Drug Information

Drug General Information
Drug ID
D0B1CM
Former ID
DNC014545
Drug Name
2-Methoxy-5-(3,4,5-trimethoxy-benzyl)-phenol
Drug Type
Small molecular drug
Indication Discovery agent Investigative [527276]
Formula
C17H20O5
Canonical SMILES
COC1=C(C=C(C=C1)CC2=CC(=C(C(=C2)OC)OC)OC)O
InChI
1S/C17H20O5/c1-19-14-6-5-11(8-13(14)18)7-12-9-15(20-2)17(22-4)16(10-12)21-3/h5-6,8-10,18H,7H2,1-4H3
InChIKey
JFZDWXGLUXEEAY-UHFFFAOYSA-N
PubChem Compound ID
372869
Target and Pathway
Target(s) Tubulin Target Info Inhibitor [527276]
Tubulin beta Target Info Inhibitor [527276]
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 527276J Med Chem. 1992 Mar 20;35(6):1058-67.Synthesis of alkoxy-substituted diaryl compounds and correlation of ring separation with inhibition of tubulin polymerization: differential enhancement of inhibitory effects under suboptimal polymerization reaction conditions.
Ref 527276J Med Chem. 1992 Mar 20;35(6):1058-67.Synthesis of alkoxy-substituted diaryl compounds and correlation of ring separation with inhibition of tubulin polymerization: differential enhancement of inhibitory effects under suboptimal polymerization reaction conditions.

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