of 8.64, 8.75 and 8.75 for 5-HT2A, 5-HT2B and 5-HT2C, respectively. Metergoline is a high-affinity ligand for the h5-HT7 receptor, with a Ki of 16 nM. Metergoline is also a reversible neural Na+ channels inhibitor. Metergoline is commonly used for the research of seasonal affective disorder, prolactin hormone regulation.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 403.52 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Metergoline |
| Grade | Research |
| SMILES | O=C(OCC1=CC=CC=C1)NC[C@H](C[C@@]23[H])CN(C)[C@]2([H])CC4=CN(C)C5=CC=CC3=C54 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.62% |
| CAS | 17692-51-2 |
| Solubility Information | DMSO : 125 mg/mL (309.77 mM; Need ultrasonic) |
| Health Hazard 1 | H302∣H312∣H332 |
| Purity Grade Notes | Research |
| Recommended Storage | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Shelf Life | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molecular Formula | C25H29N3O2 |
| Formula Weight | 403.52 |
Acrizanib, MedChemExpress
MedChemExpress Acrizanib (LHA510) is a VEGFR-2 inhibitor, with an IC50 of 17.4 nM for BaF3-VEGFR-2.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 445.4 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Acrizanib |
| Grade | Research |
| SMILES | O=C(N1C2=CC=C(OC3=NC=NC(CNC)=C3)C=C2C=C1)NC4=NN(C)C(C(F)(F)F)=C4 |
| Percent Purity | 98.23% |
| CAS | 1229453-99-9 |
| Solubility Information | DMSO : 41.67 mg/mL (93.56 mM; Need ultrasonic) |
| Synonym | LHA510 |
| 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 | C20H18F3N7O2 |
| Formula Weight | 445.4 |
Ribociclib, MedChemExpress
MedChemExpress Ribociclib (LEE01) 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.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 434.54 |
|---|---|
| Color | Light Yellow |
| Physical Form | Powder |
| Chemical Name or Material | Ribociclib |
| Grade | Research |
| SMILES | O=C(N(C)C)C(N1C2CCCC2)=CC(C1=N3)=CN=C3NC(N=C4)=CC=C4N5CCNCC5 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.52% |
| CAS | 1211441-98-3 |
| Solubility Information | DMSO : 20 mg/mL (46.03 mM; Need ultrasonic) |
| Synonym | LEE011 |
| 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 | C23H30N8O |
| Formula Weight | 434.54 |
CAY10650, MedChemExpress
MedChemExpress CAY10650 is a highly potent cytosolic phospholipase A2α (cPLA2α) inhibitor with an IC50 value of 12 nM. CAY10650 suppresses lipid droplets formation and PGE2 secretion.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 471.5 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | CAY10650 |
| Grade | Research |
| SMILES | O=C(CN1C(C=CC(C(O)=O)=C2)=C2C(C(C(C)C)=O)=C1)COC(C=C3)=CC=C3OC4=CC=CC=C4 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 1233706-88-1 |
| Solubility Information | DMSO : ≥ 43 mg/mL (91.20 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 | C28H25NO6 |
| Formula Weight | 471.5 |
GSK376501A, MedChemExpress
MedChemExpress GSK376501A is a selective peroxisome proliferator-activated receptor gamma (PPARγ) modulator for the treatment of type 2 diabetes mellitus.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
YM-90709, MedChemExpress
MedChemExpress YM-90709 is a novel IL-5 inhibitor which selectively blocks the binding of IL-5 to the IL-5 receptor (IL-5R).YM-90709 potently inhibits the binding of [125I]-IL-5 to IL-5R on human peripheral eosinophils and eosinophilic HL-60 clone 15 cells with IC50 values of 1.0 and 0.57 μM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 359.42 |
|---|---|
| Color | Orange |
| Physical Form | Solid |
| Chemical Name or Material | YM-90709 |
| Grade | Research |
| SMILES | CC(CC1=CC(OC)=C(OC)C=C12)(C)N3C2=CC4=NC5=CC=CC=C5N=C43 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.52% |
| CAS | 163769-88-8 |
| Solubility Information | DMSO : 62.5 mg/mL (173.89 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 | C22H21N3O2 |
| Formula Weight | 359.42 |
FMK, MedChemExpress
MedChemExpress FMK is a an irreversible RSK2 kinase inhibitor, that covalently modifies the C-terminal kinase domain of RSK.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 342.37 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | FMK |
| Grade | Research |
| SMILES | FCC(C1=C(C2=C(N=CN=C2N1CCCO)N)C3=CC=C(C=C3)C)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.05% |
| CAS | 821794-92-7 |
| Solubility Information | DMSO : 100 mg/mL (292.08 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 | C18H19FN4O2 |
| Formula Weight | 342.37 |
ML-098, MedChemExpress
MedChemExpress ML-098 (CID-7345532) is an activator of the GTP-binding protein Rab7 with an EC50 of 77.6 nM.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 309.36 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | ML-098 |
| Grade | Research |
| SMILES | O=C(C1=CN(CCOC2=CC(C)=CC=C2C)C3=C1C=CC=C3)O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.89% |
| CAS | 878978-76-8 |
| Solubility Information | DMSO : ≥ 29 mg/mL (93.74 mM) |
| Synonym | CID-7345532 |
| 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 | C19H19NO3 |
| Formula Weight | 309.36 |
Amcasertib, MedChemExpress
MedChemExpress Amcasertib (BBI503) is an orally active and small-molecule multi-kinase inhibitor. Amcasertib exhibits inhibitory activity against the NANOG and CD133 expression and cell viability in PC-9/GR cells. As an orally available cancer cell stemness kinase inhibitor with potential antineoplastic activity, it is currently being studied in phase I clinical trials in a number of cancers.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 539.69 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Amcasertib |
| Grade | Research |
| SMILES | O=C(C1=C(C)NC(/C=C2C(NC3=C/2C=C(C4=CSC(C5=CC=CC=C5)=N4)C=C3)=O)=C1C)NCCN(CC)CC |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.15% |
| CAS | 1129403-56-0 |
| Solubility Information | DMSO : ≥ 30 mg/mL (55.59 mM) |
| Synonym | BBI503 |
| 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 | C31H33N5O2S |
| Formula Weight | 539.69 |
(S)-Ketorolac, MedChemExpress
MedChemExpress (S)-Ketorolac is a nonsteroidal anti-inflammatory agent. (S)-ketorolac exhibits potent COX1 and COX2 enzyme inhibition.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
Learn More
| Molecular Weight (g/mol) | 255.27 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | (S)-Ketorolac |
| Grade | Research |
| SMILES | O=C(C1=CC=CC=C1)C2=CC=C3N2CC[C@@H]3C(O)=O |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.62% |
| CAS | 66635-92-5 |
| Solubility Information | DMSO : 200 mg/mL (783.48 mM; Need ultrasonic) |
| Synonym | (-)-Ketorolac |
| 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 | C15H13NO3 |
| Formula Weight | 255.27 |