EcoDrugPlus


Synonyms	5-Fluorocamalexin
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 ...

Synonyms

5-Fluorocamalexin

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	KGIGBOZMEHVLMU-UHFFFAOYSA-N
Smiles	Fc1ccc2[nH]cc(c3nccs3)c2c1
InChI	InChI=1S/C11H7FN2S/c12-7-1-2-10-8(5-7)9(6-14-10)11-13-3-4-15-11/h1-6,14H

InChI Key

KGIGBOZMEHVLMU-UHFFFAOYSA-N

Smiles

Fc1ccc2[nH]cc(c3nccs3)c2c1

InChI

InChI=1S/C11H7FN2S/c12-7-1-2-10-8(5-7)9(6-14-10)11-13-3-4-15-11/h1-6,14H

Property Name	Value
Molecular Formula	C11H7FN2S
Molecular Weight	218.25
AlogP	2.71
Hydrogen Bond Acceptor	1.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	1.0
Polar Surface Area	56.92
Molecular species	NEUTRAL
Aromatic Rings	3.0
Heavy Atoms	15.0

Property Name

Value

Molecular Formula

C11H7FN2S

Molecular Weight

218.25

AlogP

2.71

Hydrogen Bond Acceptor

1.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

1.0

Polar Surface Area

56.92

Molecular species

NEUTRAL

Aromatic Rings

3.0

Heavy Atoms

15.0

	EC50(nM)	IC50(nM)	Kd(nM)	Ki(nM)	Inhibition(%)
Leptosphaeria maculans	-	-	-	-	47-100

EC50(nM)

IC50(nM)

Kd(nM)

Ki(nM)

Inhibition(%)

Leptosphaeria maculans

47-100

Resources	Reference
ChEMBL	CHEMBL240583
PubChem	11390334
SureChEMBL	SCHEMBL12993647

Resources

Reference

ChEMBL

CHEMBL240583

PubChem

11390334

SureChEMBL

SCHEMBL12993647

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-FLUOROCAMALEXIN

Structure

Physicochemical Descriptors

Pharmacology

Cross References