2964 Results for: "5-Acetylthiophene-2-carboxaldehyde&amp"

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

Supplier: Apollo Scientific

6-(Morpholin-4-yl)pyridine-2-carboxaldehyde 97%

Supplier: Apollo Scientific

2,2,3,3-Tetrafluoro-1,4-benzodioxane-6-carboxaldehyde

Supplier: Thermo Fisher Scientific

(R)-(+)-3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde 95%

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

Supplier: Apollo Scientific

1,2-Dimethyl-1H-indole-3-carboxaldehyde 95+%

Supplier: Apollo Scientific

3-[4-(Trifluoromethyl)phenyl]-1H-pyrazole-4-carboxaldehyde

Supplier: Bioss

The protein encoded by this gene can hydrolyse substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumour suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene.

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

Supplier: Bioss

AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

Supplier: Bioss

The protein encoded by this gene can hydrolyze substrates such as AMP-morpholidate, AMP-N-alanine methyl ester, AMP-alpha-acetyl lysine methyl ester, and AMP-NH2. The encoded protein interacts with these substrates via a histidine triad motif, which is part of the loop that binds to the substrate. This gene has been found to be a tumor suppressing gene. Several transcript variants, but only one of them protein-coding, have been found for this gene. [provided by RefSeq, Dec 2012].

Supplier: Apollo Scientific

2-(2,4-Difluorophenoxy)-1-methyl-1H-indole-3-carboxaldehyde 97%

Supplier: Thermo Fisher Scientific

Uracil-5-carboxaldehyde 97%

Supplier: Bioss

AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.

Supplier: Apollo Scientific

3-(3,5-Difluorophenyl)-1H-pyrazole-4-carboxaldehyde 98%

Supplier: Apollo Scientific

2-Bromothiophene-3-carboxaldehyde 97%

Supplier: Thermo Fisher Scientific

2,5-Dimethyl-1-phenylpyrrole-3-carboxaldehyde ≥98%

Supplier: Apollo Scientific

2-[4-(Trifluoromethyl)phenyl]-1,3-thiazole-4-carboxaldehyde

Supplier: Apollo Scientific

5-Chloro-1,3-dimethyl-1H-pyrazole-4-carboxaldehyde oxime

Supplier: Apollo Scientific

3'-(Trifluoromethyl)biphenyl-4-carboxaldehyde

Supplier: Apollo Scientific

2-Methyl-4-(trifluoromethyl)-1,3-thiazole-5-carboxaldehyde 97%

Supplier: Apollo Scientific

5-(Fur-2-yl)-1-methyl-1H-pyrazole-3-carboxaldehyde 97%

Supplier: Apollo Scientific

2-Methyl-4-phenyl-1,3-thiazole-5-carboxaldehyde 97%

Supplier: Apollo Scientific

5-Fluoro-1-methyl-1H-indazole-6-carboxaldehyde

Supplier: PanReac AppliChem

Rifampicin

Supplier: Apollo Scientific

1,4-Dioxaspiro[4.5]decane-8-carboxaldehyde

Supplier: Bioss

AMP deaminase plays a critical role in energy metabolism.Involvement in diseaseDefects in AMPD3 are the cause of adenosine monophosphate deaminase deficiency erythrocyte type (AMPDDE); also known as erythrocyte AMP deaminase deficiency. AMPDDE is a metabolic disorder due to lack of activity of the erythrocyte isoform of AMP deaminase. It is a clinically asymptomatic condition characterized by a 50% increase in steady-state levels of ATP in affected cells. Individuals with complete deficiency of erythrocyte AMP deaminase are healthy and have no hematologic disorders.

Supplier: Apollo Scientific

Imidazo[1,5-a]pyridine-3-carboxaldehyde 98%

Supplier: Apollo Scientific

2-Chloro-6-ethoxyquinoline-3-carboxaldehyde