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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H14F3NO3
Molecular Weight 337.2932
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZD-6169

SMILES

C[C@](O)(C(=O)NC1=CC=C(C=C1)C(=O)C2=CC=CC=C2)C(F)(F)F

InChI

InChIKey=LVEDGSIMCSQNNX-INIZCTEOSA-N
InChI=1S/C17H14F3NO3/c1-16(24,17(18,19)20)15(23)21-13-9-7-12(8-10-13)14(22)11-5-3-2-4-6-11/h2-10,24H,1H3,(H,21,23)/t16-/m0/s1

HIDE SMILES / InChI

Molecular Formula C17H14F3NO3
Molecular Weight 337.2932
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
(-)-(9S)-9-(3-Bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637): a novel ATP-sensitive potassium channel opener efficacious in suppressing urinary bladder contractions. II. in vivo characterization.
2002-10
The involvement of L-type Ca(2+) channels in the relaxant effects of the ATP-sensitive K(+) channel opener ZD6169 on pig urethral smooth muscle.
2001-12
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:03:38 GMT 2025
Edited
by admin
on Mon Mar 31 18:03:38 GMT 2025
Record UNII
H6UIO70F5E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZD-6169
Code English
PROPANAMIDE, N-(4-BENZOYLPHENYL)-3,3,3-TRIFLUORO-2-HYDROXY-2-METHYL-, (2S)-
Preferred Name English
ZD6169
Code English
Code System Code Type Description
FDA UNII
H6UIO70F5E
Created by admin on Mon Mar 31 18:03:38 GMT 2025 , Edited by admin on Mon Mar 31 18:03:38 GMT 2025
PRIMARY
PUBCHEM
177852
Created by admin on Mon Mar 31 18:03:38 GMT 2025 , Edited by admin on Mon Mar 31 18:03:38 GMT 2025
PRIMARY
CAS
147696-46-6
Created by admin on Mon Mar 31 18:03:38 GMT 2025 , Edited by admin on Mon Mar 31 18:03:38 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> ACTIVATOR
Opens potassium channel. Test done in Guinea pigs bladder muscle. Inhibition of action potentials and phasic contractions of UBSM. The results suggest that activation of <1% of KATP channels is sufficient to inhibit significantly action potentials and the related phasic contractions.
K1/2
TARGET -> ACTIVATOR
Opens potassium channel. Test done in Guinea pigs bladder muscle. Half maximal activation of potassium current.
K1/2