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Details

Stereochemistry ACHIRAL
Molecular Formula C14H13NO4
Molecular Weight 259.2573
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of KOKUSAGININE

SMILES

COC1=C(OC)C=C2C(=C1)N=C3OC=CC3=C2OC

InChI

InChIKey=JBRXRVFXQIKPEA-UHFFFAOYSA-N
InChI=1S/C14H13NO4/c1-16-11-6-9-10(7-12(11)17-2)15-14-8(4-5-19-14)13(9)18-3/h4-7H,1-3H3

HIDE SMILES / InChI

Molecular Formula C14H13NO4
Molecular Weight 259.2573
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
28.2 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Furoquinolines and dihydrooxazole alkaloids with cytotoxic activity from the stem bark of Araliopsis soyauxii.
2019-03
Determination of antibacterial activity and metabolite profile of Ruta graveolens against Streptococcus mutans and Streptococcus sobrinus.
2018-08-07
The inhibitory effect of kokusaginine on the growth of human breast cancer cells and MDR-resistant cells is mediated by the inhibition of tubulin assembly.
2018-08-01
Chalepin: isolated from Ruta angustifolia L. Pers induces mitochondrial mediated apoptosis in lung carcinoma cells.
2016-10-12
Phytochemicals from Ruta graveolens Activate TAS2R Bitter Taste Receptors and TRP Channels Involved in Gustation and Nociception.
2015-10-16
Furoquinoline Alkaloids from the Leaves of Evodia lepta as Potential Cholinesterase Inhibitors and their Molecular Docking.
2015-08
Inhibition of hepatitis C virus replication by chalepin and pseudane IX isolated from Ruta angustifolia leaves.
2014-12
Cytotoxic Benzophenanthridine and Furoquinoline Alkaloids from Zanthoxylum buesgenii (Rutaceae).
2014
Antibacterial constituents of three Cameroonian medicinal plants: Garcinia nobilis, Oricia suaveolens and Balsamocitrus camerunensis.
2013-04-10
Furoquinoline alkaloids isolated from Balfourodendron riedelianum as photosynthetic inhibitors in spinach chloroplasts.
2013-03-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:51:37 GMT 2025
Edited
by admin
on Mon Mar 31 18:51:37 GMT 2025
Record UNII
JG1753DK5H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
KOKUSAGININE
Common Name English
NSC-103013
Preferred Name English
KOKUSAGININ
Common Name English
FURO(2,3-B)QUINOLINE, 4,6,7-TRIMETHOXY-
Systematic Name English
6,7-DIMETHOXYDICTAMNINE
Systematic Name English
4,6,7-TRIMETHOXYFURO(2,3-B)QUINOLINE
Systematic Name English
Code System Code Type Description
NSC
103013
Created by admin on Mon Mar 31 18:51:37 GMT 2025 , Edited by admin on Mon Mar 31 18:51:37 GMT 2025
PRIMARY
PUBCHEM
10227
Created by admin on Mon Mar 31 18:51:37 GMT 2025 , Edited by admin on Mon Mar 31 18:51:37 GMT 2025
PRIMARY
FDA UNII
JG1753DK5H
Created by admin on Mon Mar 31 18:51:37 GMT 2025 , Edited by admin on Mon Mar 31 18:51:37 GMT 2025
PRIMARY
EPA CompTox
DTXSID60197506
Created by admin on Mon Mar 31 18:51:37 GMT 2025 , Edited by admin on Mon Mar 31 18:51:37 GMT 2025
PRIMARY
CAS
484-08-2
Created by admin on Mon Mar 31 18:51:37 GMT 2025 , Edited by admin on Mon Mar 31 18:51:37 GMT 2025
PRIMARY