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Details

Stereochemistry ACHIRAL
Molecular Formula C21H23N3O5.C7H8O3S
Molecular Weight 569.626
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ABEXINOSTAT TOSYLATE

SMILES

CC1=CC=C(C=C1)S(O)(=O)=O.CN(C)CC2=C(OC3=CC=CC=C23)C(=O)NCCOC4=CC=C(C=C4)C(=O)NO

InChI

InChIKey=XMXZUHOHUKWCJK-UHFFFAOYSA-N
InChI=1S/C21H23N3O5.C7H8O3S/c1-24(2)13-17-16-5-3-4-6-18(16)29-19(17)21(26)22-11-12-28-15-9-7-14(8-10-15)20(25)23-27;1-6-2-4-7(5-3-6)11(8,9)10/h3-10,27H,11-13H2,1-2H3,(H,22,26)(H,23,25);2-5H,1H3,(H,8,9,10)

HIDE SMILES / InChI

Molecular Formula C21H23N3O5
Molecular Weight 397.4244
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C7H8O3S
Molecular Weight 172.202
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 15:43:37 UTC 2023
Edited
by admin
on Sat Dec 16 15:43:37 UTC 2023
Record UNII
AOH3JC92C0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ABEXINOSTAT TOSYLATE
Common Name English
2-BENZOFURANCARBOXAMIDE, 3-((DIMETHYLAMINO)METHYL)-N-(2-(4-((HYDROXYAMINO)CARBONYL)PHENOXY)ETHYL)-, 4-METHYLBENZENESULFONATE (1:1)
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C160889
Created by admin on Sat Dec 16 15:43:37 UTC 2023 , Edited by admin on Sat Dec 16 15:43:37 UTC 2023
PRIMARY
SMS_ID
100000183701
Created by admin on Sat Dec 16 15:43:37 UTC 2023 , Edited by admin on Sat Dec 16 15:43:37 UTC 2023
PRIMARY
PUBCHEM
77461142
Created by admin on Sat Dec 16 15:43:37 UTC 2023 , Edited by admin on Sat Dec 16 15:43:37 UTC 2023
PRIMARY
FDA UNII
AOH3JC92C0
Created by admin on Sat Dec 16 15:43:37 UTC 2023 , Edited by admin on Sat Dec 16 15:43:37 UTC 2023
PRIMARY
CAS
1622385-42-5
Created by admin on Sat Dec 16 15:43:37 UTC 2023 , Edited by admin on Sat Dec 16 15:43:37 UTC 2023
PRIMARY
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ACTIVE MOIETY