KEGG   COMPOUND: C00483
Entry
C00483                      Compound                               
Name
Tyramine;
2-(p-Hydroxyphenyl)ethylamine
Formula
C8H11NO
Exact mass
137.0841
Mol weight
137.18
Structure
Reaction
R00736 R02382 R02383 R02384 R02385 R08436 R10902
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        1.4.3.-         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
KNApSAcK: C00001435
PDB-CCD: AEF[PDBj]
NIKKAJI: J4.123H
LinkDB
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
111.15
Structure
Remark
Same as: D08040
Reaction
R01167 R02150 R02152 R02155 R07643
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
map04082  Neuroactive ligand signaling
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
Network
nt06037  Histidine metabolism
nt06544  Neuroactive ligand signaling
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)
    HRH2
     D08040  Histamine (DCF)
    HRH3
     D08040  Histamine (DCF)
    HRH4
     D08040  Histamine (DCF)
Other DBs
CAS: 51-45-6
PubChem: 3678
KNApSAcK: C00001414
PDB-CCD: HSM[PDBj]
NIKKAJI: J4.117C
LinkDB
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
85.15
Structure
Reaction
R03994 R09052
Pathway
map00960  Tropane, piperidine and pyridine alkaloid biosynthesis
map04974  Protein digestion and absorption
Enzyme
2.3.1.145
Other DBs
CAS: 110-89-4
PubChem: 4880
PDB-CCD: PIP[PDBj]
NIKKAJI: J2.884C
LinkDB
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
102.18
Structure
Reaction
R00462 R03666 R06740 R08359 R08418 R08419 R08421 R09048
R12214 R12305
Pathway
map00310  Lysine degradation
map00470  D-Amino acid 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
map01120  Microbial metabolism in diverse environments
map04974  Protein digestion and absorption
Module
M00956  Lysine degradation, bacteria, L-lysine => succinate
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
KNApSAcK: C00001403
PDB-CCD: LB9[PDBj] N2P[PDBj]
NIKKAJI: J5.771A
LinkDB
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
88.1000
Mol weight
88.15
Structure
Reaction
R00018 R00670 R01151 R01152 R01153 R01154 R01155 R01156
R01157 R01399 R01919 R01920 R01944 R07414 R08714 R09074
R09077 R09079 R09256 R09257 R12304 R13286
Pathway
map00330  Arginine and proline metabolism
map00470  D-Amino acid 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
map04148  Efferocytosis
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
Network
nt06033  Glycine, serine and arginine metabolism
nt06535  Efferocytosis
Enzyme
1.4.3.10        1.4.3.22        1.5.1.43        1.5.3.13        
1.5.3.17        1.14.13.252     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
KNApSAcK: C00001428
PDB-CCD: 58I[PDBj] PUT[PDBj]
NIKKAJI: J1.979H
LinkDB
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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