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Details

Stereochemistry ACHIRAL
Molecular Formula C30H29N3O
Molecular Weight 447.5708
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MN-18

SMILES

CCCCCC1=CC=C(CN2N=C(C(=O)NC3=CC=CC4=CC=CC=C34)C5=C2C=CC=C5)C=C1

InChI

InChIKey=BLOQUZQMKJZVQE-UHFFFAOYSA-N
InChI=1S/C30H29N3O/c1-2-3-4-10-22-17-19-23(20-18-22)21-33-28-16-8-7-14-26(28)29(32-33)30(34)31-27-15-9-12-24-11-5-6-13-25(24)27/h5-9,11-20H,2-4,10,21H2,1H3,(H,31,34)

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.233 nM [EC50]
2.028 nM [EC50]
Name Type Language
MN-18
Common Name English
1H-INDAZOLE-3-CARBOXAMIDE, N-1-NAPHTHALENYL-1-PENTYL-
Systematic Name English
N-(NAPHTHALEN-1-YL)-1-PENTYL-1H-INDAZOLE-3-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-MN-18
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
Code System Code Type Description
CAS
1391484-80-2
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY
FDA UNII
GP2N1PG5X2
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY
WIKIPEDIA
MN-18
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY MN 18 is an indazole-based synthetic cannabinoid that is presumed to be a potent agonist of the CB1 receptor and has been sold online as a designer drug. It is the indazole core analogue of NNE1. Given the known metabolic liberation (and presence as an impurity) of amantadine in the related compound APINACA, it is suspected that metabolic hydrolysis of the amide group of MN-18 may release 1-naphthylamine, a known carcinogen. MN-18 is banned in Sweden.
MANUFACTURER PRODUCT INFORMATION
MN-18
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY MN-18 is a synthetic cannabinoid modeled after AKB48 (APINACA, Item No. 11566), with the adamantyl group replaced by a naphthalenyl group. The physiological and toxicological properties of this compound are unknown. This product is intended for forensic and research applications.
EPA CompTox
DTXSID301010033
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY
PUBCHEM
154925762
Created by admin on Sat Dec 16 11:50:39 GMT 2023 , Edited by admin on Sat Dec 16 11:50:39 GMT 2023
PRIMARY