MC-7404

Details

Stereochemistry	ACHIRAL
Molecular Formula	C29H21BrN4O2
Molecular Weight	537.407
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

BrC1=CC=C(C=C1)C(=O)C2=NC(=CC3=C2NC4=CC=CC=C34)C(=O)NCCC5=CNC6=C5C=CC=C6

InChI

InChIKey=DLOFNWDJTXTZPF-UHFFFAOYSA-N

InChI=1S/C29H21BrN4O2/c30-19-11-9-17(10-12-19)28(35)27-26-22(21-6-2-4-8-24(21)33-26)15-25(34-27)29(36)31-14-13-18-16-32-23-7-3-1-5-20(18)23/h1-12,15-16,32-33H,13-14H2,(H,31,36)

HIDE SMILES / InChI

Molecular Formula	C29H21BrN4O2
Molecular Weight	537.407
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 19:53:35 UTC 2023` Edited by `admin` on `Sat Dec 16 19:53:35 UTC 2023`
Record UNII	74V87G4R62
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

MC-7404

Code

English

MC7404

Common Name

English

1-(4-bromobenzoyl)-N-[2-(1H-indol-3-yl)ethyl]-9H-pyrido[3,4-b]indole-3-carboxamide

Systematic Name

English

Code System Code Type Description

FDA UNII

74V87G4R62

Created by admin on Sat Dec 16 19:53:35 UTC 2023 , Edited by admin on Sat Dec 16 19:53:35 UTC 2023

PRIMARY

PUBCHEM

167312403

Created by admin on Sat Dec 16 19:53:35 UTC 2023 , Edited by admin on Sat Dec 16 19:53:35 UTC 2023

PRIMARY

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TARGET -> INHIBITOR

Comments:

Inhibits the activation of STAT3 signaling resulting from tyrosine residue phosphorylation (Y705) leads to aberrant oncogene transcription.

Amount: