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	RRZSMNDLJQXDPI-UHFFFAOYSA-N
Smiles	COC(=O)c1c(C)nn(c1OCCCOc2c(C(=O)OC)c(C)nn2c3ccccc3)c4ccccc4
InChI	InChI=1S/C27H28N4O6/c1-18-22(26(32)34-3)24(30(28-18)20-12-7-5-8-13-20)36-16-11-17-37-25-23(27(33)35-4)19(2)29-31(25)21-14-9-6-10-15-21/h5-10,12-15H,11,16-17H2,1-4H3

InChI Key

RRZSMNDLJQXDPI-UHFFFAOYSA-N

Smiles

COC(=O)c1c(C)nn(c1OCCCOc2c(C(=O)OC)c(C)nn2c3ccccc3)c4ccccc4

InChI

InChI=1S/C27H28N4O6/c1-18-22(26(32)34-3)24(30(28-18)20-12-7-5-8-13-20)36-16-11-17-37-25-23(27(33)35-4)19(2)29-31(25)21-14-9-6-10-15-21/h5-10,12-15H,11,16-17H2,1-4H3

Property Name	Value
Molecular Formula	C27H28N4O6
Molecular Weight	504.53
AlogP	4.49
Hydrogen Bond Acceptor	8.0
Number of Rotational Bond	12.0
Polar Surface Area	106.7
Molecular species	NEUTRAL
Aromatic Rings	4.0
Heavy Atoms	37.0

Property Name

Value

Molecular Formula

C27H28N4O6

Molecular Weight

504.53

AlogP

4.49

Hydrogen Bond Acceptor

8.0

Number of Rotational Bond

12.0

Polar Surface Area

106.7

Molecular species

NEUTRAL

Aromatic Rings

4.0

Heavy Atoms

37.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Rattus norvegicus	-	-	-	-	15.1-24.4

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Rattus norvegicus

15.1-24.4

Resources	Reference
ChEMBL	CHEMBL2238204
PubChem	76308218

Resources

Reference

ChEMBL

CHEMBL2238204

PubChem

76308218

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...

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Last update: Monday, 3 November 2025

DIMETHYL 5,5'-(PROPANE-1,3-DIYLBIS(OXY))BIS(3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBOXYLATE)

Structure

Physicochemical Descriptors

Pharmacology

Cross References