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.
All Product Categories
-
Isotope-Labeled Compounds Related Products (11098)
Related Products (11098)
-
4-Hydroxy alverine-d5 hydrochloride
0 ImagesCat. No.: HY-132330S14-Hydroxy alverine-d5 (hydrochloride) is the deuterium labeled 4-Hydroxy alverine hydrochloride.
-
Avatrombopag-d8 hydrochloride
0 ImagesCat. No.: HY-13463BSSynonyms: AKR-501-d8 hydrochloride; E5501-d8 hydrochloride; YM477-d8 hydrochlorideAvatrombopag-d8 (hydrochloride) is deuterium labeled Avatrombopag (hydrochloride). Avatrombopag (AKR-501) hydrochloride is an orally active, nonpeptide thrombopoietin (TPO) receptor agonist (EC50=3.3 nM). Avatrombopag hydrochloride mimics the biological activities of TPO. Avatrombopag hydrochloride increases platelet production by activating the intracellular signaling system, and promotes production of platelets and megakaryocytes from hemopoietic precursor cells. Avatrombopag hydrochloride is a substrate of cytochrome P450 (CYP) 2C9 and CYP3A.
-
N-Acetyl-D-mannosamine-13C-1
0 ImagesCat. No.: HY-128850S2Synonyms: N-Acetylmannosamine-13C-1; ManNAc-13C-1N-Acetyl-D-mannosamine-13C-1 is the 13C labeled N-Acetyl-D-mannosamine. N-Acetyl-D-mannosamine (ManNAc) is an essential precursor of N-acetylneuraminic acid (NeuAc), the specific monomer of bacterial capsular polysialic acid (PA)-
m-Terphenyl-d14
0 ImagesCat. No.: HY-W009659SCAS No.: 17714-84-0m-Terphenyl-d14 is the deuterium labeled m-Terphenyl (HY-W009659). m-Terphenyl is a non-chlorinated trisphenyl compound and is commonly used as the basic structure for industrial raw materials (such as plastic additives).
-
Acetic acid-13C-1 sodium
0 ImagesCat. No.: HY-Y0817SCAS No.: 13291-89-9Synonyms: Anhydrous sodium acetate-13C-1Acetic acid-13C-1 sodium is the 13C-labeled Acetic acid sodium.
-
Prothionamide-d5
0 ImagesCat. No.: HY-B0306SCAS No.: 1330261-26-1Synonyms: Protionamide-d5Prothionamide-d5 is deuterium labeled Prothionamide (HY-B0306). Prothionamide is an orally active thioamide antibacterial agent. Prothionamide is a substrate of OCT1 with a Km value of 805.8 μM. Prothionamide reacts with NAD to form a covalent adduct, with the adduct being a tight-binding inhibitor of Mycobacterium tuberculosis and Mycobacterium leprae InhA. Prothionamide can effectively inhibit the growth of Mycobacterium tuberculosis (MIC = ~0.5 µg/mL) and Mycobacterium leprae. Prothionamide is used in the research of tuberculosis and leprosy.
-
2-Methoxyestradiol-13C,d3
0 ImagesCat. No.: HY-12033SCAS No.: 1217470-09-12-Methoxyestradiol-13C,d3 is the 13C- and deuterium labeled 2-Methoxyestradiol. 2-Methoxyestradiol (2-ME2), an orally active endogenous metabolite of 17β-estradiol (E2), is an apoptosis inducer and an angiogenesis inhibitor with potent antineoplastic activity. 2-Methoxyestradiol also destablize microtubules. 2-Methoxyestradio, also a potent superoxide dismutase (SOD) inhibitor and a ROS-generating agent, induces autophagy in the transformed cell line HEK293 and the cancer cell lines U87 and HeLa.
-
Estetrol-d3
0 ImagesCat. No.: HY-W744272Estetrol-d3 is the deuterium labeled Estetrol (HY-15731). Estetrol, an orally active estrogen synthesized exclusively during pregnancy by the human fetal liver, is a selective nuclear?estrogen receptor?modulator. Estetrol binds?ERα?as well as?ERβ?(with a fourfold lower affinity). Estetrol increases?eNOS?expression/activity and NO synthesis in endothelial cells. Estetrol exerts estrogenic actions on the endometrium or the central nervous system but presents antagonistic effects on the breast. Estetrol can be used in contraception and menopausal hormone research.
-
Cefadroxil-d4 trifluoroacetate
0 ImagesCat. No.: HY-B1190S1Synonyms: BL-S 578-d4 trifluoroacetateCefadroxil-d4 (trifluoroacetate) is deuterium labeled Cefadroxil.
-
Moxifloxacin-d3-1 hydrochloride
0 ImagesCat. No.: HY-66011AS3CAS No.: 1246816-75-0Synonyms: BAY 12-8039-d3-1Moxifloxacin-d3-1 hydrochloride (BAY 12-8039-d3-1) is a deuterium labeled Moxifloxacin (HY-66011A). Moxifloxacin is an orally active 8-methoxyquinolone antimicrobial for use in the treatment of acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and community-acquired pneumonia.
-
N6-Lauroyl Cordycepin-d23
0 ImagesCat. No.: HY-W741469N6-Lauroyl Cordycepin-d23 is the deuterium labeled N6-Lauroyl Cordycepin (HY-N7812).
-
Hexadecanoate-d2 potassium
0 ImagesCat. No.: HY-W134007S2CAS No.: 203805-86-1Hexadecanoate-d2 (potassium) is the deuterium labeled Hexadecanoate.
-
4,5,6,7-Tetrabromoisobenzofuran-1,3-dione-13C6
0 ImagesCat. No.: HY-W750399Synonyms: Tetrabromophthalic anhydride-13C64,5,6,7-Tetrabromoisobenzofuran-1,3-dione-13C6 (Tetrabromophthalic anhydride-13C6) is the 13C-labeled 4,5,6,7-Tetrabromoisobenzofuran-1,3-dione (HY-W010833).
-
D-Fructose-d2
0 ImagesCat. No.: HY-N7092S16CAS No.: 285979-75-1Synonyms: D(-)-Fructose-d2D-Fructose-d2 is the deuterium labeled D-Fructose. D-Fructose (D(-)-Fructose) is a naturally occurring monosaccharide found in many plants.
-
[U-15N]-ApoA1
![[U-15N]-ApoA1](https://file.medchemexpress.com/product_pic/hy-187271s.gif "Click to View [U-15N]-ApoA1 Product Detail")
0 ImagesCat. No.: HY-187271S[U-15N]-ApoA1 is the 15N-labeled ApoA1. Reduced serum levels of apolipoprotein A1 (ApoA1) are closely associated with cardiovascular diseases, such as coronary heart disease. This isotope can be used in NMR studies to investigate disease mechanisms and in mass spectrometry analysis.
-
2,6-Diaminoheptanedioic acid-15N2
0 ImagesCat. No.: HY-128746S12,6-Diaminoheptanedioic acid-15N2 is 15N labeled 2,6-Diaminoheptanedioic acid (HY-128746). 2,6-Diaminoheptanedioic acid is an endogenous metabolite.
-
Ethyl 3-hydroxybutyrate-d5
0 ImagesCat. No.: HY-W012701SCAS No.: 1206486-01-2Ethyl 3-hydroxybutyrate-d5 is the deuterium labeled Ethyl 3-hydroxybutyrate (HY-W012701). Ethyl 3-hydroxybutyrate is a fragrance found in wine and Tribolium castaneum.
-
Moclobemide-d8
0 ImagesCat. No.: HY-B0534SCAS No.: 2309010-25-9Synonyms: Ro111163-d8Moclobemide-d8 (Ro111163-d8) is the deuterium labeled Moclobemide. Moclobemide (Ro111163) is a brain-penetrant and reversible monoamine oxidase (MAO-A) inhibitor with an IC50 of 6.061 μM for hMAO-A.Moclobemide up-regulates proliferation of hippocampal progenitor cells in chronically stressed mice.
-
N-Desmethyl Pimavanserin-d9 hydrochloride
0 ImagesCat. No.: HY-135392SCAS No.: 2712363-60-3Synonyms: AC-279-d9 hydrochlorideN-Desmethyl Pimavanserin-d9 hydrochloride (AC-279-d9 hydrochloride) is the deuterium labeled N-Desmethyl Pimavanserin (HY-135392). N-Desmethyl Pimavanserin is the active metabolite of Pimavanserin. Pimavanserin is a selective inverse agonist of the 5-HT2A receptor with pIC50 and pKd of 8.73 and 9.3, respectively.
