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Results for "

Methoxyethyl

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Amino Acid Derivatives (1) Angiotensin Receptor (1) Apolipoprotein (3) Apoptosis (1) Biochemical Assay Reagents (2) DNA/RNA Synthesis (6) Drug Intermediate (1) Drug Metabolite (1) Endogenous Metabolite (2) GCGR (2) Glucocorticoid Receptor (2) HBV (1) HCV (2) HSP (2) Huntingtin (3) Isotope-Labeled Compounds (6) MicroRNA (1) Nucleoside Antimetabolite/Analog (57) Orthopoxvirus (1) Ras (1) Reference Standards (2) Ser/Thr Kinase (1) TNF Receptor (1) Transthyretin (TTR) (2) Vasopressin Receptor (1) Virus Protease (1)
By Research Areas:	Cancer (47) Cardiovascular Disease (3) Endocrinology (2) Infection (4) Inflammation/Immunology (3) Metabolic Disease (6) Neurological Disease (9)
Click Chemistry:	Azide (3)
Oligonucleotides:	A (15) Nucleosides and their Analogs (54) C (8) Nucleoside Phosphoramidites (1) U (19) G (8) I (5) Antisense Oligonucleotides (27)

Inhibitors & Agonists

Fluorescent Dye

Biochemical Assay Reagents

Peptides

Natural
Products

Isotope-Labeled Compounds

Click Chemistry

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-W048495

*2'-O-(2-Methoxyethyl)-uridine*	Nucleoside Antimetabolite/Analog	Cancer
2'-O-(2-Methoxyethyl)-uridine is a synthetic oligonucleotide conversed from uridine. 2'-O-(2-Methoxyethyl)-uridine has the potential for chemotherapeutic agents development .

HY-132579

Tominersen RG6042; IONIS-HTTRx	Huntingtin	Neurological Disease
Tominersen (RG6042) is a second-generation 2′-O-(2-methoxyethyl) antisense oligonucleotide that targets huntingtin protein (HTT) mRNA and potently suppresses HTT production. Tominersen improves survival and reduces brain atrophy in mice. Tominersen can be used for the research of Huntington’s disease (HD) .

HY-W048496

*2'-O-(2-Methoxyethyl)-cytidine*	Nucleoside Antimetabolite/Analog	Cancer
2'-O-(2-Methoxyethyl)-cytidine is a synthetic oligonucleotide derived from uridine. 2'-O-(2-Methoxyethyl)-cytidine has good hybridization properties and high stability, and can be used in the research of oligonucleotide chemotherapeutic agents .

HY-W013849S

*Bis(2-methoxyethyl) phthalate-3,4,5,6-d4*	Isotope-Labeled Compounds	Others
Bis(2-methoxyethyl) phthalate-3,4,5,6-d₄ is the deuterium labeled Bis(2-methoxyethyl) phthalate .

HY-154285

*3’-O-(2-Methoxyethyl) uridine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl) uridine is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents .

HY-152516

*2’-O-(2-Methoxyethyl) inosine*	Nucleoside Antimetabolite/Analog	Cancer
2’-O-(2-Methoxyethyl) inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152577

*3’-O-(2-Methoxyethyl) inosine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl) inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154434

*3’-O-(2-Methoxyethyl)-5-methyluridine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl)-5-methyluridine is a thymidine analog. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis .

HY-152480

*3’-O-(2-Methoxyethyl)-5-methylcytidine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl)-5-methylcytidine is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .

HY-42084R

*4-(2-Methoxyethyl)phenol (Standard)* p-Hydroxyphenethyl methyl ether (Standard)	Biochemical Assay Reagents Reference Standards	Others
4-(2-Methoxyethyl)phenol (Standard) is the analytical standard of 4-(2-Methoxyethyl)phenol. This product is intended for research and analytical applications. 4-(2-Methoxyethyl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-W033132

*N-(2-Methoxyethyl)-N-methylglycine*	Amino Acid Derivatives	Others
N-(2-Methoxyethyl)-N-methylglycine is a glycine derivative that can be used for compound synthesis .

HY-W048491

*2′-O-(2-Methoxyethyl)adenosine*	DNA/RNA Synthesis	Others
2′-O-(2-Methoxyethyl)adenosine is a compound can be used in the synthesis of oligonucleotides .

HY-152482

*3’-O-(2-Methoxyethyl)-2-thiouridine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl)-2-thiouridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152549

*2’-O-(2-Methoxyethyl)-2-aminoadenosine*	Nucleoside Antimetabolite/Analog	Others
2’-O-(2-Methoxyethyl)-2-aminoadenosine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-N1871

*4-(2-Hydroxy-1-methoxyethyl)-1,2-benzenediol*	Others	Inflammation/Immunology
4-(2-Hydroxy-1-methoxyethyl)-1,2-benzenediol is a phenylethanoid isolated from the stem bark of Syringa reticulate (Bl.) Hara (Oleaceae) with expectorant and antiasthmatic activity .

HY-23789

*2′-O-(2-Methoxyethyl)guanosine* 2'-O-MOE-rG	Nucleoside Antimetabolite/Analog DNA/RNA Synthesis	Others
2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG) is a 2'-O-methoxyethyl-modified nucleoside analogue and an important intermediate in the synthesis of nucleic acid drugs. 2′-O-(2-Methoxyethyl)guanosine neither effectively phosphorylated by cytosolic nucleoside kinases, nor are they incorporated into cellular DNA or RNA .

HY-152646

*3’-O-(2-Methoxyethyl)-2-aminoadenosine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl)-2-aminoadenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .

HY-152573

*N1-Methyl-3’-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
N1-Methyl-3’-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152571

*N1-Methyl-2’-O-(2-methoxyethyl) inosine*	Nucleoside Antimetabolite/Analog	Cancer
N1-Methyl-2’-O-(2-methoxyethyl) inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152575

*N6-Methyl-3’-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
N6-Methyl-3’-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152569

*N1-Methyl-2’-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
N1-Methyl-2’-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152570

*N6-Methyl-2’-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
N6-Methyl-2’-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152567

*N1-Methyl-2’-O-(2-methoxyethyl) guanosine*	Nucleoside Antimetabolite/Analog	Cancer
N1-Methyl-2’-O-(2-methoxyethyl) guanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152587

*N1-Methyl-3’-O-(2-methoxyethyl) inosine*	Nucleoside Antimetabolite/Analog	Cancer
N1-Methyl-3’-O-(2-methoxyethyl) inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152568

*N7-Methyl-2’-O-(2-methoxyethyl) guanosine*	Nucleoside Antimetabolite/Analog	Cancer
N7-Methyl-2’-O-(2-methoxyethyl) guanosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154173

*3’-O-(t-Butyldimethylsilyl)-2’-O-(2-methoxyethyl) uridine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(t-Butyldimethylsilyl)-2’-O-(2-methoxyethyl) uridine is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents .

HY-154240

*2-Amino-2’,3’-bis-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
2-Amino-2’,3’-bis-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154385

*4’,5’-Didehydro-2’-O-(2-methoxyethyl)-5-methyluridine*	Nucleoside Antimetabolite/Analog	Cancer
4’,5’-Didehydro-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154290

*N3,5-Dimethyl-2’-O-(2-methoxyethyl) uridine*	Nucleoside Antimetabolite/Analog	Cancer
N3,5-Dimethyl-2’-O-(2-methoxyethyl) uridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-132608

Inotersen sodium ISIS-420915 sodium	Transthyretin (TTR)	Neurological Disease
Inotersen (ISIS-420915) sodium is a 2′-O-methoxyethyl-modified antisense oligonucleotide. Inotersen sodium inhibits the production of transthyretin (TTR) protein by targeting the TTR RNA transcript and reduces the levels of the TTR transcript. Inotersen sodium can be used for the research of hereditary TTR amyloidosis polyneuropathy .

HY-154449

*N4-Benzoyl-3’-O-(2-methoxyethyl)-5-methylcytidine*	Nucleoside Antimetabolite/Analog	Cancer
N4-Benzoyl-3’-O-(2-methoxyethyl)-5-methylcytidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-42084

*4-(2-Methoxyethyl)phenol* p-Hydroxyphenethyl methyl ether	Biochemical Assay Reagents	Others
4-(2-Methoxyethyl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-152382

*3’-O-(2-Methoxyethyl)cytidine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(2-Methoxyethyl)cytidine is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .

HY-154386

*5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine*	Nucleoside Antimetabolite/Analog	Cancer
5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc . 5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine 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.

HY-154543

*5’-O-(4,4’-Dimethoxytrityl)-3’-O-(2-methoxyethyl) uridine*	Nucleoside Antimetabolite/Analog	Cancer
5’-O-(4,4’-Dimethoxytrityl)-3’-O-(2-methoxyethyl) uridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-WAA0006

*5-(2-Methoxyethyl)-7-methyl-2,5,7-triazaspiro[3.4]octan-6-one hydrochloride*	Drug Intermediate	Others
5-(2-Methoxyethyl)-7-methyl-2,5,7-triazaspiro[3.4]octan-6-one hydrochloride is a drug intermediate for synthesis of various active compounds.

HY-154552

*2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine*	Nucleoside Antimetabolite/Analog	Cancer
2’-O-Acetyl-5’-O-benzoyl-3’-O-(2-methoxyethyl) uridine is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents .

HY-154384

*5’-Deoxy-5’-iodo-2’-O-(2-methoxyethyl)-5-methyluridine*	Nucleoside Antimetabolite/Analog	Cancer
5’-Deoxy-5’-iodo-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154365

*5’-O-(4,4’-Dimethoxy trityl)-2’-O-(2-methoxyethyl) inosine*	Nucleoside Antimetabolite/Analog	Cancer
5’-O-(4,4’-Dimethoxy trityl)-2’-O-(2-methoxyethyl) inosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154260

*N6-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
N6-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl) adenosine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154441

*N4-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl)-5-methylcytidine*	Nucleoside Antimetabolite/Analog	Cancer
N4-Benzoyl-3'-O-DMT-2'-O-(2-methoxyethyl)-5-methylcytidine is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .

HY-154450

*N4-Benzoyl-5’-O-DMT-3’-O-(2-methoxyethyl)-5-methylcytidine*	Nucleoside Antimetabolite/Analog	Cancer
N4-Benzoyl-5’-O-DMT-3’-O-(2-methoxyethyl)-5-methylcytidine is a cytidine analog. Cytidine analogs have a mechanism of inhibiting DNA methyltransferases (such as Zebularine, HY-13420), and have potential anti-metabolic and anti-tumor activities .

HY-154228

*3’-O-(4,4’-Dimethoxy trityl)-2’-O-(2-methoxyethyl)-5-methyluridine*	Nucleoside Antimetabolite/Analog	Cancer
3’-O-(4,4’-Dimethoxy trityl)-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-154353

*5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine*	Nucleoside Antimetabolite/Analog	Cancer
5’-O-(4,4’-Dimethoxytrityl)-2’-O-(2-methoxyethyl) adenosine is an adenosine analog. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. Its popular products are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .

HY-152525

*5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine*	Nucleoside Antimetabolite/Analog	Others
5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine is a thymidine analogue. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis . 5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine 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.

HY-152493

*3’-O-(2-Methoxyethyl)guanosine*	Nucleoside Antimetabolite/Analog	Others
3’-O-(2-Methoxyethyl)guanosine is a guanosine analogue. Some guanosine analogs have immunostimulatory activity. In some animal models, they also induce type I interferons, producing antiviral effects. Studies have shown that the functional activity of guanosine analogs is dependent on the activation of Toll-like receptor 7 (TLR7) .

HY-152498

*3’-O-(2-Methoxyethyl)adenosine*	Nucleoside Antimetabolite/Analog	Others
3’-O-(2-Methoxyethyl)adenosine is an adenosine analogue. Adenosine analogs mostly act as smooth muscle vasodilators and have also been shown to inhibit cancer progression. The popular products in this series are adenosine phosphate, Acadesine (HY-13417), Clofarabine (HY-A0005), Fludarabine phosphate (HY-B0028) and Vidarabine (HY-B0277) .

HY-152444

*5-Hydroxymethyl-2’-O-(2-methoxyethyl)uridine*	Nucleoside Antimetabolite/Analog	Others
5-Hydroxymethyl-2’-O-(2-methoxyethyl)uridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

HY-152363

*N3-Methyl-2’-O-(2-methoxyethyl)uridine*	Nucleoside Antimetabolite/Analog	Others
N3-Methyl-2’-O-(2-methoxyethyl)uridine is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents .

HY-154121

*2’-O-(2-Methoxyethyl)guanosine 5’-triphosphate ammonium*	Nucleoside Antimetabolite/Analog	Cancer
2’-O-(2-Methoxyethyl)guanosine 5’-triphosphate (ammonium) is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc .

Cat. No.	Product Name	Type

HY-150236

FITC-labeled Tominersen sodium	Dyes
FITC-labeled Tominersen (sodium) is the Tominersen labeled with FITC. Tominersen (RG6042) is a second-generation 2′-O-(2-methoxyethyl) antisense oligonucleotide that targets huntingtin protein (HTT) mRNA and potently suppresses HTT production. Tominersen improves survival and reduces brain atrophy in mice. Tominersen can be used for the research of Huntington’s disease (HD).

Cat. No.	Product Name	Type

HY-23789

*2′-O-(2-Methoxyethyl)guanosine* 2'-O-MOE-rG	Gene Sequencing and Synthesis
2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG) is a 2'-O-methoxyethyl-modified nucleoside analogue and an important intermediate in the synthesis of nucleic acid drugs. 2′-O-(2-Methoxyethyl)guanosine neither effectively phosphorylated by cytosolic nucleoside kinases, nor are they incorporated into cellular DNA or RNA .

HY-42084

*4-(2-Methoxyethyl)phenol* p-Hydroxyphenethyl methyl ether	Biochemical Assay Reagents
4-(2-Methoxyethyl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-42084R

*4-(2-Methoxyethyl)phenol (Standard)* p-Hydroxyphenethyl methyl ether (Standard)	Biochemical Assay Reagents
4-(2-Methoxyethyl)phenol (Standard) is the analytical standard of 4-(2-Methoxyethyl)phenol. This product is intended for research and analytical applications. 4-(2-Methoxyethyl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No.	Product Name	Target	Research Area

HY-P3066

SKF 100398 d(CH2)5Tyr(Et)VAVP	Vasopressin Receptor	Metabolic Disease
SKF 100398 (d(CH2)5Tyr(Et)VAVP), an arginine vasopressin (AVP) analogue, is a specific antagonist of the antidiuretic effect of exogenous and endogenous AVP .

HY-W033132

*N-(2-Methoxyethyl)-N-methylglycine*	Amino Acid Derivatives	Others
N-(2-Methoxyethyl)-N-methylglycine is a glycine derivative that can be used for compound synthesis .

HY-P10828

MAPI	Virus Protease	Infection Inflammation/Immunology
MAPI is a polypeptide irreversible 3C cysteine protease (SV3CP) inhibitor. MAPI inhibits SV3CP by covalently binding its C-terminal Michael-acceptor extension to the active site thiol of SV3CP Cys 139. MAPI is promising for research of noroviruses infection .

HY-P4756

*N-(2-Carbamoyl-ethyl)-Val-Leu-anilide*	Peptides	Others
N-(2-Carbamoyl-ethyl)-Val-Leu-anilide is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N1871

*4-(2-Hydroxy-1-methoxyethyl)-1,2-benzenediol*	Oleaceae Source classification Syringa reticulata Polyphenols Plants	Others
4-(2-Hydroxy-1-methoxyethyl)-1,2-benzenediol is a phenylethanoid isolated from the stem bark of Syringa reticulate (Bl.) Hara (Oleaceae) with expectorant and antiasthmatic activity .

HY-113291R

5'-Deoxyadenosine (Standard)	Structural Classification Natural Products Human Gut Microbiota Metabolites Microorganisms Source classification Endogenous metabolite	Reference Standards Endogenous Metabolite Orthopoxvirus
4-(2-Methoxyethyl)phenol (Standard) is the analytical standard of 4-(2-Methoxyethyl)phenol. This product is intended for research and analytical applications. 4-(2-Methoxyethyl)phenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

HY-147406

Tonlamarsen ION-904	Cardiovascular Disease Structural Classification Natural Products Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields	Endogenous Metabolite
Tonlamarsen is a angiotensinogen synthesis reducer, with antihypertensive activity .

Cat. No.	Product Name	Chemical Structure

HY-W013849S

*Bis(2-methoxyethyl) phthalate-3,4,5,6-d4*
Bis(2-methoxyethyl) phthalate-3,4,5,6-d₄ is the deuterium labeled Bis(2-methoxyethyl) phthalate .

HY-W336012S

Metoprolol EP impurity O-d7 hydrochloride
Metoprolol EP impurity O-d₇ (hydrochloride) is the deuterium labeled 3,3'-(Isopropylazanediyl)bis(1-(4-(2-methoxyethyl)phenoxy)propan-2-ol) .

HY-W714698

Dimethachlor ethane sulfonic acid sodium salt-d6
Dimethachlor ethane sulfonic acid sodium salt-d₆ is the deuterium labeled Sodium 2-((2,6-dimethylphenyl)(2-methoxyethyl)amino)-2-oxoethane-1-sulfonate (HY-W714703).

HY-W714228S

*2-(2-Hydroxy-N-(2-(methoxy-d3)ethyl)acetamido)-3-methylbenzoic acid*
2-(2-Hydroxy-N-(2-(methoxy-d₃)ethyl)acetamido)-3-methylbenzoic acid is deuterium labeled 2-(2-Hydroxy-N-(2-methoxyethyl)acetamido)-3-methylbenzoic acid .

HY-W714702S

*2-((2,6-Dimethylphenyl)(2-(methoxy-d3)ethyl)amino)-2-oxoacetic acid*
2-((2,6-Dimethylphenyl)(2-(methoxy-d₃)ethyl)amino)-2-oxoacetic acid is deuterium labeled 2-((2,6-Dimethylphenyl)(2-methoxyethyl)amino)-2-oxoacetic acid .

HY-W714703S

*Sodium 2-((2,6-dimethylphenyl)(2-(methoxy-d3)ethyl)amino)-2-oxoethane-1-sulfonate*
Sodium 2-((2,6-dimethylphenyl)(2-(methoxy-d₃)ethyl)amino)-2-oxoethane-1-sulfonate is deuterium labeled Sodium 2-((2,6-dimethylphenyl)(2-methoxyethyl)amino)-2-oxoethane-1-sulfonate .

Cat. No.	Product Name		Classification

HY-154386

*5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine*		Azide
5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc . 5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)-5-methyluridine 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.

HY-152525

*5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine*		Azide
5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine is a thymidine analogue. Analogs of this series have insertional activity towards replicated DNA. They can be used to label cells and track DNA synthesis . 5-(Azidomethyl)-2’-O-(2-methoxyethyl)uridine 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.

HY-154383

*5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)uridine*		Azide
5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)uridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc . 5’-Azido-5’-deoxy-2’-O-(2-methoxyethyl)uridine 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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