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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H18O9
Molecular Weight 354.3087
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NEOCHLOROGENIC ACID

SMILES

O[C@@H]1C[C@@](O)(C[C@@H](OC(=O)\C=C\C2=CC(O)=C(O)C=C2)[C@H]1O)C(O)=O

InChI

InChIKey=CWVRJTMFETXNAD-NXLLHMKUSA-N
InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24,15(22)23)6-11(19)14(12)21/h1-5,11-12,14,17-19,21,24H,6-7H2,(H,22,23)/b4-2+/t11-,12-,14+,16-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H18O9
Molecular Weight 354.3087
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 22:08:29 UTC 2023
Edited
by admin
on Fri Dec 15 22:08:29 UTC 2023
Record UNII
O4601UER1Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEOCHLOROGENIC ACID
Common Name English
NEOCHLOROGENIC ACID (CONSTITUENT OF ST. JOHN'S WORT) [DSC]
Common Name English
CYCLOHEXANECARBOXYLIC ACID, 3-((3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-1,4,5-TRIHYDROXY-, (1R-(1.ALPHA.,3.ALPHA.(E),4.ALPHA.,5.BETA.))-
Common Name English
(1R-(1.ALPHA.,3.ALPHA.,4.ALPHA.,5.BETA.))-3-((3-(3,4-DIHYDROXYPHENYL)-1-OXOALLYL)OXY)-1,4,5-TRIHYDROXYCYCLOHEXANECARBOXYLIC ACID
Common Name English
(E)-NEOCHLOROGENIC ACID
Common Name English
CYCLOHEXANECARBOXYLIC ACID, 3-(((2E)-3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPEN-1-YL)OXY)-1,4,5-TRIHYDROXY-, (1R,3R,4S,5R)-
Systematic Name English
3-CQA
Common Name English
CYCLOHEXANECARBOXYLIC ACID, 3-((3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-1,4,5-TRIHYDROXY-, (1R-(1.ALPHA.,3.ALPHA.,4.ALPHA.,5.BETA.))-
Common Name English
3-O-(E)-CAFFEOYLQUINIC ACID
Common Name English
Code System Code Type Description
CAS
342811-68-1
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
WIKIPEDIA
NEOCHLOROGENIC ACID
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
MESH
C473200
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
PUBCHEM
5280633
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
CAS
906-33-2
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
FDA UNII
O4601UER1Z
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
ECHA (EC/EINECS)
212-997-1
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
CHEBI
16384
Created by admin on Fri Dec 15 22:08:30 UTC 2023 , Edited by admin on Fri Dec 15 22:08:30 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
The water-soluble fraction was repeatedly chromatographed over MCI gel CHP20P, Sephadex LH-20, and YMC ODSA to yield the compound.
CONSTITUENT ALWAYS PRESENT -> PARENT
Methanol extracts of stevia dry leaves were directly used for LC-MS analysis. Efficient separation and resolution were achieved with diphenyl packing and acetonitrile/water as solvent in the HPLC method. Negative ion mode was used for all MS measurements.
PARENT -> CONSTITUENT ALWAYS PRESENT