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Home/Compounds/Research Reagent/1-(4-Methoxyphenyl)-2-methyl-3-nitro-1H-indol-6-ol
C16H14N2O4
298.29 g/mol
Research ReagentWarning

ID-8

CAS147591-46-6
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

ID-8 is a chemical compound used as a research reagent, specifically as an inhibitor of DYRK kinases. It is primarily employed in laboratory studies to investigate the biological roles of DYRK enzymes.

research reagent for DYRK inhibition studies

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Related Compounds

ReferenceSame Category

[(1R,8S)-bicyclo[6.1.0]non-4-yn-9-yl]methyl N-[2-(2-{2-[({[(1R,8S)-bicyclo[6.1.0]non-4-yn-9-yl]methoxy}carbonyl)amino]ethoxy}ethoxy)ethyl]carbamate

CAS1476737-97-9

research compound

ReferenceSame Category

N-tert-butyl-1H-indazole-7-carboxamide

CAS1476776-76-7

research compound

ReferenceSame Category

Goserelin EP Impurity E

CAS147688-42-4

research compound

ReferenceSame Category

1H-indole-2-carboxylic acid

CAS1477-50-5

research compound

Referencesame scaffold

1-(2,6-Dichlorophenyl)-2-indolinone

CAS172371-96-9

pharmaceutical intermediate

Referencesame scaffold

UK 5099

CAS56396-35-1

research compound

Referencesame scaffold

1-(3,5-Difluorophenyl)-3-(1-methylethyl)-1H-indole-2-methanol

CAS886362-94-3

research compound

Safety Reference

Harmful
Harmful
Environmental Hazard
Environmental Hazard
Warning
H302Harmful if swallowed
H400Very toxic to aquatic life
Identifiers
IUPAC Name

1-(4-methoxyphenyl)-2-methyl-3-nitroindol-6-ol

InChIKey

VVZNWYXIOADGSW-UHFFFAOYSA-N

SMILES

CC1=C(C2=C(N1C3=CC=C(C=C3)OC)C=C(C=C2)O)[N+](=O)[O-]

Synonyms (9)
  • ID-8
  • AH-262/34226056
  • Cambridge id 5280205
  • ID 8-d3
  • ID-8, >=98% (HPLC)

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