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

Details

Stereochemistry UNKNOWN
Molecular Formula C7H15N
Molecular Weight 113.2007
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NANOFIN

SMILES

CC1CCCC(C)N1

InChI

InChIKey=SDGKUVSVPIIUCF-UHFFFAOYSA-N
InChI=1S/C7H15N/c1-6-4-3-5-7(2)8-6/h6-8H,3-5H2,1-2H3

HIDE SMILES / InChI
Nanofin is a ganglion blocker alkaloid having nicotinic acetylcholine receptor antagonist action. It has an antihypertensive effect used for mild to moderate hypertension. It was also used for the treatment of eczema and neurodermatitis.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Nicotinic acetylcholine receptor
PubMed

PubMed

TitleDatePubMed
Active site directed docking studies: synthesis and pharmacological evaluation of cis-2,6-dimethyl piperidine sulfonamides as inhibitors of acetylcholinesterase.
2009-10
Combined experimental and computational study of the thermochemistry of methylpiperidines.
2006-05-12
Development of an efficient strategy for the synthesis of the ETB receptor antagonist BQ-788 and some related analogues.
2005-08
Mechanism of hydrodenitrogenation on phosphides and sulfides.
2005-02-17
Patents
Name Type Language
NSC-63890
Preferred Name English
NANOFIN
INN  
INN  
Official Name English
nanofin [INN]
Common Name English
2,6-LUPETIDINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C66886
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C76789
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
INN
1085
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
PUBCHEM
68843
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
NSC
63890
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
SMS_ID
100000084465
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID8048527
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
EVMPD
SUB09149MIG
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
FDA UNII
329I5805BP
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
MESH
C008581
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104431
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
WIKIPEDIA
2,6-Dimethylpiperidine
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
CAS
504-03-0
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-981-6
Created by admin on Mon Mar 31 18:29:44 GMT 2025 , Edited by admin on Mon Mar 31 18:29:44 GMT 2025
PRIMARY