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Details

Stereochemistry RACEMIC
Molecular Formula C19H18F3N5O
Molecular Weight 389.3743
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SCH-51866

SMILES

[H][C@@]12CCC[C@]1([H])N3C(=N2)N(C)C(=O)C4=C3NC(CC5=CC=C(C=C5)C(F)(F)F)=N4

InChI

InChIKey=JOSMPBVYYKRYLG-OLZOCXBDSA-N
InChI=1S/C19H18F3N5O/c1-26-17(28)15-16(27-13-4-2-3-12(13)23-18(26)27)25-14(24-15)9-10-5-7-11(8-6-10)19(20,21)22/h5-8,12-13H,2-4,9H2,1H3,(H,24,25)/t12-,13+/m1/s1

HIDE SMILES / InChI

Molecular Formula C19H18F3N5O
Molecular Weight 389.3743
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
cGMP-phosphodiesterase antagonists inhibit Ca2+-influx in Dictyostelium discoideum and bovine cyclic-nucleotide-gated-channel.
2005 Apr 18
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:47:01 GMT 2023
Edited
by admin
on Sat Dec 16 08:47:01 GMT 2023
Record UNII
F8GU4PSP29
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SCH-51866
Common Name English
CYCLOPENT(4,5)IMIDAZO(2,1-B)PURIN-4(1H)-ONE, 5,6A,7,8,9,9A-HEXAHYDRO-5-METHYL-2-((4-(TRIFLUOROMETHYL)PHENYL)METHYL)-, (6AR,9AS)-REL-
Systematic Name English
Code System Code Type Description
CAS
167298-74-0
Created by admin on Sat Dec 16 08:47:01 GMT 2023 , Edited by admin on Sat Dec 16 08:47:01 GMT 2023
PRIMARY
EPA CompTox
DTXSID001045744
Created by admin on Sat Dec 16 08:47:01 GMT 2023 , Edited by admin on Sat Dec 16 08:47:01 GMT 2023
PRIMARY
PUBCHEM
15473392
Created by admin on Sat Dec 16 08:47:01 GMT 2023 , Edited by admin on Sat Dec 16 08:47:01 GMT 2023
PRIMARY
WIKIPEDIA
SCH-51866
Created by admin on Sat Dec 16 08:47:01 GMT 2023 , Edited by admin on Sat Dec 16 08:47:01 GMT 2023
PRIMARY
FDA UNII
F8GU4PSP29
Created by admin on Sat Dec 16 08:47:01 GMT 2023 , Edited by admin on Sat Dec 16 08:47:01 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY