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 (10875):

Cat. No.	Product Name	Effect	Purity	Chemical Structure

HY-W012791S1

2-(Methylamino)acetic acid-d₅ hydrochloride
2-(Methylamino)acetic acid-d₅ (hydrochloride) is the deuterium labeled 2-(Methylamino)acetic acid.

HY-163712S

17-Epiestriol-d₅-1
17-Epiestriol-d₅-1 is the deuterium labeled 17-Epiestriol (HY-163712). 17-Epiestriol is an estrogen metabolite and a selective estrogen receptor (ER) β agonist. 17-epiestriol inhibits the mRNA and protein expression of the vascular cell adhesion molecule VCAM-1 induced by tumor necrosis factor α (TNFα). 17-epiestriol also inhibits TNFα-induced VCAM-1 expression and prevents NF-κB migration to the nucleus. 17-Epiestriol also induces the mRNA and protein expression of endothelial nitric oxide synthase.

HY-144216S

(S)-Cetirizine-d₄ dihydrochloride
(S)-Cetirizine-d₄ (dihydrochloride) is the deuterium labeled (S)-Cetirizine dihydrochloride.

HY-W738640

N,N-dimethyl-N′-p-tolylsulfamide-d₇
N,N-dimethyl-N′-p-tolylsulfamide-d₇ (4-Dimethylaminosulfotoluidide-d₇; N,N-Dimethyl-N-Tolylsulfonyldiamide-d₇) is the deuterium labeled N,N-dimethyl-N′-p-tolylsulfamide (HY-W286414).

HY-N0379S2

D-Mannose-¹⁸O
D-Mannose-¹⁸O is the ¹⁸O labeled D-Mannose. D-Mannose is a carbohydrate, which plays an important role in human metabolism, especially in the glycosylationof specific prote.

HY-166950S

2,2′,3,4,4′,6-Hexabromo diphenyl ether-¹³C₁₂
2,2′,3,4,4′,6-Hexabromo diphenyl ether-¹³C₁₂ is ¹³C labeled 2,2′,3,4,4′,6-Hexabromo diphenyl ether.

HY-W654377

Triptolide-d₃(major) (>90%)
Triptolide-d₃ (major) (>90%) is the deuterium labeled Triptolide (HY-32735). Triptolide is a diterpenoid triepoxide extracted from the root of Tripterygium wilfordii with immunosuppressive, anti-inflammatory, antiproliferative and antitumour effects. Triptolide is a NF-κB activation inhibitor.

HY-W008579S

1,5-Bis(3,4-dimethoxyphenyl)penta-1,4-dien-3-one-d₁₂
1,5-Bis(3,4-dimethoxyphenyl)penta-1,4-dien-3-one-d₁₂ is the deuterium labeled 1,5-Bis(3,4-dimethoxyphenyl)penta-1,4-dien-3-one.

HY-143907S

Atorvastatin EP impurity H-d₅
Atorvastatin EP impurity H-d₅ is the deuterium labeled Atorvastatin EP impurity H.

HY-W415746S

Nonyltriphenylphosphonium bromide-d₅
Nonyltriphenylphosphonium bromide-d₅ is the deuterium labeled Nonyltriphenylphosphonium bromide.

HY-146845S

17:0-22:4 PE-d₅
17:0-22:4 PE-d₅ is deuterium labeled 17:0-22:4 PE.

HY-N0059S3

D-Arabinose-¹³C-3
D-Arabinose-¹³C-3 is the ¹³C 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).

HY-100642S1

3-O-Methyltolcapone-d₄
3-O-Methyltolcapone-d₄ (Ro 40-7591 d₄) is a deuterium labeled 3-O-Methyltolcapone (HY-174062). 3-O-Methyltolcapone (Ro 40-7591) is a metabolite of Tolcapone (HY-17406). Tolcapone (Ro 40-7592) is a selective, potent and orally active COMT inhibitor with an IC₅₀of 773 nM. Tolcapone can inhibits α-syn and Aβ₄₂ oligomerization and fibrillogenesis. Tolcapone can cause oxidative stress and induce cancer cells apoptosis and ROS production. Tolcapone can be used for the researches of cancer and neurological disease, such as Parkinson disease and neuroblastoma.

HY-146717S

N-Acetyl-S-(3-hydroxypropyl)-L-cysteine-d₆ dicyclohexylamine
N-Acetyl-S-(3-hydroxypropyl)-L-cysteine-d₆ (dicyclohexylamine) is the deuterium labeled N-Acetyl-S-(3-hydroxypropyl)-L-cysteine.

HY-W743303

8-Nitro-1-pyrenol-d₈
8-Nitro-1-pyrenol-d₈ is the deuterium labeled 8-Nitro-1-pyrenol.

HY-W008625S

1-Bromohexadecane-16,16,16-d₃		98.8%
1-Bromohexadecane-16,16,16-d₃ is the deuterium labeled 1-Bromohexadecane.

HY-W010179S

2-Methoxynaphthalene-d₇
2-Methoxynaphthalene-d₇ is the deuterium labeled 2-Methoxynaphthalene.

HY-W110702S

1-Bromotridecane-d₂₇
1-Bromotridecane-d₂₇ is the deuterium labeled 1-Bromotridecane.

HY-151895S

(±)-1-Hexadecanoyl-3-chloropropane-dd₅-diol		98.1%
(±)-1-Hexadecanoyl-3-chloropropane-dd₅-diol is the deuterium labeled (±)-1-Hexadecanoyl-3-chloropropane-diol.

HY-10284S3

Linagliptin-d₃-1
Linagliptin-d3-1 (BI 1356-d3-1) is the deuterium labeled Linagliptin (HY-10284). Linagliptin is a highly potent, selective DPP-4 inhibitor with IC₅₀ of 1 nM.

Name
Email *

	Sorry, but the email address you supplied was invalid.