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Details

Stereochemistry ABSOLUTE
Molecular Formula C14H19FN2O2
Molecular Weight 266.3113
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of S-14001

SMILES

FC1=CC2=C(NCCC2)C(OC[C@@H]3CNCCO3)=C1

InChI

InChIKey=OAZZVPWZWPKSGF-LBPRGKRZSA-N
InChI=1S/C14H19FN2O2/c15-11-6-10-2-1-3-17-14(10)13(7-11)19-9-12-8-16-4-5-18-12/h6-7,12,16-17H,1-5,8-9H2/t12-/m0/s1

HIDE SMILES / InChI

Molecular Formula C14H19FN2O2
Molecular Weight 266.3113
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 19:38:17 GMT 2025
Edited
by admin
on Wed Apr 02 19:38:17 GMT 2025
Record UNII
B949D6H8KP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
S-14001
Common Name English
S14001
Preferred Name English
Quinoline, 6-fluoro-1,2,3,4-tetrahydro-8-(2-morpholinylmethoxy)-, (S)-
Systematic Name English
Code System Code Type Description
CAS
135912-10-6
Created by admin on Wed Apr 02 19:38:17 GMT 2025 , Edited by admin on Wed Apr 02 19:38:17 GMT 2025
PRIMARY
PUBCHEM
131937
Created by admin on Wed Apr 02 19:38:17 GMT 2025 , Edited by admin on Wed Apr 02 19:38:17 GMT 2025
PRIMARY
FDA UNII
B949D6H8KP
Created by admin on Wed Apr 02 19:38:17 GMT 2025 , Edited by admin on Wed Apr 02 19:38:17 GMT 2025
PRIMARY
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ACTIVE MOIETY
Dual effects on adrenergic neurotransmission in the canine saphenous vein: (a) an inhibitory action on the neuronal accumulation; and (b) a pharmacological displacement of the transmitter from adrenergic nerve terminals.