156 Results for "

modifiers

" in MedChemExpress (MCE) Product Catalog:
Products (156)

156 Results for "modifiers" in MCE Product Catalog:

Cat. No.: HY-186239
CAS No.: 94113-57-2
Domaines de recherche:  

Others

Azophloxine-1,7-disulfonate disodium (CML) is a bio-based surfactant prepared from lignocellulosic biomass. Azophloxine-1,7-disulfonate disodium can serve as a modifier for Fe3O4 nanoparticles to load gold nanoparticles .
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Cat. No.: HY-W1061745
Domaines de recherche:  

Others

PC Spacer C6 Phosphoramidite is a photocleavable C6 spacer phosphoramidite modifier for oligonucleotide synthesis and can be used to introduce a photocleavable C6 spacer into oligonucleotides. PC Spacer C6 Phosphoramidite can be used to construct modified oligonucleotides containing photocleavable sites.
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Cat. No.: HY-100360R
CAS No.: 1502816-23-0
Domaines de recherche:  

Cancer

MS049 (Standard) is the analytical standard of MS049 (HY-100360). This product is intended for research and analytical applications. MS049, a chemical probe, is a potent, selective, and cell-active dual inhibitor of PRMT4 and PRMT6 with IC50s of 34 nM and 43 nM, respectively. MS049 reduces levels of Med12me2a and H3R2me2a in HEK293 cells. MS049 is not toxic and does not affect the growth of HEK293 cells .
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Cat. No.: HY-185930
CAS No.: 3119104-59-2
Target:  

CCR

Domaines de recherche:  

Neurological Disease

Reftinirsen inapertide is a CNOT3 inhibitor. CNOT3 is a non-catalytic subunit of the CCR4-NOT complex, serving as a direct transcriptional repressor and penetrance modifier of PRPF31. Reftinirsen inapertide can be used for the research of retinal dystrophies associated with prpf31 mutations .
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Cat. No.: HY-185797
Domaines de recherche:  

Others

TCO Phosphoramidite is a nucleic acid phosphoramidite modifier containing a trans-cyclooctene (TCO) reactive group. TCO Phosphoramidite enables nucleic acid fragment ligation via the inverse electron demand Diels-Alder (IEDDA) bioorthogonal reaction between TCO and tetrazine (Tz), and it can be used for research on oligonucleotide and RNA modification and assembly .
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Cat. No.: HY-P5790
Target:  

Sodium Channel

Domaines de recherche:  

Neurological Disease

μ-TRTX-Hd1a, a spider venom, is a selective NaV 1.7 inhibitor. μ-TRTX-Hd1a is a gating modifier that inhibits human NaV 1.7 by interacting with the S3b-S4 paddle motif in channel domain II .
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Cat. No.: HY-174712
Target:  

mRNA

Domaines de recherche:  

Cancer

Human FGF1 mRNA encodes the human Fibroblast growth factor 1 (FGF1) protein, a member of fibroblast growth factor (FGF) family. FGF1 functions as a modifier of endothelial cell migration and proliferation, as well as an angiogenic factor. It also acts as a mitogen for a variety of mesoderm- and neuroectoderm-derived cells in vitro, thus is thought to be involved in organogenesis.
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Cat. No.: HY-W014069
CAS No.: 71310-21-9
Synonyms: 11-Thioundecanoic acid; MUA; MUDA
11-Mercaptoundecanoic acid (11-Thioundecanoic acid; MUA; MUDA) is a self-assembled monolayer membrane composed of long-chain alkane chains and carboxyl-containing thioalcohols and can be used as a metal surface modifier. 11-Mercaptoundecanoic acid is widely applied in the research of molecular probes, self-assembled membranes, nanomaterials, and biological materials, etc .
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Cat. No.: HY-B0180AR
CAS No.: 99011-78-6
Synonyms: R 837 hydrochloride (Standard)
Imiquimod (hydrochloride) (Standard) is the analytical standard of Imiquimod (hydrochloride). This product is intended for research and analytical applications. Imiquimod hydrochloride (R 837 hydrochloride), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod hydrochloride exhibits antiviral and antitumor effects in vivo. Imiquimod hydrochloride can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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Cat. No.: HY-B0180BR
CAS No.: 896106-16-4
Imiquimod (maleate) (Standard) is the analytical standard of Imiquimod (maleate). This product is intended for research and analytical applications. Imiquimod maleate (R 837 maleate), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod maleate exhibits antiviral and antitumor effects in vivo. Imiquimod maleate can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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Cat. No.: HY-B0180R
CAS No.: 99011-02-6
Synonyms: R 837 (Standard)
Imiquimod (Standard) is the analytical standard of Imiquimod. This product is intended for research and analytical applications. Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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Cat. No.: HY-B0180S2
Synonyms: R 837-d7
Imiquimod-d7 (R 837-d7) is deuterium labeled Imiquimod. Imiquimod (R 837), an immune response modifier, is a selective toll like receptor 7 (TLR7) agonist. Imiquimod exhibits antiviral and antitumor effects in vivo. Imiquimod can be used for the research of external genital, perianal warts, cancer and COVID-19 .
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Cat. No.: HY-W145516
CAS No.: 9000-30-0
Guar gum is an orally active nonionic galactomannan polysaccharide. It is present in the endosperm of Cyamopsis tetragonolobus seeds. Guar gum reduces cholesterol levels, regulates body weight, and acts as a thickener and viscosity modifier by forming hydrogen-bonded aqueous solutions. It serves as a rate-controlling excipient in compound delivery systems, and finds applications in the food, tissue engineering, nanosensing and industrial fields .
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Cat. No.: HY-123650
CAS No.: 78859-42-4
Pureté:  99.06%
Synonyms: 5'-p-Fluorosulfonylbenzoyladenosine
Domaines de recherche:  

Cancer

FSBA (5'-p-Fluorosulfonylbenzoyladenosine) hydrochloride is a covalent modifier and affinity labeling reagent for adenine nucleotide-binding proteins. FSBA hydrochloride covalently attaches to the nucleotide-binding sites of pyruvate kinase, glutamate dehydrogenase, and p56 lck, and to a lysine residue in the ATP-binding site of cAMP-dependent protein kinase, causing loss of enzymatic activity. FSBA hydrochloride can be used for the research of T lymphoma .
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Cat. No.: HY-W190743
CAS No.: 1527515-88-3
Br-PEG8-OH is a PEG derivative that consists of a bromine atom (Br), eight PEG units, and a hydroxyl group (-OH). The bromine group is a common functional group in chemical reactions and can be used for alkylation reactions, coupling reactions, or the introduction of other functional groups. Br-PEG8-OH can be used as a polymer-based material or as a modifier for biomolecules .
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Cat. No.: HY-W250112
CAS No.: 8068-05-1
Lignin alkali acts as a decomposer, depolymerizer and structural modifier. Lignin alkali is recovered from lignocellulosic biomass via alkaline pretreatment. Lignin alkali consists of p-hydroxyphenyl, guaiacyl and syringyl propanoid units. Lignin alkali can be custom-converted into high-value-added chemicals and materials. Lignin alkali exhibits significant application potential in the fields of biomass refining and high-value utilization .
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Cat. No.: HY-W704600
CAS No.: 2846-04-0
Synonyms: TG(18:0/18:1/18:0)
Domaines de recherche:  

Others

1,3-Distearoyl-2-oleoyl glycerol (TG(18:0/18:1/18:0)) is a triglyceride that can be isolated from native fats such as such as kokum, shea butter and mango kernel fat. 1,3-Distearoyl-2-oleoyl glycerol is widely used in the chocolate industry as a cocoa butter modifier and an anti-blooming agent .
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Cat. No.: HY-134595
CAS No.: 2416910-70-6
Target:  

E1/E2/E3 Enzyme

Domaines de recherche:  

Cancer

SENP1-IN-2 is a specific deSUMOylation protease 1 (SENP1) inhibitor extracted from patent CN110627860, Compound 30. SENP1-IN-2 is developed for tumor radiosensitivity enhancement .
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Cat. No.: HY-134596
CAS No.: 2416910-59-1
Pureté:  99.92%
Target:  

E1/E2/E3 Enzyme

Domaines de recherche:  

Cancer

SENP1-IN-3 is a specific deSUMOylation protease 1 (SENP1) inhibitor extracted from patent CN110627860, Compound 17. SENP1-IN-3 is developed for tumor radiosensitivity enhancement .
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Cat. No.: HY-134597
CAS No.: 2416910-64-8
Pureté:  ≥98.0%
Target:  

E1/E2/E3 Enzyme

Domaines de recherche:  

Cancer

SENP1-IN-4 is a specific deSUMOylation protease 1 (SENP1) inhibitor extracted from patent CN110627860, Compound 21. SENP1-IN-4 is developed for tumor radiosensitivity enhancement .
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