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Filtered Search Results
LDN-212854, MedChemExpress
MedChemExpress LDN-212854 is a bone morphogenetic protein (BMP) inhibitor that potently inhibits ALK2 (IC50: 1.3 nM). LDN-212854 also inhibits ALK1 (IC50: 2.40 nM). LDN-212854 can be used in the research of fibrodysplasia ossificans progressive and cancers, such as hepatocellular carcinoma (HCC).
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| Molecular Weight (g/mol) | 406.48 |
|---|---|
| Color | Light Yellow |
| Physical Form | Solid |
| Chemical Name or Material | LDN-212854 |
| Grade | Research |
| SMILES | C12=C(C3=C4N=CC(C5=CC=C(N6CCNCC6)C=C5)=CN4N=C3)C=CC=C1N=CC=C2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 99.65% |
| CAS | 1432597-26-6 |
| Solubility Information | DMSO : ≥ 30 mg/mL (73.80 mM) |
| Health Hazard 1 | H301 |
| 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 | C25H22N6 |
| Formula Weight | 406.48 |
Citarinostat, MedChemExpress
MedChemExpress Citarinostat (ACY241) is a second generation potent, orally active and high-selective HDAC6 inhibitor with an IC50 of 2.6 nM (IC50s of 35 nM, 45 nM, 46 nM and 137 nM for HDAC1, HDAC2, HDAC3 and HDAC8, respectively). Citarinostat has anticancer effects.
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| Molecular Weight (g/mol) | 467.95 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Citarinostat |
| Grade | Research |
| SMILES | O=C(C1=CN=C(N(C2=CC=CC=C2Cl)C3=CC=CC=C3)N=C1)NCCCCCCC(NO)=O |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 95.0% |
| CAS | 1316215-12-9 |
| Solubility Information | DMSO : ≥ 30 mg/mL (64.11 mM) |
| Synonym | ACY241 |
| 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 | C24H26ClN5O3 |
| Formula Weight | 467.95 |
ABT-046, MedChemExpress
MedChemExpress ABT-046 is a potent, selective, and orally efficacious acyl CoA:diacylglycerol acyltransferase 1 (DGAT-1) inhibitor (IC50= 8 nM).
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| Molecular Weight (g/mol) | 350.41 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | ABT-046 |
| Grade | Research |
| SMILES | NC1=C(C2=CC=C([C@H]3CC[C@H](CC(O)=O)CC3)C=C2)C=NC4=CC=NN41 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.13% |
| CAS | 1031336-60-3 |
| Solubility Information | DMSO : 66.67 mg/mL (190.26 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 | C20H22N4O2 |
| Formula Weight | 350.41 |
CZ415, MedChemExpress
MedChemExpress CZ415 is a potent and highly selective mTOR inhibitor with a pIC50 of 8.07. CZ415 inhibits mTORC1 and mTORC2 protein complex.
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| Molecular Weight (g/mol) | 459.56 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | CZ415 |
| Grade | Research |
| SMILES | O=C(NCC)NC(C=C1)=CC=C1C2=NC3=C(CS(C3(C)C)(=O)=O)C(N4[C@@H](C)COCC4)=N2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.74% |
| CAS | 1429639-50-8 |
| Solubility Information | DMSO : 100 mg/mL (217.60 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 | C22H29N5O4S |
| Formula Weight | 459.56 |
BMS-833923, MedChemExpress
MedChemExpress BMS-833923 (XL-139) is an orally bioavailable small-molecule inhibitor of Smoothened with potential antineoplastic activity; inhibits BODIPY cyclopamine binding to SMO in a dose-dependent manner with an IC50 of 21 nM.
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| Molecular Weight (g/mol) | 473.57 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | BMS-833923 |
| Grade | Research |
| SMILES | O=C(NC1=CC(CNC)=CC=C1C)C2=CC=C(NC3=NC(C4=CC=CC=C4)=C5C=CC=CC5=N3)C=C2 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.21% |
| CAS | 1059734-66-5 |
| Solubility Information | DMSO : 50 mg/mL (105.58 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | XL-139 |
| 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 | C30H27N5O |
| Formula Weight | 473.57 |
MK-8617, MedChemExpress
MedChemExpress MK-8617 is an orally active pan-inhibitor of hypoxia-inducible factor prolyl hydroxylase 1-3 (HIF PHD1-3) with an IC50 of 1 nM for PHD2.
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| Molecular Weight (g/mol) | 443.45 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | MK-8617 |
| Grade | Research |
| SMILES | O=C(C1=CN=C(C2=NN=CC=C2)N=C1O)NC(C3=CC=C(OC)C=C3)C4=CC=C(OC)C=C4 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 98.02% |
| CAS | 1187990-87-9 |
| Solubility Information | DMSO : 6 mg/mL (13.53 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 | C24H21N5O4 |
| Formula Weight | 443.45 |
LDC000067, MedChemExpress
MedChemExpress LDC000067 is a highly specific CDK9 inhibitor with an IC50 value of 44±10 nM in vitro.
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| Molecular Weight (g/mol) | 370.43 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | LDC000067 |
| Grade | Research |
| SMILES | O=S(CC1=CC=CC(NC2=NC=NC(C3=CC=CC=C3OC)=C2)=C1)(N)=O |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.58% |
| CAS | 1073485-20-7 |
| Solubility Information | DMSO : ≥ 47 mg/mL (126.88 mM) |
| Synonym | LDC067 |
| 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 | C18H18N4O3S |
| Formula Weight | 370.43 |
BML-284, MedChemExpress
MedChemExpress BML-284 is a potent and cell-permeable Wnt signaling activator. BML-284 induces TCF-dependent transcriptional activity with an EC50 of 700 nM.
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| Molecular Weight (g/mol) | 350.37 |
|---|---|
| Color | White |
| Physical Form | Powder |
| Chemical Name or Material | BML-284 |
| Grade | Research |
| SMILES | NC1=NC(C2=CC=CC(OC)=C2)=CC(NCC3=CC=C(OCO4)C4=C3)=N1 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 97.48% |
| CAS | 853220-52-7 |
| Solubility Information | DMSO : ≥ 100 mg/mL (285.41 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 | C19H18N4O3 |
| Formula Weight | 350.37 |
Filorexant, MedChemExpress
MedChemExpress Filorexant (MK-6096) is an orally bioavailable potent and selective reversible antagonist of OX1 and OX2 receptor(<3 nM in binding).
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| Molecular Weight (g/mol) | 420.48 |
|---|---|
| Color | Light Brown |
| Physical Form | Powder |
| Chemical Name or Material | Filorexant |
| Grade | Research |
| SMILES | CC1=CC(C(N2C[C@H](COC3=CC=C(F)C=N3)CC[C@H]2C)=O)=C(C4=NC=CC=N4)C=C1 |
| For Use With (Application) | Neuroscience-Neuromodulation |
| Percent Purity | 98.95% |
| CAS | 1088991-73-4 |
| Solubility Information | DMSO : 100 mg/mL (237.82 mM; Need ultrasonic) |
| Synonym | MK-6096 |
| 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 | C24H25FN4O2 |
| Formula Weight | 420.48 |
GDC-0349, MedChemExpress
MedChemExpress GDC-0349 is a potent and selective ATP-competitive mTOR inhibitor with a Ki of 3.8 nM. GDC-0349 inhibits of both mTORC1 and mTORC2 complexes.
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| Molecular Weight (g/mol) | 452.55 |
|---|---|
| Color | Yellow |
| Physical Form | Solid |
| Chemical Name or Material | GDC-0349 |
| Grade | Research |
| SMILES | O=C(NCC)NC(C=C1)=CC=C1C2=NC3=C(CCN(C4COC4)C3)C(N5[C@@H](C)COCC5)=N2 |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 95.0% |
| CAS | 1207360-89-1 |
| Solubility Information | DMSO : ≥ 100 mg/mL (220.97 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 | C24H32N6O3 |
| Formula Weight | 452.55 |
PF-4840154, MedChemExpress
MedChemExpress PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel with EC50s of 97 and 23 nM, respectively. PF-4840154 elicits TrpA1-mediated nocifensive behaviour in mouse.
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| Molecular Weight (g/mol) | 466.62 |
|---|---|
| Color | Off-White |
| Physical Form | Solid |
| Chemical Name or Material | PF-4840154 |
| Grade | Research |
| SMILES | O=C(C1=CN=C(N2CCN(CC3COCCC3)CC2)N=C1NCC(C)C)NCC4=CC=CC=C4 |
| For Use With (Application) | COVID-19-immunoregulation |
| Percent Purity | 99.0% |
| CAS | 1332708-14-1 |
| Solubility Information | DMSO : 50 mg/mL (107.15 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 | C26H38N6O2 |
| Formula Weight | 466.62 |
Pyrimethamine, MedChemExpress
MedChemExpress Pyrimethamine(RP4753) is a medication used for protozoal infections; interferes with tetrahydrofolic acid synthesis from folic acid by inhibiting the enzyme dihydrofolate reductase (DHFR).
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| Molecular Weight (g/mol) | 248.71 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | Pyrimethamine |
| Grade | Research |
| SMILES | NC1=NC(N)=C(C2=CC=C(Cl)C=C2)C(CC)=N1 |
| For Use With (Application) | COVID-19-anti-virus |
| Percent Purity | 99.9% |
| CAS | 58-14-0 |
| Solubility Information | DMSO : 20 mg/mL (80.41 mM; Need ultrasonic) |
| Health Hazard 1 | H302 |
| Synonym | Pirimecidan Pirimetamin RP 4753 |
| 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 | C12H13ClN4 |
| Formula Weight | 248.71 |
KDM4D-IN-1, MedChemExpress
MedChemExpress KDM4D-IN-1 is a new histone lysine demethylase 4D (KDM4D) inhibitor with an IC50 value of 0.41±0.03 μM.
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| Molecular Weight (g/mol) | 225.21 |
|---|---|
| Color | Earth Yellow |
| Physical Form | Solid |
| Chemical Name or Material | KDM4D-IN-1 |
| Grade | Research |
| SMILES | OC1=NC2=C(C#N)C(C)=NN2C3=C1C=CC=N3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 99.91% |
| CAS | 2098902-68-0 |
| Solubility Information | DMSO : 7.14 mg/mL (31.70 mM; Need ultrasonic) |
| 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 | C11H7N5O |
| Formula Weight | 225.21 |
EPZ015666, MedChemExpress
MedChemExpress EPZ015666 (GSK3235025) is an orally available inhibitor of PRMT5 with an IC50 of 22 nM.
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| Molecular Weight (g/mol) | 383.44 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | EPZ015666 |
| Grade | Research |
| SMILES | O=C(NC[C@H](O)CN1CCC(C=CC=C2)=C2C1)C3=CC(NC4COC4)=NC=N3 |
| For Use With (Application) | Cancer-programmed cell death |
| Percent Purity | 98.96% |
| CAS | 1616391-65-1 |
| Solubility Information | DMSO : 100 mg/mL (260.80 mM; Need ultrasonic) |
| Synonym | GSK3235025 |
| 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 | C20H25N5O3 |
| Formula Weight | 383.44 |
mTOR inhibitor-3, MedChemExpress
MedChemExpress mTOR inhibitor-3 is a remarkably selective mTOR inhibitor with a Ki of 1.5 nM. mTOR inhibitor-3 suppresses mTORC1 and mTORC2 in cellular and in vivo pharmacokinetic (PK)/pharmacodynamic (PD) experiments.
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| Molecular Weight (g/mol) | 474.56 |
|---|---|
| Color | White |
| Physical Form | Solid |
| Chemical Name or Material | mTOR inhibitor-3 |
| Grade | Research |
| SMILES | O=C(NC1=CC=C(C2=NC(N3[C@@H](C)COCC3)=C4C(CN(C5=NC=CC=N5)CC4)=N2)C=C1)NCC |
| For Use With (Application) | Cancer-Kinase/protease |
| Percent Purity | 98.58% |
| CAS | 1207358-59-5 |
| Solubility Information | DMSO : 50 mg/mL (105.36 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 | C25H30N8O2 |
| Formula Weight | 474.56 |