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ملاتونین

File:Melatonin.svg · Wikimedia Commons · See Wikimedia Commons

EntityQ180912· pop 73· linked from 1,555 articles

ملاتونین

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Also known as MLT, N-[2-(5-methoxyindol-3-yl)ethyl]acetamide, 5-methoxy-N-acetyltryptamine, Melovine, {N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-} Acetamide, N-(2-(5-Methoxyindol-3-yl)ethyl)-Acetamide, N-Acetyl-5-methoxy-tryptamine, N-[2-(5-Methoxyindol-3-yl)ethyl]-Acetamide

هورمونی که در غدهٔ کوچکی در مغز تولید می‌شود و چرخه‌ی خواب و بیداری بدن را تنظیم می‌کند

OverviewAI-generated

Melatonin is a chemical compound with the formula C₁₃H₁₆N₂O₂. Its IUPAC name is N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide. The substance has a mass of 232.121 and a weight of 232.28. It carries a charge of 0 and features two hydrogen bond donors and two hydrogen bond acceptors. The calculated xlogp value is 0.8, while the topological polar surface area (TPSA) is 54.1.

The defined daily dose for melatonin is 2.0. The compound is associated with a PubMed query count of 37218. It is referenced by 1,555 other encyclopedia articles.

Synthesized by Vinony from 20 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C13H16N2O2
Molecular weight
232.28 g/mol
IUPAC name
N-[2-(5-methoxy-1H-indol-3-yl)ethyl]acetamide
SMILES
CC(=O)NCCC1=CNC2=C1C=C(C=C2)OC
InChIKey
DRLFMBDRBRZALE-UHFFFAOYSA-N
XLogP
0.8
Polar surface area
54.1 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Research

37,218 papers

via PubMed

Wikidata facts

Subclass of
hormone
Has part
carbon
Mass
232.121
Has use
medication
Show 11 more facts
medical condition treated
jet lag
Commons category
Melatonin
chemical formula
C₁₃H₁₆N₂O₂
topic's main category
Category:Melatonin
canonical SMILES
CC(=O)NCCC1=CNC2=C1C=C(C=C2)OC
isomeric SMILES
C/C(=N\CCC1=CNC2=C1C=C(C=C2)OC)/O
defined daily dose
2.0
subject has role
primary metabolite
different from
melanin
Sources (11)

via Wikidata · CC0

Gallery (15)