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Filtered Search Results
eMolecules 49672-69-7 | 1,?4-?Dioxaspiro[4.5]?decan-?7-?amine | MFCD19373870 | 1g
Medchem Express | STING agonist-3 (trihydrochloride) | 5mg | 784543614 | HY-103665A | | 860.200 | C37H45Cl3N12O6
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Medchemexpress LLC Niemann-Pick C2 (NPC2) protein | >95.0% | 5 UG
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Recombinant rat Niemann-Pick C2 (NPC2) protein produced in HEK293 cells with a C-terminal 6xHis tag. Supplied lyophilized for biochemical and cell biology research into cholesterol trafficking and lipid metabolism; available in small research quantities such as 5 μg.
- Recombinant protein expressed in HEK293 cells.
- C-terminal 6xHis tag for detection and purification.
- Sequence corresponds to residues E20-G149 of rat NPC2.
- Lyophilized from 0.22 μm filtered PBS, pH 7.4.
- Purity greater than 95% by reducing SDS-PAGE.
- Store at -20°C; reconstituted material stable short term at 4°C.
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eMolecules Chem-Impex Trifluoroethanol 10kg 342449200 04832 0 000 75-89-8 MFCD00004672 100 040 C2H3F3O
Chem-Impex Trifluoroethanol 10kg 342449200 04832 0 000 75-89-8 MFCD00004672 100 040 C2H3F3O
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eMolecules 1,1,1,3,3,3-Hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol | 449804-09-5 | | 1g
Apollo Scientific | 1,1,1,3,3,3-Hexafluoro-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propan-2-ol | 1g | 562429211 | PC32786 | 95.000 | 449804-09-5 | | 370.100 | C15H17BF6O3
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Medchemexpress LLC Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct | 95464-05-4 | 98.5% | 816.64 | 100 G
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Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl2, a phosphine ligand palladium(II) complex. It serves as a versatile precatalyst for various cross-coupling reactions.
- Stabilizes reaction intermediates and lowers reaction activation energy in coupling reactions.
- Useful in Suzuki-Miyaura coupling reaction studies.
- Efficiently catalyzes various cross-coupling reactions.
- Suitable for modifying complex bioactive molecules containing free amino groups.
- Product can be purified by column chromatography before biological activity testing.
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eMolecules 3 6-DICHLORO-4-FLUOROPYR 100MG
5000192375 3 6-DICHLORO-4-FLUOROPYR 100MG
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eMolecules 3 6-DICHLORO-4-FLUOROPYR 250MG
5000192546 3 6-DICHLORO-4-FLUOROPYR 250MG
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Chemscene CHEMSCENE
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5000576361 DICHLORO 1 3-BIS DIPHENYLP 1KG
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Medchemexpress LLC HY-103349 5mg Medchemexpress, PETCM CAS:10129-56-3 Purity:>98%
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Medchemexpress, HY-103349 5mg PETCM CAS:10129-56-3 PETCM is an activator of caspase-3. PETCM can induces cell apoptosis and stimulate apoptosome formation in HeLa cell cytosols. 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 2,6-Dichloro-3-cyanopyridine | 40381-90-6 | 173.00 | 5 G
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2,6-Dichloro-3-cyanopyridine is a biochemical reagent. It can be used as a biological material or organic compound for life science related research.
- For research use only.
- Available in solid appearance.
- Color is white to off-white.
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Medchemexpress LLC Ethyl 3-[(tert-butylcarbamoyl)(N-[(4-chlorophenyl)methyl]formamido)methyl]-6-chloro-1H-indole-2-carboxylate | 1364488-67-4 | 98.3% | 50 MG
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YH239-EE is the ethyl ester of a small-molecule MDM2/p53 antagonist used in vitro to disrupt the p53-MDM2 interaction, inducing cell-cycle arrest and apoptosis in p53 wild-type acute myeloid leukemia (AML) cell lines. Supplied as a high-purity solid and available in multiple sizes and solution formats for cellular and biochemical assays.
- Antagonizes the p53-MDM2 interaction in vitro.
- Induces cell-cycle arrest and apoptosis in p53 wild-type AML cells.
- High purity (98.3%) solid, white to off-white, suitable for research assays.
- Available in multiple quantities and as a 10 mM solution in DMSO for cell-based studies.
- Molecular weight 504.41 g/mol; formula C25H27Cl2N3O4.
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Apexbio Technology LLC YH239-EE 1364488-67-4 50mg
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YH239-EE (CAS 1364488-67-4) is a small molecule antagonist of the p53-MDM2 interaction By disrupting the binding between p53 a tumor suppressor transcription factor and its negative regulator MDM2 YH239-EE reactivates p53 signaling pathways In acute myeloid leukemia (AML) cell models such as OCI-AML-3 MOLM-13 and NB4 YH239-EE inhibits cell proliferation and induces cell cycle arrest accompanied by significant accumulation of sub-G1 populations It promotes apoptosis with rates observed up to 13 1-fold over control in NB4 cells and activates caspase 3/7 in MOLM-13 cells Enantiomers display distinct biological activity with EC50 values of 7 5 M and 25 2 M YH239-EE serves as a valuable tool for studying p53-MDM2 modulation in cancer research
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eMolecules Chem-Impex 3-(Amidinothio)-1-propanesulfonic acid 1kg 272388741 27890 0 000 21668-81-5 MFCD00085942 198 260 C4H10N2O3S2
Chem-Impex 3-(Amidinothio)-1-propanesulfonic acid 1kg 272388741 27890 0 000 21668-81-5 MFCD00085942 198 260 C4H10N2O3S2
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eMolecules 2-BROMOETHANOL 5G
5000158493 2-BROMOETHANOL 5G
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eMolecules 3-BROMO-1-PROPANOL 25G
5000216673 3-BROMO-1-PROPANOL 25G
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