How Many Carbons Does the Molecule X Have? It Is a Stimulant From the Nightshade Family of Plants.

Monoisotopic Mass

162.11570

InChI

InChI=1S/C10H14N2/c1-12-7-three-5-10(12)9-4-ii-6-11-8-9/h2,4,6,viii,10H,three,5,7H2,1H3/t10-/m0/s1

InChIKey

SNICXCGAKADSCV-JTQLQIEISA-North

SMILES

C=1C=C([C@]2(Northward(CCC2)C)[H])C=NC1

Metabolite of Species	Details
Nicotiana tabacum (NCBI:txid4097)	See: PubMed

Roles Classification
Chemical Role(southward):	Bronsted base A molecular entity capable of accepting a hydron from a donor (Br o nsted acid). (via organic amino chemical compound )
Biological Role(s):	teratogenic amanuensis A role played by a chemical compound in biological systems with adverse consequences in embryo developments, leading to nascency defects, embryo death or contradistinct development, growth retardation and functional defect. immunomodulator Biologically active substance whose activity affects or plays a role in the functioning of the immune system. mitogen A chemical substance that encourages a jail cell to commence cell segmentation, triggering mitosis. establish metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. xenobiotic A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and diverse compounds that have been introduced into the environment by artificial ways. neurotoxin A poison that interferes with the functions of the nervous arrangement. nicotinic acetylcholine receptor agonist An agonist that selectively binds to and activates a nicotinic acetylcholine receptor. metabolite Whatever intermediate or production resulting from metabolism. The term 'metabolite' subsumes the classes commonly known equally primary and secondary metabolites. (via alkaloid )
Application(southward):	biomarker A substance used as an indicator of a biological state. immunomodulator Biologically active substance whose activity affects or plays a role in the performance of the allowed system. peripheral nervous system drug A drug that acts principally at i or more sites inside the peripheral neuroeffector systems, the autonomic system, and motor nerve-skeletal system. psychotropic drug A loosely defined group of drugs that take effects on psychological function. anxiolytic drug Anxiolytic drugs are agents that alleviate anxiety, tension, and anxiety disorders, promote sedation, and have a calming issue without affecting clarity of consciousness or neurologic conditions. nicotinic acetylcholine receptor agonist An agonist that selectively binds to and activates a nicotinic acetylcholine receptor. phytogenic insecticide An insecticide chemical compound naturally occurring in plants.

View more via ChEBI Ontology

IUPAC Name

iii-[(iiDue south)-1-methylpyrrolidin-2-yl]pyridine

Synonyms	Sources
(−)-nicotine	ChemIDplus
(-)-3-(ane-Methyl-2-pyrrolidyl)pyridine	HMDB
(-)-3-(N-Methylpyrrolidino)pyridine	HMDB
(R)-3-(1-Methyl-2-pyrrolidinyl)pyridine	HMDB
(Due south)-(−)-nicotine	NIST Chemistry WebBook
(S)-3-(1-methylpyrrolidin-2-yl)pyridine	KEGG Chemical compound
(Southward)-three-(N-methylpyrrolidin-2-yl)pyridine	IUBMB
(South)-Nicotine	KEGG Compound
(Due south)-nicotine	ChemIDplus
one-Methyl-2-(3-pyridyl)pyrrolidine	HMDB
3-(1-Methyl-2-pyrollidinyl)pyridine	HMDB
3-(i-Methylpyrrolidin-2-yl)pyridine	HMDB
3-(two-(N-methylpyrrolidinyl))pyridine	NIST Chemical science WebBook
three-(N-methylpyrollidino)pyridine	NIST Chemistry WebBook
Fifty(−)-nicotine	IUBMB
50-3-(1-Methyl-2-pyrrolidyl)pyridine	HMDB
L-Nicotine	HMDB
Nicotine	KEGG Chemical compound
Nicotine	HMDB

Manual Xrefs	Databases
1920	DrugCentral
485	BPDB
C00002057	KNApSAcK
C00745	KEGG Compound
D03365	KEGG DRUG
DB00184	DrugBank
HMDB0001934	HMDB
LSM-2093	LINCS
NCT	PDBeChem
Nicotine	Wikipedia
NICOTINE	MetaCyc
View more database links

Registry Numbers	Types	Sources
3604351	Beilstein Registry Number	Beilstein
54-eleven-5	CAS Registry Number	KEGG Chemical compound
54-xi-5	CAS Registry Number	ChemIDplus
54-11-v	CAS Registry Number	NIST Chemistry WebBook
82109	Reaxys Registry Number	Reaxys
82109	Beilstein Registry Number	Beilstein

Citations	Types	Sources
11209966	PubMed citation	Europe PMC
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14761239	PubMed citation	Europe PMC
14975706	PubMed commendation	Europe PMC
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15380834	PubMed citation	Europe PMC
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15707677	PubMed commendation	Europe PMC
15734728	PubMed commendation	Europe PMC
15826609	PubMed citation	Europe PMC
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21945235	PubMed commendation	Europe PMC
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22030716	PubMed commendation	Europe PMC
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Last Modified

25 July 2017

bartleyhateep.blogspot.com

Source: https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI%3A17688

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