carbamoyl

H3B-120 is a highly selective, competitive, and allosteric carbamoyl phosphate synthetase 1 (CPS1) inhibitor with an IC50 of 1.5 μM and a Ki of 1.4 μM, exhibiting anti-cancer activity.

2-((Azido-PEG8-carbamoyl)methoxy)acetic acid is a polyethylene glycol (PEG) derivative used as a linker in the synthesis of proteolysis targeting chimeras (PROTACs) [1].

m-((3-Chloro-4-(3-(2,4,6-triamino-5-pyrimidinyl)propoxy)phenyl)carbamoyl)benzenesulfonyl fluoride is a bioactive chemical.

m-((3-Chloro-4-(3-(2,4,6-triamino-5-pyrimidinyl)propoxy)phenyl)carbamoyl)benzenesulfonyl fluoride monoethanesulfonate can be used in related research in the field of life sciences. Its product number is T33123 and CAS number is 22478-95-1.

(-)-Sitagliptin carbamoyl glucuronide is a minor phase II metabolite of the dipeptidyl peptidase 4 (DPP-4) inhibitor (-)-sitagliptin . (-)-Sitagliptin carbamoyl glucuronide is formed by N-carbamoyl glucuronidation and has been found in rat and dog plasma following administration of (-)-sitagliptin.

N-Carbamoyl-DL-aspartic acid (Ureidosuccinic acid) is an intermediary product in pyrimidine biosynthesis.

[(2,6-Dimethylphenyl)Carbamoyl]Formic acid is a useful organic compound for research related to life sciences. The catalog number is T66191 and the CAS number is 2903-48-2.

(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-carbamoyl-2,6-dimethylphenyl)propanoic acid is a useful organic compound for research related to life sciences. The catalog number is T66476 and the CAS number is 623950-02-7.

Carbamoyl phosphate dilithium salt acts as an anti-sickling agent and plays a significant role in the urea cycle. It modifies the terminal valine residues of hemoglobin S in red blood cells through formylation, thereby disrupting the sickling process. The lithium cations present in Carbamoyl phosphate dilithium salt contribute to its toxicity.

3β-[N-(N′,N′-Dimethylaminoethyl)carbamoyl]cholesterol is a lipid utilized in research for cancer gene therapy and vaccine delivery systems.

2-Carbamoyl-3-hydroxy-1,4-naphthoquinone is a natural product for research related to life sciences. The catalog number is TN5790 and the CAS number is 103646-20-4.

N-Carbamoyl-L-aspartic acid, an intermediate in pyrimidine metabolism, can be utilized to measure the enzyme activity of dihydroorotase (DHOse) [1] [2].

3-(S)-(1-Carbamoyl-1,1-diphenylmethyl)pyrrolidine tartrate is a pharmaceutical intermediate used in the synthesis of various active compounds.

N-Carbamoyl-alanine-CoA (N-Carbamoyl-alanine-coenzyme A) is a derivative of coenzyme A.

N-Carbamoyl-L-aspartate-CoA (N-Carbamoyl-L-aspartate-coenzyme A) is a derivative of coenzyme A.

Ethyl 2-carbamoyloxybenzoate, abbreviated as ECXB, is a compound used as a molecular structural unit. It is a synthetic derivative of benzoyloxybenzoic acid and has been used in the synthesis of drugs, the study of biochemical and physiological effects of compounds, the study of drug metabolism, and the study of the effects of drugs on the body.

Descarbamoyl cefuroxime is also an intermediate in the synthesis of cephalosporin antibiotics. Decarbamyl cefuroxime is a degradation product of cefuroxime.

Bromoacetamido-PEG9-ethylcarbamoyl-C12-Boc is a polyethylene glycol (PEG) derived linker used in synthesizing proteolysis-targeting chimeras (PROTACs) [1].

Bromoacetamido-PEG9-ethylcarbamoyl-C4-Boc is a polyethylene glycol (PEG)-based proteolysis targeting chimera (PROTAC) linker used in the synthesis of PROTACs[1].

Bromoacetamido-PEG9-ethylcarbamoyl-C8-Boc represents a PEG-based PROTAC linker suitable for synthesizing PROTACs[1].

Decarbamoylmitomycin C, an analog of Mitomycin C (MC), functions as a DNA alkylating agent. It is capable of activating chromatin relaxation by the ataxia-telangiectasia and Rad3-related protein (ATR) in a p53-independent manner.

Ammonium, (m-(N-methylcarbamoylmethoxy)phenyl)trimethyl-, methylsulfate is a bioactive chemical.

Valeranilide, 2-chloro-3'-hydroxy-, methylcarbamate (ester) is a bioactive chemical.

S-(N-PhenethylthiocarbaMoyl)-L-cysteine (PEITC-Cys) is an anticarcinogenic agent that exhibits antileukemic activity by inhibiting DNA synthesis in HL60 cells [1] and acts as an inhibitor of P450 [2].