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Filtered Search Results
Medchemexpress LLC (E/Z)-ZINC09659342 | 591726-26-0 | 99.7% | C23H15F3N2O4 | 1 ML
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(E/Z)-ZINC09659342 is an inhibitor of Lbc-RhoA interaction. This compound appears as a solid with an orange to red color and has a purity of 99.71%. It is intended for research use only.
- Inhibits Lbc-RhoA interaction
- Solid form, orange to red color
- Soluble in DMSO (≥ 50 mg/mL)
- Powder storage: -20°C for 3 years, 4°C for 2 years
- Solution storage: -80°C for 6 months, -20°C for 1 month
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Abcam Ro 31-8220 mesylate (Bisindolylmaleimide I x ), Protein kinase inhibitor, 10MG
MW 553.7 Da, Purity >98%. Widely used as a cell-permeable, reversible, competitive protein kinase C inhibitor. Also potently inhibits wide range of kinases inlcuding RSK1, RSK2, PRK2, PKCα, PKD1, MSK1, GSK3β, CDK2-cyclin A and PIM3, as well as PKCα. Also available in simple stock solutions (ab146723) - add 1 ml of water to get an exact, ready-to-use concentration.
The product is subject to the following: Abcam Restricted Use Statement
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000295461 Z -LFM-A13 10MG
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Medchemexpress LLC Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) | 138516-31-1 | 99.7% | 10 MG
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Bisindolylmaleimide VIII acetate (Ro 31-7549 acetate) is a potent and selective protein kinase C (PKC) inhibitor. It demonstrates inhibitory effects on various PKC isoforms including PKC-α, PKC-βI, PKC-βII, PKC-γ, and PKC-ε. This compound is known to facilitate Fas-mediated apoptosis and has shown promise in inhibiting T cell-mediated autoimmune diseases.
- Potent and selective protein kinase C (PKC) inhibitor
- Inhibits PKC-α, PKC-βI, PKC-βII, PKC-γ, and PKC-ε isoforms
- Facilitates Fas-mediated apoptosis
- Inhibits T cell-mediated autoimmune diseases
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Aat Bioquest AAT BIOQUEST
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NC3968171 XFD430 C5 MALEIMIDE
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Sigma Aldrich Fine Chemicals Biosciences Maleimide Activated KLH5MG
Maleimide Activated KLH is provided in lyophilized ready to-use form eliminating the need for time-consuming activation and purification steps of the carrier protein. Maleimide Activated KLH contains approximately 160-320 maleimide groups for each KLH molecule. The conjugation reaction with a cysteine containing peptide is performed at pH 6.6-7.0. The extent of conjugation can then be determined by a colorimetric assay with Ellmans reagent to detect unreacted thiol groups in the cysteine-containing peptide.
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Medchemexpress LLC Carbonic anhydrase 8 protein, mouse, His-tagged | >95.0% | 5 UG
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Recombinant mouse carbonic anhydrase 8 (CA8) is a His-tagged protein intended for research use in biochemical assays, antibody validation, and structural studies. The protein has an approximate molecular weight of 35 kDa, is supplied at microgram-scale quantities, and is characterized for purity by SDS-PAGE.
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Medchemexpress LLC Boc-NH-PEG7-azide | 100MG
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Boc-NH-PEG7-azide | 100MG
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eMolecules Pharmablock tert-butyl (2S 3S)-3-amino-2-methyl-pyrrolidine-1-carboxylate 250mg 761744142 PBB1341 0 000 1192608-69-7 200 282 C10H20N2O2
Pharmablock tert-butyl (2S 3S)-3-amino-2-methyl-pyrrolidine-1-carboxylate 250mg 761744142 PBB1341 0 000 1192608-69-7 200 282 C10H20N2O2
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TARGETMOL CHEMICALS INC BISINDOLYLMALEIMIDE IV 10MG
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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Bisindolylmaleimide IV is a protein kinase C (PKC) cell permeable inhibitor( IC50 0.10 - 0.55 uM)purity: 98%
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Medchemexpress LLC (Rac)-Idroxioleic acid (2-hydroxyoleic acid) | 56472-29-8 | 99.9% | 25 MG
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(Rac)-Idroxioleic acid (2-Hydroxyoleic acid) is a synthetic oleic acid (OA) derivative. It functions by binding to the plasma membrane and altering lipid organization. This compound has demonstrated anti-tumor effects.
- Binds to the plasma membrane and alters lipid organization.
- Exhibits anti-tumor effects.
- Impairs Jurkat cell growth in a time- and concentration-dependent manner (IC50 of approximately 40 μM).
- Induces proteolytic cleavage of PARP, a molecular marker of apoptosis.
- Significantly inhibits tumor growth in nude mice in a xenograft model.
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Chemscene CHEMSCENE
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5000579100 S-1-BOC-3-AMINOPYRROLIDINE 10G
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Medchemexpress LLC 4,7,10-trioxa-11-thiadodecanoic acid, 1,1-dimethylethyl ester, 11,11-dioxide | 1312309-62-8 | ≥97.0% | C12H24O7S | 100 MG
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Ms-PEG2-C2-Boc is a PEG-based PROTAC linker. PROTACs are molecules that exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins by connecting a ligand for an E3 ubiquitin ligase with a ligand for the target protein via a linker.
- Can be used in the synthesis of PROTACs.
- PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein.
- PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
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Medchemexpress LLC BCN-endo-PEG7-maleim |5mg
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BCN-endo-PEG7-maleimide is an ADC Linker containing 7 PEG units BCN-endo-PEG7-maleimide contains the lyophilic bidentate macrocyclic ligand endo-BCN which can further synthesize macrocyclic complexes In click chemistry endo-BCN can react with molecules containing azide groups to form stable triazoles in the absence of catalysts
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Medchemexpress LLC (E/Z)-ZINC09659342 | 591726-26-0 | 99.7% | C23H15F3N2O4 | 25 MG
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(E/Z)-ZINC09659342 is an inhibitor of Lbc-RhoA interaction. It is provided as an orange to red solid with a purity of 99.7% and is intended for research use only. This compound targets Ras and is involved in the GPCR/G Protein and MAPK/ERK pathways.
- Inhibits Lbc-RhoA interaction
- Targets Ras and related pathways (GPCR/G Protein, MAPK/ERK)
- Molecular formula: C23H15F3N2O4
- Molecular weight: 440.37
- Purity: 99.7%
- Solubility in DMSO: ≥ 50 mg/mL
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