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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H32F6N2O2
Molecular Weight 542.5563
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PNU-157706

SMILES

C[C@]12CC[C@H]3[C@@H](CC[C@H]4NC(=O)C=C[C@]34C)[C@@H]1CC[C@@H]2C(=O)NC(C5=CC=CC=C5)(C(F)(F)F)C(F)(F)F

InChI

InChIKey=CUHBWKJGTVFTMR-QKONGSNMSA-N
InChI=1S/C28H32F6N2O2/c1-24-14-12-19-17(8-11-21-25(19,2)15-13-22(37)35-21)18(24)9-10-20(24)23(38)36-26(27(29,30)31,28(32,33)34)16-6-4-3-5-7-16/h3-7,13,15,17-21H,8-12,14H2,1-2H3,(H,35,37)(H,36,38)/t17-,18-,19-,20+,21+,24-,25+/m0/s1

HIDE SMILES / InChI

Molecular Formula C28H32F6N2O2
Molecular Weight 542.5563
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:42:02 GMT 2025
Edited
by admin
on Mon Mar 31 21:42:02 GMT 2025
Record UNII
RVW8CZ26BK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1H-INDENO(5,4-F)QUINOLINE-7-CARBOXAMIDE, 2,4A,4B,5,6,6A,7,8,9,9A,9B,10,11,11A-TETRADECAHYDRO-4A,6A-DIMETHYL-2-OXO-N-(2,2,2-TRIFLUORO-1-PHENYL-1-(TRIFLUOROMETHYL)ETHYL)-, (4AR,4BS,6AS,7S,9AS,9BS,11AR)-
Preferred Name English
PNU-157706
Code English
1H-INDENO(5,4-F)QUINOLINE-7-CARBOXAMIDE, 2,4A,4B,5,6,6A,7,8,9,9A,9B,10,11,11A-TETRADECAHYDRO-4A,6A-DIMETHYL-2-OXO-N-(2,2,2-TRIFLUORO-1-PHENYL-1-(TRIFLUOROMETHYL)ETHYL)-, (4AR-(4A.ALPHA.,4B.BETA.,6A.ALPHA.,7.ALPHA.,9A.BETA.,9B.ALPHA.,11A.BETA.))-
Systematic Name English
(4AR,4BS,6AS,7S,9AS,9BS,11AR)-2,4A,4B,5,6,6A,7,8,9,9A,9B,10,11,11A-TETRADECAHYDRO-4A,6A-DIMETHYL-2-OXO-N-(2,2,2-TRIFLUORO-1-PHENYL-1-(TRIFLUOROMETHYL)ETHYL)-1H-INDENO(5,4-F)QUINOLINE-7-CARBOXAMIDE
Systematic Name English
PNU157706
Code English
Code System Code Type Description
FDA UNII
RVW8CZ26BK
Created by admin on Mon Mar 31 21:42:02 GMT 2025 , Edited by admin on Mon Mar 31 21:42:02 GMT 2025
PRIMARY
PUBCHEM
9915313
Created by admin on Mon Mar 31 21:42:02 GMT 2025 , Edited by admin on Mon Mar 31 21:42:02 GMT 2025
PRIMARY
CAS
208995-99-7
Created by admin on Mon Mar 31 21:42:02 GMT 2025 , Edited by admin on Mon Mar 31 21:42:02 GMT 2025
SUPERSEDED
CAS
188754-67-8
Created by admin on Mon Mar 31 21:42:02 GMT 2025 , Edited by admin on Mon Mar 31 21:42:02 GMT 2025
PRIMARY
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ACTIVE MOIETY