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serotonin

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komponim kimik

External resources

numri CAS
Proleksis enciklopedija ID
startrek.com Database ID
Encyclopædia Britannica Online ID
science/serotonin

referuar si: serotonin

Treccani ID
serotonina

referuar si: serotonina

ChEMBL ID
Gran Enciclopèdia Catalana ID
identifikues i BNF
Römpp online ID
WordNet 3.1 Synset ID
14832443-n
JSTOR topic ID (archived)
Great Russian Encyclopedia Online ID (old version)
PatientsLikeMe treatment ID
ECHA Substance Infocard ID
PDB structure ID
NALT ID
Encyclopedia of China (Third Edition) ID
130040

referuar si: 5-羟色胺

51610

referuar si: 5-羟色胺

tema kryesore: mjekësi

De Agostini ID
serotonìna

referuar si: serotonìna

Treccani's Enciclopedia Italiana ID
serotonina

vëllimi i librit: III Appendice

data e publikimit: 1961

referuar si: SEROTONINA

emri i autorit si varg: A. E. R., G.

Freebase ID
Reaxys registry number
143524[15]
AccessScience ID
Store medisinske leksikon ID
serotonin

mapping relation type: përputhje e përpiktë

Encyclopedia of China (Second Edition) ID
UniChem compound ID
Probes And Drugs ID
MeSH tree code
Know Your Meme ID
J9U ID
PDB ligand ID
SPLASH
KEGG ID
Hrvatska enciklopedija ID
Encyclopædia Universalis ID
GND ID
numri CE
Gran Enciclopèdia Catalana ID (former scheme)
OpenAlex ID
DeCS ID
ChemSpider ID
YSO ID
InChIKey
ScienceDirect topic ID
InChI
Brockhaus Enzyklopädie online ID
DSSTox substance ID
ChEBI ID
28790[3][25][26]

mapping relation type: përputhje e përpiktë

KNApSAcK ID
Golden ID
SureChEMBL ID
Guide to Pharmacology Ligand ID
MeSH descriptor ID
D012701

referuar si: Serotonin

Lex ID
DrugBank ID
KBpedia ID
NDL Authority ID
PubChem CID
WikiSkripta article ID
Microsoft Academic ID
Library of Congress ID
DSSTOX compound identifier
AGROVOC ID
BNCF Thesaurus ID
NE.se ID
Gmelin number
1861995
MassBank accession ID
Human Metabolome Database ID
Great Russian Encyclopedia portal ID
RxNorm ID
UNII

instancë e

type of chemical entity

nënklasë e

tryptamine alkaloid

pjesë e

G protein-coupled serotonin receptor activity[32]

subjekti ka rol: reactant

serotonin binding[32]

subjekti ka rol: reactant

serotonin receptor activity[32]

subjekti ka rol: reactant

serotonin biosynthetic process from tryptophan[32]

subjekti ka rol: product

response to serotonin[32]

subjekti ka rol: reactant

cellular response to serotonin[32]

subjekti ka rol: reactant

serotonin:sodium symporter activity[32]

subjekti ka rol: cargo

serotonin transport[32]

subjekti ka rol: cargo

synaptic transmission, serotonergic[32]

subjekti ka rol: participant

serotonin uptake[33]

subjekti ka rol: cargo

serotonin metabolic process[33]

subjekti ka rol: participant

serotonin biosynthetic process[33]

subjekti ka rol: product

serotonin catabolic process[33]

subjekti ka rol: reactant

strukturë kimike

image of molecular model or crystal lattice model

përshkruan: space-filling model

masa

176,095 dalton[34]

zbulues

Arda Green[35]
Maurice M. Rapport

formula kimike

C₁₀H₁₂N₂O[21]

kanonikja SMILES

C1=CC2=C(C=C1O)C(=CN2)CCN[21]

electric dipole moment

2,98 debye

melting point

167,5 Celcius

boiling point

416±30 Celcius

pKa

10,4

found in taxon

Panaeolus cyanescens[42]
Panaeolus goossensiae[42]
Panaeolus semiovatus[42]
Panaeolus antillarum[42]
Tovaria pendula[43][44]
Mimosa somnians[45]
Hyrtios reticulatus[46]
Amorphophallus konjac[47][48]
Aplysia californica[49]
Araujia sericifera[50]
Cnidoscolus texanus[51]
Corallistes undulatus[52]
Hypericum perforatum[53]
arra[54]
Mamestra brassicae[55]
Ranunculus sceleratus[56]
Theobroma cacao[57]
Amanita citrina[58]
Bufo bufo[59]
Bufo gargarizans[59]
Panaeolus campanulatus[60]
Panaeolus papilionaceus[60]
Paramuricea clavata[61]
Hyrtios[64]
Copelandia[42]
Sophora flavescens[65]
Mus musculus[67][68]
Hippophae rhamnoides[69]
Nitraria schoberi[70]
Phaseolus vulgaris[72]
Musa cavendishii[73]
Solanum[75]
Rhodospirillum rubrum[76]

reagon fizikisht me

5-hydroxytryptamine receptor 1A[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 1B[77]

subjekti ka rol: agonist

5-hydroxytryptamine (serotonin) receptor 1B[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 1D[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 1E[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 1F[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 2A[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 2B[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 2C[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 3A[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 4[77]

subjekti ka rol: agonist

5 hydroxytryptamine (serotonin) receptor 4[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 5A[77]

subjekti ka rol: agonist

5-hydroxytryptamine (serotonin) receptor 5A[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 6[77]

subjekti ka rol: agonist

5-hydroxytryptamine receptor 7[77]

subjekti ka rol: agonist

5-hydroxytryptamine (serotonin) receptor 7[77]

subjekti ka rol: agonist

Dopamine receptor D1[77]

subjekti ka rol: agonist

Dopamine receptor D5[77]

subjekti ka rol: agonist

Solute carrier family 36 member 1[77]

subjekti ka rol: agonist

subjekti ka rol

serotonin receptor agonists[78]
neurotransmitter
primary metabolite[79]

kategoria në Commons

Serotonin

kategoria kryesore

Category:Serotonin

Reference

  1. ^ a b c d Global Substance Registration System, 19 nëntor 2016, anglisht, serotonin, 333DO1RDJY
  2. ^ CAS Common Chemistry, 9 prill 2021, https://commonchemistry.cas.org/detail?cas_rn=50-67-9, QZAYGJVTTNCVMB-UHFFFAOYSA-N
  3. ^ a b ChEMBL, 19 nëntor 2016, anglisht, SEROTONIN, CHEMBL39
  4. ^ ECHA Substance Infocard database, 27 dhjetor 2018, 100.000.054, 3-(2-aminoethyl)indol-5-ol, CAS no.: 50-67-9
  5. ^ Protein Data Bank, 19 tetor 2016, anglisht, 3Q6K, 3Q6K
  6. ^ Protein Data Bank, 19 tetor 2016, anglisht, 3ADV, 3ADV
  7. ^ Protein Data Bank, 19 tetor 2016, anglisht, 2QEH, 2QEH
  8. ^ Protein Data Bank, 19 tetor 2016, anglisht, 2YMD, 2YMD
  9. ^ Protein Data Bank, 19 tetor 2016, anglisht, 4DUF, 4DUF
  10. ^ Protein Data Bank, 19 tetor 2016, anglisht, 4DTW, 4DTW
  11. ^ Protein Data Bank, 19 tetor 2016, anglisht, 3BRN, 3BRN
  12. ^ Protein Data Bank, 19 tetor 2016, anglisht, 4DUE, 4DUE
  13. ^ Protein Data Bank, 19 tetor 2016, anglisht, 3NK1, 3NK1
  14. ^ Freebase Data Dumps, 28 tetor 2013
  15. ^ a b ChEBI, 19 tetor 2016, anglisht, serotonin, 28790
  16. ^ UniChem
  17. ^ Biblioteka Kombëtare e Izraelit
  18. ^ OpenAlex, 26 janar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  19. ^ ChemSpider, 19 nëntor 2016, anglisht, 5013, Serotonin
  20. ^ YSO-Wikidata mapping project
  21. ^ a b c d e PubChem, 19 nëntor 2016, anglisht, 5202, serotonin
  22. ^ ChEBI release 2020-09-01
  23. ^ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  24. ^ a b c d e f QZAYGJVTTNCVMB-UHFFFAOYSA-N, InChIKey
  25. ^ ChEBI release 2019-10-02
  26. ^ InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10/h1-2,5-6,12-13H,3-4,11H2, International Chemical Identifier
  27. ^ a b c inferred from InChIKey
  28. ^ https://golden.com/wiki/Serotonin-MNGYY, 10 shtator 2022
  29. ^ IUPHAR/BPS Guide to PHARMACOLOGY, 19 nëntor 2016, anglisht, 5, 5-hydroxytryptamine
  30. ^ KBpedia, 9 korrik 2020
  31. ^ Nuovo soggettario
  32. ^ a b c d e f g h i Gene Ontology release 2019-11-16
  33. ^ a b c d Gene Ontology release 2020-05-02
  34. ^ PubChem, 19 tetor 2016, anglisht, 5202, serotonin
  35. ^ The Biographical Dictionary of Women in Science, 525, 1
  36. ^ New alkaloids from Peganum harmala
  37. ^ Biosynthesis of serotonin and β-carboline alkaloids in hairy root cultures of Peganum harmala
  38. ^ Accumulation of beta-Carboline Alkaloids and Serotonin by Cell Cultures of Peganum harmala L: I. CORRELATION BETWEEN PLANTS AND CELL CULTURES AND INFLUENCE OF MEDIUM CONSTITUENTS
  39. ^ Hairy Root Cultures of Peganum harmala II. Characterization of Cell Lines and Effect of Culture Conditions on the Accumulation of ß-Carboline Alkaloids and Serotonin
  40. ^ New natural products from Peganum harmala
  41. ^ Accumulation of β-Carboline Alkaloids and Serotonin by Cell Cultures of Peganum harmala
  42. ^ a b c d e Species identification and chemical analysis of psychoactive fungi in the Hawaiian islands
  43. ^ 1-acetyl-S-indolylmethylglucosinolate in Seedlings of Tovaria pendula Ruiz et Pav.
  44. ^ Serotonin and indoleglucosinolate in Tovaria pendula
  45. ^ The Occurrence of Tryptamine and N-Methyltryptamine in Mimosa somnians
  46. ^ 5-hydroxytryptamine-derived alkaloids from two marine sponges of the genus Hyrtios
  47. ^ Cis-N-(p-Coumaroyl)serotonin from Konnyaku, Amorphophallus konjac K. Koch
  48. ^ Peroxynitrite scavenging activities of aromatic compounds isolated from Konnyaku, Amorphophallus konjac K.Koch
  49. ^ Coexistence of Several Putative Neurotransmitters in Single Identified Neurons of 'Aplysia'
  50. ^ Constituents of Araujia sericifera
  51. ^ Chemical contents of stinging trichomes ofCnidoscolus texanus
  52. ^ Pteridines, Sterols, and Indole Derivatives from the Lithistid Sponge Corallistes undulatus of the Coral Sea
  53. ^ Mammalian neurohormones: potential significance in reproductive physiology of St. John's wort (Hypericum perforatum L.)?
  54. ^ Serotonin Biosynthesis and Its Regulation in Seeds of Juglans regia L.
  55. ^ Melatonin in the Testis of the Cabbage Armyworm, Mamestra brassicae
  56. ^ Identification of tryptamine derivatives in Ranunculus sceleratus L
  57. ^ Tetrahydro-beta-carbolines, potential neuroactive alkaloids, in chocolate and cocoa.
  58. ^ INVESTIGATION OF THE ALKALOIDS OFAMANITASPECIES1– II.AMANITA. CITRINAANDAMANITA PORPHYRIA
  59. ^ a b Quality evaluation of traditional Chinese drug toad venom from different origins through a simultaneous determination of bufogenins and indole alkaloids by HPLC.
  60. ^ a b Quantitative determination of serotonin in Panaeolus species
  61. ^ Antifouling properties of simple indole and purine alkaloids from the Mediterranean gorgonian Paramuricea clavata.
  62. ^ Recon 2.2: from reconstruction to model of human metabolism
  63. ^ A community-driven global reconstruction of human metabolism.
  64. ^ 5-Hydroxyindole-type alkaloids, as Candida albicans isocitrate lyase inhibitors, from the tropical sponge Hyrtios sp.
  65. ^ Correction: Chae, H.S., et al. Anti-Inflammatory Effects of 6,8-Diprenyl-7,4'-dihydroxyflavanone from Sophora tonkinensis on Lipopolysaccharide-Stimulated RAW 264.7 Cells. Molecules. 2016, 21, 1049.
  66. ^ Punica granatum (pomegranate) and its potential for prevention and treatment of inflammation and cancer
  67. ^ Flavonoids ofAtraphaxis muschketovii
  68. ^ Keine GEMA-Gebühren für Hintergrundmusik
  69. ^ Polyphenols from the leaves of Hippophae rhamnoides
  70. ^ Chemical Characterization and Pharmacological Activity of Nazlinin, a Novel Indole Alkaloid from Nitraria schoberi
  71. ^ Salt stress-induced seedling growth inhibition coincides with differential distribution of serotonin and melatonin in sunflower seedling roots and cotyledons
  72. ^ Metabolite Profiling of Root Exudates of Common Bean under Phosphorus Deficiency
  73. ^ Chip electrophoresis of active banana ingredients with label-free detection utilizing deep UV native fluorescence and mass spectrometry
  74. ^ Metabolomics of capsicum ripening reveals modification of the ethylene related-pathway and carbon metabolism
  75. ^ a b c HPLC analysis of serotonin, tryptamine, tyramine, and the hydroxycinnamic acid amides of serotonin and tyramine in food vegetables
  76. ^ The occurrence of hydroxy-derivatives of phytoene and phytofluene in diphenylamine-inhibited cultures of Rhodospirillum rubrum
  77. ^ a b c d e f g h i j k l m n o p q r s t IUPHAR/BPS Guide to PHARMACOLOGY, 17 gusht 2016, 5, anglisht
  78. ^ Medical Subject Headings, 15 mars 2018, D012701
  79. ^ Reactome, https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT