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Details

Stereochemistry ACHIRAL
Molecular Formula C23H27FN2O4
Molecular Weight 414.4699
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of S-777469

SMILES

CCC1=C(C)C=C(C(=O)NC2(CCCCC2)C(O)=O)C(=O)N1CC3=CC=C(F)C=C3

InChI

InChIKey=JIYXOJFSPOFZPY-UHFFFAOYSA-N
InChI=1S/C23H27FN2O4/c1-3-19-15(2)13-18(20(27)25-23(22(29)30)11-5-4-6-12-23)21(28)26(19)14-16-7-9-17(24)10-8-16/h7-10,13H,3-6,11-12,14H2,1-2H3,(H,25,27)(H,29,30)

HIDE SMILES / InChI

Molecular Formula C23H27FN2O4
Molecular Weight 414.4699
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Shionogi developed S 777469 as a selective cannabinoid 2 receptor agonist for the atopic dermatitis treatment. This drug successfully completed phase II clinical trial, where was evaluate its safety and efficacy in patients with atopic dermatitis. However, information about the further development of S 777469 is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Discovery of S-777469: an orally available CB2 agonist as an antipruritic agent.
2012 Apr 15
S-777469, a novel cannabinoid type 2 receptor agonist, suppresses itch-associated scratching behavior in rodents through inhibition of itch signal transmission.
2015
The Inhibitory Effect of S-777469, a Cannabinoid Type 2 Receptor Agonist, on Skin Inflammation in Mice.
2017
Patents

Sample Use Guides

S-777469 400 mg BID (two 200 mg tablets of S-777469 and two tablets of placebo BID)
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:19:28 UTC 2023
Edited
by admin
on Fri Dec 15 16:19:28 UTC 2023
Record UNII
88NI79737I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
S-777469
Common Name English
Code System Code Type Description
PUBCHEM
57331749
Created by admin on Fri Dec 15 16:19:28 UTC 2023 , Edited by admin on Fri Dec 15 16:19:28 UTC 2023
PRIMARY
WIKIPEDIA
S-777,469
Created by admin on Fri Dec 15 16:19:28 UTC 2023 , Edited by admin on Fri Dec 15 16:19:28 UTC 2023
PRIMARY
FDA UNII
88NI79737I
Created by admin on Fri Dec 15 16:19:28 UTC 2023 , Edited by admin on Fri Dec 15 16:19:28 UTC 2023
PRIMARY
EPA CompTox
DTXSID301336647
Created by admin on Fri Dec 15 16:19:28 UTC 2023 , Edited by admin on Fri Dec 15 16:19:28 UTC 2023
PRIMARY
CAS
885496-53-7
Created by admin on Fri Dec 15 16:19:28 UTC 2023 , Edited by admin on Fri Dec 15 16:19:28 UTC 2023
PRIMARY
Related Record Type Details
METABOLITE INACTIVE -> PARENT
MAJOR
FECAL; PLASMA; URINE
Related Record Type Details
ACTIVE MOIETY