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Filtered Search Results
Medchemexpress LLC 1-Boc-3-aminopyrrolidine | 186550-13-0 | 99.9% | 186.25 | 10 G
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1-Boc-3-Aminopyrrolidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is intended for research use only.
- Biochemical reagent for life science research
- Suitable as a biological material
- Suitable as an organic compound
- Not for sale to patients
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Medchemexpress LLC Mal-PEG2-C2-Boc | 500MG
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Mal-PEG2-C2-Boc | 500MG
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Medchemexpress LLC Boc-Met-Leu-Phe-OH trifluoroacetate | 00-00-0 | MFCD00037435 | 99.5% | 623.68 g·mol⁻¹ | C27H40F3N3O8S | 10 MG
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Boc-MLF TFA is a protected tripeptide (Boc-Met-Leu-Phe-OH trifluoroacetate) used as a formyl peptide receptor antagonist in biochemical and cell-signaling research. It can inhibit signaling through formyl peptide receptor-like 1 (FPRL1) at higher concentrations. The material is supplied as a solid and in pre-made DMSO solutions and is for research use only.
- Formyl peptide receptor antagonist peptide
- Inhibits FPRL1 signaling at higher concentrations
- Reported purity approximately 99.5% by manufacturer
- Available as solid and as pre-dissolved DMSO solutions
- Molecular weight approximately 623.68 g·mol⁻¹ (TFA salt)
- Intended for research use only; not for clinical or patient use
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC N-(Azido-PEG2)-N-Boc-PEG4-acid | 2093153-82-1 | C22H42N4O10 | 100 MG
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N-(Azido-PEG2)-N-Boc-PEG4-acid is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent due to its Azide group, which allows it to undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
- Utilized in the synthesis of PROTACs
- Functions as a click chemistry reagent with an Azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
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Medchemexpress LLC (Z)-Guggulsterone | 39025-23-5 | 99.4% | 312.45 | 10 MG
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(Z)-Guggulsterone is a constituent of the Indian Ayurvedic medicinal plant *Commiphora mukul*. It inhibits the growth of human prostate cancer cells by causing apoptosis and inhibits angiogenesis by suppressing the VEGF-VEGF-R2-Akt signaling axis. It also acts as a potent FXR antagonist and reduces ACE2 expression and SARS-CoV-2 infection.
- Inhibits growth of human prostate cancer cells by causing apoptosis
- Inhibits angiogenesis by suppressing the VEGF-VEGF-R2-Akt signaling axis
- Acts as a potent FXR antagonist
- Reduces ACE2 expression
- Reduces SARS-CoV-2 infection
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Aobchem (Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 250mg
(Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 250mg
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AARON CHEMICALS LLC
NC3909337 3-3 4IMETHOXYPHENYLPROPION
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Ambeed AMBEED
5000894179 N-CBZ-3-PIPERIDINECARBOXAL 1GR
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Ambeed AMBEED
5000891229 CBZ-NH-PEG4-C2-ACID 250MG
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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 Z-3578 | 5MG
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Z-3578 | 5MG
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Ambeed AMBEED
5000883928 1-CBZ-4-METHYLSULFONYLOX 5G
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Ambeed AMBEED
5000895570 1-CBZ-AMINO-2-METHYLAMIN 250MG
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Apexbio Technology LLC Z-FA-FMK 105637-38-5;197855-65-5 10mg
Z-FA-FMK is a peptidyl fluoromethyl ketone inhibitor targeting cysteine proteases specifically cathepsins such as cathepsin B and certain caspases It does not require a P1 aspartate residue for inhibition Mechanistically Z-FA-FMK suppresses the enzyme activity of effector caspases (including caspases-2 -3 -6 and -7) but shows minimal impact on initiator caspases (caspase-8 and caspase-10) and only partial attenuation of caspase-9 activity As a negative control inhibitor Z-FA-FMK is regularly applied in apoptosis research to differentiate specific caspase-dependent signaling pathways and to assess the role of cathepsins and caspases in biological contexts such as cell death mechanisms and related pathways
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![Medchemexpress LLC N-(2,4-dimethylphenyl)-2,2,2-trifluoro-N-[(E)-(3-methoxyphenyl)methylideneamino]acetamide | 1146963-51-0 | MFCD25976644 | 99.8% | C18H17F3N2O2 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000259460.png-250.jpg)
Medchemexpress LLC N-(2,4-dimethylphenyl)-2,2,2-trifluoro-N-[(E)-(3-methoxyphenyl)methylideneamino]acetamide | 1146963-51-0 | MFCD25976644 | 99.8% | C18H17F3N2O2 | 10MG
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(E/Z)-J147 (N-(2,4-dimethylphenyl)-2,2,2-trifluoro-N-[(E)-(3-methoxyphenyl)methylideneamino]acetamide) is a small-molecule research compound investigated for neuroprotective and cognitive-enhancing effects. It readily crosses the blood-brain barrier and has reported activity against monoamine oxidase B and the dopamine transporter. The material is supplied as a high-purity solid for laboratory use.
- High purity: 99.8% by supplier specification.
- Powder form, off-white to pink in color.
- Recommended solvent: DMSO soluble at ≥100 mg/mL.
- Storage: powder stable at -20°C (long term) and 4°C (short term).
- Demonstrated neuroprotective activity and blood-brain barrier penetration.
- For research use only; not for human or clinical use.
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