KEGG   COMPOUND: C00483
Entry
C00483                      Compound                               

Name
Tyramine;
2-(p-Hydroxyphenyl)ethylamine
Formula
C8H11NO
Exact mass
137.0841
Mol weight
137.179
Structure
Reaction
Pathway
map00350  Tyrosine metabolism
map00680  Methane metabolism
map00950  Isoquinoline alkaloid biosynthesis
map01060  Biosynthesis of plant secondary metabolites
map01063  Biosynthesis of alkaloids derived from shikimate pathway
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
map01240  Biosynthesis of cofactors
map04080  Neuroactive ligand-receptor interaction
map04974  Protein digestion and absorption
Module
M00935  Methanofuran biosynthesis
Enzyme
1.4.3.4         1.4.3.21        1.4.9.2         1.14.13.-       
1.14.18.1       2.1.1.27        2.3.1.110       4.1.1.25        
4.1.1.28        6.3.4.24
Brite
Compounds with biological roles [BR:br08001]
 Peptides
  Amines
   Biogenic amines
    C00483  Tyramine
Phytochemical compounds [BR:br08003]
 Alkaloids
  Alkaloids derived from tyrosine
   Tyramine derivatives
    C00483  Tyramine
Other DBs
CAS: 51-67-2
PubChem: 3766
ChEBI: 15760
ChEMBL: CHEMBL11608
KNApSAcK: C00001435
PDB-CCD: AEF[PDBj]
3DMET: B01260
NIKKAJI: J4.123H
KCF data

ATOM        10
            1   C8y C    25.9700  -18.5500
            2   C8x C    25.9700  -19.9500
            3   C8x C    24.7800  -17.8500
            4   C1b C    27.2300  -17.8500
            5   C8x C    24.7800  -20.6500
            6   C8x C    23.5900  -18.4800
            7   C1b C    28.4200  -18.6200
            8   C8y C    23.5900  -19.9500
            9   N1a N    29.6100  -17.9200
            10  O1a O    22.3300  -20.5800
BOND        10
            1     1   2 2
            2     1   3 1
            3     1   4 1
            4     2   5 1
            5     3   6 2
            6     4   7 1
            7     5   8 2
            8     7   9 1
            9     8  10 1
            10    6   8 1

» Japanese version

KEGG   COMPOUND: C00388
Entry
C00388                      Compound                               

Name
Histamine;
1H-Imidazole-4-ethanamine;
2-(4-Imidazolyl)ethylamine
Formula
C5H9N3
Exact mass
111.0796
Mol weight
111.1451
Structure
Remark
Same as: D08040
Reaction
Pathway
map00340  Histidine metabolism
map01065  Biosynthesis of alkaloids derived from histidine and purine
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
map04080  Neuroactive ligand-receptor interaction
map04664  Fc epsilon RI signaling pathway
map04721  Synaptic vesicle cycle
map04750  Inflammatory mediator regulation of TRP channels
map04971  Gastric acid secretion
map04974  Protein digestion and absorption
map05310  Asthma
map07227  Histamine H2/H3 receptor agonists/antagonists
Enzyme
1.4.3.22        2.1.1.8         2.3.1.-         4.1.1.22        
6.3.2.18
Brite
Compounds with biological roles [BR:br08001]
 Peptides
  Amines
   Biogenic amines
    C00388  Histamine
 Hormones and transmitters
  Other hormones
   Histamine
    C00388  Histamine
  Neurotransmitters
   Biogenic amines
    C00388  Histamine
Target-based classification of drugs [BR:br08310]
 G Protein-coupled receptors
  Rhodopsin family
   Histamine
    HRH1
     D08040  Histamine (DCF) <US>
    HRH2
     D08040  Histamine (DCF) <US>
    HRH3
     D08040  Histamine (DCF) <US>
    HRH4
     D08040  Histamine (DCF) <US>
Other DBs
CAS: 51-45-6
PubChem: 3678
ChEBI: 18295
ChEMBL: CHEMBL90
KNApSAcK: C00001414
PDB-CCD: HSM[PDBj]
3DMET: B00101
NIKKAJI: J4.117C
KCF data

ATOM        8
            1   C8x C    23.1586  -15.5543
            2   C8y C    22.7262  -16.8922
            3   N4x N    22.0251  -14.7305
            4   N5x N    21.3183  -16.8922
            5   C8x C    20.8859  -15.5543
            6   C1b C    23.9290  -17.5823
            7   C1b C    25.1361  -16.8834
            8   N1a N    26.3433  -17.5753
BOND        8
            1     2   4 1
            2     3   5 1
            3     4   5 2
            4     2   6 1
            5     1   2 2
            6     6   7 1
            7     1   3 1
            8     7   8 1

» Japanese version

KEGG   COMPOUND: C01746
Entry
C01746                      Compound                               

Name
Piperidine;
Azacyclohexane;
Hexahydropyridine
Formula
C5H11N
Exact mass
85.0891
Mol weight
85.1475
Structure
Reaction
Pathway
map00960  Tropane, piperidine and pyridine alkaloid biosynthesis
map04974  Protein digestion and absorption
Enzyme
Other DBs
CAS: 110-89-4
PubChem: 4880
ChEBI: 18049
ChEMBL: CHEMBL15487
PDB-CCD: PIP[PDBj]
3DMET: B00341
NIKKAJI: J2.884C
KCF data

ATOM        6
            1   C1x C    26.5234  -22.8300
            2   C1x C    25.3238  -22.1217
            3   C1x C    27.7421  -22.1217
            4   C1x C    25.3238  -20.7179
            5   C1x C    27.7421  -20.7179
            6   N1x N    26.5234  -20.0224
BOND        6
            1     1   2 1
            2     1   3 1
            3     2   4 1
            4     3   5 1
            5     4   6 1
            6     5   6 1

» Japanese version

KEGG   COMPOUND: C01672
Entry
C01672                      Compound                               

Name
Cadaverine;
1,5-Pentanediamine;
1,5-Diaminopentane;
Pentamethylenediamine
Formula
C5H14N2
Exact mass
102.1157
Mol weight
102.1781
Structure
Reaction
Pathway
map00310  Lysine degradation
map00480  Glutathione metabolism
map00960  Tropane, piperidine and pyridine alkaloid biosynthesis
map01060  Biosynthesis of plant secondary metabolites
map01064  Biosynthesis of alkaloids derived from ornithine, lysine and nicotinic acid
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
map01120  Microbial metabolism in diverse environments
map04974  Protein digestion and absorption
Enzyme
1.4.3.21        2.5.1.16        2.6.1.82        4.1.1.18        
4.1.1.116
Other DBs
CAS: 462-94-2
PubChem: 4816
ChEBI: 18127
ChEMBL: CHEMBL119296
KNApSAcK: C00001403
PDB-CCD: N2P[PDBj]
3DMET: B00334
NIKKAJI: J5.771A
KCF data

ATOM        7
            1   C1b C    22.1200  -15.8411
            2   C1b C    20.9104  -16.5424
            3   C1b C    23.3296  -16.5424
            4   C1b C    19.6946  -15.8411
            5   C1b C    24.5454  -15.8411
            6   N1a N    18.4850  -16.5424
            7   N1a N    25.7550  -16.5424
BOND        6
            1     1   2 1
            2     1   3 1
            3     2   4 1
            4     3   5 1
            5     4   6 1
            6     5   7 1

» Japanese version

KEGG   COMPOUND: C00134
Entry
C00134                      Compound                               

Name
Putrescine;
1,4-Butanediamine;
1,4-Diaminobutane;
Tetramethylenediamine;
Butane-1,4-diamine
Formula
C4H12N2
Exact mass
88.1
Mol weight
88.1515
Structure
Reaction
Pathway
map00330  Arginine and proline metabolism
map00472  D-Arginine and D-ornithine metabolism
map00480  Glutathione metabolism
map00960  Tropane, piperidine and pyridine alkaloid biosynthesis
map01060  Biosynthesis of plant secondary metabolites
map01064  Biosynthesis of alkaloids derived from ornithine, lysine and nicotinic acid
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
map02010  ABC transporters
map04974  Protein digestion and absorption
Module
M00133  Polyamine biosynthesis, arginine => agmatine => putrescine => spermidine
M00134  Polyamine biosynthesis, arginine => ornithine => putrescine
M00135  GABA biosynthesis, eukaryotes, putrescine => GABA
M00136  GABA biosynthesis, prokaryotes, putrescine => GABA
Enzyme
1.4.3.10        1.4.3.22        1.5.1.43        1.5.3.13        
1.5.3.17        2.1.1.53        2.1.3.6         2.3.1.57        
2.3.1.138       2.3.1.-         2.5.1.16        2.5.1.44        
2.5.1.45        2.6.1.29        2.6.1.82        2.6.1.113       
3.5.1.53        3.5.1.62        3.5.3.11        4.1.1.17        
4.1.1.116       6.3.1.11
Brite
Compounds with biological roles [BR:br08001]
 Peptides
  Amines
   Biogenic amines
    C00134  Putrescine
Other DBs
CAS: 110-60-1
PubChem: 3434
ChEBI: 17148
ChEMBL: CHEMBL46257
KNApSAcK: C00001428
PDB-CCD: PUT[PDBj]
3DMET: B00037
NIKKAJI: J1.979H
KCF data

ATOM        6
            1   C1b C    25.0120  -16.1708
            2   C1b C    26.2280  -15.4692
            3   C1b C    23.8016  -15.4692
            4   C1b C    27.4384  -16.1708
            5   N1a N    22.5913  -16.1708
            6   N1a N    28.6487  -15.4692
BOND        5
            1     1   2 1
            2     1   3 1
            3     2   4 1
            4     3   5 1
            5     4   6 1

» Japanese version

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