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4-Methoxybenzaldehyde-d<sub>1</sub>

" in MedChemExpress (MCE) Product Catalog:

2469

Inhibitors & Agonists

9

Biochemical Assay Reagents

8

Peptides

1

Inhibitory Antibodies

7

Natural
Products

10

Recombinant Proteins

2406

Isotope-Labeled Compounds

3

Antibodies

13

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-RS13999
    SUB1 Human Pre-designed siRNA Set A

    		Small Interfering RNA (siRNA) Others

    SUB1 Human Pre-designed siRNA Set A contains three designed siRNAs for SUB1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

    SUB1 Human Pre-designed siRNA Set A
    SUB1 Human Pre-designed siRNA Set A
  • HY-146227
    DNA topoisomerase II inhibitor 1

    		Topoisomerase Apoptosis Cancer
    DNA topoisomerase II inhibitor 1 (compound 8ed) is a potent DNA topoisomerase II inhibitor. DNA topoisomerase II inhibitor 1 shows anti-proliferative activity. DNA topoisomerase II inhibitor 1 induces apoptosis and cell cycle arrest at sub G1 phase [1].
    DNA topoisomerase II inhibitor <em>1</em>
  • HY-Y0740S
    4-Methoxybenzaldehyde-d1

    		Endogenous Metabolite Others
    4-Methoxybenzaldehyde-d1 is the deuterium labeled 4-Methoxybenzaldehyde[1]. 4-Methoxybenzaldehyde is a naturally occurring fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking[2].
    <em>4-Methoxybenzaldehyde</em>-d<em>1</em>
  • HY-Y0740S1
    4-Methoxybenzaldehyde-d3

    		Endogenous Metabolite Others
    4-Methoxybenzaldehyde-d3 is the deuterium labeled 4-Methoxybenzaldehyde[1]. 4-Methoxybenzaldehyde is a naturally occurring fragrant phenolic compound. 4-Methoxybenzaldehyde has been found in many plant species including horseradish, anise, star anise. 4-Methoxybenzaldehyde is a possible neurotoxicant and it has shown effects that include mortality, attractancy, and interference with host seeking[2].
    <em>4-Methoxybenzaldehyde</em>-d3
  • HY-I0637S
    Isovanillin-d3

    3-Hydroxy-4-Methoxybenzaldehyde-d<sub>3sub>

    		 Isotope-Labeled Compounds
    Isovanillin-d3 is the deuterium labeled Isovanillin[1]. Isovanillin is an aldehyde oxidase inhibitor[2]. Antispasmodic activities[3]. Antidiarrheal activities[4].
    Isovanillin-d3
  • HY-B0389S3
    D-Glucose-d1-1

    Glucose-d<sub>1sub>-1; D-(+)-Glucose-d<sub>1sub>-1; Dextrose-d<sub>1sub>-1

    		 Endogenous Metabolite Metabolic Disease
    D-Glucose-d-11 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic and abiotic stress response[1].
    D-Glucose-d<em>1</em>-<em>1</em>
  • HY-B0389S1
    D-Glucose-d1

    Glucose-d<sub>1sub>; D-(+)-Glucose-d<sub>1sub>; Dextrose-d<sub>1sub>

    		 Isotope-Labeled Compounds Endogenous Metabolite Metabolic Disease Cancer
    D-Glucose-d is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molec
    D-Glucose-d<em>1</em>
  • HY-125833
    Alpha-Naphthoflavone
    5 Publications Verification

    		 Cytochrome P450 Aryl Hydrocarbon Receptor Apoptosis Cancer
    Alpha-Naphthoflavone is an orally active flavonoid that is a potent, competitive inhibitor of aromatase< b>aromatase. < b > IC < sub > 50 < / sub > < / b > and < b > K < sub > I < / sub > < / b > value were 0.5 and 0.2 microns. Alpha-Naphthoflavone can inhibit cell proliferation and induce apoptosis [1] [4].
    Alpha-Naphthoflavone
  • HY-41700S2
    D-Alanine-d1

    (R)-Alanine-d<sub>1sub>; Ba 2776-d<sub>1sub>; D-α-Alanine-d<sub>1sub>

    		 Isotope-Labeled Compounds Endogenous Metabolite
    D-Alanine-d is the deuterium labeled D-Alanine. D-Alanine is a weak GlyR (inhibitory glycine receptor) and PMBA agonist, with an EC50 of 9 mM for GlyR[1].
    D-Alanine-d<em>1</em>
  • HY-N0378S5
    D-Mannitol-d1

    Mannitol-d<sub>1sub>; Mannite-d<sub>1sub>

    		 Isotope-Labeled Compounds Apoptosis Endogenous Metabolite Metabolic Disease Cancer
    D-Mannitol-d is the deuterium labeled D-Mannitol.
    D-Mannitol-d<em>1</em>
  • HY-B0389S8
    D-Glucose-d1-4

    Glucose-d<sub>1sub>-4; D-(+)-Glucose-d<sub>1sub>-4; Dextrose-d<sub>1sub>-4

    		 Isotope-Labeled Compounds Endogenous Metabolite Metabolic Disease
    D-Glucose-d-44 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic and abiotic stress response[1].
    D-Glucose-d<em>1</em>-<em>4</em>
  • HY-B0389S7
    D-Glucose-d1-3

    Glucose-d<sub>1sub>-3; D-(+)-Glucose-d<sub>1sub>-3; Dextrose-d<sub>1sub>-3

    		 Endogenous Metabolite Metabolic Disease
    D-Glucose-d-33 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic and abiotic stress response[1].
    D-Glucose-d<em>1</em>-3
  • HY-B0389S4
    D-Glucose-d1-2

    Glucose-d<sub>1sub>-2; D-(+)-Glucose-d<sub>1sub>-2; Dextrose-d<sub>1sub>-2

    		 Isotope-Labeled Compounds Endogenous Metabolite Metabolic Disease
    D-Glucose-d1-2 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic and abiotic stress response[1].
    D-Glucose-d<em>1</em>-2
  • HY-B0389S2
    D-Glucose-d12-1

    Glucose-d<sub>12sub>-1; D-(+)-Glucose-d<sub>12sub>-1; Dextrose-d<sub>12sub>-1

    		 Isotope-Labeled Compounds Endogenous Metabolite Metabolic Disease
    D-Glucose-d12-12 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling molecules in relation to both cellular metabolic status and biotic and abiotic stress response[1].
    D-Glucose-d12-<em>1</em>
  • HY-19696S2
    Tauroursodeoxycholate-d4-1

    Tauroursodeoxycholic acid-d<sub>4sub>-1; TUDCA-d<sub>4sub>-1; UR 906-d<sub>4sub>-1

    		 Isotope-Labeled Compounds ERK Caspase Endogenous Metabolite Apoptosis
    Tauroursodeoxycholate-d4-1 is the deuterium labeled Tauroursodeoxycholate. Tauroursodeoxycholate (Tauroursodeoxycholic acid) is an endoplasmic reticulum (ER) stress inhibitor. Tauroursodeoxycholate significantly reduces expression of apoptosis molecules, such as caspase-3 and caspase-12. Tauroursodeoxycholate also inhibits ERK.
    Tauroursodeoxycholate-d<em>4</em>-<em>1</em>
  • HY-B0389S23
    D-Glucose-d2-1

    Glucose-d<sub>2sub>-1; D-(+)-Glucose-d<sub>2sub>-1; Dextrose-d<sub>2sub>-1

    		 Endogenous Metabolite Metabolic Disease Cancer
    D-Glucose-d2-1 is the deuterium labeled D-Glucose. D-Glucose (Glucose), a monosaccharide, is an important carbohydrate in biology. D-Glucose is a carbohydrate sweetener and critical components of the general metabolism, and serve as critical signaling mol
    D-Glucose-d2-<em>1</em>
  • HY-109037S2
    Mavacamten-d1

    MYK461-d<sub>1sub>; SAR439152-d<sub>1sub>

    		 Isotope-Labeled Compounds Myosin Cardiovascular Disease
    Mavacamten-d1 (MYK461-d1; SAR439152-d1) is deuterium labeled Mavacamten (HY-109037). Mavacamten (MYK461) is an orally active modulator of cardiac myosin, with IC50s of 490, 711 nM for bovine cardiac and human cardiac, respectively.
    Mavacamten-d<em>1</em>
  • HY-B0763S2
    Ibudilast-d7-1

    KC-404-d<sub>7sub>-1; AV-411-d<sub>7sub>-1; MN-166-d<sub>7sub>-1

    		 Phosphodiesterase (PDE)
    Ibudilast-d7-1 is the deuterium labeled Ibudilast[1]. Ibudilast (KC-404;AV-411;MN-166) is a cyclic AMP phosphodiesterase (PDE) inhibitor. Ibudilast has platelet anti-aggregatory effects. Ibudilast can be used for the research of asthma for its inhibitory effects on tracheal smooth muscle contractility. Ibudilast may be a useful neuroprotective and anti-dementia agent counteracting neurotoxicity in activated microglia[2].
    Ibudilast-d7-<em>1</em>
  • HY-B0141S6
    Estradiol-d2-1

    β-Estradiol-d<sub>2sub>-1; E2-d<sub>2sub>-1; 17β-Estradiol-d<sub>2sub>-1; 17β-Oestradiol-d<sub>2sub>-1

    		 Isotope-Labeled Compounds Estrogen Receptor/ERR Endogenous Metabolite Neurological Disease Inflammation/Immunology
    Estradiol-d2-1 is the deuterium labeled Estradiol. Estradiol is a steroid sex hormone vital to the maintenance of fertility and secondary sexual characteristics in females. Estradiol upregulates IL-6 expression through the estrogen receptor β (ERβ) pathway[1][2][3][4].
    Estradiol-d2-<em>1</em>
  • HY-B0511S
    Biotin-d2-1

    Vitamin B7 d<sub>2sub>-1; Vitamin H d<sub>2sub>-1; D-Biotin d<sub>2sub>-1

    		 Endogenous Metabolite Metabolic Disease
    Biotin-d2-1 is the deuterium labeled Biotin. Biotin is an enzyme co-factor present in minute amounts in every living cell.
    Biotin-d2-<em>1</em>
  • HY-B0152S
    Adenine-d1

    6-Aminopurine-d<sub>1sub>; Vitamin B4-d<sub>1sub>

    		 DNA/RNA Synthesis Endogenous Metabolite Cancer
    Adenine-d is the deuterium labeled Adenine. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3].
    Adenine-d<em>1</em>
  • HY-B1411S1
    i-Inositol-d1

    myo-Inositol-d<sub>1sub>; meso-Inositol-d<sub>1sub>

    		 Endogenous Metabolite Others
    i-Inositol-d is the deuterium labeled i-Inositol[1].
    i-Inositol-d<em>1</em>
  • HY-B0479S1
    Thiamphenicol-d3-1

    Thiophenicol-d<sub>3sub>-1; Dextrosulphenidol-d<sub>3sub>-1

    		 Isotope-Labeled Compounds Infection
    Thiamphenicol-d3-1 (Thiophenicol-d3-1; Dextrosulphenidol-d3-1) is the deuterium-labeled Thiamphenicol (HY-B0479) [1]. Thiamphenicol (Thiophenicol), a methyl-sulfonyl derivative of Chloramphenicol, is a broad-spectrum antimicrobial antibiotic. Thiamphenicol acts by binding to the 50S ribosomal subunit, leading to inhibition of protein synthesis and bacteriostatic effect (against Gram-negative, Gram-positive aerobic and anaerobic bacteria) .
    Thiamphenicol-d3-<em>1</em>
  • HY-14648S1
    Dexamethasone-d5-1

    Hexadecadrol-d<sub>5sub>-1; Prednisolone F-d<sub>5sub>-1

    		 Isotope-Labeled Compounds Glucocorticoid Receptor SARS-CoV Autophagy Complement System Mitophagy Bacterial Antibiotic Infection Inflammation/Immunology Endocrinology Cancer
    Dexamethasone-d5-1 is deuterium labeled Dexamethasone. Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18 expression on monocytes. Dexamethasone is highly effective in the control of COVID-19 infection. Dexamethasone inhibits production of exosomes containing inflammatory microRNA-155 in lipopolysaccharide-induced macrophage inflammatory responses.
    Dexamethasone-d5-<em>1</em>
  • HY-B0234S4
    Estrone-d2-1

    E1-d<sub>2sub>-1; Oestrone-d<sub>2sub>-1

    		 Isotope-Labeled Compounds Estrogen Receptor/ERR Endogenous Metabolite
    Estrone-d2-1 is the deuterium labeled Estrone. Estrone (E1) is a natural estrogenic hormone. Estrone is the main representative of the endogenous estrogens and is produced by several tissues, especially adipose tissue. Estrone is the result of the process of aromatization of androstenedione that occurs in fat cells[1][2].
    Estrone-d2-<em>1</em>
  • HY-14648S5
    Dexamethasone-d3-1

    Hexadecadrol-d<sub>3sub>-1; Prednisolone F-d<sub>3sub>-1

    		 Isotope-Labeled Compounds Cancer
    Dexamethasone-d3-1 (Hexadecadrol-d3-1; Prednisolone F-d3-1) is a deuterium labeled Dexamethasone (HY-14648). Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18 expression on monocytes. Dexamethasone is highly effective in the control of COVID-19 infection. Dexamethasone inhibits production of exosomes containing inflammatory microRNA-155 in lipopolysaccharide-induced macrophage inflammatory responses.
    Dexamethasone-d3-<em>1</em>
  • HY-13966S
    2-Deoxy-D-glucose-d1

    2-DG-d<sub>1sub>; 2-Deoxy-D-arabino-hexose-d<sub>1sub>; D-Arabino-2-deoxyhexose-d<sub>1sub>

    		 Isotope-Labeled Compounds Apoptosis Hexokinase HSV Cancer
    2-Deoxy-D-glucose-d is the deuterium labeled 2-Deoxy-D-glucose. 2-Deoxy-D-glucose is a glucose analog that acts as a competitive inhibitor of glucose metabolism, inhibiting glycolysis via its actions on hexokinase[1][2].
    2-Deoxy-D-glucose-d<em>1</em>
  • HY-G0016S1
    N-Acetyl dapsone-d4-1

    MADDS-d<sub>4sub>-1; Monoacetyldapsone-d<sub>4sub>-1

    		 Isotope-Labeled Compounds Inflammation/Immunology
    N-acetyl Dapsone-d4-1 is the deuterium labeled N-acetyl Dapsone, which is a metabolite of Dapsone.
    N-Acetyl dapsone-d<em>4</em>-<em>1</em>
  • HY-13593S1
    Chlorambucil-d8-1

    CB-1348-d<sub>8sub>-1; WR-139013-d<sub>8sub>-1

    		 Isotope-Labeled Compounds DNA Alkylator/Crosslinker Cancer
    Chlorambucil-d8-1 is the deuterium labeled Chlorambucil. Chlorambucil (CB-1348), an orally active antineoplastic agent, is a bifunctional alkylating agent belonging to the nitrogen mustard group. Chlorambucil can be used for the research of lymphocytic leukemia, ovarian and breast carcinomas, and Hodgkin’s disease[1][2][3][4].
    Chlorambucil-d8-<em>1</em>
  • HY-10162S3
    Olaparib-d4-1

    AZD2281-d<sub>4sub>-1; KU0059436-d<sub>4sub>-1

    		 Isotope-Labeled Compounds PARP Autophagy Mitophagy Cancer
    Olaparib-d4-1 is the deuterium labeled Olaparib. Olaparib (AZD2281; KU0059436) is a potent and orally active PARP inhibitor with IC50s of 5 and 1 nM for PARP1 and PARP2, respectively. Olaparib is an autophagy and mitophagy activator[1][2][3][4].
    Olaparib-d<em>4</em>-<em>1</em>
  • HY-50898S3
    Lapatinib-d4-1

    GW572016-d<sub>4sub>-1; GW2016-d<sub>4sub>-1

    		 Isotope-Labeled Compounds EGFR Autophagy Ferroptosis Cancer
    Lapatinib-d4-1 is deuterium labeled Lapatinib. Lapatinib (GW572016) is a potent inhibitor of the ErbB-2 and EGFR tyrosine kinase domains with IC50 values against purified EGFR and ErbB-2 of 10.2 and 9.8 nM, respectively[1].
    Lapatinib-d<em>4</em>-<em>1</em>
  • HY-70057S1
    Safinamide-d4-1

    FCE 26743-d<sub>4sub>-1; EMD 1195686-d<sub>4sub>-1

    		 Isotope-Labeled Compounds Monoamine Oxidase Neurological Disease
    Safinamide-d4-1 is deuterium labeled Safinamide. Safinamide is a potent, selective, and reversible monoamine oxidase B (MAO-B) inhibitor (IC50=0.098 µM) over MAO-A (IC50=580 µM)[1]. Safinamide also blocks sodium channels and modulates glutamate (Glu) release, showing a greater affinity at depolarized (IC50=8 µM) than at resting (IC50=262 µM) potentials. Safinamide has neuroprotective and neurorescuing effects and can be used for the study of parkinson disease, ischemia stroke etc.al[2][3].
    Safinamide-d<em>4</em>-<em>1</em>
  • HY-B0400S7
    D-Sorbitol-d1-2

    Sorbitol-d<sub>1sub>-2; D-Glucitol-d<sub>1sub>-2

    		 Endogenous Metabolite Others
    D-Sorbitol-d-2 is the deuterium labeled D-Sorbitol. D-Sorbitol (Sorbitol) is a six-carbon sugar alcohol and can used as a sugar substitute. D-Sorbitol can be used as a stabilizing excipient and/or isotonicity agent, sweetener, humectant, thickener and di
    D-Sorbitol-d<em>1</em>-2
  • HY-B0400S8
    D-Sorbitol-d2-1

    Sorbitol-d<sub>2sub>-1; D-Glucitol-d<sub>2sub>-1

    		 Endogenous Metabolite Others
    D-Sorbitol-d2-1 is the deuterium labeled D-Sorbitol. D-Sorbitol (Sorbitol) is a six-carbon sugar alcohol and can used as a sugar substitute. D-Sorbitol can be used as a stabilizing excipient and/or isotonicity agent, sweetener, humectant, thickener and di
    D-Sorbitol-d2-<em>1</em>
  • HY-100442S1
    Paquinimod-d5-1

    ABR-215757-d<sub>5sub>-1; ABR 25757-d<sub>5sub>-1

    		 SARS-CoV Isotope-Labeled Compounds Metabolic Disease Inflammation/Immunology
    Paquinimod-d5-1 is a deuterated analog of Paquinimod (HY-100442). Paquinimod (ABR 215757) is a specific and orally active inhibitor of S100A8/S100A9. Paquinimod rescues the pneumonia with substantial reduction of viral loads in SARS-CoV-2-infected mice [1] .
    Paquinimod-d5-<em>1</em>
  • HY-W016577S4
    1-Bromoheptane-d1

    n-Heptyl bromide-d<sub>1sub>

    		 Isotope-Labeled Compounds Others
    1-Bromoheptane-d1 is the deuterium labeled 1-Bromoheptane[1].
    <em>1</em>-Bromoheptane-d<em>1</em>
  • HY-W099504S2
    1-Heptanol-d1

    n-Heptyl alcohol-d<sub>1sub>

    		 Isotope-Labeled Compounds Others
    1-Heptanol-d1 is the deuterium labeled 1-Heptanol[1].
    <em>1</em>-Heptanol-d<em>1</em>
  • HY-10585S4
    Valproic acid-d4-1

    VPA-d<sub>4sub>-1; 2-Propylpentanoic Acid-d<sub>4sub>-1

    		 Isotope-Labeled Compounds HDAC Autophagy Mitophagy HIV Notch Endogenous Metabolite Cancer
    Valproic acid-d4-1 is the deuterium labeled Valproic acid. Valproic acid (VPA; 2-Propylpentanoic Acid) is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches[1][2].
    Valproic acid-d<em>4</em>-<em>1</em>
  • HY-108506S2
    Licarbazepine-d4-1

    BIA 2-005-d<sub>4sub>-1; GP 47779-d<sub>4sub>-1

    		 Isotope-Labeled Compounds Sodium Channel Neurological Disease
    Licarbazepine-d4-1 is deuterium labeled Licarbazepine. Licarbazepine (BIA 2-005; GP 47779) is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects[1].
    Licarbazepine-d<em>4</em>-<em>1</em>
  • HY-A0095S1
    Flibanserin-d4-1

    BIMT-17-d<sub>4sub>-1; BIMT-17BS-d<sub>4sub>-1

    		 Isotope-Labeled Compounds 5-HT Receptor Neurological Disease
    Flibanserin-d4-1 is deuterium labeled Flibanserin. Flibanserin (BIMT-17) is a full agonist of the serotonin 5-HT1A receptor (Ki=1 nM) and an antagonist of 5-HT2A (49 nM). Flibanserin binds to dopamine D4 receptors (4-24 nM), and has negligible affinity for a variety of other neurotransmitter receptors and ion channels. Flibanserin is efficacious in treating hypoactive sexual desire disorder (HSDD)[1][2].
    Flibanserin-d<em>4</em>-<em>1</em>
  • HY-15592S2
    Cabotegravir-d3-1

    GSK-1265744-d<sub>3sub>-1; S/GSK1265744-d<sub>3sub>-1

    		 Isotope-Labeled Compounds HIV Integrase Infection
    Cabotegravir d3-1 (GSK-1265744-d3-1) is a deuterium substitute of Cabotegravir. Cabotegravir is a potent HIV integrase inhibitor used in AIDS research [1]
    Cabotegravir-d3-<em>1</em>
  • HY-157440
    AChE/Aβ-IN-3

    		Amyloid-β Reactive Oxygen Species Cholinesterase (ChE) Neurological Disease
    AChE/Aβ-IN-3 (compound AM5) is a dual inhibitor of AChE and Amyloid-β aggregation with IC50<.sub> values of 1.29 and 4.93 μM, respectively. AChE/Aβ-IN-3 has antioxidant properties that scavenge ROS and restore their normal levels. AChE/Aβ-IN-3 can be used in the study of neurological diseases, such as Alzheimer's disease [1].
    AChE/Aβ-IN-3
  • HY-N0210S6
    D-Galactose-d1-1

    D-(+)-Galactose-d<sub>1sub>-1

    		 Isotope-Labeled Compounds Endogenous Metabolite Neurological Disease
    D-Galactose-d-1 is the deuterium labeled D-Galactose. D-Galactose is a natural aldohexose and C-4 epimer of glucose.
    D-Galactose-d<em>1</em>-<em>1</em>
  • HY-144290
    ARN25068

    		GSK-3 DYRK Neurological Disease
    ARN25068 is a sub-micromolar inhibitor of the three protein kinases, GSK-3β, FYN and DYRK1A to tackle tau hyperphosphorylation [1].
    ARN25068
  • HY-B1716S1
    L-5-Hydroxytryptophan-d3-1

    L-5-HTP-d<sub>3sub>-1; Oxitriptan-d<sub>3sub>-1

    		 Endogenous Metabolite
    L-5-Hydroxytryptophan-d3-1 is the deuterium labeled L-5-Hydroxytryptophan[1]. L-5-Hydroxytryptophan (L-5-HTP), a naturally occurring amino acid and a dietary supplement for use as an antidepressant, appetite suppressant, and sleep aid, is the immediate precursor of the neurotransmitter serotonin and a reserpine antagonist[2]. L-5-Hydroxytryptophan (L-5-HTP) is used to treat fibromyalgia, myoclonus, migraine, and cerebellar ataxia[3][4][5][6].
    L-5-Hydroxytryptophan-d3-<em>1</em>
  • HY-B1659S3
    Glycerol-d1

    Glycerin-d<sub>1sub>

    		 Endogenous Metabolite Cardiovascular Disease Inflammation/Immunology Cancer
    Glycerol-d is the deuterium labeled Glycerol. Glycerol is used in sample preparation and gel formation for polyacrylamide gel electrophoresis.
    Glycerol-d<em>1</em>
  • HY-N7118
    Clindamycin hydrochloride monohydrate

    		Bacterial Antibiotic Infection Cancer
    Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1) or alpha-haemolysin (Hla) [1].
    Clindamycin hydrochloride monohydrate
  • HY-Y1139S
    Pimelic acid-d4

    Heptanedioic acid-d<sub>4sub>; 1,5-Pentanedicarboxylic acid-d<sub>4sub>; 1,7-Heptanedioic acid-d<sub>4sub>

    		 Endogenous Metabolite Metabolic Disease
    Pimelic acid-d4 is the deuterium labeled Pimelic acid[1]. Pimelic acid is the organic compound and its derivatives are involved in the biosynthesis of the amino acid called lysine.
    Pimelic acid-d<em>4</em>
  • HY-129946
    Dopamine D2 receptor antagonist-1

    		Dopamine Receptor Neurological Disease
    Dopamine D2 receptor antagonist-1 is a negative allosteric modulator (NAM) of the dopamine D2 receptor (D2R) with sub-mM affinity [1].
    Dopamine D2 receptor antagonist-<em>1</em>
  • HY-163129
    BPU

    		Apoptosis MMP Cancer
    BPU arrests cell cycle progression in the sub-G1 phase. BPU is an anticancer agent through inhibiting blood vessel formation in tumor tissues [1].
    BPU

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