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-32208S

tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate-d₄
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate-d₄ is the deuterium labeled tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate[1].

HY-132636S

(Rac)-5-Carboxy tolterodine-d₁₄
(Rac)-5-Carboxy Tolterodine-d₁₄ is the deuterium labeled (Rac)-5-Carboxy Tolterodine.

HY-135336AS1

(S)-Verapamil-d₆ (hydrochloride)
(S)-Verapamil-d₆ ((S)-(-)-Verapamil-d₆) hydrochloride is the deuterium labeled (S)-Verapamil hydrochloride. (S)-Verapamil hydrochloride (S(-)-Verapamil hydrochloride) inhibits leukotriene C4 (LTC4) and calcein transport by MRP1. (S)-Verapamil hydrochloride leads to the death of potentially resistant tumor cells.

HY-118788S

N-Desmethyl rosiglitazone-d₄
N-Desmethyl rosiglitazone-d₄ is the deuterium labeled N-Desmethyl rosiglitazone.

HY-132763S

N-Benzyloxycarbonyl (S)-Lisinopril-d₅
N-Benzyloxycarbonyl (S)-Lisinopril-d₅ Ethyl Methyl Diester is the deuterium labeled N-Benzyloxycarbonyl (S)-Lisinopril Ethyl Methyl Diester.

HY-12772S1

(2R,4S)-Hydroxy Itraconazole-d₈
(2R,4S)-Hydroxy Itraconazole-d₈ is the deuterium labeled (2R,4S)-Hydroxy Itraconazole[1].

HY-141788S

rel-4-Nitrobenzyl (2S,4R)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate-d₆
rel-4-Nitrobenzyl (2S,4R)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate-d₆ is the deuterium labeled rel-4-Nitrobenzyl (2S,4R)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate.

HY-W013376S

Norcyclizine-d₈
Norcyclizine-d₈ is the deuterium labeled Norcyclizine.

HY-141758S

Defluoro linezolid-d₃
Defluoro Linezolid-d₃ is the deuterium labeled Defluoro Linezolid.

HY-Z4206S

Deacetamidine cyano dabigatran-d₃ ethyl ester
Deacetamidine Cyano Dabigatran-d₃ Ethyl Ester is the deuterium labeled Deacetamidine Cyano Dabigatran Ethyl Ester.

HY-B1272AS1

Desipramine-d₃
Desipramine-d₃ is the deuterium labeled Desipramine (HY-B1272A). Desipramine is a first-generation tricyclic antidepressant. Desipramine selectively binds to norepinephrine transporter and blocks neuronal norepinephrine reuptake. Desipramine activates MAPK signaling via ERK1/2, JNK, and p38, represses NF-κB and AP-1 activity, and induces apoptosis via ROS elevation, mitochondrial membrane potential reduction, and intracellular calcium increase. Desipramine also shows anyi-inflammatory activity, inhibiting TNF-α production. Desipramine can be used for the research of hepatocellular cancer, inflammation, and neurological diseases.

HY-A0115S

Ramiprilat-d₃ (Mixture of Diastereomers)
Ramiprilat-d₃ (Mixture of Diastereomers) is the deuterium labeled Ramiprilat (Mixture of Diastereomers).

HY-B0346S

Propylthiouracil-d₅
Propylthiouracil-d₅ is the deuterium labeled Propylthiouracil. Propylthiouracil (6-Propyl-2-thiouracil) is a thyroperoxidase and 5'-deiodinase inhibitor.

HY-B0265S

Nimodipine-d₇		99.35%
Nimodipine-d₇ is the deuterium labeled Nimodipine. Nimodipine (BAY-e 9736) is an orally active, well-tolerated and light-sensitive dihydropyridine calcium antagonist. Nimodipine can be used for the research of cerebrovascular disorders.

HY-132728S

1-[(2R)-N’-Boc-2-amino-2-cyclohexylacetyl]-N-(4’-cyanobenzyl)-2-L-azetidinecarboxamide-d₁₁
1-[(2R)-N’-Boc-2-amino-2-cyclohexylacetyl]-N-(4’-cyanobenzyl)-2-L-azetidinecarboxamide-d₁₁ is the deuterium labeled 1-[(2R)-N’-Boc-2-amino-2-cyclohexylacetyl]-N-(4’-cyanobenzyl)-2-L-azetidinecarboxamide.

HY-B0412S1

Estriol-d
Estriol-d is the deuterium labeled Estriol. Estriol is an antagonist of the G-protein coupled estrogen receptor in estrogen receptor-negative breast cancer cells.

HY-132627S

iso-Colchicine-d₃
iso-Colchicine-d₃ is the deuterium labeled iso-Colchicine.

HY-132690S

N-Demethyl Trimebutine-d₅ hydrochloride
N-Demethyl Trimebutine-d₅ (hydrochloride) is the deuterium labeled N-Demethyl Trimebutine hydrochloride.

HY-17503S2

(S)-Metoprolol-d₇
(S)-Metoprolol-d₇ is the deuterium labeled Metoprolol. Metoprolol (Toprol) is a selective β1 receptor blocker used in treatment of several diseases of the cardiovascular system, especially hypertension[1][2].

HY-B1118S

Secnidazole-d₆
Secnidazole-d₆ is the deuterium labeled Secnidazole. Secnidazole (RP-14539;PM-185184) is an orally active azole antibiotic with a longer half-life than metronidazole (HY-B0318). Secnidazole is against the vaginosis-associated bacteria and has the potential for bacterial vaginosis research.

Name
Email *

	Sorry, but the email address you supplied was invalid.