1. Signaling Pathways
  2. Others
  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 (9621):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N6779S
    Patulin-13C7
    Patulin-13C7 (Terinin-13C7) is the 13C labeled Patulin (HY-N6779). Patulin (Terinin) is a mycotoxin produced by fungi including the Aspergillus, Penicillium, and Byssochlamys species, is suspected to be clastogenic, mutagenic, teratogenic and cytotoxic. Patulin induces autophagy-dependent apoptosis through lysosomal-mitochondrial axis, and causes DNA damage.
    Patulin-<sup>13</sup>C<sub>7</sub>
  • HY-W008642S
    (Leu-13C6,15N)-Leu-OH
    (Leu-13C6,15N)-Leu-OH TFA is a C13 and N15 labeled Leu-Leu-OH TFA. Leu-Leu-OH, a Leu derivative, is a dipeptide.
    (Leu-<sup>13</sup>C<sub>6</sub>,<sup>15</sup>N)-Leu-OH
  • HY-B1912S1
    Amidosulfuron-13C2,d6
    Amidosulfuron-13C2,d6 is the 13C- and deuterium labeled Amidosulfuron.
    Amidosulfuron-<sup>13</sup>C<sub>2</sub>,d<sub>6</sub>
  • HY-B0615AS
    Moricizine-d8 Hydrochloride
    Moricizine-d8 (Hydrochloride) is the deuterium labeled Moricizine Hydrochloride (HY-B0615A). Moricizine Hydrochloride is an orally active Class I antiarrhythmic agent. Moricizine Hydrochloride decreases the maximum rate of phase 0 depolarization; increases rates of phase 2 and 3 repolarization, decreases action potential duration, and decreases effective refractory period.
    Moricizine-d<sub>8</sub> Hydrochloride
  • HY-146721S
    Epicholesterol-2,2,3,4,4,6-d6
    Epicholesterol-2,2,3,4,4,6-d6 is the deuterium labeled Epicholesterol-2,2,3,4,4,6.
    Epicholesterol-2,2,3,4,4,6-d<sub>6</sub>
  • HY-W704006
    1-(3,4-Bis(benzyloxy)phenyl)ethane-1,2-diol-d5
    1-(3,4-Bis(benzyloxy)phenyl)ethane-1,2-diol-d5 is the deuterium labeled 1-(3,4-Bis(benzyloxy)phenyl)ethane-1,2-diol (HY-W704007).
    1-(3,4-Bis(benzyloxy)phenyl)ethane-1,2-diol-d<sub>5</sub>
  • HY-W741478
    Bis(triisopropylsilyl) 2-oleoyl glycerol-d5
    Bis(triisopropylsilyl) 2-oleoyl glycerol-d5 is the deuterium labeled 1,3-O-Bis(triisopropylsilyl) 2-Oleoyl Glycerol (HY-W741480).
    Bis(triisopropylsilyl) 2-oleoyl glycerol-</sub>d<sub>5</sub>
  • HY-12767S1
    Carvedilol metabolite 4-Hydroxyphenyl Carvedilol-d4
    Carvedilol metabolite 4-Hydroxyphenyl Carvedilol-d4 is deuterated labeled Carvedilol metabolite 4-Hydroxyphenyl Carvedilol (HY-12767). 4-Hydroxyphenyl Carvedilol is a metabolite of Carvedilol.
    Carvedilol metabolite 4-Hydroxyphenyl Carvedilol-d<sub>4</sub>
  • HY-112586S1
    Sulfaethoxypyridazine-13C6
    Sulfaethoxypyridazine-13C6 is the 13C6 labeled Sulfaethoxypyridazine. Sulfaethoxypyridazine is a sulfonamide antibacterial agent. Sulfaethoxypyridazine is a sulfonamide that is used in veterinary medicine as feedstuffs.
    Sulfaethoxypyridazine-<sup>13</sup>C<sub>6</sub>
  • HY-18252S
    Avanafil-13C,d3
    Avanafil-13C,d3 is the 13C- and deuterium labeled Avanafil.
    Avanafil-<sup>13</sup>C,d<sub>3</sub>
  • HY-B0409S
    Clonidine-d4
    Clonidine-d4 is the deuterium labeled Clonidine. Clonidine hydrochloride is an agonist of α2-adrenoceptor and potent antihypertensive agent.
    Clonidine-d<sub>4</sub>
  • HY-N0117AS1
    (Z)-Indirubin-d8
    (Z)-Indirubin-d8 is the deuterium labeled (Z)-Indirubin.
    (Z)-Indirubin-d<sub>8</sub>
  • HY-139811S
    Glimepiride-d4
    Glimepiride-d4 is the deuterium labeled Glimepiride.
    Glimepiride-d<sub>4</sub>
  • HY-W726534
    5-Methyl-1-(methyl-d3)-1H-pyrazole-4-sulfonamide
    5-Methyl-1-(methyl-d3)-1H-pyrazole-4-sulfonamide is the deuterium labeled 5-Methyl-1-(methyl)-1H-pyrazole-4-sulfonamide.
    5-Methyl-1-(methyl-d3)-1H-pyrazole-4-sulfonamide
  • HY-17396S
    Butenafine-13C,d3 hydrochloride
    Butenafine-13C,d3 (hydrochloride) is the 13C- and deuterium labeled. Butenafine Hydrochloride (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase.
    Butenafine-<sup>13</sup>C,d<sub>3</sub> hydrochloride
  • HY-B2219S8
    Stearic acid-d
    Stearic acid-d is the deuterium labeled Stearic acid. Stearic acid is a long chain dietary saturated fatty acid which exists in many animal and vegetable fats and oils.
    Stearic acid-d
  • HY-B0843AS
    Metalaxyl-M-d6
    Metalaxyl-M-d6 ((R)-Metalaxyl-d6) is the deuterium labeled Metalaxyl-M (HY-B0843A). Metalaxyl-M ((R)-Metalaxyl) is an orally active and selective inhibitor of fungal RNA polymerase, which exerts fungicidal activity by selectively interfering with the synthesis of fungal ribosomal RNA. Metalaxyl-M can also be used to induce inflammation in hepatocytes and regulate tryptophan metabolism. Metalaxyl-M can be used in ecotoxicology studies.
    Metalaxyl-M-d<sub>6</sub>
  • HY-117275S1
    Meclofenamic acid-13C6
    Meclofenamic acid-13C6 is the 13C6 labeled Meclofenamic acid. Meclofenamic Acid (Meclofenamate), a non-steroidal, anti-inflammatory agent, is a highly selective fat mass and obesity-associated (FTO) enzyme inhibitor. Meclofenamic Acid competes with FTO binding for the m(6)A-containing nucleic acid. Meclofenamic acid is a non-selective gap-junction blocker.
    Meclofenamic acid-<sup>13</sup>C<sub>6</sub>
  • HY-B0144S
    Pitavastatin-d4 hemicalcium
    Pitavastatin-d4 (hemicalcium) is deuterium labeled Pitavastatin (Calcium). Pitavastatin Calcium (NK-104 hemicalcium) is a potent hydroxymethylglutaryl-CoA (HMG-CoA) reductase inhibitor. Pitavastatin Calcium (NK-104 hemicalcium) inhibits cholesterol synthesis from acetic acid with an IC50 of 5.8 nM in HepG2 cells. Pitavastatin Calcium is an efficient hepatocyte low-density lipoprotein-cholesterol (LDL-C) receptor inducer. Anti-cancer activity[1][2][3].
    Pitavastatin-d<sub>4</sub> hemicalcium
  • HY-W009204S2
    Fmoc-Ala-OH-1-13C
    Fmoc-Ala-OH-1-13C is the 13C labeled Fmoc-Ala-OH.
    Fmoc-Ala-OH-1-<sup>13</sup>C