Tetracarboxylic acids and derivatives
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Filtered Search Results
SGC3027, MedChemExpress
MedChemExpress SGC3027 is a histone methyltransferase inhibitor. SGC3027 is the first potent, selective and cell active chemical probe for PRMT7.
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EDO-S101, MedChemExpress
MedChemExpress EDO-S101 (Tinostamustine) is a pan HDAC inhibitor; inhibits HDAC6, HDAC1, HDAC2 and HDAC3 with IC50 values of 6 nM, 9 nM, 9 nM and 25 nM, respectively.
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| Molecular Weight (g/mol) | 415.36 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | EDO-S101 |
| Grade | Research |
| SMILES | O=C(NO)CCCCCCC1=NC2=CC(N(CCCl)CCCl)=CC=C2N1C |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.0% |
| CAS | 1236199-60-2 |
| Solubility Information | DMSO : 100 mg/mL (240.76 mM; Need ultrasonic) |
| Synonym | Tinostamustine |
| 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 | C19H28Cl2N4O2 |
| Formula Weight | 415.36 |
EGTA-AM, MedChemExpress
MedChemExpress EGTA-AM is a membrane permeable form of EGTA, can be passively loaded into cells to generate intracellular EGTA; EGTA-AM is also a Ca2+ chelator with slow chelating dynamics.
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BAPTA-AM, MedChemExpress
MedChemExpress BAPTA-AM is a well-known membrane permeable Ca2+ chelator. BAPTA-AM inhibits hERG channels, hKv1.3 and hKv1.5 channels in HEK 293 cells with IC50s of 1.3 μM, 1.45 μM and 1.23 μM, respectively.
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| Molecular Weight (g/mol) | 764.68 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | BAPTA-AM |
| Grade | Research |
| SMILES | O=C(OCOC(C)=O)CN(C(C=CC=C1)=C1OCCOC(C=CC=C2)=C2N(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O |
| Percent Purity | 98.38% |
| CAS | 126150-97-8 |
| Solubility Information | DMSO : 50 mg/mL (65.39 mM; Need ultrasonic) ∣H2O : < 0.1 mg/mL (ultrasonic) (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 | C34H40N2O18 |
| Formula Weight | 764.68 |
(+)-JQ-1, MedChemExpress
MedChemExpress (+)-JQ-1 (JQ1) is a potent, specific, and reversible BET bromodomain inhibitor, with IC50s of 77 and 33 nM for the first and second bromodomain (BRD4(1/2)). (+)-JQ-1 also activates autophagy.
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| Molecular Weight (g/mol) | 456.99 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | (+)-JQ-1 |
| Grade | Research |
| SMILES | O=C(C[C@H]1C2=NN=C(N2C3=C(C(C4=CC=C(C=C4)Cl)=N1)C(C)=C(S3)C)C)OC(C)(C)C |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.65% |
| CAS | 1268524-70-4 |
| Solubility Information | DMSO : ≥ 45 mg/mL (98.47 mM) |
| Synonym | JQ1 |
| 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 | C23H25ClN4O2S |
| Formula Weight | 456.99 |
Empagliflozin, MedChemExpress
MedChemExpress Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2.
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| Molecular Weight (g/mol) | 450.91 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | Empagliflozin |
| Grade | Research |
| SMILES | ClC(C=CC([C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C2)=C2CC(C=C3)=CC=C3O[C@H]4CCOC4 |
| For Use With (Application) | Metabolism-sugar/lipid metabolism |
| Percent Purity | 98.74% |
| CAS | 864070-44-0 |
| Solubility Information | DMSO : 50 mg/mL (110.89 mM; Need ultrasonic) ∣H2O : 0.11 mg/mL (0.24 mM; Need ultrasonic and warming) |
| Synonym | BI 10773 |
| 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 | C23H27ClO7 |
| Formula Weight | 450.91 |
ARQ 531, MedChemExpress
MedChemExpress ARQ 531 (MK-1026) is a reversible non-covalent and orally active inhibitor of Bruton’s Tyrosine Kinase (BTK), with IC50s of 0.85 nM and 0.39 nM for WT-BTK and C481S-BTK, respectively.
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| Molecular Weight (g/mol) | 478.93 |
|---|---|
| Color | Off-White |
| Physical Form | Powder |
| Chemical Name or Material | ARQ 531 |
| Grade | Research |
| SMILES | O=C(C1=C(C=C(OC2=CC=CC=C2)C=C1)Cl)C3=CNC4=NC=NC(N[C@@H]5CC[C@@H](CO)OC5)=C34 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.52% |
| CAS | 2095393-15-8 |
| Solubility Information | DMSO : ≥ 50 mg/mL (104.40 mM) |
| Health Hazard 1 | H302∣H315∣H319∣H335 |
| Synonym | MK-1026 |
| 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 | C25H23ClN4O4 |
| Formula Weight | 478.93 |
Rupatadine Fumarate, MedChemExpress
MedChemExpress Rupatadine (UR-12592) Fumarate is a potent, orally active and long-lasting dual PAF/H1 antagonist, with Kis of 0.55 μM and 0.1 μM, respectively. Rupatadine Fumarate can be used for the research of allergic rhinitis and urticaria.
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| Molecular Weight (g/mol) | 532.03 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Rupatadine Fumarate |
| Grade | Research |
| SMILES | CC1=CN=CC(CN2CC/C(CC2)=C3C4=CC=C(Cl)C=C4CCC5=CC=CN=C5\3)=C1.O=C(O)/C=C/C(O)=O |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.15% |
| CAS | 182349-12-8 |
| Solubility Information | DMSO : 30 mg/mL (56.39 mM; Need ultrasonic and warming) |
| Health Hazard 1 | H302 |
| Synonym | UR-12592 Fumarate |
| 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 | C30H30ClN3O4 |
| Formula Weight | 532.03 |
BAPTA, MedChemExpress
MedChemExpress BAPTA is a non-permeable, selective extracellular calcium chelator, with 105-fold greater affinity for Ca2+ than Mg2+. BAPTA is a valuable tool to study the role of calcium in cell signaling.
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| Molecular Weight (g/mol) | 476.43 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | BAPTA |
| Grade | Research |
| SMILES | O=C(O)CN(C1=CC=CC=C1OCCOC2=CC=CC=C2N(CC(O)=O)CC(O)=O)CC(O)=O |
| Percent Purity | 97.0% |
| CAS | 85233-19-8 |
| Solubility Information | 1M NaOH : 100 mg/mL (209.89 mM; ultrasonic and adjust pH to 11 with NaOH) ∣DMSO : 15.62 mg/mL (32.79 mM; ultrasonic and warming and heat to 60°C) |
| 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 | C22H24N2O10 |
| Formula Weight | 476.43 |