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Details

Stereochemistry ACHIRAL
Molecular Formula C24H21NO3
Molecular Weight 371.4284
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of N-(5-(4-(3-FURYL)PHENYL)-3-PHENYL-2-PENTEN-4-YN-1-YL)SARCOSINE

SMILES

CN(C\C=C(\C#CC1=CC=C(C=C1)C2=COC=C2)C3=CC=CC=C3)CC(O)=O

InChI

InChIKey=KIGCTKNPXSPYMQ-XKZIYDEJSA-N
InChI=1S/C24H21NO3/c1-25(17-24(26)27)15-13-22(20-5-3-2-4-6-20)12-9-19-7-10-21(11-8-19)23-14-16-28-18-23/h2-8,10-11,13-14,16,18H,15,17H2,1H3,(H,26,27)/b22-13-

HIDE SMILES / InChI

Molecular Formula C24H21NO3
Molecular Weight 371.4284
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 02:59:46 GMT 2023
Edited
by admin
on Sat Dec 16 02:59:46 GMT 2023
Record UNII
26M82RK6TE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-(5-(4-(3-FURYL)PHENYL)-3-PHENYL-2-PENTEN-4-YN-1-YL)SARCOSINE
Systematic Name English
2-(((E)-5-(4-(3-FURYL)PHENYL)-3-PHENYL-PENT-2-EN-4-YNYL)-METHYL-AMINO)ACETIC ACID
Systematic Name English
R-213129
Code English
R213129
Code English
GLYCINE, N-(5-(4-(3-FURANYL)PHENYL)-3-PHENYL-2-PENTEN-4-YN-1-YL)-N-METHYL-
Systematic Name English
Code System Code Type Description
PUBCHEM
9929349
Created by admin on Sat Dec 16 02:59:46 GMT 2023 , Edited by admin on Sat Dec 16 02:59:46 GMT 2023
PRIMARY
FDA UNII
26M82RK6TE
Created by admin on Sat Dec 16 02:59:46 GMT 2023 , Edited by admin on Sat Dec 16 02:59:46 GMT 2023
PRIMARY
CAS
337510-16-4
Created by admin on Sat Dec 16 02:59:46 GMT 2023 , Edited by admin on Sat Dec 16 02:59:46 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY
R213129 dose levels were selected based on exposure levels that blocked the GlyT1 sites >50% in preclinical experiments. Forty-three of the 45 included subjects completed the study. Scopolamine significantly affected almost every central nervous system parameter measured in this study. R213129 alone compared with placebo did not elicit pharmacodynamic changes. R213129 had some small effects on scopolamine-induced central nervous system impairments. Scopolamine-induced finger tapping impairment was further enhanced by 3 mg R213129 with 2.0 taps/10 seconds (95% CI -4.0, -0.1), electroencephalography alpha power was increased by 10 mg R213129 with respectively 12.9% (0.7, 26.6%), scopolamine-induced impairment of the Stroop test was partly reversed by 10 mg R213129 with 59 milliseconds (-110, -7).