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Filtered Search Results
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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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.
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| 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 |
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.
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| 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 |
Vinburnine, MedChemExpress
MedChemExpress Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator.
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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.
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| 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 |
RG7713, MedChemExpress
MedChemExpress RG7713 (RO5028442) is a highly potent and selective Brain-Penetrant Vasopressin 1a (V1a) receptor antagonist with Kis of 1 nM (hV1a) and 39 nM (mV1a).
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| Molecular Weight (g/mol) | 437.96 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | RG7713 |
| Grade | Research |
| SMILES | O=C(C1=CN(CCN(C)C)C2=C1C=CC(Cl)=C2)N3CCC4(C(C=CC=C5)=C5CO4)CC3 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 99.79% |
| CAS | 920022-47-5 |
| Solubility Information | DMSO : 20 mg/mL (45.67 mM; Need ultrasonic) |
| Synonym | RO5028442 |
| 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 | C25H28ClN3O2 |
| Formula Weight | 437.96 |
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.
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| 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 |
JNJ-7777120, MedChemExpress
MedChemExpress JNJ-7777120 is a selective H4R antagonist with Ki of 4 ±1 nM, exhibits >1000-fold selectivity over the other histamin receptors.
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| Molecular Weight (g/mol) | 277.75 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | JNJ-7777120 |
| Grade | Research |
| SMILES | O=C(C(N1)=CC2=C1C=CC(Cl)=C2)N3CCN(C)CC3 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.0% |
| CAS | 459168-41-3 |
| Solubility Information | DMSO : ≥ 50 mg/mL (180.02 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 | C14H16ClN3O |
| Formula Weight | 277.75 |
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.
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| 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 |
LY2452473, MedChemExpress
MedChemExpress LY2452473 is an orally bioavailable, selective androgen receptor modulator (SARM).
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Molecular Weight (g/mol) | 374.44 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | LY2452473 |
| Grade | Research |
| SMILES | O=C(N[C@@H]1CC(N(C2=C3C=C(C=C2)C#N)CC4=NC=CC=C4)=C3C1)OC(C)C |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.13% |
| CAS | 1029692-15-6 |
| Solubility Information | DMSO : 62.5 mg/mL (166.92 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 | C22H22N4O2 |
| Formula Weight | 374.44 |
AZ191, MedChemExpress
MedChemExpress AZ191 is a potent inhibitor that selectively inhibits DYRK1B with IC50 of 17 nM.
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| Molecular Weight (g/mol) | 429.52 |
|---|---|
| Color | Brown |
| Physical Form | Solid |
| Chemical Name or Material | AZ191 |
| Grade | Research |
| SMILES | CN1C2=CN=CC=C2C(C3=NC(NC4=CC=C(N5CCN(C)CC5)C=C4OC)=NC=C3)=C1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.7% |
| CAS | 1594092-37-1 |
| Solubility Information | DMSO : ≥ 30 mg/mL (69.85 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 | C24H27N7O |
| Formula Weight | 429.52 |
KY1220, MedChemExpress
MedChemExpress KY1220 is a compound that destabilizes both β-catenin and Ras, via targeting the Wnt/β-catenin pathway; with an IC50 of 2.1 μM in HEK293 reporter cells.
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| Molecular Weight (g/mol) | 314.32 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | KY1220 |
| Grade | Research |
| SMILES | O=C(/C(N1)=C/C2=CC=CN2C3=CC=C([N+]([O-])=O)C=C3)NC1=S |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 292168-79-7 |
| Solubility Information | DMSO : ≥ 100 mg/mL (318.15 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 | C14H10N4O3S |
| Formula Weight | 314.32 |
GSK376501A, MedChemExpress
MedChemExpress GSK376501A is a selective peroxisome proliferator-activated receptor gamma (PPARγ) modulator for the treatment of type 2 diabetes mellitus.
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UNC2025, MedChemExpress
MedChemExpress UNC2025 is a potent, ATP-competitive and highly orally active Mer/Flt3 inhibitor with IC50 values of 0.74 nM and 0.8 nM, respectively. UNC2025 is >45-fold selectivity for MERTK relative to Axl (IC50= 122 nM; Ki = 13.3 nM). UNC2025 exhibits an excellent PK properties, and can be used for the investigation of acute leukemia.
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| Molecular Weight (g/mol) | 476.66 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | UNC2025 |
| Grade | Research |
| SMILES | CN1CCN(CC2=CC=C(C3=CN([C@@H]4CC[C@@H](O)CC4)C5=NC(NCCCC)=NC=C53)C=C2)CC1 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 96.86% |
| CAS | 1429881-91-3 |
| Solubility Information | DMSO : 33.33 mg/mL (69.92 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 | C28H40N6O |
| Formula Weight | 476.66 |
MDL-29951, MedChemExpress
MedChemExpress MDL-29951 is a novel glycine antagonist of NMDA receptor activation, with Ki of 0.14 μM for [3H]glycine binding in vitro and in vivo.
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| Molecular Weight (g/mol) | 302.11 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | MDL-29951 |
| Grade | Research |
| SMILES | O=C(O)CCC1=C(C(O)=O)NC2=C1C(Cl)=CC(Cl)=C2 |
| For Use With (Application) | Neuroscience-Neurodegeneration |
| Percent Purity | 99.5% |
| CAS | 130798-51-5 |
| Solubility Information | DMSO : ≥ 50 mg/mL (165.50 mM) |
| Health Hazard 1 | H302∣H317 |
| 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 | C12H9Cl2NO4 |
| Formula Weight | 302.11 |