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 Inhibitors (4)

Isotope-Labeled Compounds Related Products (10876):

Cat. No.	Product Name	Effect	Purity	Chemical Structure

HY-N0221S1

Daurisoline-d₅
Daurisoline-d₅ is the deuterium labeled Daurisoline (HY-N0221). Daurisoline is a bis-benzylisoquinoline alkaloid that can be isolated from Menispermum dauricum and Rhizoma Menispermi. Daurisoline exerts a blocking effect on hERG and has antiarrhythmic effects. Daurisoline is a potent autophagy blocker that can be used for the research of cancer.

HY-B1833S

Afloqualone-d₇
Afloqualone-d₇ (HQ-495-d₇) is deuterium labeled Afloqualone. Afloqualone (HQ-495) is an orally active central muscle relaxant and antivertiginous agent that can increase the sensitivity of GABA receptors in neurons of the lateral vestibular nucleus. Afloqualone (HQ-495) can be used in the research of low back pain and neck-arm-shoulder syndrome.

HY-W585914S

2-(3-Sec-butyl-5-tert-butyl-2-hydroxyphenyl)benzotriazole-d₄
2-(3-Sec-butyl-5-tert-butyl-2-hydroxyphenyl)benzotriazole-d₄ is deuterium labeled 2-(3-Sec-butyl-5-tert-butyl-2-hydroxyphenyl)benzotriazole.

HY-113280S

Pyridoxol 5'-phosphate-d₃
Pyridoxol 5'-phosphate-d₃ is deuterium labeled Pyridoxine 5'-phosphate.

HY-17404S1

Cilnidipine-d₄
Cilnidipine-d₄ (FRC-8653-d₄) is deuterium labeled Cilnidipine. Cilnidipine is a long-acting, second-generation dihydropyridine Ca²⁺-channel blocker on L and N-type Ca²⁺ channel. Antihypertensive effects.

HY-W185208S

Chloridazon metabolite B1-d₃
Chloridazon metabolite B1-d₃ (Methyldesphenylchloridazon-d₃) is deuterium labeled 5-Amino-4-chloro-2-methyl-2,3-dihydropyridazin-3-one.

HY-132476S

N-Methyl Gatifloxacin-d₃
N-Methyl Gatifloxacin-d₃ is the deuterium labeled N-Methyl Gatifloxacin.

HY-116780S

Prothipendyl-d₆ hydrochloride
Prothipendyl-d₆ (hydrochloride) is the deuterium labeled Prothipendyl hydrochloride.

HY-126358S

Acetylcarnitine-d₃
Acetylcarnitine-d₃ is the deuterium labeled Acetylcarnitine (HY-126358). Acetylcarnitine is an endogenous metabolite.

HY-17405S

Alarelin-(Leu-¹³C₆,¹⁵N) TFA
Alarelin-(Leu-sup>13C₁₀,¹⁵N) TFA is the ¹³C- and ¹⁵N-labeled Alarelin TFA.

HY-169220S

RORγ/DHODH-IN-1
RORγ/DHODH-IN-1 (compound 1404), a deuterium labeled compound, is a dual RORγ and DHODH inhibitor with IC₅₀ values of 9.7 nM and 100 nM, repaectively. RORγ/DHODH-IN-1 blocks the replication of SARS-CoV-2, HCMV, and non-enveloped DNA virus (HAdV5).

HY-W707384

Candesartan Cilexetil-d₁₁
Candesartan Cilexetil-d₁₁ (TCV-116-d₁₁) is deuterium labeled Candesartan Cilexetil. Candesartan Cilexetil (TCV-116) is an angiotensin II receptor inhibitor. Candesartan Cilexetil ameliorates the pulmonary fibrosis and has antiviral and skin wound healing effect. Candesartan Cilexetil can be used for the research of high blood pressure.

HY-B0395S

Sitafloxacin-d₄
Sitafloxacin-d₄ (DU6859a-d₄) is deuterium labeled Sitafloxacin. Sitafloxacin (DU6859a) is a potent, orally active fluoroquinolone antibiotic. Sitafloxacin shows antichlamydial activity and antibacterial activities against a broad range of gram-positive and gram-negative bacteria, including anaerobic bacteria, as well as against atypical pathogens. Sitafloxacin can be used for the research of respiratory tract infection and urinary tract infection.

HY-W753532

Bisphenol B-¹³C₁₂
Bisphenol B-¹³C₁₂ is ¹³C labeled Bisphenol B.

HY-B0679S

Lubiprostone-d₇
Lubiprostone-d₇ (RU-0211-d7) is the deuterium labeled Lubiprostone. Lubiprostone (SPI-0211) increases intestinal fluid secretion through generation of CIC-2/CFTR and activation of cAMP signaling pathway. Lubiprostone inhibits myeloperoxidase (MPO) activity, downregulates Indomethacin (HY-14397)-induced iNOS and TNFα expression. Lubiprostone can be used for chronic constipation research.

HY-15149S2

Romidepsin-d₇
Romidepsin-d₇ (FK 228-d₇) is deuterium labeled Romidepsin. Romidepsin (FK 228) is a Histone deacetylase (HDAC) inhibitor with anti-tumor activities. Romidepsin (FK 228) inhibits HDAC1, HDAC2, HDAC4, and HDAC6 with IC₅₀s of 36 nM, 47 nM, 510 nM and 1.4 μM, respectively. Romidepsin (FK 228) is produced by Chromobacterium violaceum, induces cell G2/M phase arrest and apoptosis.

HY-W010476S1

2,3,5-Trimethylpyrazine-d₃
2,3,5-Trimethylpyrazine-d₃ is deuterated labeled 2,3,5-Trimethylpyrazine (HY-W010476). 2,3,5-Trimethylpyrazine is an endogenous metabolite.

HY-109591S

Oleoyl coenzyme A-¹³C₁₈ lithium
Oleoyl coenzyme A-¹³C₁₈ (lithium) is the ¹³C labeled Oleoyl Coenzyme A lithium. Oleoyl coenzyme A (Oleoyl-CoA) is a thioester of oleic acid and coenzyme A. Oleoyl coenzyme A has a role as an Escherichia coli metabolite and a mouse metabolite.

HY-P0058S

Pramlintide-(Ala-¹³C₃,¹⁵N)
Pramlintide-(Ala-¹³C₃,¹⁵N) is the ¹³C- and ¹⁵N-labeled Pramlintide. Pramlintide is a polypeptide analogue of human amylin. Pramlintide, an antidiabetic agent, is antineoplastic in colorectal cancer.

HY-146899S

CER6-2’R-d₉		99.0%
CER6-2’R-d₉ is deuterium labeled CER6-2’R.

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