U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C14H13NO2
Molecular Weight 227.2585
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLINDERSINE

SMILES

CC1(C)OC2=C(C=C1)C(=O)NC3=C2C=CC=C3

InChI

InChIKey=PXNMNABLQWUMCX-UHFFFAOYSA-N
InChI=1S/C14H13NO2/c1-14(2)8-7-10-12(17-14)9-5-3-4-6-11(9)15-13(10)16/h3-8H,1-2H3,(H,15,16)

HIDE SMILES / InChI

Molecular Formula C14H13NO2
Molecular Weight 227.2585
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Haplophytin-A and B: the alkaloidal constituents of Haplophyllum acutifolium.
2001 Aug
Photo-activated DNA binding and antimicrobial activities of furoquinoline and pyranoquinolone alkaloids from rutaceae.
2004 Jun
Isolation and identification of antifungal and antialgal alkaloids from Haplophyllum sieversii.
2005 Oct 5
Screening of 14 alkaloids isolated from Haplophyllum A. Juss. for their cytotoxic properties.
2006 Apr 21
Transition metal complexes of quinolino[3,2-b]benzodiazepine and quinolino[3,2-b]benzoxazepine: synthesis, characterization, and antimicrobial studies.
2007
Effects of proximity on the relaxation dynamics of flindersine and 6(5H)-phenanthridinone.
2007 Jan 18
Static and dynamic interaction of a naturally occurring photochromic molecule with bovine serum albumin studied by UV-visible absorption and fluorescence spectroscopy.
2008 Dec 25
Boolean and fuzzy logic gates based on the interaction of flindersine with bovine serum albumin and tryptophan.
2008 Nov 27
Secondary metabolites and cytotoxic activities from the stem bark of Zanthoxylum nitidum.
2009 Jun
Antibacterial and antifungal activity of Flindersine isolated from the traditional medicinal plant, Toddalia asiatica (L.) Lam.
2009 Jun 25
Cytotoxic activity and cell cycle analysis of quinoline alkaloids isolated from Haplophyllum canaliculatum Boiss.
2009 Nov
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:43:50 UTC 2023
Edited
by admin
on Fri Dec 15 19:43:50 UTC 2023
Record UNII
6A8PD12CKP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLINDERSINE
MI  
Common Name English
2,2'-DIMETHYL-.ALPHA.-PYRANO(5',6',3,4)-2(1H)-QUINOLONE
Common Name English
FLINDERSINE [MI]
Common Name English
NSC-94655
Code English
2,6-DIHYDRO-2,2-DIMETHYL-5H-PYRANO(3,2-C)QUINOLIN-5-ONE
Systematic Name English
Code System Code Type Description
CAS
523-64-8
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY
FDA UNII
6A8PD12CKP
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY
PUBCHEM
68230
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY
MESH
C539535
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY
NSC
94655
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY
MERCK INDEX
m5403
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID80200324
Created by admin on Fri Dec 15 19:43:50 UTC 2023 , Edited by admin on Fri Dec 15 19:43:50 UTC 2023
PRIMARY