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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H22O4
Molecular Weight 266.3328
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ANHYDRODIHYDROARTEMISNIN

SMILES

[H][C@]12OC=C(C)[C@]3([H])CC[C@@H](C)[C@]4([H])CC[C@@](C)(OO[C@@]134)O2

InChI

InChIKey=UKXCIQFCSITOCY-VLDCTWHGSA-N
InChI=1S/C15H22O4/c1-9-4-5-11-10(2)8-16-13-15(11)12(9)6-7-14(3,17-13)18-19-15/h8-9,11-13H,4-7H2,1-3H3/t9-,11+,12+,13-,14-,15+/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H22O4
Molecular Weight 266.3328
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 6 / 6
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:43:18 GMT 2023
Edited
by admin
on Sat Dec 16 08:43:18 GMT 2023
Record UNII
0YH8NQO930
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ANHYDRODIHYDROARTEMISNIN
Common Name English
9,10-ANHYDRODEHYDROARTEMISININ
Common Name English
3,12-EPOXY-12H-PYRANO(4,3-J)-1,2-BENZODIOXEPIN, 3,4,5,5A,6,7,8,8A-OCTAHYDRO-3,6,9-TRIMETHYL-, (3R,5AS,6R,8AS,12R,12AR)-
Systematic Name English
(3R,5AS,6R,8AS,12R,12AR)-3,4,5,5A,6,7,8,8A-OCTAHYDRO-3,6,9-TRIMETHYL-3,12-EPOXY-12H-PYRANO(4,3-J)-1,2-BENZODIOXEPIN(+)-9,10
Common Name English
ANHYDRODIHYDROARTEMISININ
Common Name English
ARTESUNATE RELATED COMPOUND C
Common Name English
Code System Code Type Description
PUBCHEM
393517
Created by admin on Sat Dec 16 08:43:18 GMT 2023 , Edited by admin on Sat Dec 16 08:43:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID50327855
Created by admin on Sat Dec 16 08:43:18 GMT 2023 , Edited by admin on Sat Dec 16 08:43:18 GMT 2023
PRIMARY
CAS
82596-30-3
Created by admin on Sat Dec 16 08:43:18 GMT 2023 , Edited by admin on Sat Dec 16 08:43:18 GMT 2023
PRIMARY
FDA UNII
0YH8NQO930
Created by admin on Sat Dec 16 08:43:18 GMT 2023 , Edited by admin on Sat Dec 16 08:43:18 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
In the chromatogram obtained with solution (1): the area of any peak corresponding to impurity C, when multiplied by a correction factor of 0.07, is not greater than 0.2 times the area of the principal peak obtained with solution (4) (0.2%) the sum of the corrected area of any peak corresponding to impurity C and the areas of all other peaks, other than the principal peak, is not greater than twice the area of the principal peak obtained with solution (4) (2.0%).
PARENT -> IMPURITY
PARENT -> IMPURITY
PARENT -> IMPURITY