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Others Related Products (76524)
Related Products (76524)
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18:1 SM (d18:1/18:1)-d9
0 ImagesCat. No.: HY-146929SCAS No.: 2342574-42-718:1 SM (d18:1/18:1)-d9 is deuterium labeled 18:1 SM (d18:1/18:1).
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16:1 SM (d18:1/16:1)-d9
0 ImagesCat. No.: HY-146930SCAS No.: 2342574-45-016:1 SM (d18:1/16:1)-d9 is deuterium labeled 16:1 SM (d18:1/16:1).
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Linoleoyl LPA-d5
0 ImagesCat. No.: HY-146955SLinoleoyl LPA-d5 is deuterium labeled Linoleoyl LPA.
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3-O-Methyl-D-glucose-13C
0 Images3-O-Methyl-D-glucose-13C is the 13C labeled 3-O-Methyl-D-glucose.
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Fmoc-Lys(5-FITC)-OH
0 ImagesCat. No.: HY-147104CAS No.: 1095493-05-2Fmoc-Lys(5-FITC)-OH is a marker for polypeptides or proteins. FITC is a fluorescence probe for the labeling of amines. FITC is a pH- and Cu2+-sensitive fluorescence dye.
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4-[3-(Trifluoromethyl)diazirin-3-yl] benzoic acid N-hydroxysuccinimide ester
0 Images4-[3-(Trifluoromethyl)diazirin-3-yl] benzoic acid N-hydroxysuccinimide ester is a photoactivated bifunctional cross-linker. 4-[3-(Trifluoromethyl)diazirin-3-yl] benzoic acid N-hydroxysuccinimide ester can be used for researching a strategy of rapid and accurate structure generation in support of antigen engineering programs.
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5-(3-Hydroxybenzylidene)-rhodanine
0 Images5-(3-Hydroxybenzylidene)-rhodanine, a derivative of rhodanine, can be used as an algicidal agent.
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- BBR-BODIPY
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Schnurri-3 inhibitor-1
0 ImagesSchnurri-3 inhibitor-1 is a potent schnurri-3 inhibitor which is an essential regulator of adult bone formation. Schnurri-3 inhibitor-1 can inhibit Shn3 with EF1alpha promoter in osteoblast cell line Shn3FFL with an AC50 value of 2.09 μM. Schnurri-3 inhibitor-1 can be used to research osteoporosis.
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Wnt/β-catenin agonist 3 hydrochloride
0 ImagesCat. No.: HY-148055APurity: 99.92%Wnt/β-catenin agonist 3 hydrochloride is a Wnt/β-catenin signalling pathway agonist. Wnt/β-catenin agonist 3 (compound 98) can be used for the research of osteoporosis.
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Thr-Val-Leu
0 ImagesThr-Val-Leu is a central nervous system tripeptide and reduces Thr-Val-Leu content in schizophrenic brain tissue.
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lucPpy-IN-1
0 ImageslucPpy-IN-1 (compound 9) is an ATP-dependent luciferase from Photinus pyralis (lucPpy) inhibitor with an IC50 value of 4.0 μM. lucPpy-IN-1 can be used for the research of target’s agentgability.
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- Litronesib Racemate
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Pomalidomide-5'-PEG5-C2-COOH
0 ImagesPomalidomide-5'-PEG5-C2-COOH is an active compound. Pomalidomide-5'-PEG5-C2-COOH can be used for the research of various biochemical.
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18β-Glycyrrhetyl-3-O-sulfate-d3
0 ImagesCat. No.: HY-148682S2Synonyms: Glycyrrhetic acid 3-O-hydrogen sulfate-d318β-Glycyrrhetyl-3-O-sulfate-d3 is the deuterium labeled 18β-Glycyrrhetyl-3-O-sulfate (HY-148682).
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(S)-Zavondemstat
0 ImagesCat. No.: HY-148807BSynonyms: (S)-QC8222 free base; (S)-TACH 101 free base(S)-Zavondemstat is the S-enantiomer of Zavondemstat (HY-148807). Zavondemstat is an inhibitor of histone lysine demethylase 4D (KDM4D) with antineoplastic activity[1].
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AzGGK TFA
0 ImagesCat. No.: HY-148835APurity: 99.77%AzGGK TFA is an unnatural amino acid. AzGGK TFA is site-specifically incorporated into proteins via genetic-code expansion. AzGGK TFA can be used as a site-specific probe for ubiquitylation and SUMOylation. AzGGK TFA is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Sulfo DBCO-PEG3-NHS ester
0 ImagesCat. No.: HY-148840Sulfo DBCO-PEG3-NHS ester is a click chemistry reagent containing an azide group. Sulfo DBCO-PEG3-NHS ester is an analog of DBCO-Acid with PEG linker and a DBCO group. The DBCO group is commonly used for copper-free Click Chemistry reactions due to its strain promoted high energy. The hydrophilic PEG chain and sulfo group increase water solubility. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. Reagent grade, for research use only.
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Akt1&PKA-IN-1
0 ImagesCat. No.: HY-148868CAS No.: 1334107-58-2Akt1&PKA-IN-1 is a potent dual Akt/PKA inhibitor with IC50 values of 0.03 , 0.11 μM, and 9.8 μM for PKAa, Akt, and CDK2, respectively. Akt1&PKA-IN-1 is selective for cyclin-dependent kinase 2 (CDK2).
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SNAP-Biotin
0 ImagesCat. No.: HY-148958CAS No.: 471918-16-8SNAP-Biotin is a cell-permeable SNAP-tag-targeted labeling reagent. SNAP-Biotin undergoes an irreversible covalent reaction with SNAP-tag to transfer biotin to the tag. SNAP-Biotin enables the detection of SNAP-tag fusion proteins via a streptavidin-HRP immunoblotting system and achieves biotinylation of SNAP-tag fusion proteins. SNAP-Biotin is applicable to triple-negative breast cancer-related research.
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