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Filtered Search Results
eMolecules MALEIMIDE 25G
5000190114 MALEIMIDE 25G
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Selleck Chemical LLC ACT-1016-0707-E1941-25MG
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ACT-1016-0707 (LPA1 receptor antagonist 2) is an orally active and selective antagonist of LPA1 Receptor with IC50 of 3 1 nM for hLPAR1 in tango assay It has the potential to treat fibrotic diseases
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Medchemexpress LLC TMEM219/IGFBP-3R Hu 20ug | 20ug
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The TMEM219/IGFBP-3R protein was identified as an IGFBP3-specific cell death receptor and a potential mediator of caspase-8-dependent apoptosis upon ligand binding This protein actively binds to IGFBP3 forming a key molecular interaction that may initiate the apoptosis signaling pathway TMEM219/IGFBP-3R Protein Human (HEK293 Fc) is the recombinant human-derived TMEM219/IGFBP-3R protein expressed by HEK293 with C-hFc labeled tag
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Cayman Chemical N-EthylmaleImIde 10g
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A modifier of protein sulfhydryl groups; has commonly been used to inactivate cysteine-containing enzymes in vitro; inhibits prolyl endopeptidase (IC50 = 6.3 µM); alkylates Cys519 in Kv7.4 and activates Kv7.2, Kv7.4, and Kv7.5 in CHO cells at 50 µM
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LUMIPROBE BDP TMR MALEIMIDE 1MG
NC3363881 BDP TMR MALEIMIDE 1MG
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eMolecules EMOLECULES INC
5000470811 3R-3-TERT-BUTOXYCARBON 100G
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Medchemexpress LLC PROTAC BET degrader- 10mg | 3031993-61-7 | 10 MG
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PROTAC BET degrader-3 is a bifunctional proteolysis targeting chimera that recruits the von Hippel-Lindau (VHL) E3 ligase to BET-family bromodomains to induce targeted degradation of BET proteins. It is supplied as a research-grade powder for preclinical studies.
- Targets BET proteins via VHL-mediated degradation.
- Molecular formula C53H64N12O9S.
- Molecular weight 1045.22 g·mol⁻¹.
- Purity 99.11% (HPLC).
- Powder form; store at -20°C, shelf life 3 years.
- For research use only; not for human or clinical use.
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eMolecules Oakwood Chemical N-Boc-6-bromohexylamine 250mg 649421964 037106 0 000 142356-33-0 MFCD06201019 280 206 C11H22BrNO2
Oakwood Chemical N-Boc-6-bromohexylamine 250mg 649421964 037106 0 000 142356-33-0 MFCD06201019 280 206 C11H22BrNO2
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eMolecules EMOLECULES INC
5000483709 1-TERT-BUTOXYCARBONYL-3 3-D 1G
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Medchemexpress LLC S R S -AHPC-amido-C | 50MG
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S R S -AHPC-amido-C | 50MG
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eMolecules EMOLECULES INC
5000489822 9H-FLUOREN-9-YLMETHYL 2 25G
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SANTA CRUZ BIOTECHNOLOGY FUMARATE HYDRATASE CLONE J-13
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NC2379339 FUMARATE HYDRATASE CLONE J-13
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eMolecules Chem-Impex 2-Amino-2-(hydroxymethyl)-1 3-propanediol 1kg 272384824 00298 0 000 77-86-1 MFCD00004679 121 136 C4H11NO3
Chem-Impex 2-Amino-2-(hydroxymethyl)-1 3-propanediol 1kg 272384824 00298 0 000 77-86-1 MFCD00004679 121 136 C4H11NO3
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Medchemexpress LLC (Rac)-IBT6A | 1412418-47-3 | 98.18% | 100 MG
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(Rac)-IBT6A is a racemate of IBT6A, an impurity of Ibrutinib. This product can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct. Ibrutinib is known as a selective, irreversible Btk inhibitor with an IC50 of 0.5 nM.
- Targets Btk
- Functions via Protein Tyrosine Kinase/RTK pathway
- Can be stored as powder at -20°C for 3 years or 4°C for 2 years
- Can be stored in solvent at -80°C for 2 years or -20°C for 1 year
- Soluble in DMSO at 50 mg/mL
- Used in the synthesis of Ibrutinib and Ibrutinib-based activity-based probes (ABPs)
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Medchemexpress LLC BAY-298 | 2471978-97-7 | 99.9% | 50 MG
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BAY-298 is an orally active and selective antagonist of the luteinizing hormone receptor (LH-R). It exhibits IC50 values of 96 nM for human LH (hLH), 23 nM for rat LH (rLH), and 78 nM for cynomolgus monkey LH (cLH). This compound has demonstrated the ability to reduce sex hormone levels and is intended for research use only.
- Orally active and selective LH-R antagonist
- Inhibits human, rat, and cynomolgus monkey LH-R
- Reduces sex hormone levels
- For research use only
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