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Filtered Search Results
Medchemexpress LLC HY-10043 10mg Medchemexpress, gamma-secretase modulator 1 CAS:1172637-87-4 Purity:>98%
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Medchemexpress, HY-10043 10mg gamma-secretase modulator 1 CAS:1172637-87-4 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC M-89 | 2363165-42-6 | 99.1% | 50 MG
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M-89 is a highly potent and specific menin inhibitor that targets the menin-mixed lineage leukemia (Menin-MLL) protein-protein interaction. It has potential for studying MLL leukemia by inhibiting cell growth in leukemia cell lines and inducing apoptosis. It is for research use only.
- Highly potent and specific menin inhibitor
- Inhibits menin-MLL protein-protein interaction
- Potential for studying MLL leukemia
- Inhibits cell growth in leukemia cell lines carrying MLL fusion
- Induces time- and dose-dependent apoptosis in MV4;11 cells
- Stabilizes cellular menin protein in MV4;11 and MOLM-13 cells
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eMolecules 1825355-56-3 | Medchem Express | Ribocil-C | 5mg | 446269873 | HY-19488A | 419.51 | C21H21N7OS
Ambeed | (3-Bromo-45-dimethylphenyl)boronic acid | 100mg | 714083990 | A1536329 | 2828439-67-2 | 228.880 | C8H10BBrO2
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eMolecules 1213362-28-7 | (R)-3-(4-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | MFCD07784070 | 185.650 | C9H12ClNO | 97.000 | N[C@H](CCO)c1ccc(Cl)cc1 | 1g | 112525513
(R)-3-(4-CHLOROPHENYL)-BETA-ALANINOL | AstaTech | 1213362-28-7 | MFCD07784070 | 185.650 | C9H12ClNO | 97.000 | N[C@H](CCO)c1ccc(Cl)cc1 | 1g | 112525513
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Medchemexpress LLC HY-101085 10mg Medchemexpress, SKL2001 CAS:909089-13-0 Purity:>98%
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Medchemexpress, HY-101085 10mg SKL2001 CAS:909089-13-0 SKL2001 is an agonist of the Wnt/β-catenin pathway, with anti-cancer activity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1246560-33-7 | Medchem Express | VS-5584 | 5mg | 446267557 | HY-16585 | MFCD25372027 | 354.418 | C17H22N8O
Medchem Express | M-110 | 5mg | 446261904 | HY-12830 | 1395048-49-3 | MFCD28053523 | 445.950 | C22H28ClN5O3
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eMolecules 65039-08-9 | 1-Ethyl-3-methylimidazolium bromide | Chem-Impex | MFCD03427610 | 191.072 | C6H11BrN2 | 99.000 | [Br-].CCn1cc[n+](C)c1 | 25g | 386904216
1-Ethyl-3-methylimidazolium bromide | Chem-Impex | 65039-08-9 | MFCD03427610 | 191.072 | C6H11BrN2 | 99.000 | [Br-].CCn1cc[n+](C)c1 | 25g | 386904216
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eMolecules 6775-78-6 | 6-Chloroimidazo[1,2-b]pyridazine | Combi-Blocks | MFCD07778345 | 153.570 | C6H4ClN3 | 98.000 | Clc1ccc2nccn2n1 | 5g | 117534047
6-Chloroimidazo[1,2-b]pyridazine | Combi-Blocks | 6775-78-6 | MFCD07778345 | 153.570 | C6H4ClN3 | 98.000 | Clc1ccc2nccn2n1 | 5g | 117534047
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Medchemexpress LLC HY-108940 10mg Medchemexpress, GlyRS-IN-1 CAS:112921-11-6 Purity:>98%
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Medchemexpress, HY-108940 10mg GlyRS-IN-1 CAS:112921-11-6 GlyRS-IN-1 is a glycyl-tRNA synthase (GlyRS) inhibitor extracted from patent WO 2017066459 A1. GlyRS-IN-1 can also inhibit the growth of bacteria. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 60246-64-2 | 3-[(2-Aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one | Oakwood Chemicals | MFCD00174834 | 333.450 | C21H19NOS | 0.000 | Nc1ccccc1SC(CC(=O)c1ccccc1)c1ccccc1 | 10mg | 480157686
3-[(2-Aminophenyl)sulfanyl]-1,3-diphenylpropan-1-one | Oakwood Chemicals | 60246-64-2 | MFCD00174834 | 333.450 | C21H19NOS | 0.000 | Nc1ccccc1SC(CC(=O)c1ccccc1)c1ccccc1 | 10mg | 480157686
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Medchemexpress LLC Tenofovir amibufenamide | 1571076-26-0 | 99.7% | C22H31N6O5P | 10MG
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Tenofovir amibufenamide is an orally active tenofovir prodrug used in antiviral research to inhibit hepatitis B virus (HBV). It is applied in preclinical studies of chronic hepatitis B to evaluate tenofovir-based antiviral activity and pharmacology.
- Orally active tenofovir prodrug suitable for in vivo and in vitro studies.
- Demonstrated inhibition of hepatitis B virus replication.
- Used in chronic hepatitis B research applications.
- High purity (99.7%).
- Molecular formula C22H31N6O5P, molecular weight 490.49 g/mol.
- Available in small research-scale quantities for preclinical use.
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eMolecules 35899-54-8 | SIBA | MFCD00056008 | 50mg
Pharmablock | (3R)-NN-dimethylpyrrolidin-3-amine dihydrochloride | 500mg | 551228355 | PB95540-1 | 864448-61-3 | MFCD08704347 | 187.110 | C6H16Cl2N2
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eMolecules 1380288-87-8 | Medchem Express | Pinometostat | 5mg | 446266072 | HY-15593 | MFCD24849416 | 562.719 | C30H42N8O3
ChemScene | 4-(2-Methoxyethyl)benzaldehyde | 100mg | 761228891 | CS-0616362 | 1781092-86-1 | 164.204 | C10H12O2
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eMolecules 51036-79-4 | 2-(2-IMIDAZOLYL)ETHANOL | AstaTech | MFCD06655989 | 112.132 | C5H8N2O | 97.000 | OCCc1ncc[nH]1 | 1g | 248473110
2-(2-IMIDAZOLYL)ETHANOL | AstaTech | 51036-79-4 | MFCD06655989 | 112.132 | C5H8N2O | 97.000 | OCCc1ncc[nH]1 | 1g | 248473110
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Medchemexpress LLC 2-[4-[[4-hydroxy-3-[2-(4-nitrophenyl)ethynyl]-5-propan-2-ylphenyl]methyl]-3,5-dimethylphenoxy]aceti | 447415-26-1 | 99.4% | C28H27NO6 | 10MG
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NH-3 is an orally active, reversible thyroid hormone receptor (THR) antagonist that inhibits hormone binding and cofactor recruitment; it shows potent THR inhibition (IC50 55 nM) and contains an alkyne group enabling copper-catalyzed azide-alkyne cycloaddition for click chemistry applications.
- Orally active, reversible thyroid hormone receptor antagonist.
- Potent THR inhibition with reported IC50 of 55 nM.
- Contains an alkyne group for copper-catalyzed click chemistry.
- High purity suitable for research use (≈99.4%).
- Available as powder and DMSO solution formats for flexibility in assays.
- Recommended storage conditions provided to preserve stability.
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