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  3. Isotope-Labeled Compounds

Isotope-Labeled Compounds

Isotope-labeled compounds are chemical substances in which some atoms in their molecules are replaced by isotope atoms. The range of stable isotope products can cover from gases to complex molecules. Isotope-labeled compounds could provide a site-specific investigation of structures, making molecules easily detectable by mass spectrometry and NMR, and maintaining the physico-chemical properties of the target molecule at the same time. MCE isotope-labeled compounds are all stable isotope-labeled compounds and are non-radioactive labeled substances. MCE isotope-labeled compounds are unique tools for identifying and understanding biological and chemical processes. Stable isotope-labeled products are now getting more and more popular among scientists. The scope of application is gradually penetrating into various scientific fields, such as life sciences, food and medicine, agriculture, environment, geology, etc. Stable isotope-labeled compounds have a wide range of applications in the Life Science areas, such as Metabolomics, Proteomics, Clinical studies, Deuterium drugs, etc.

Isotope-Labeled Compounds Related Products (10876):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-W778954
    2,2-Dimethyl-1,3-dioxolane-4-methanol-13C3
    2,2-Dimethyl-1,3-dioxolane-4-methanol-13C3 ((2,2-Dimethyl-[1,3] dioxane-4-yl)-methanol-13C3) is the 13C-labeled 2,2-Dimethyl-1,3-dioxolane-4-methanol (HY-Y1372).
    2,2-Dimethyl-1,3-dioxolane-4-methanol-<sup>13</sup>C<sub>3</sub>
  • HY-W702292
    (R)-(+)-Verapamil-d6 hydrochloride
    (R)-(+)-Verapamil-d6 (hydrochloride) is deuterium labeled (R)-Verapamil (hydrochloride). (R)-Verapamil hydrochloride ((R)-(+)-Verapamil hydrochloride) is a P-Glycoprotein inhibitor. (R)-Verapamil hydrochloride blocks MRP1 mediated transport, resulting in chemosensitization of MRP1-overexpressing cells to anticancer agents.
    (R)-(+)-Verapamil-d<sub>6</sub> hydrochloride
  • HY-150981S
    1,2-O-Isopropylidene-a-D-glucofuranuronic-6-13C acid, γ-lactone
    1,2-O-Isopropylidene-a-D-glucofuranuronic-6-13C acid, γ-lactone is the 13C labeled 1,2-O-Isopropylidene-β-L-idofuranuronic acid, γ-lactone.
    1,2-O-Isopropylidene-a-D-glucofuranuronic-6-<sup>13</sup>C acid, γ-lactone
  • HY-131104AS
    Brombuterol-d9 hydrochloride
    Brombuterol-d9 (hydrochloride) is a deuterium labeled Brombuterol hydrochloride. Brombuterol hydrochloride is a β-adrenergic receptor agonist.
    Brombuterol-d<sub>9</sub> hydrochloride
  • HY-W742688
    Crotonobetaine Hydrochloride-d9
    Crotonobetaine Hydrochloride-d9 is the deuterium labeled Levocarnitine Impurity 6 (HY-Z12757).
    Crotonobetaine Hydrochloride-d<sub>9</sub>
  • HY-W750404
    (-)-Carvone-d4
    (-)-Carvone-d4 is the deuterium labeled (-)-Carvone (HY-W017423). (-)-Carvone is an insect neurotoxin and a irreversible acetylcholinesterase (AChE) inhibitor. (-)-Carvone can be used as a bird repellent, inhibits larval growth, decreases pupatation rate, and increases mortality of larvae.
    (-)-Carvone-d<sub>4<sub>
  • HY-13004S
    Maraviroc-d6
    Maraviroc-d6 (UK-427857-d6) is the deuterium labeled Maraviroc. Maraviroc (UK-427857) is a selective CCR5 antagonist with activity against human HIV.
    Maraviroc-d<sub>6</sub>
  • HY-N0059S5
    D-Arabinose-d5
    D-Arabinose-d5 is the deuterium labeled D-Arabinose (HY-N0059). D-Arabinose is is an orally active antidepressant and a growth inhibitor of C. elegans (IC50 is 7.5 mM). D-Arabinose can penetrate the blood-brain barrier, selectively interfere with the metabolism of D-ribose and D-fructose, and inhibit the growth of nematodes. D-Arabinose can also inhibit the synthesis of cell biofilm and exert antibacterial activity. D-Arabinose activates the ACSS2-PPARγ/TFEB-CRTC1 axis through the lysosomal AXIN-LKB1-AMPK pathway, inducing CRTC1 transcription, exerts antidepressant-like activity. D-Arabinose is the ring-opened form of the aldopentose D-?Arabinose (HY-N7082).
    D-Arabinose-d<sub>5</sub>
  • HY-113405S
    21-Desoxycortisol-d4
    21-Desoxycortisol-d4 is the deuterium labeled 21-Desoxycortisol.
    21-Desoxycortisol-d<sub>4</sub>
  • HY-W739665
    9-(2-Hydroxypropyl)adenine-d6
    9-(2-Hydroxypropyl)adenine-d6 is the deuterium labeled 9-(2-Hydroxypropyl)adenine (HY-W751009).
    9-(2-Hydroxypropyl)adenine-d<sub>6</sub>
  • HY-P60514S1
    NQVS-(Leu-13C6,15N)-SCA-(Val-13C5,15N)-K TFA
    NQVS-(Leu-13C6,15N)-SCA-(Val-13C5,15N)-K TFA is the 13C- and 15N-labeled NQVSSCAK TFA.
    NQVS-(Leu-<sup>13</sup>C<sub>6</sub>,<sub>15</sub>N)-SCA-(Val-<sup>13</sup>C<sub>5</sub>,<sub>15</sub>N)-K TFA
  • HY-144953S
    Abiraterone sulfate-d4 sodium
    Abiraterone sulfate-d4 sodium is the deuterium labeled Abiraterone sulfate sodium (HY-131936). Abiraterone sulfate is a metabolite of Abiraterone (HY-148377). Abiraterone is a potent and irreversible?CYP17A1 inhibitor?with antiandrogen activity.
    Abiraterone sulfate-d<sub>4</sub> sodium
  • HY-16168AS2
    Degarelix-d7 TFA-1
    Degarelix-d7 TFA-1 (FE 200486-d7 TFA-1) is the deuterium labeled Degarelix TFA. Degarelix acetate (FE 200486) is a decapeptide that shows high affinity/selectivity to human gonadotropin-releasing hormone (GnRH) receptor (IC50 = 3 nM). Degarelix acetate Degarelix acetate (FE 200486) is used for the research of prostate cancer.
    Degarelix-d<sub>7</sub> TFA-1
  • HY-B0343AS
    Sarafloxacin-d8 hydrochloride
    Sarafloxacin-d8 (A-56620-d8) hydrochloride is the deuterium labeled Sarafloxacin hydrochloride. Sarafloxacin hydrochloride (A-56620 hydrochloride) is a quinolone antibiotic drug.
    Sarafloxacin-d<sub>8</sub> hydrochloride
  • HY-B1148AS
    Furaltadone-d5
    Furaltadone-d5 is the deuterium labeled Furaltadone (HY-B1148A). Furaltadone, a nitrofuran agent, has the potential for the study in infections of chickens with salmonella enteritidis. Furaltadone is inhibitory and bactericidal in vitro for staphylococci .
    Furaltadone-d<sub>5</sub>
  • HY-Y0215S
    5-Azacytosine-13C,15N2
    5-Azacytosine-13C,15N2 is the 13C- and 15N-labeled 5-Azacytosine.
    5-Azacytosine-<sup>13</sup>C,<sup>15</sup>N<sub>2</sub>
  • HY-141987S
    2-Hydroxy atorvastatin-d5
    2-Hydroxy atorvastatin-d5 (Atorvastatin impurity K-d5) is the deuterium labeled 2-Hydroxy atorvastatin. 2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt. Atorvastatin is a potent HMG-CoA reductase inhibitor with an IC50 value of 8 nM.
    2-Hydroxy atorvastatin-d<sub>5</sub>
  • HY-Y1051S
    (Chlorocarbonyl)cyclohexane-d11
    (Chlorocarbonyl)cyclohexane-d11 is the deuterium labeled (Chlorocarbonyl)cyclohexane.
    (Chlorocarbonyl)cyclohexane-d<sub>11</sub>
  • HY-W779018
    Xylose-13C2
    Xylose-13C2 (D-(+)-Xylose-13C2) is the 13C-labeled Xylose. Xylose (D-(+)-Xylose) is a natural pentose sugar that is catalyzed by xylose isomerase to form xylulose, which is a key step in the anaerobic ethanol fermentation of Xylose. Xylose can be used by microorganisms to produce fuels, chemicals, and bulk industrial enzymes. Xylose provides the substances and energy for cells, as a carbon source for the biosynthesis of high-value chemicals and biofuel. Xylose can be used to fully explore lignocellulose resources and provide a new direction for microbia fermentation.
    Xylose-<sup>13</sup>C<sub>2</sub>
  • HY-A0090S
    Nitrofurantoin-13C3
    Nitrofurantoin-13C3 is the 13C labeled Nitrofurantoin (HY-A0090). Nitrofurantoin is a potent and orally active broad-spectrum beta-lactamase antimicrobial agent. Nitrofurantoin acts as an antibiotic and can be used for the study of urinary tract infections (UTIs), including cystitis and kidney infections.
    Nitrofurantoin-<sup>13</sup>C<sub>3</sub>