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	JPGSTHKGEJVSML-MXWIWYRXSA-N
Smiles	CCCCCCC(=O)Oc1ccc(\C=C\C(=O)CC(=O)\C=C\c2ccc(OC(=O)CCCCCC)c(OC)c2)cc1OC
InChI	InChI=1S/C35H44O8/c1-5-7-9-11-13-34(38)42-30-21-17-26(23-32(30)40-3)15-19-28(36)25-29(37)20-16-27-18-22-31(33(24-27)41-4)43-35(39)14-12-10-8-6-2/h15-24H,5-14,25H2,1-4H3/b19-15+,20-16+

InChI Key

JPGSTHKGEJVSML-MXWIWYRXSA-N

Smiles

CCCCCCC(=O)Oc1ccc(\C=C\C(=O)CC(=O)\C=C\c2ccc(OC(=O)CCCCCC)c(OC)c2)cc1OC

InChI

InChI=1S/C35H44O8/c1-5-7-9-11-13-34(38)42-30-21-17-26(23-32(30)40-3)15-19-28(36)25-29(37)20-16-27-18-22-31(33(24-27)41-4)43-35(39)14-12-10-8-6-2/h15-24H,5-14,25H2,1-4H3/b19-15+,20-16+

Property Name	Value
Molecular Formula	C35H44O8
Molecular Weight	592.72
AlogP	8.56
Hydrogen Bond Acceptor	8.0
Number of Rotational Bond	22.0
Polar Surface Area	105.2
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	43.0

Property Name

Value

Molecular Formula

C35H44O8

Molecular Weight

592.72

AlogP

8.56

Hydrogen Bond Acceptor

8.0

Number of Rotational Bond

22.0

Polar Surface Area

105.2

Molecular species

NEUTRAL

Aromatic Rings

2.0

Heavy Atoms

43.0

Targets	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Enzyme Isomerase	-	2900	-	-	-

Targets

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Enzyme Isomerase

2900

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Homo sapiens	-	2900	-	-	-

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Homo sapiens

2900

Resources	Reference
ChEMBL	CHEMBL2259878
PubChem	76311989

Resources

Reference

ChEMBL

CHEMBL2259878

PubChem

76311989

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

DI-O-HEPTANOYLCURCUMIN

Structure

Physicochemical Descriptors

Pharmacology

Cross References