U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H10O8
Molecular Weight 258.1816
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEGLATONE

SMILES

[H][C@]12OC(=O)[C@@H](OC(C)=O)[C@@]1([H])OC(=O)[C@@H]2OC(C)=O

InChI

InChIKey=ZOZKYEHVNDEUCO-DKXJUACHSA-N
InChI=1S/C10H10O8/c1-3(11)15-7-5-6(18-9(7)13)8(10(14)17-5)16-4(2)12/h5-8H,1-2H3/t5-,6-,7-,8+/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H10O8
Molecular Weight 258.1816
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 http://www.ncbi.nlm.nih.gov/pubmed/6614934

Aceglatone (Glucaron/ 2.5-Di-O-acetyl-D-glucaro-1,4:6,3-dilactone/ DAGDL ) is a non-toxic natural inhibitor of beta-glucuronidase. Is an antineoplastic drug available in Japan, which is used for preventive therapy after preservative operation against bladder cancer.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Enhancement by phenothiazine and 2,5-di-O-acetyl-D-glucosaccharo-(1,4)(6,3)-dilactone of bladder carcinogenicity of N-[4-(5-nitro-2-furyl)-2-thiazolyl]-formamide in rats.
1984 Aug
Patents

Patents

Sample Use Guides

aceglatone 2.25 g/day for three doses
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:46:14 GMT 2023
Edited
by admin
on Sat Dec 16 16:46:14 GMT 2023
Record UNII
347Q3OOJ13
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACEGLATONE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
2,5-DI-O-ACETYL-D-GLUCARO-1,4:6,3-DILACTONE
Common Name English
D-GLUCARIC ACID 1,4:6,3-DILACTONE DIACETATE
Common Name English
aceglatone [INN]
Common Name English
2,5-DI-O-ACETYL-D-GLUCOSACCHARO-1,4:6,3-DILACTONE
Common Name English
ACEGLATONE [JAN]
Common Name English
Aceglatone [WHO-DD]
Common Name English
GLUCARON
Brand Name English
ACEGLATONE [MI]
Common Name English
ACEGLATONE [MART.]
Common Name English
D-GLUCARIC ACID DI-.GAMMA.-LACTONE DIACETATE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C1017
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2103781
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
PUBCHEM
636372
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
DRUG CENTRAL
45
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
MESH
C038936
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
INN
3151
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
FDA UNII
347Q3OOJ13
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
EVMPD
SUB05207MIG
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
NCI_THESAURUS
C984
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
SMS_ID
100000087911
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
WIKIPEDIA
ACEGLATONE
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
MERCK INDEX
m1
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID0048848
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
CAS
642-83-1
Created by admin on Sat Dec 16 16:46:14 GMT 2023 , Edited by admin on Sat Dec 16 16:46:14 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY