Pyrroles
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Pevonedistat, MedChemExpress
MedChemExpress Pevonedistat (MLN4924) is a potent and selective NEDD8-activating enzyme (NAE) inhibitor with an IC50 of 4.7 nM.
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| Molecular Weight (g/mol) | 443.52 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Pevonedistat |
| Grade | Research |
| SMILES | O=S(OC[C@@H]1C[C@@H](N2C3=NC=NC(N[C@H]4CCC5=C4C=CC=C5)=C3C=C2)C[C@@H]1O)(N)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 905579-51-3 |
| Solubility Information | DMSO : 62.5 mg/mL (140.92 mM; Need ultrasonic) |
| Synonym | MLN4924 |
| 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 | C21H25N5O4S |
| Formula Weight | 443.52 |
SB269652, MedChemExpress
MedChemExpress SB269652 is the first drug-like allosteric modulator of the dopamine D2 receptor (D2R); a new chemical probe that can differentiate D2R monomers from dimers or oligomers depending on the observed pharmacology.
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KW-8232 free base, MedChemExpress
MedChemExpress KW-8232 free base, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2.
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Verdiperstat, MedChemExpress
MedChemExpress Verdiperstat (AZD3241) is a selective, irreversible and orally active myeloperoxidase (MPO) inhibitor, with an IC50 of 630 nM, and can be used in the research of neurodegenerative brain disorders.
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| Molecular Weight (g/mol) | 253.32 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Verdiperstat |
| Grade | Research |
| SMILES | O=C(N1)C(NC=C2)=C2N(CCOC(C)C)C1=S |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.6% |
| CAS | 890655-80-8 |
| Solubility Information | DMSO : 150 mg/mL (592.14 mM; Need ultrasonic) |
| Synonym | AZD3241 |
| 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 | C11H15N3O2S |
| Formula Weight | 253.32 |
CMK, MedChemExpress
MedChemExpress CMK is a RSK2 kinase inhibitor which exhibits similar potency but less chemical stability compared with FMK.
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| Molecular Weight (g/mol) | 358.82 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | CMK |
| Grade | Research |
| SMILES | NC1=C(C2=NC=N1)C(C3=CC=C(C=C3)C)=C(N2CCCO)C(CCl)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.2% |
| CAS | 821794-90-5 |
| Solubility Information | DMSO : 150 mg/mL (418.04 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 | C18H19ClN4O2 |
| Formula Weight | 358.82 |
(R)-BPO-27, MedChemExpress
MedChemExpress (R)-BPO-27, the R enantiomer of BPO-27, is a potent, orally active and ATP-competitive CFTR inhibitor with an IC50 of 4 nM.
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| Molecular Weight (g/mol) | 548.34 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | (R)-BPO-27 |
| Grade | Research |
| SMILES | O=C(C1=CC=C(O[C@@H](C2=CC=C(Br)O2)C3=C(N(C)C4=O)C(C(N4C)=O)=C(C5=CC=CC=C5)N36)C6=C1)O |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 99.86% |
| CAS | 1415390-47-4 |
| Solubility Information | DMSO : ≥ 14.28 mg/mL (26.04 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 | C26H18BrN3O6 |
| Formula Weight | 548.34 |
GSK503, MedChemExpress
MedChemExpress GSK503 is a potent and specific inhibitor of EZH2 methyltransferase with Kiapp values of 3 to 27 nM.
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| Molecular Weight (g/mol) | 526.67 |
|---|---|
| Color | Light Gray |
| Physical Form | Solid |
| Chemical Name or Material | GSK503 |
| Grade | Research |
| SMILES | O=C(C1=CC(C2=CC=C(N3CCN(C)CC3)N=C2)=CC4=C1C(C)=CN4C(C)C)NCC5=C(C)C=C(C)NC5=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.73% |
| CAS | 1346572-63-1 |
| Solubility Information | DMSO : ≥ 44 mg/mL (83.54 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 | C31H38N6O2 |
| Formula Weight | 526.67 |
ALB-127158(a), MedChemExpress
MedChemExpress ALB-127158(a) is a potent and selective melanin concentrating hormone 1 (MCH1) receptor antagonist.
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| Molecular Weight (g/mol) | 404.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | ALB-127158(a) |
| Grade | Research |
| SMILES | O=C1C=C(OCC2=NC=C(F)C=C2)C=CN1C3=CC4=C(C=C3)C(CNCC5)=C5N4C |
| For Use With (Application) | Metabolism-protein/nucleotide metabolism |
| Percent Purity | 99.6% |
| CAS | 1173154-32-9 |
| Solubility Information | Ethanol : 2 mg/mL (4.95 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 | C23H21FN4O2 |
| Formula Weight | 404.44 |
Tivantinib, MedChemExpress
MedChemExpress Tivantinib is a highly selective c-Met tyrosine kinase inhibitor with a Ki of 355 nM.
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| Molecular Weight (g/mol) | 369.42 |
|---|---|
| Color | Brown |
| Physical Form | Solid |
| Chemical Name or Material | Tivantinib |
| Grade | Research |
| SMILES | O=C(NC1=O)[C@@H](C2=CN3C4=C(C=CC=C42)CCC3)[C@@H]1C5=CNC6=C5C=CC=C6 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.99% |
| CAS | 905854-02-6 |
| Solubility Information | DMSO : ≥ 100 mg/mL (270.69 mM) |
| Synonym | ARQ 197 |
| 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 | C23H19N3O2 |
| Formula Weight | 369.42 |
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 |
EPZ004777, MedChemExpress
MedChemExpress EPZ004777 is a potent, selective DOT1L inhibitor with an IC50 of 0.4 nM.
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| Molecular Weight (g/mol) | 539.67 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | EPZ004777 |
| Grade | Research |
| SMILES | NC1=C2C(N([C@H]3[C@H](O)[C@H](O)[C@@H](CN(C(C)C)CCCNC(NC4=CC=C(C(C)(C)C)C=C4)=O)O3)C=C2)=NC=N1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.02% |
| CAS | 1338466-77-5 |
| Solubility Information | DMSO : 80 mg/mL (148.24 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 | C28H41N7O4 |
| Formula Weight | 539.67 |
Optovin, MedChemExpress
MedChemExpress Optovin is a reversible photoactivated TRPA1 ligand that enables light-mediated neuronal excitation. Optovin activates TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues.
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| Molecular Weight (g/mol) | 315.41 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | Optovin |
| Grade | Research |
| SMILES | O=C1NC(S/C1=C\C2=C(C)N(C3=CC=CN=C3)C(C)=C2)=S |
| Percent Purity | 96.47% |
| CAS | 348575-88-2 |
| Solubility Information | DMSO : ≥ 37 mg/mL (117.31 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 | C15H13N3OS2 |
| Formula Weight | 315.41 |
Forodesine, MedChemExpress
MedChemExpress Forodesine (BCX-1777) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. Forodesine is a potent human lymphocyte proliferation inhibitor. Forodesine could induce apoptosis in leukemic cells by increasing the dGTP levels.
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NVP-AEW541, MedChemExpress
MedChemExpress NVP-AEW541 (AEW541) is a potent inhibitor of IGF-1R with IC50 of 0.15 μM, also inhibits InsR, with IC50 of 0.14 μM.
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| Molecular Weight (g/mol) | 439.55 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | NVP-AEW541 |
| Grade | Research |
| SMILES | NC1=C2C(N([C@@H]3C[C@@H](C3)CN4CCC4)C=C2C5=CC=CC(OCC6=CC=CC=C6)=C5)=NC=N1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.45% |
| CAS | 475489-16-8 |
| Solubility Information | DMSO : 50 mg/mL (113.75 mM; Need ultrasonic) |
| Synonym | AEW541 |
| 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 | C27H29N5O |
| Formula Weight | 439.55 |
AZD1981, MedChemExpress
MedChemExpress AZD1981 is a potent and selective CRTh2 antagonist; displaces radio-labelled PGD2 from human recombinant DP2 with high potency (pIC50 = 8.4).
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| Molecular Weight (g/mol) | 388.87 |
|---|---|
| Color | Gray |
| Physical Form | Solid |
| Chemical Name or Material | AZD1981 |
| Grade | Research |
| SMILES | O=C(O)CN1C(C)=C(SC2=CC=C(Cl)C=C2)C3=C1C=CC=C3NC(C)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.81% |
| CAS | 802904-66-1 |
| Solubility Information | DMSO : ≥ 31 mg/mL (79.72 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 | C19H17ClN2O3S |
| Formula Weight | 388.87 |