Unsaturated hydrocarbons
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- (162)
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- (1)
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- (23)
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- (16)
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- (2)
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- (2)
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- (1)
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Filtered Search Results
Promega Corporation JANELIA FLUOR 503 HALOTAG LIGA
PRHT1010 JANELIA FLUOR 503 HALOTAG LIGA
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eMolecules 536-20-9 | Pyridine-2,4,6-tricarboxylic acid | ChemScene | MFCD00778565 | 211.129 | C8H5NO6 | 95.000 | OC(=O)c1cc(nc(c1)C(O)=O)C(O)=O | 100mg | 718356514
Pyridine-2,4,6-tricarboxylic acid | ChemScene | 536-20-9 | MFCD00778565 | 211.129 | C8H5NO6 | 95.000 | OC(=O)c1cc(nc(c1)C(O)=O)C(O)=O | 100mg | 718356514
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Aobchem AOBCHEM
5001074608 2-BROMO-4-TRICYCLO 3.3.1.13 7
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Medchemexpress LLC 5-IODOPENT-1-YNE 250 mg
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5-IODOPENT-1-YNE 250MG
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Medchemexpress LLC 1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-N-(6-phenyl-3-pyridazinyl)-7H-purine-7-acetamide | 1638250-96-0 | MFCD29472267 | ≥95.0% | 391.4 | C19H17N7O3 | 10 MG
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ETC-159 is a potent, orally available porcupine (PORCN) inhibitor used in research to block Wnt ligand secretion and Wnt/β-catenin signaling. It inhibits β-catenin reporter activity with a reported IC50 of 2.9 nM and has been evaluated in preclinical and early clinical studies for Wnt-dependent cancers. Typical supplier purity is ≥95% and the compound is supplied as a crystalline solid.
- Potent PORCN inhibition with low nanomolar activity.
- Orally bioavailable for in vivo research applications.
- Blocks Wnt ligand secretion and downstream β-catenin signaling.
- Reported β-catenin reporter IC50 ~2.9 nM.
- High purity (≥95%) and crystalline solid form.
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Indofine Chemical Lycopene, 5 Mg
LYCOPENE 5 MG, Herbal Standards, C40H56, MW: 536.88, >98% by UV, 502-65-8, MFCD00017350
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Avanti Polar Lipids 16 1 9-CIS PC 25MG
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NC3073642 16 1 9-CIS PC 25MG
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Ambeed AMBEED
5000949215 VE-821 5MG
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Ambeed AMBEED
5000950364 VE-821 50MG
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Aobchem AOBCHEM
5001005958 PHENYLMETHYL 3-CYCLOPENTENE-1-
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Aobchem AOBCHEM
5001006494 PHENYLMETHYL 3-CYCLOPENTENE-1-
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Medchemexpress LLC Bay 65-1942 hydrochloride | 600734-06-3 | 99.4% | C22H26ClN3O4 | 100 MG
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Bay 65-1942 hydrochloride is an ATP-competitive and selective IKKβ inhibitor. This compound is intended for research use only. In vitro studies show that delivery of Bay 65-1942 prior to ischemia significantly decreases left ventricular infarct size. In vivo, it demonstrates synergistic inhibition of cell viability and induces caspase 3/7 activation when combined with AZD6244 in MYL-R cells.
- Acts as an ATP-competitive and selective IKKβ inhibitor
- Decreases left ventricular infarct size in vitro
- Attenuates CK-MB levels in vivo
- Demonstrates synergistic inhibition of cell viability with AZD6244
- Induces caspase 3/7 activation with AZD6244
- Suitable for research applications
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eMolecules 3-CYCLOPENTENE-1-OL 10G
5000163297 3-CYCLOPENTENE-1-OL 10G
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eMolecules 287944-10-9 | Cyclopentene-1-boronic acid, pinacol ester | Combi-Blocks, Inc. | MFCD08669391 | 194.080 | C11H19BO2 | 95.000 | CC1(C)OB(OC1(C)C)C1=CCCC1 | 500g | 854190032
Cyclopentene-1-boronic acid, pinacol ester | Combi-Blocks, Inc. | 287944-10-9 | MFCD08669391 | 194.080 | C11H19BO2 | 95.000 | CC1(C)OB(OC1(C)C)C1=CCCC1 | 500g | 854190032
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Medchemexpress LLC Tau protein (592-597), human TFA | 2703746-44-3 | 95.2% | 868.94 | 50 MG
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Tau protein (592-597), human TFA is a peptide fragment of human Tau protein. The dysfunction of Tau protein is involved in neurodegeneration and dementia.
- Peptide fragment of human Tau protein.
- Involved in neurodegeneration and dementia research.
- Purity of 95.17%.
- Molecular weight of 868.94.
- White to off-white solid appearance.
- Powder storage: 2 years at -80°C, 1 year at -20°C.
- In solvent storage: 6 months at -80°C, 1 month at -20°C (sealed storage, away from moisture).
- Soluble in H2O at ≥ 2 mg/mL.
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