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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H12O6
Molecular Weight 180.1559
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IDOSE, D-

SMILES

OC[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)C=O

InChI

InChIKey=GZCGUPFRVQAUEE-ZXXMMSQZSA-N
InChI=1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4-,5+,6+/m1/s1

HIDE SMILES / InChI

Molecular Formula C6H12O6
Molecular Weight 180.1559
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/17629262

Idose is an aldohexose isomeric with galactose. Idose can influence to the stability of phospholipid bilayers and topical application of idose accelerated the skin barrier recovery

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
L-Idose: an attractive substrate alternative to D-glucose for measuring aldose reductase activity.
2015 Jan 24
Patents

Patents

Sample Use Guides

The effects of topical application of Idose on barrier recovery after barrier disruption by tape stripping were investigated. All experiments were performed on 7- to 10-week-old male hairless mice (HR-1, Hoshino, Japan). Measurement of skin barrier function, disruption of the barrier and application of test samples were carried out under anaesthesia with nembutal. Permeability barrier function was evaluated by measurement of transepidermal water loss (TEWL) with an electric moisture analyser (Meeco, Warrington, PA, USA). For barrier recovery experiments, skin on both flanks was treated by repeated tape stripping until the TEWL reached 7–10 mg ⁄ cm2 per h. Immediately after tape stripping, 100 mkm of 0.1 m aqueous solution of Idose was applied. TEWL was then measured at the same sites at 1, 3, 6 and 24 h thereafter. Barrier disruption was done between 7:00AM and 8:00AM and the barrier recovery rate was evaluated immediately, to avoid the effect of circadian rhythm.
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:37:47 UTC 2023
Edited
by admin
on Sat Dec 16 09:37:47 UTC 2023
Record UNII
N1T50P1RZ2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IDOSE, D-
Systematic Name English
IDOSE D-FORM [MI]
Common Name English
IDOSE, (+)-
Systematic Name English
D-IDOSE
Systematic Name English
Code System Code Type Description
PUBCHEM
111123
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY
EPA CompTox
DTXSID901015881
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY
CAS
5978-95-0
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY
ECHA (EC/EINECS)
227-780-7
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY
CAS
552-76-1
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
ALTERNATIVE
CAS
41847-68-1
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
ALTERNATIVE
MERCK INDEX
m6200
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY Merck Index
FDA UNII
N1T50P1RZ2
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY
CHEBI
28014
Created by admin on Sat Dec 16 09:37:47 UTC 2023 , Edited by admin on Sat Dec 16 09:37:47 UTC 2023
PRIMARY