TDR Targets

Basic information

Technical information

Name: Unnamed compound
MW: 514.04 | Formula: C25H28ClN5O3S
H donors: 1 H acceptors: 3 LogP: 3.48 Rotable bonds: 6
Rule of 5 violations (Lipinski): 2
SMILES: Clc1ccc2c(c1)cc([nH]2)S(=O)(=O)N1CCN(CC1)C(=O)c1ccc(cc1)C(=N)N1CCCCC1
InChi: 1S/C25H28ClN5O3S/c26-21-8-9-22-20(16-21)17-23(28-22)35(33,34)31-14-12-30(13-15-31)25(32)19-6-4-18(5-7-19)24(27)29-10-2-1-3-11-29/h4-9,16-17,27-28H,1-3,10-15H2
InChiKey: HZDFOLZBDXXSNA-UHFFFAOYSA-N

Network

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Target Layer

Model Organisms

Species	Viewmode
Arabidopsis thaliana
Caenorhabditis elegans
Dictyostelium discoideum
Drosophila melanogaster
Escherichia coli
Homo sapiens
Mus musculus
Oryza sativa
Saccharomyces cerevisiae
Schmidtea mediterranea
Other organisms

TDR Pathogens:

Species	Viewmode
Brugia malayi
Chlamydia trachomatis
Echinococcus granulosus
Entamoeba histolytica
Echinococcus multilocularis
Giardia lamblia
Leishmania major
Loa Loa (eye worm)
Mycobacterium leprae
Mycobacterium tuberculosis
Mycobacterium ulcerans
Onchocerca volvulus
Plasmodium falciparum
Plasmodium vivax
Schistosoma mansoni
Trypanosoma brucei
Trypanosoma cruzi
Toxoplasma gondii
Treponema pallidum
Trichomonas vaginalis
Wolbachia endosymbiont of Brugia malayi

Other Pathogens:

Species	Viewmode
Babesia bovis
Candida albicans
Cryptosporidium hominis
Cryptosporidium parvum
Leishmania braziliensis
Leishmania donovani
Leishmania infantum
Leishmania mexicana
Neospora caninum
Plasmodium berghei
Plasmodium knowlesi
Plasmodium yoelii
Schistosoma japonicum
Trypanosoma brucei gambiense
Trypanosoma congolense
Theileria parva

Compound Layer

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Clustering layers

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species	Target name	Source	Bibliographic reference
Homo sapiens	coagulation factor X	Starlite/ChEMBL	References

Predicted pathogen targets for this compound

By orthology

No druggable targets predicted by orthology data

By sequence similarity to non orthologous known druggable targets

No druggable targets predicted by sequence similarity

Ranking Plot

Putative Targets List

Species	Potential target	Raw	Global	Species
Treponema pallidum	ATP-dependent RNA helicase	0.0103	1	0.5
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Loa Loa (eye worm)	ctsf protein	0.0022	0.0629	0.0629
Leishmania major	eukaryotic initiation factor 4a, putative	0.0103	1	1
Echinococcus multilocularis	cathepsin L cysteine protease	0.0022	0.0629	0.0629
Onchocerca volvulus		0.0022	0.0629	0.0629
Echinococcus multilocularis	cathepsin L cysteine protease	0.0022	0.0629	0.0629
Onchocerca volvulus	Cathepsin F homolog	0.0022	0.0629	0.0629
Brugia malayi	Papain family cysteine protease containing protein	0.0022	0.0629	0.0629
Loa Loa (eye worm)	fibroinase	0.0022	0.0629	0.0629
Onchocerca volvulus		0.0022	0.0629	0.0629
Loa Loa (eye worm)	cysteine protease	0.0022	0.0629	0.0629
Echinococcus granulosus	cathepsin L cysteine proteinase	0.0022	0.0629	0.0629
Leishmania major	eukaryotic initiation factor 4a, putative	0.0103	1	1
Entamoeba histolytica	DEAD/DEAH box helicase, putative	0.0103	1	1
Toxoplasma gondii	eukaryotic initiation factor-4A, putative	0.0103	1	1
Trypanosoma cruzi	Eukaryotic initiation factor 4A-1	0.0103	1	1
Loa Loa (eye worm)	Papain cysteine protease/cathepsin propeptide inhibitor-containing protein	0.0022	0.0629	0.0629
Onchocerca volvulus		0.0022	0.0629	0.0629
Trichomonas vaginalis	DEAD box ATP-dependent RNA helicase, putative	0.0103	1	1
Loa Loa (eye worm)	hypothetical protein	0.0022	0.0629	0.0629
Mycobacterium tuberculosis	Probable cold-shock DeaD-box protein A homolog DeaD (ATP-dependent RNA helicase dead homolog)	0.0103	1	0.5
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Echinococcus multilocularis	eukaryotic initiation factor 4A III	0.0103	1	1
Echinococcus multilocularis	cysteine protease	0.0022	0.0629	0.0629
Onchocerca volvulus	Cathepsin L homolog	0.0022	0.0629	0.0629
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Echinococcus multilocularis	cathepsin l cysteine peptidase	0.0022	0.0629	0.0629
Onchocerca volvulus	Eukaryotic initiation factor 4A homolog	0.0103	1	1
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Echinococcus multilocularis	cathepsin l cysteine peptidase	0.0022	0.0629	0.0629
Schistosoma mansoni	cathepsin F (C01 family)	0.0022	0.0629	0.0629
Echinococcus multilocularis	cysteine protease	0.0022	0.0629	0.0629
Onchocerca volvulus	Cathepsin L homolog	0.0022	0.0629	0.0629
Brugia malayi	Cathepsin L-like precursor	0.0022	0.0629	0.0629
Echinococcus multilocularis	eukaryotic initiation factor 4A	0.0103	1	1
Loa Loa (eye worm)	hypothetical protein	0.0103	1	1
Trypanosoma brucei	Eukaryotic initiation factor 4A-1	0.0103	1	1
Onchocerca volvulus		0.0022	0.0629	0.0629
Schistosoma mansoni	DEAD box ATP-dependent RNA helicase	0.0103	1	1
Echinococcus granulosus	cathepsin l1	0.0022	0.0629	0.0629
Schistosoma mansoni	cathepsin F (C01 family)	0.0022	0.0629	0.0629
Onchocerca volvulus		0.0022	0.0629	0.0629
Plasmodium falciparum	eukaryotic initiation factor 4A	0.0103	1	1
Loa Loa (eye worm)	papain family cysteine protease containing protein	0.0022	0.0629	0.0629
Giardia lamblia	Translation initiation factor eIF-4A, putative	0.0103	1	0.5
Trichomonas vaginalis	DEAD box ATP-dependent RNA helicase, putative	0.0103	1	1
Onchocerca volvulus		0.0022	0.0629	0.0629
Toxoplasma gondii	cathepsin CPL	0.0022	0.0629	0.0629
Echinococcus granulosus	cathepsin l cysteine peptidase	0.0022	0.0629	0.0629
Echinococcus granulosus	eukaryotic initiation factor 4A III	0.0103	1	1
Schistosoma mansoni	DEAD box ATP-dependent RNA helicase	0.0103	1	1
Trypanosoma cruzi	Eukaryotic initiation factor 4A-1	0.0103	1	1
Onchocerca volvulus		0.0022	0.0629	0.0629
Echinococcus granulosus	eukaryotic initiation factor 4A	0.0103	1	1
Plasmodium vivax	RNA helicase-1, putative	0.0103	1	1
Trichomonas vaginalis	DEAD box ATP-dependent RNA helicase, putative	0.0103	1	1

Activities

Activity type	Activity value	Assay description	Source	Reference
IC50 (binding)	= 120 nM	In vitro inhibitory activity against Coagulation factor X was determined	ChEMBL.	15080981
IC50 (binding)	= 120 nM	In vitro inhibitory activity against Coagulation factor X was determined	ChEMBL.	15080981

Phenotypes

Whole-cell/tissue/organism interactions

We have no records of whole-cell/tissue assays done with this compound What does this mean?

Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.

Annotated phenotypes:

We have no manually annotated phenotypes for this drug. What does this mean? / Care to help?

In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.

In any case, if you have information about papers containing relevant validation data for this target, please log in using your TDR Targets username and password and send them to us using the corresponding form in this page (only visible to registered users) or contact us.

External resources for this compound

No external resources registered for this compound

Bibliographic References

1 literature reference was collected for this gene.

If you have references for this compound, please enter them in a user comment (below) or Contact us.

Detailed information for compound 104608