Drug General Information
Drug ID
D00CPM
Former ID
DNC014570
Drug Name
2-(4-Methoxy-phenyl)-1H-indole-3-carbaldehyde
Drug Type
Small molecular drug
Indication Discovery agent Investigative [534765]
Structure
Download
2D MOL

3D MOL

Formula
C16H13NO2
Canonical SMILES
COC1=CC=C(C=C1)C2=C(C3=CC=CC=C3N2)C=O
InChI
1S/C16H13NO2/c1-19-12-8-6-11(7-9-12)16-14(10-18)13-4-2-3-5-15(13)17-16/h2-10,17H,1H3
InChIKey
QIMWZVMNUAWWSJ-UHFFFAOYSA-N
PubChem Compound ID
Target and Pathway
Target(s) Tubulin Target Info Inhibitor [534765]
Tubulin beta Target Info Inhibitor [534765]
KEGG Pathway Phagosome
Gap junction
Pathogenic Escherichia coli infection
NetPath Pathway FSH Signaling Pathway
TCR Signaling Pathway
EGFR1 Signaling Pathway
PANTHER Pathway Cytoskeletal regulation by Rho GTPase
Huntington disease
Reactome Regulation of PLK1 Activity at G2/M Transition
Loss of Nlp from mitotic centrosomes
Recruitment of mitotic centrosome proteins and complexes
Loss of proteins required for interphase microtubule organization?from the centrosome
Anchoring of the basal body to the plasma membrane
WikiPathways Parkin-Ubiquitin Proteasomal System pathway
Pathogenic Escherichia coli infection
Mitotic G2-G2/M phases
References
Ref 534765J Med Chem. 1998 Dec 3;41(25):4965-72.Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerization.
Ref 534765J Med Chem. 1998 Dec 3;41(25):4965-72.Methoxy-substituted 3-formyl-2-phenylindoles inhibit tubulin polymerization.

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