U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H12N2.2C6H3N3O7
Molecular Weight 606.4128
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORNICOTINE DIPICRATE

SMILES

C1CN[C@@H](C1)C2=CN=CC=C2.OC3=C(C=C(C=C3[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O.OC4=C(C=C(C=C4[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O

InChI

InChIKey=IIJVAJGRPUJGSK-WWPIYYJJSA-N
InChI=1S/C9H12N2.2C6H3N3O7/c1-3-8(7-10-5-1)9-4-2-6-11-9;2*10-6-4(8(13)14)1-3(7(11)12)2-5(6)9(15)16/h1,3,5,7,9,11H,2,4,6H2;2*1-2,10H/t9-;;/m0../s1

HIDE SMILES / InChI
Nornicotine is a natural alkaloid produced by plants in the genus Nicotiana and is structurally related to nicotine. Nornicotine is the direct precursor of tobacco-specific nitrosamine N'-nitrosonornicotine, which is a highly potent human carcinogen. Nornicotine is an active nicotine metabolite, which accumulates in brain to pharmacologically relevant concentrations following repeated nicotine administration to rats. Nornicotine stimulated DA release from nucleus accumbens in a nicotinic receptor-mediated manner, further supporting the hypothesis that nornicotine contributes to tobacco dependence. Nornicotine is present in Nicotiana tobaccum in both S(-) and R(+) enantiomeric forms. Nornicotine enantiomeric forms appear to differ in analgesic potency and side effects. Exposure to nornicotine results in additional activation of α7-type receptors, which may be important for effects on cognition and attention. Likewise, the effects of nornicotine on α6-containing receptors may contribute to the reinforcing effects of nicotine, and therefore, is relevant to dependence on tobacco. In contrast to nicotine, nornicotine had relatively low activity on receptors other than those containing α7 or α6 subunits. Yaupon Therapeutics was developing Nornicotine as a once a day oral drug for smoking cessation. However this development was discontinued.

Approval Year

PubMed

PubMed

TitleDatePubMed
Simultaneous analysis of nicotine, nicotine metabolites, and tobacco alkaloids in serum or urine by tandem mass spectrometry, with clinically relevant metabolic profiles.
2002 Sep
The addition of five minor tobacco alkaloids increases nicotine-induced hyperactivity, sensitization and intravenous self-administration in rats.
2009 Nov
Patents

Sample Use Guides

Rats: 5 mg/kg s.c. The 5 mg/kg dose was chosen based on a previous report suggesting that this dose was behaviorally active.
Route of Administration: Other
In Vitro Use Guide
Curator's Comment: Rat nucleus accumbens slices were preloaded with [3H]DA and superfused for 60 min in the absence and presence of a range of alkaloid concentrations. Superfusate samples were collected and alkaloid-evoked [3H]overflow was determined. S(-)-Nornicotine (EC(50) value = 3.0 uM), R(+)-nornicotine (EC(50) value = 0.48 uM), and S(-)-nicotine (EC(50) value = 70 nM) evoked [3H]overflow in a concentration-dependent manner. For each nornicotine enantiomer, 0.3 uM was the lowest concentration to evoke significant [3H]overflow. https://www.ncbi.nlm.nih.gov/pubmed/11755112
The effects of nornicotine on specific combinations of neuronal nicotinic acetylcholine receptor (nAChR) subunits expressed in Xenopus oocytes were studied. Of the nAChR subtypes studied, it was found that α7 receptors were very responsive to nornicotine (EC50≈ 17 uM Imax 50% compared to ACh). nAChRs containing the ligand-binding domain of the α6 subunits (in the form of an α6/α3 chimera) were also strongly responsive to nornicotine (EC50≈ 4 uM Imax50% compared to ACh).
Name Type Language
NORNICOTINE DIPICRATE
Common Name English
PYRIDINE, 3-(2-PYRROLIDINYL)-, (S)-, COMPD. WITH 2,4,6-TRINITROPHENOL (1:2)
Systematic Name English
PYRIDINE, 3-(2S)-2-PYRROLIDINYL-, COMPD. WITH 2,4,6-TRINITROPHENOL (1:2)
Systematic Name English
NICOTINE, 1'-DEMETHYL-, DIPICRATE
Systematic Name English
NORNICOTINE, DIPICRATE
Common Name English
Code System Code Type Description
FDA UNII
NCU3KH6Q5Y
Created by admin on Sat Dec 16 10:06:31 GMT 2023 , Edited by admin on Sat Dec 16 10:06:31 GMT 2023
PRIMARY
PUBCHEM
126961347
Created by admin on Sat Dec 16 10:06:31 GMT 2023 , Edited by admin on Sat Dec 16 10:06:31 GMT 2023
PRIMARY
CAS
6255-01-2
Created by admin on Sat Dec 16 10:06:31 GMT 2023 , Edited by admin on Sat Dec 16 10:06:31 GMT 2023
PRIMARY