EcoDrugPlus


Molecule Category	Free-form
Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Molecule Category

Free-form

Source

Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


InChI Key	CMQGCWMEXQRWSS-KTKRTIGZSA-N
Smiles	COc1cc(\C=C/c2ccccc2)cc(OC)c1OC
InChI	InChI=1S/C17H18O3/c1-18-15-11-14(12-16(19-2)17(15)20-3)10-9-13-7-5-4-6-8-13/h4-12H,1-3H3/b10-9-

InChI Key

CMQGCWMEXQRWSS-KTKRTIGZSA-N

Smiles

COc1cc(\C=C/c2ccccc2)cc(OC)c1OC

InChI

InChI=1S/C17H18O3/c1-18-15-11-14(12-16(19-2)17(15)20-3)10-9-13-7-5-4-6-8-13/h4-12H,1-3H3/b10-9-

Property Name	Value
Molecular Formula	C17H18O3
Molecular Weight	270.32
AlogP	3.77
Hydrogen Bond Acceptor	3.0
Number of Rotational Bond	5.0
Polar Surface Area	27.69
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C17H18O3

Molecular Weight

270.32

AlogP

3.77

Hydrogen Bond Acceptor

3.0

Number of Rotational Bond

5.0

Polar Surface Area

27.69

Heavy Atoms

20.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	36307.81	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

36307.81

Resources	Reference
ChEMBL	CHEMBL87162
PubChem	5388756
SureChEMBL	SCHEMBL9184995

Resources

Reference

ChEMBL

CHEMBL87162

PubChem

5388756

SureChEMBL

SCHEMBL9184995

EcoDrug+ was developed under the PREMIER Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

(Z)-2-PHENYL-1-(3,4,5-TRIMETHOXYPHENYL)ETHENE

Structure

Physicochemical Descriptors

Pharmacology

Cross References