3-(1-(4-METHOXYBENZENESULFONYL)-2,3-DIHYDRO-1H-INDOL-5-YL)-N-HYDROXYACRYLAMIDE

COC1=CC=C(C=C1)S(=O)(=O)N2CCC3=C2C=CC(\C=C\C(=O)NO)=C3

InChIKey=LMFNVOGHSBJWLX-YCRREMRBSA-N

InChI=1S/C18H18N2O5S/c1-25-15-4-6-16(7-5-15)26(23,24)20-11-10-14-12-13(2-8-17(14)20)3-9-18(21)19-22/h2-9,12,22H,10-11H2,1H3,(H,19,21)/b9-3+

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

PubMed

Title	Date	PubMed
1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines histone deacetylase inhibitors are potent cytokine release suppressors.	2013-07-08	23788254

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:28:59 GMT 2025` Edited by `admin` on `Mon Mar 31 21:28:59 GMT 2025`
Record UNII	2237262Z7U
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

3-(1-(4-METHOXYBENZENESULFONYL)-2,3-DIHYDRO-1H-INDOL-5-YL)-N-HYDROXYACRYLAMIDE

Preferred Name

English

Code System Code Type Description

EPA CompTox

DTXSID401129776

Created by admin on Mon Mar 31 21:28:59 GMT 2025 , Edited by admin on Mon Mar 31 21:28:59 GMT 2025

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FDA UNII

2237262Z7U

Created by admin on Mon Mar 31 21:28:59 GMT 2025 , Edited by admin on Mon Mar 31 21:28:59 GMT 2025

PRIMARY

PUBCHEM

53385599

Created by admin on Mon Mar 31 21:28:59 GMT 2025 , Edited by admin on Mon Mar 31 21:28:59 GMT 2025

PRIMARY

CAS

1338320-95-8

Created by admin on Mon Mar 31 21:28:59 GMT 2025 , Edited by admin on Mon Mar 31 21:28:59 GMT 2025

PRIMARY