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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H34N4O3S
Molecular Weight 518.67
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BN-80933

SMILES

CC1=C(O)C(C)=C2CC[C@](C)(OC2=C1C)C(=O)N3CCN(CC3)C4=CC=C(NC(=N)C5=CC=CS5)C=C4

InChI

InChIKey=STCYUKSGPHEXDI-LJAQVGFWSA-N
InChI=1S/C29H34N4O3S/c1-18-19(2)26-23(20(3)25(18)34)11-12-29(4,36-26)28(35)33-15-13-32(14-16-33)22-9-7-21(8-10-22)31-27(30)24-6-5-17-37-24/h5-10,17,34H,11-16H2,1-4H3,(H2,30,31)/t29-/m0/s1

HIDE SMILES / InChI

Molecular Formula C29H34N4O3S
Molecular Weight 518.67
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Neuroprotective effects of (S)-N-[4-[4-[(3,4-Dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)carbonyl]-1-piperazinyl]phenyl]-2-thiophenecarboximid-amide (BN 80933), an inhibitor of neuronal nitric-oxide synthase and an antioxidant, in model of transient focal cerebral ischemia in mice.
2003 Aug
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:35:29 GMT 2023
Edited
by admin
on Sat Dec 16 08:35:29 GMT 2023
Record UNII
98L2F93VSI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BN-80933
Common Name English
2-THIOPHENECARBOXIMIDAMIDE, N-(4-(4-(((2S)-3,4-DIHYDRO-6-HYDROXY-2,5,7,8-TETRAMETHYL-2H-1-BENZOPYRAN-2-YL)CARBONYL)-1-PIPERAZINYL)PHENYL)-
Systematic Name English
PIPERAZINE, 1-(((2S)-3,4-DIHYDRO-6-HYDROXY-2,5,7,8-TETRAMETHYL-2H-1-BENZOPYRAN-2-YL)CARBONYL)-4-(4-((IMINO-2-THIENYLMETHYL)AMINO)PHENYL)-
Systematic Name English
(+)-BN-80933
Common Name English
Code System Code Type Description
FDA UNII
98L2F93VSI
Created by admin on Sat Dec 16 08:35:29 GMT 2023 , Edited by admin on Sat Dec 16 08:35:29 GMT 2023
PRIMARY
PUBCHEM
6918419
Created by admin on Sat Dec 16 08:35:29 GMT 2023 , Edited by admin on Sat Dec 16 08:35:29 GMT 2023
PRIMARY
CAS
214348-10-4
Created by admin on Sat Dec 16 08:35:29 GMT 2023 , Edited by admin on Sat Dec 16 08:35:29 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY