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Filtered Search Results
eMolecules 451-82-1 | 2-Fluorophenylacetic acid | Ambeed | MFCD00004315 | 154.140 | C8H7FO2 | 98.000 | OC(=O)Cc1ccccc1F | 5g | 490510646
2-Fluorophenylacetic acid | Ambeed | 451-82-1 | MFCD00004315 | 154.140 | C8H7FO2 | 98.000 | OC(=O)Cc1ccccc1F | 5g | 490510646
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Strem, An Ascensus Company CAS 1198080-53-3. 50mg. 1-(2R)-1-[(11bR)-Dinaphtho[21-d12-f][132]dioxaphosphepin-4-yloxy]propan-2-yl-3-phenylurea min. 97% UREAPhos. MFCD18827627
CAS 1198080-53-3. 50mg. 1-(2R)-1-[(11bR)-Dinaphtho[21-d12-f][132]dioxaphosphepin-4-yloxy]propan-2-yl-3-phenylurea min. 97% UREAPhos. MFCD18827627. Molecular Weight 508.50. Molecular Formula C30H25N2O4P. Color/form white pwdr. Strem 15-2200. http//www.strem.com/catalog/v/15-2200/
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eMolecules 2095064-06-3 | Medchem Express | Posenacaftor (sodium) | 5mg | 596608012 | HY-109187A | 467.497 | C27H26NNaO5
AbaChemScene | 5-Cyclopropyl-1H-pyrazole-3-carboxylic acid | 1g | 410744092 | CS-0037041 | 401629-04-7 | MFCD04967194 | 152.153 | C7H8N2O2
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Medchemexpress LLC HY-107324 10mg Medchemexpress, β-Elemene CAS:515-13-9 Purity:>98%
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Medchemexpress, HY-107324 10mg β-Elemene CAS:515-13-9 β-Elemene ((-)-β-Elemene; Levo-β-elemene) is isolated from natural plant Curcuma wenyujin with an antitumor activity. β-Elemene can induce cell apoptosis. 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 HY-100315 10mg Medchemexpress, Tyrosine kinase-IN-1 CAS:705946-27-6 Purity:>98%
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Medchemexpress, HY-100315 10mg Tyrosine kinase-IN-1 CAS:705946-27-6 Tyrosine kinase-IN-1 is a multi-targeted tyrosine kinase inhibitor with IC 50 s of 4, 20, 4, 2 nM for KDR , Flt-1 , FGFR1 and PDGFRα , respectively. 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 N-Benzyllinolenamide | 883715-18-2 | 5 MG
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N-Benzyllinolenamide is a natural macamide isolated from Lepidium meyenii. It functions as an inhibitor of fatty acid amide hydrolase (FAAH) with an IC50 of 41.8 μM. It is for research use only and not intended for sale to patients. The product is an off-white to light yellow solid. It is also an alkaloid from plants.
- Natural macamide isolated from Lepidium meyenii.
- Functions as an inhibitor of fatty acid amide hydrolase (FAAH).
- For research use only.
- Off-white to light yellow solid.
- Alkaloid from plants.
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eMolecules 153774-39-1 | Allyl 3-amino-4-fluorobenzoate | MFCD20723071 | 250mg
Medchem Express | Abemaciclib metabolite M20 | 5mg | 506403951 | HY-129336 | 2138499-06-4 | 522.605 | C27H32F2N8O
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Medchemexpress LLC 6-methoxy-2-(5-methyl-2-furanyl)-N-(1-methyl-4-piperidinyl)-7-[3-(1-pyrrolidinyl)propoxy]-4-quinolin | 1846570-31-7 | 98.7% | 478.63 g/mol | C28H38N4O3 | 50 MG
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CM-272 is a reversible small-molecule inhibitor that selectively targets the histone methyltransferase G9a and DNA methyltransferases (DNMTs), showing antiproliferative and pro-apoptotic activity in preclinical cancer models and inducing immunogenic responses.
- Dual inhibition of G9a and DNA methyltransferases enables epigenetic modulation.
- Low-nanomolar potency against primary target with measurable activity on DNMT isoforms.
- Demonstrated antiproliferative and pro-apoptotic effects in cellular and animal studies.
- High chemical purity suitable for research applications.
- Available in small milligram quantities for in vitro and in vivo experiments.
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eMolecules 120635-25-8 | Medchem Express | Mofegiline (hydrochloride) | 5mg | 446267652 | HY-16677A | MFCD00890215 | 233.69 | C11H14ClF2N
ChemScene | 4-Bromo-1-methyl-1H-pyrrole-2-carbonitrile | 100mg | 572188304 | CS-0095366 | 1289207-30-2 | MFCD18917074 | 185.024 | C6H5BrN2
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Medchemexpress LLC HY-12305 10mg Medchemexpress, Q-VD-OPh CAS:1135695-98-5 Purity:>98%
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Medchemexpress, HY-12305 10mg Q-VD-OPh CAS:1135695-98-5 Q-VD-OPh is an irreversible pan-caspase inhibitor with potent antiapoptotic properties; inhibits caspase 7 with an IC50 of 48 nM and 25-400 nM for other caspases including caspase 1, 3, 8, 9, 10, and 12. Q-VD-OPh can inhibits HIV infection. Q-VD-OPh is able to cross the blood-brain barrier. 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 913835-80-0 | (2-Bromo-6-fluorophenyl)boronic acid | Ambeed | MFCD05664309 | 218.820 | C6H5BBrFO2 | 97.000 | OB(O)c1c(F)cccc1Br | 1g | 552693452
(2-Bromo-6-fluorophenyl)boronic acid | Ambeed | 913835-80-0 | MFCD05664309 | 218.820 | C6H5BBrFO2 | 97.000 | OB(O)c1c(F)cccc1Br | 1g | 552693452
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Medchemexpress LLC EGFR-IN-17 100mg | 2817679-31-3 | 568.01 g/mol | C27H31ClN7O3P | 100 MG
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EGFR-IN-17 is a potent, selective small-molecule inhibitor of the epidermal growth factor receptor (EGFR) developed to overcome C797S-mediated resistance. It exhibits sub-nanomolar biochemical potency against mutant EGFR and is supplied as a high-purity solid for in vitro research use.
- Sub-nanomolar potency against mutant EGFR (reported IC50 0.0002 μM).
- Active against C797S/T790M/L858R EGFR mutants.
- High purity (≈98.2%) solid for laboratory use.
- Soluble in DMSO; sonication or warming may improve solubility.
- Multiple package sizes available for small-scale research.
- Storage recommendations provided for powder and solution formats.
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eMolecules 359625-79-9 | Medchem Express | Roluperidone | 5mg | 446269862 | HY-19469 | MFCD28502826 | 366.436 | C22H23FN2O2
AstaTech | (1-((13-DIOXOLAN-2-YL)METHYL)-1H-PYRAZOL-4-YL)BORONIC ACID PINACOL ESTER | 0.1g | 721956111 | 29371 | 95.000 | 864754-17-6 | MFCD08272028 | 280.130 | C13H21BN2O4
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Medchemexpress LLC Abemaciclib metabolite M18 | 2704316-81-2 | 98.01% | 10 MG
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Abemaciclib metabolite M18 (LSN3106729) is a metabolite of Abemaciclib and acts as a CDK inhibitor with antitumor activity. It has been utilized in conjunction with a CRBN ligand to engineer a PROTAC CDK4/6 degrader. The primary mechanism of action for CDK4/6 inhibitors involves the inhibition of retinoblastoma (RB) protein phosphorylation, leading to the induction of cell cycle arrest.
- Acts as a CDK inhibitor with antitumor activity.
- Utilized in conjunction with a CRBN ligand to engineer a PROTAC CDK4/6 degrader.
- Inhibits retinoblastoma (RB) protein phosphorylation.
- Induces cell cycle arrest.
- Promotes T-cell persistence and increases immunologic memory in mice that receive tumor-specific CD8+ T cells.
- Appears as an off-white to light yellow solid.
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eMolecules 202865-69-8 | (5-BROMO-2-FLUOROPHENYL)METHANAMINE HCL | MFCD00143426 | 5g
Ambeed | H-D-Dap(Boc)-OMe | 1g | 571783013 | A159875 | 363191-25-7 | MFCD11100944 | 218.253 | C9H18N2O4
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