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	PJPFICFWZAOAQQ-UHFFFAOYSA-N
Smiles	C(CCNc1c2CCCCc2nc3sc4CCCCc4c13)CNc5c6CCCCc6nc7sc8CCCCc8c57
InChI	InChI=1S/C34H42N4S2/c1-5-15-25-21(11-1)31(29-23-13-3-7-17-27(23)39-33(29)37-25)35-19-9-10-20-36-32-22-12-2-6-16-26(22)38-34-30(32)24-14-4-8-18-28(24)40-34/h1-20H2,(H,35,37)(H,36,38)

InChI Key

PJPFICFWZAOAQQ-UHFFFAOYSA-N

Smiles

C(CCNc1c2CCCCc2nc3sc4CCCCc4c13)CNc5c6CCCCc6nc7sc8CCCCc8c57

InChI

InChI=1S/C34H42N4S2/c1-5-15-25-21(11-1)31(29-23-13-3-7-17-27(23)39-33(29)37-25)35-19-9-10-20-36-32-22-12-2-6-16-26(22)38-34-30(32)24-14-4-8-18-28(24)40-34/h1-20H2,(H,35,37)(H,36,38)

Property Name	Value
Molecular Formula	C34H42N4S2
Molecular Weight	570.85
AlogP	9.37
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	7.0
Polar Surface Area	106.32
Molecular species	BASE
Aromatic Rings	4.0
Heavy Atoms	40.0

Property Name

Value

Molecular Formula

C34H42N4S2

Molecular Weight

570.85

AlogP

9.37

Hydrogen Bond Acceptor

4.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

7.0

Polar Surface Area

106.32

Molecular species

BASE

Aromatic Rings

4.0

Heavy Atoms

40.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Rattus norvegicus	-	-	-	-	35.67

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Rattus norvegicus

35.67

Resources	Reference
ChEMBL	CHEMBL2299372
PubChem	76320637

Resources

Reference

ChEMBL

CHEMBL2299372

PubChem

76320637

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

BUTANE-1,4-DIAMINO-N,N'-DIYL-11,11'-BIS(1,2,3,4,7,8,9,1'-OCTAHYDRO[1]BENZOTHIENO[2,3-B]QUINOLINE

Structure

Physicochemical Descriptors

Pharmacology

Cross References