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Details

Stereochemistry ACHIRAL
Molecular Formula C21H17NO9S2
Molecular Weight 491.491
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULISATIN

SMILES

CC1=CC=CC2=C1NC(=O)C2(C3=CC=C(OS(O)(=O)=O)C=C3)C4=CC=C(OS(O)(=O)=O)C=C4

InChI

InChIKey=URNFTLVCQLRCMN-UHFFFAOYSA-N
InChI=1S/C21H17NO9S2/c1-13-3-2-4-18-19(13)22-20(23)21(18,14-5-9-16(10-6-14)30-32(24,25)26)15-7-11-17(12-8-15)31-33(27,28)29/h2-12H,1H3,(H,22,23)(H,24,25,26)(H,27,28,29)

HIDE SMILES / InChI

Molecular Formula C21H17NO9S2
Molecular Weight 491.491
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulisatin (also known as DAN-603) is an indolinone derivative patented by Andreu, Dr., S. A. as a laxative. In preclinical models, Sulisatin increases selectively the colon motility without modifying the speed of gastric, intestinal (small intestine) and caecal emptying in rats. Sulisatin is unable to inhibit water absorption in rat colon while small amounts of Sulisatin may inhibit it significantly.

Approval Year

PubMed

PubMed

TitleDatePubMed
Study of the laxative properties of the disodium salt of the sulfuric diester of 3,3-bis-(4-hydroxyphenyl)-7-methyl-2-indolinone (DAN-603 in the rat.
1976 Mar
Patents

Patents

Sample Use Guides

In Vivo Use Guide
rat 1.5, 3 and 6 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:20:51 GMT 2023
Edited
by admin
on Fri Dec 15 17:20:51 GMT 2023
Record UNII
5EOG8KQT0Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULISATIN
INN   MI   WHO-DD  
INN  
Official Name English
SULISATIN [MI]
Common Name English
sulisatin [INN]
Common Name English
Sulisatin [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29697
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
Code System Code Type Description
INN
3885
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
MESH
C012120
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
FDA UNII
5EOG8KQT0Y
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
EVMPD
SUB10745MIG
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
DRUG CENTRAL
2535
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
NCI_THESAURUS
C74275
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
MERCK INDEX
m947
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY Merck Index
CAS
54935-03-4
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
SMS_ID
100000083768
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
PUBCHEM
41238
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID80203451
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104944
Created by admin on Fri Dec 15 17:20:51 GMT 2023 , Edited by admin on Fri Dec 15 17:20:51 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY