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Filtered Search Results
eMolecules E3 LIGASE LIGAND 1A | 1948273-02-6 | | 0.25g
AstaTech | E3 LIGASE LIGAND 1A | 0.25g | 573027259 | AT10808 | 95.000 | 1948273-02-6 | | 444.590 | C23H32N4O3S
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5000426781 Z-VDVAD-FMK 25MG
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![eMolecules 4-Chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine | 71149-52-5 | MFCD09746275 | 5g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502138595.JPG-250.jpg)
eMolecules 4-Chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine | 71149-52-5 | MFCD09746275 | 5g
Ambeed | 4-Chloro-2-methyl-7H-pyrrolo[2,3-d]pyrimidine | 5g | 525201686 | A383893 | | 71149-52-5 | MFCD09746275 | 167.600 | C7H6ClN3
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Medchemexpress LLC (Z)-3-propyl-2-(o-tolylimino)thiazolidin-4-one | 1228116-62-8 | MFCD31560466 | 100mg
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(Z)-3-propyl-2-(o-tolylimino)thiazolidin-4-one is a drug impurity
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Medchemexpress LLC E/Z-HA155 25mg | 1229652-22-5 | 463.29 | C24H19BFNO5S | 25 MG
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A potent autotaxin (ATX) type I inhibitor for laboratory research, (E/Z)-HA155 is used to study cancer, fibrotic disease, inflammation, pain, and angiogenesis. The product is supplied as a high-purity solid and includes supporting structural and stability data for experimental use.
- Potent autotaxin (ATX) type I inhibitor for mechanistic and pharmacology studies.
- High purity suitable for analytical and biological assays.
- Supplied as a solid 25 mg quantity for small-scale experiments.
- Stable when stored as a powder at -20°C for extended periods.
- Structural identifiers and formula provided for computational and analytical workflows.
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Medchemexpress LLC S -3-N-Cbz-Amino-su 100mg
(S)-3-N-Cbz-Amino-succinimide (Compound 1d) is an antiepileptic agent that can inhibit pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced tonic convulsions in mice[1]
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Medchemexpress LLC Bcn-endo-PEG7-maleimide | 95.0% | 695.80 g/mol | C34H53N3O12 | 10 MG
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BCN-endo-PEG7-maleimide is a BCN-based click chemistry linker containing a seven-unit polyethylene glycol (PEG7) spacer and a terminal maleimide for selective thiol conjugation. It is designed for bioconjugation, antibody-drug conjugate linker assembly, and other strain-promoted click chemistry applications.
- Contains an endo-BCN moiety for strain-promoted click reactions.
- Includes a PEG7 spacer to improve solubility and flexibility.
- Has a terminal maleimide for selective conjugation to thiol groups.
- Suitable for bioconjugation and antibody-drug conjugate linker synthesis.
- Offered in small-scale research pack sizes for discovery workflows.
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5000352945 BOC-NH-PEG2-NH-BOC 500MG
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5000352941 AZIDO-PEG6-ACID 500MG
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5000352849 AZIDO-PEG3-C-BOC 250MG
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Medchemexpress LLC (E/Z)-IT-603 | 292168-90-2 | 99.9% | 1 ML
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(E/Z)-IT-603 is a mixture of E-IT-603 and Z-IT-603 that acts as an IκBα/c-Rel inhibitor and is supplied as a 10 mM solution in DMSO for research use.
- Provided as a 1 mL solution in DMSO.
- Concentration 10 mM in DMSO.
- Purity 99.9%.
- Molecular weight 329.17 g/mol; formula C11H9BrN2O3S.
- CAS number 292168-90-2.
- Reported c-Rel IC50 approximately 3 μM.
- Store in solution at -80°C for up to 6 months.
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5000379270 S R S -AHPC-C8-NH2 100MG
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Enzo Life Sciences SB-415286 (5mg). CAS: 264218-23-7
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Potent and selective inhibitor of GSK-3β (IC50=78nM). Stimulates glycogen synthesis in human liver cells and mimics other actions of insulin. Protects primary neurons from death induced by PI-3 kinase pathway inhibition suggesting therapeutic potential in neurodegenerative diseases and stroke. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO, ethanol or methanol. Long Term Storage: -20°C.
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Enzo Life Sciences Go-6983 (0.5mg). CAS: 133053-19-7
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PKC inhibitor. Has been shown to selectively inhibit several PKC isoenzymes (IC50 = 7nM for PKCα and PKCβ; 6nM for PKCγ; 10nM for PKCδ; 60nM for PKCζ). The compound does not effectively inhibit PKCµ (IC50=20 µM) and therefore can be used to differentiate PKCµ from other isoforms. Purity: ≥95% (HPLC). Solubility: Soluble in DMSO. Long Term Storage: -20°C.
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Revvity Health Sciences Inc HTRF Anti-Europium TBP Maleimide Labeling Reagent, 100 µg
HTRF Anti-Europium TBP Maleimide Labeling Reagent, 100 µg
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