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	ROMQPDPUYFSPFF-UHFFFAOYSA-N
Smiles	COc1cc(NC(=C2C(=O)OC(C)(C)OC2=O)NCCCCCCCCc3ccc(OCCC(C)C)cc3)cc(OC)c1OC
InChI	InChI=1S/C35H50N2O8/c1-24(2)19-21-43-27-17-15-25(16-18-27)14-12-10-8-9-11-13-20-36-32(30-33(38)44-35(3,4)45-34(30)39)37-26-22-28(40-5)31(42-7)29(23-26)41-6/h15-18,22-24,36-37H,8-14,19-21H2,1-7H3

InChI Key

ROMQPDPUYFSPFF-UHFFFAOYSA-N

Smiles

COc1cc(NC(=C2C(=O)OC(C)(C)OC2=O)NCCCCCCCCc3ccc(OCCC(C)C)cc3)cc(OC)c1OC

InChI

InChI=1S/C35H50N2O8/c1-24(2)19-21-43-27-17-15-25(16-18-27)14-12-10-8-9-11-13-20-36-32(30-33(38)44-35(3,4)45-34(30)39)37-26-22-28(40-5)31(42-7)29(23-26)41-6/h15-18,22-24,36-37H,8-14,19-21H2,1-7H3

Property Name	Value
Molecular Formula	C35H50N2O8
Molecular Weight	626.78
AlogP	7.6
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	19.0
Polar Surface Area	113.58
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	45.0

Property Name

Value

Molecular Formula

C35H50N2O8

Molecular Weight

626.78

AlogP

7.6

Hydrogen Bond Acceptor

10.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

19.0

Polar Surface Area

113.58

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

45.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	3499.45-3500	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

3499.45-3500

Resources	Reference
ChEMBL	CHEMBL2235998

Resources

Reference

ChEMBL

CHEMBL2235998

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, Volume 54, Issue D1, 6 January 2026, Pages D1397–D1404, https://doi.org/10.1093/nar/gkaf1251

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

Last update: Monday, 3 November 2025

5-((8-(4-(ISOPENTYLOXY)PHENYL)OCTYLAMINO)(3,4,5-TRIMETHOXYPHENYLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE

Structure

Physicochemical Descriptors

Pharmacology

Cross References