5,6-O-BENZYLIDENE-L-ASCORBIC ACID

[H][C@]1(COC(O1)C2=CC=CC=C2)[C@@]3([H])OC(=O)C(O)=C3O

InChIKey=SWTGJCNCBUCXSS-ISUZDFFFSA-N

InChI=1S/C13H12O6/c14-9-10(15)12(16)19-11(9)8-6-17-13(18-8)7-4-2-1-3-5-7/h1-5,8,11,13-15H,6H2/t8-,11+,13?/m0/s1

Stereochemistry	EPIMERIC
Additional Stereochemistry	No
Defined Stereocenters	2 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

PubMed

Title	Date	PubMed
Sodium benzylideneascorbate induces apoptosis in HIV-replicating U1 cells.	1994 Aug 29	8076675

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:52:43 GMT 2023` Edited by `admin` on `Fri Dec 15 15:52:43 GMT 2023`
Record UNII	T544M6Z94A
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

5,6-O-BENZYLIDENE-L-ASCORBIC ACID

Common Name

English

L-ASCORBIC ACID, 5,6-O-BENZYLIDENE-

Common Name

English

L-ASCORBIC ACID, 5,6-O-(PHENYLMETHYLENE)-

Common Name

English

Code System Code Type Description

CAS

20664-60-2

Created by admin on Fri Dec 15 15:52:43 GMT 2023 , Edited by admin on Fri Dec 15 15:52:43 GMT 2023

PRIMARY

EPA CompTox

DTXSID50942865

Created by admin on Fri Dec 15 15:52:43 GMT 2023 , Edited by admin on Fri Dec 15 15:52:43 GMT 2023

PRIMARY

PUBCHEM

54682464

Created by admin on Fri Dec 15 15:52:43 GMT 2023 , Edited by admin on Fri Dec 15 15:52:43 GMT 2023

PRIMARY

FDA UNII

T544M6Z94A

Created by admin on Fri Dec 15 15:52:43 GMT 2023 , Edited by admin on Fri Dec 15 15:52:43 GMT 2023

PRIMARY