KEGG   COMPOUND: C02210Help
Entry
C02210                      Compound                               

Name
beta-Endorphin
Sequence
Tyr Gly Gly Phe Met Thr Ser Glu Lys Ser Gln Thr Pro Leu Val Thr
Leu Phe Lys Asn Ala Ile Ile Lys Asn Ala Tyr Lys Lys Gly Glu
  Organism
Human [HSA:5443] [UP:COLI_HUMAN]
  Type
Peptide
Pathway
Neuroactive ligand-receptor interaction
Estrogen signaling pathway
Brite
Compounds with biological roles [BR:br08001]
 Hormones and transmitters
  Peptide hormones
   beta-Endorphin
    C02210  beta-Endorphin
Bioactive peptides [BR:br08005]
 Pituitary hormones
  Proopiomelanocortin-derived peptide
   C02210  Endorphin beta
Target-based classification of compounds [BR:br08010]
 G Protein-coupled receptors
  Rhodopsin family: peptide receptors
   Opioid
    delta-opioid receptor
     C02210  beta-Endorphin
    mu-opioid receptor
     C02210  beta-Endorphin
BRITE hierarchy
Other DBs
CAS: 
60617-12-1
PubChem: 
ChEBI: 
NIKKAJI: 

» Japanese version

KEGG   COMPOUND: C11684Help
Entry
C11684                      Compound                               

Name
MET-enkephalin;
Methionine enkephalin
Formula
C27H35N5O7S
Exact mass
573.2257
Mol weight
573.6611
Structure
Mol fileKCF fileDB searchJmolKegDraw
Sequence
Tyr Gly Gly Phe Met
  Organism
Human [HSA:5179] [UP:PENK_HUMAN]
  Type
Peptide
Pathway
Neuroactive ligand-receptor interaction
Brite
Compounds with biological roles [BR:br08001]
 Hormones and transmitters
  Peptide hormones
   Enkephalin
    C11684  Met-enkephalin
Bioactive peptides [BR:br08005]
 Neuropeptides
  Endogenous opioid peptide
   C11684  Met-enkephalin
Target-based classification of compounds [BR:br08010]
 G Protein-coupled receptors
  Rhodopsin family: peptide receptors
   Opioid
    delta-opioid receptor
     C11684  Met-enkephalin
    mu-opioid receptor
     C11684  MET-enkephalin
BRITE hierarchy
Other DBs
CAS: 
58569-55-4
PubChem: 
ChEBI: 
ChEMBL: 
NIKKAJI: 
KCF data Show

ATOM        40
            1   C8x C    17.2009  -20.4310
            2   C8y C    15.9810  -19.7318
            3   C8x C    15.9783  -18.3358
            4   C8x C    17.1916  -17.6278
            5   C8y C    18.4128  -18.3357
            6   C8x C    18.4122  -19.7390
            7   O1a O    14.7710  -20.4385
            8   C1b C    19.6280  -17.6378
            9   C1c C    19.6272  -16.2396
            10  N1a N    18.4130  -15.5380
            11  C5a C    20.8341  -15.5399
            12  N1b N    22.0460  -16.2374
            13  C1b C    23.2578  -15.5328
            14  C5a C    24.4698  -16.2303
            15  N1b N    25.6746  -15.5257
            16  C1b C    26.8866  -16.2234
            17  C5a C    28.0984  -15.5188
            18  N1b N    29.3103  -16.2163
            19  C1c C    30.5223  -15.5117
            20  C5a C    31.7341  -16.2092
            21  N1b N    32.9460  -15.5045
            22  C1c C    34.1580  -16.2023
            23  C6a C    35.3628  -15.4976
            24  O5a O    20.8310  -14.1379
            25  O5a O    24.4728  -17.6325
            26  O5a O    28.0953  -14.1167
            27  C1b C    30.5192  -14.1096
            28  C8y C    31.7329  -13.4094
            29  C8x C    32.9457  -14.1061
            30  C8x C    34.1587  -13.4070
            31  C8x C    34.1563  -12.0033
            32  C8x C    32.9310  -11.3017
            33  C8x C    31.7231  -12.0117
            34  O5a O    31.7371  -17.6114
            35  C1b C    34.1629  -17.5974
            36  C1b C    32.9570  -18.2991
            37  S2a S    32.9617  -19.6942
            38  C1a C    31.7560  -20.3958
            39  O6a O    36.5746  -16.1887
            40  O6a O    35.3542  -14.1018
BOND        41
            1     5   8 1
            2     9   8 1 #Down
            3     4   5 1
            4     2   3 1
            5     5   6 2
            6    19  20 1
            7    20  21 1
            8    21  22 1
            9    22  23 1
            10   11  12 1
            11   12  13 1
            12   11  24 2
            13   13  14 1
            14   14  25 2
            15   17  26 2
            16   14  15 1
            17   19  27 1 #Up
            18   15  16 1
            19   27  28 1
            20   28  29 2
            21   16  17 1
            22   29  30 1
            23   30  31 2
            24   17  18 1
            25   31  32 1
            26   32  33 2
            27   33  28 1
            28   18  19 1
            29   20  34 2
            30   11   9 1
            31   22  35 1 #Down
            32    9  10 1
            33   35  36 1
            34    6   1 1
            35   36  37 1
            36    1   2 2
            37   37  38 1
            38    2   7 1
            39    3   4 2
            40   23  39 1
            41   23  40 2

» Japanese version

KEGG   COMPOUND: C01574Help
Entry
C01574                      Compound                               

Name
Dynorphin;
Dynorphin A
Sequence
Tyr Gly Gly Phe Leu Arg Arg Ile Arg Pro Lys Leu Lys Trp Asp Asn
Gln
  Organism
Human [HSA:5173] [UP:PDYN_HUMAN]
  Type
Peptide
Pathway
Neuroactive ligand-receptor interaction
Brite
Compounds with biological roles [BR:br08001]
 Hormones and transmitters
  Peptide hormones
   Dynorphin
    C01574  Dynorphin A
Bioactive peptides [BR:br08005]
 Neuropeptides
  Endogenous opioid peptide
   C01574  Dynorphin A
Target-based classification of compounds [BR:br08010]
 G Protein-coupled receptors
  Rhodopsin family: peptide receptors
   Opioid
    kappa-opioid receptor
     C01574  Dynorphin A
    mu-opioid receptor
     C01574  Dynorphin
BRITE hierarchy
Other DBs
CAS: 
74913-18-1
PubChem: 
ChEBI: 

» Japanese version

KEGG   COMPOUND: C01516Help
Entry
C01516                      Compound                               

Name
Morphine
Formula
C17H19NO3
Exact mass
285.1365
Mol weight
285.3377
Structure
Mol fileKCF fileDB searchJmolKegDraw
Remark
Same as: 
Reaction
Pathway
Isoquinoline alkaloid biosynthesis
Drug metabolism - cytochrome P450
Biosynthesis of alkaloids derived from shikimate pathway
Metabolic pathways
Biosynthesis of secondary metabolites
Neuroactive ligand-receptor interaction
Enzyme
1.1.1.218       1.1.1.247       1.14.11.32      1.14.14.1       
2.4.1.17
Brite
Phytochemical compounds [BR:br08003]
 Alkaloids
  Alkaloids derived from tyrosine
   Isoquinoline alkaloids
    C01516  Morphine
Anatomical Therapeutic Chemical (ATC) classification [BR:br08303]
 N NERVOUS SYSTEM
  N02 ANALGESICS
   N02A OPIOIDS
    N02AA Natural opium alkaloids
     N02AA01 Morphine
      D08233  Morphine (BAN)
USP drug classification [BR:br08302]
 Analgesics
  Opioid Analgesics, Long-acting
   Morphine
    D08233  Morphine (BAN)
Target-based classification of drugs [BR:br08310]
 G Protein-coupled receptors
  Rhodopsin family
   Opioid
    mu-opioid receptor
     Morphine
      D08233  Morphine (BAN)
Major components of natural products [BR:br08323]
 Crude drugs
  Opium, powdered
   C01516  Morphine
Phytochemicals used as drugs [BR:br08306]
 Alkaloids
  Alkaloids derived from tyrosine
   Isoquinoline alkaloids
    D08233  Morphine (BAN)
BRITE hierarchy
Other DBs
CAS: 
57-27-2
PubChem: 
ChEBI: 
ChEMBL: 
KNApSAcK: 
PDB-CCD: 
3DMET: 
NIKKAJI: 
KCF data Show

ATOM        21
            1   C1z C    21.5384  -23.5506
            2   C8y C    21.5384  -22.2288
            3   C1y C    22.7210  -24.2462
            4   C1y C    20.4253  -24.1767
            5   C1x C    22.7210  -22.9245
            6   C8y C    20.4253  -21.6027
            7   C8y C    22.7210  -21.6027
            8   C1y C    23.8341  -23.5506
            9   C2x C    22.7210  -25.4984
            10  O2x O    19.1036  -22.8548
            11  C1y C    20.4253  -25.4984
            12  C1x C    24.9471  -22.9245
            13  C8y C    20.4253  -20.2809
            14  C1x C    23.8341  -22.2983
            15  C8x C    22.7210  -20.2809
            16  N1y N    24.9471  -24.2462
            17  C2x C    21.5384  -26.1941
            18  O1a O    19.3123  -26.1941
            19  C8x C    21.6080  -19.6549
            20  O1a O    19.3123  -19.6549
            21  C1a C    26.3437  -24.2462
BOND        25
            1     1   2 1
            2     1   3 1
            3     1   4 1
            4     1   5 1 #Up
            5     2   6 2
            6     2   7 1
            7     3   8 1
            8     3   9 1
            9     4  10 1 #Down
            10    4  11 1
            11    5  12 1
            12    6  13 1
            13    7  14 1
            14    7  15 2
            15    8  16 1 #Up
            16    9  17 2
            17   11  18 1 #Down
            18   13  19 2
            19   13  20 1
            20    6  10 1
            21    8  14 1
            22   11  17 1
            23   12  16 1
            24   15  19 1
            25   16  21 1

» Japanese version

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