Details
Stereochemistry | ACHIRAL |
Molecular Formula | C26H26N2O3 |
Molecular Weight | 414.4962 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C(=O)C2=CN(CCN3CCOCC3)C4=C2C=CC=C4)C5=C1C=CC=C5
InChI
InChIKey=QWHSUXWDDKWTOG-UHFFFAOYSA-N
InChI=1S/C26H26N2O3/c1-30-25-11-10-22(19-6-2-3-8-21(19)25)26(29)23-18-28(24-9-5-4-7-20(23)24)13-12-27-14-16-31-17-15-27/h2-11,18H,12-17H2,1H3
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P21554|||Q5UB37 Gene ID: 1268.0 Gene Symbol: CNR1 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/15974991 |
10.0 nM [Ki] |
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WIKIPEDIA |
Designer-drugs-JWH-198
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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J53IGM38PB
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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DTXSID40168133
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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JWH-198
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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PRIMARY | JWH 198 is a synthetic cannabinoid (CB) which binds the central CB1 receptor with high affinity (Ki = 10 nM).1 This aminoalkylindole shares structural features with the antinociceptive CB1 agonists pravadoline (Item No. 10006973) and WIN 55,212-2.1 The physiological and toxicological properties of this compound have not been investigated. | ||
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166599-76-4
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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10319620
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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JWH-198
Created by
admin on Sat Dec 16 11:17:34 GMT 2023 , Edited by admin on Sat Dec 16 11:17:34 GMT 2023
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PRIMARY | JWH-198 is a drug from the aminoalkylindole family which acts as a cannabinoid receptor agonist. It was invented by the pharmaceutical company Sanofi-Winthrop in the early 1990s. JWH-198 has a binding affinity at the CB1 receptor of 10nM, binding around four times more tightly than the parent compound JWH-200, which has no substitution on the naphthoyl ring.(1) It has been used mainly in molecular modelling of the cannabinoid receptors. |
ACTIVE MOIETY