NCBI Taxonomy: 577015

Bridelia balansae (ncbi_taxid: 577015)

found 21 associated metabolites at species taxonomy rank level.

Ancestor: Bridelia

Child Taxonomies: none taxonomy data.

Adenine

7H-purin-6-amine

C5H5N5 (135.0545)


Adenine is the parent compound of the 6-aminopurines, composed of a purine having an amino group at C-6. It has a role as a human metabolite, a Daphnia magna metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a purine nucleobase and a member of 6-aminopurines. It derives from a hydride of a 9H-purine. A purine base and a fundamental unit of adenine nucleotides. Adenine is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Adenine is a natural product found in Fritillaria cirrhosa, Annona purpurea, and other organisms with data available. Adenine is a purine nucleobase with an amine group attached to the carbon at position 6. Adenine is the precursor for adenosine and deoxyadenosine nucleosides. Adenine is a purine base. Adenine is found in both DNA and RNA. Adenine is a fundamental component of adenine nucleotides. Adenine forms adenosine, a nucleoside, when attached to ribose, and deoxyadenosine when attached to deoxyribose; it forms adenosine triphosphate (ATP), a nucleotide, when three phosphate groups are added to adenosine. Adenosine triphosphate is used in cellular metabolism as one of the basic methods of transferring chemical energy between chemical reactions. Purine inborn errors of metabolism (IEM) are serious hereditary disorders, which should be suspected in any case of neonatal fitting, failure to thrive, recurrent infections, neurological deficit, renal disease, self-mutilation and other manifestations. Investigation usually starts with uric acid (UA) determination in urine and plasma. (OMIM 300322, 229600, 603027, 232400, 232600, 232800, 201450, 220150, 232200, 162000, 164050, 278300). (A3372, A3373). Adenine is a metabolite found in or produced by Saccharomyces cerevisiae. A purine base and a fundamental unit of ADENINE NUCLEOTIDES. See also: adenine; dextrose, unspecified form (component of) ... View More ... Adenine is a purine base. Adenine is found in both DNA and RNA. Adenine is a fundamental component of adenine nucleotides. Adenine forms adenosine, a nucleoside, when attached to ribose, and deoxyadenosine when attached to deoxyribose; it forms adenosine triphosphate (ATP), a nucleotide, when three phosphate groups are added to adenosine. Adenosine triphosphate is used in cellular metabolism as one of the basic methods of transferring chemical energy between chemical reactions. Purine inborn errors of metabolism (IEM) are serious hereditary disorders, which should be suspected in any case of neonatal fitting, failure to thrive, recurrent infections, neurological deficit, renal disease, self-mutilation and other manifestations. Investigation usually starts with uric acid (UA) determination in urine and plasma. (OMIM 300322, 229600, 603027, 232400, 232600, 232800, 201450, 220150, 232200, 162000, 164050, 278300). (PMID: 17052198, 17520339). Widespread throughout animal and plant tissue, purine components of DNA, RNA, and coenzymes. Vitamin The parent compound of the 6-aminopurines, composed of a purine having an amino group at C-6. Adenine (/ˈædɪnɪn/) (symbol A or Ade) is a purine nucleobase. It is one of the four nucleobases in the nucleic acids of DNA, the other three being guanine (G), cytosine (C), and thymine (T). Adenine derivatives have various roles in biochemistry including cellular respiration, in the form of both the energy-rich adenosine triphosphate (ATP) and the cofactors nicotinamide adenine dinucleotide (NAD), flavin adenine dinucleotide (FAD) and Coenzyme A. It also has functions in protein synthesis and as a chemical component of DNA and RNA.[2] The shape of adenine is complementary to either thymine in DNA or uracil in RNA. The adjacent image shows pure adenine, as an independent molecule. When connected into DNA, a covalent bond is formed between deoxyribose sugar and the bottom left nitrogen (thereby removing the existing hydrogen atom). The remaining structure is called an adenine residue, as part of a larger molecule. Adenosine is adenine reacted with ribose, as used in RNA and ATP; Deoxyadenosine is adenine attached to deoxyribose, as used to form DNA. Adenine forms several tautomers, compounds that can be rapidly interconverted and are often considered equivalent. However, in isolated conditions, i.e. in an inert gas matrix and in the gas phase, mainly the 9H-adenine tautomer is found.[3][4] Purine metabolism involves the formation of adenine and guanine. Both adenine and guanine are derived from the nucleotide inosine monophosphate (IMP), which in turn is synthesized from a pre-existing ribose phosphate through a complex pathway using atoms from the amino acids glycine, glutamine, and aspartic acid, as well as the coenzyme tetrahydrofolate. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3].

   

N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine

(3-Methyl-but-2-enyl)-(7(9)H-purin-6-yl)-amine

C10H13N5 (203.1171)


N6-prenyladenine, also known as isopentenyladenine or ip, is a member of the class of compounds known as 6-alkylaminopurines. 6-alkylaminopurines are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. N6-prenyladenine is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). N6-prenyladenine can be found in a number of food items such as lime, lemon thyme, nectarine, and napa cabbage, which makes n6-prenyladenine a potential biomarker for the consumption of these food products. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D003583 - Cytokinins Acquisition and generation of the data is financially supported in part by CREST/JST. CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 74 6-(γ,γ-Dimethylallylamino)purine is a plant growth substance. 6-(γ,γ-Dimethylallylamino)purine is a plant growth substance.

   

Triacanthine

3-(3-methylbut-2-en-1-yl)-3H-purin-6-amine

C10H13N5 (203.1171)


   

CHEMBL298115

CHEMBL298115

C10H13N5 (203.1171)


   

3-(3-methylbut-2-en-1-yl)-3H-purin-6-amine

3-(3-methylbut-2-en-1-yl)-3H-purin-6-amine

C10H13N5 (203.1171)


   

Adenine

Adenine

C5H5N5 (135.0545)


COVID info from PDB, Protein Data Bank, COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2357 INTERNAL_ID 2357; CONFIDENCE Reference Standard (Level 1) MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; GFFGJBXGBJISGV_STSL_0142_Adenine_0125fmol_180430_S2_LC02_MS02_16; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3].

   

Adenin

InChI=1\C5H5N5\c6-4-3-5(9-1-7-3)10-2-8-4\h1-2H,(H3,6,7,8,9,10

C5H5N5 (135.0545)


COVID info from PDB, Protein Data Bank, COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3]. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis[1][2][3].

   

N(6)-dimethylallyladenine

N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine

C10H13N5 (203.1171)


A 6-isopentenylaminopurine in which has the isopentenyl double bond is located between the 2 and 3 positions of the isopentenyl group. D006133 - Growth Substances > D010937 - Plant Growth Regulators > D003583 - Cytokinins 6-(γ,γ-Dimethylallylamino)purine is a plant growth substance. 6-(γ,γ-Dimethylallylamino)purine is a plant growth substance.

   

9-(3-methylbut-2-en-1-yl)purin-6-amine

9-(3-methylbut-2-en-1-yl)purin-6-amine

C10H13N5 (203.1171)


   

(2e)-3-methylhexadec-2-en-1-yl (6s,8r)-6,8,11-trimethyldodecanoate

(2e)-3-methylhexadec-2-en-1-yl (6s,8r)-6,8,11-trimethyldodecanoate

C32H62O2 (478.475)


   

(2s,3s,4s,5s)-2-{[(2r,3r,4s)-6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy}oxane-3,4,5-triol

(2s,3s,4s,5s)-2-{[(2r,3r,4s)-6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy}oxane-3,4,5-triol

C25H32O10 (492.1995)


   

(3ar,11as)-3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

(3ar,11as)-3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

C31H50O (438.3861)


   

(2e)-3-methylhexadec-2-en-1-yl (10s,12r)-10,12,15-trimethylhexadecanoate

(2e)-3-methylhexadec-2-en-1-yl (10s,12r)-10,12,15-trimethylhexadecanoate

C36H70O2 (534.5376)


   

3-methylhexadec-2-en-1-yl 6,8,11-trimethyldodecanoate

3-methylhexadec-2-en-1-yl 6,8,11-trimethyldodecanoate

C32H62O2 (478.475)


   

1-(3-methylbut-2-en-1-yl)purin-6-amine

1-(3-methylbut-2-en-1-yl)purin-6-amine

C10H13N5 (203.1171)


   

5-(3-methylbut-2-en-1-yl)-1h-pyrrolo[3,4-d]imidazole-4,6-dione

5-(3-methylbut-2-en-1-yl)-1h-pyrrolo[3,4-d]imidazole-4,6-dione

C10H11N3O2 (205.0851)


   

3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

C31H50O (438.3861)


   

(2e)-3-methylhexadec-2-en-1-yl 10,12,15-trimethylhexadecanoate

(2e)-3-methylhexadec-2-en-1-yl 10,12,15-trimethylhexadecanoate

C36H70O2 (534.5376)


   

3-methylhexadec-2-en-1-yl 10,12,15-trimethylhexadecanoate

3-methylhexadec-2-en-1-yl 10,12,15-trimethylhexadecanoate

C36H70O2 (534.5376)


   

(1r,3ar,3br,5ar,9as,9bs,11as)-3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

(1r,3ar,3br,5ar,9as,9bs,11as)-3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylidenehept-1-en-2-yl)-dodecahydrocyclopenta[a]phenanthren-7-one

C31H50O (438.3861)


   

(2e)-3-methylhexadec-2-en-1-yl 6,8,11-trimethyldodecanoate

(2e)-3-methylhexadec-2-en-1-yl 6,8,11-trimethyldodecanoate

C32H62O2 (478.475)