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Nabilon

Structure via PubChem · Public domain (PubChem)

EntityQ419079· pop 23· linked from 1,419 articles

Also known as LY 109514, LY-109514

Racemat

In the Vinony graph

Vinony's link graph records 1,419 inbound references to Nabilon, and connects out to cannabinoids, tetrahydrocannabinol and antiemetic.

Vinony files it under Analgesics, Antiaggressive drugs and Appetite stimulants.

Vinony links it to 22 Wikipedia language editions.

Chemical data

Formula
C24H36O3
Molecular weight
372.5 g/mol
IUPAC name
(6aR,10aR)-1-hydroxy-6,6-dimethyl-3-(2-methyloctan-2-yl)-7,8,10,10a-tetrahydro-6aH-benzo[c]chromen-9-one
SMILES
CCCCCCC(C)(C)C1=CC(=C2[C@@H]3CC(=O)CC[C@H]3C(OC2=C1)(C)C)O
InChIKey
GECBBEABIDMGGL-RTBURBONSA-N
XLogP
6.4
Polar surface area
46.5 Ų
H-bond donors
1
H-bond acceptors
3
Formal charge
0

via PubChem

Wikidata facts

Instance of
medication
Mass
372.266445
Show 6 more facts
subject has role
anxiolytic
chemical formula
C₂₄H₃₆O₃
Commons category
Nabilone
medical condition treated
vomiting
canonical SMILES
CCCCCCC(C)(C)C1=CC2=C(C3CC(=O)CCC3C(O2)(C)C)C(=C1)O
defined daily dose
3
Sources (3)

via Wikidata · CC0

Article · Deutsch

Nabilon ist ein vollsynthetisches Derivat des Δ9-Tetrahydrocannabinols. Nabilon wurde 1975 von Eli Lilly als Tranquilizer und Antiemetikum patentiert.

Abstract from DBpedia / Wikipedia · CC BY-SA

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