Detailed information for compound 1600711

Basic information

Technical information
  • TDR Targets ID: 1600711
  • Name: N-[(4-chlorophenyl)methyl]-2-(3-fluoro-4-meth anesulfonamidophenyl)propanamide
  • MW: 384.853 | Formula: C17H18ClFN2O3S
  • H donors: 2 H acceptors: 3 LogP: 2.9 Rotable bonds: 7
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C(C(c1ccc(c(c1)F)NS(=O)(=O)C)C)NCc1ccc(cc1)Cl
  • InChi: 1S/C17H18ClFN2O3S/c1-11(17(22)20-10-12-3-6-14(18)7-4-12)13-5-8-16(15(19)9-13)21-25(2,23)24/h3-9,11,21H,10H2,1-2H3,(H,20,22)
  • InChiKey: XVKVWVSICFWXTJ-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • N-[(4-chlorophenyl)methyl]-2-(3-fluoro-4-methanesulfonamido-phenyl)propanamide
  • N-(4-chlorobenzyl)-2-(3-fluoro-4-methanesulfonamido-phenyl)propionamide
  • N-[(4-chlorophenyl)methyl]-2-[3-fluoro-4-(methylsulfonylamino)phenyl]propanamide

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Rattus norvegicus Vanilloid receptor 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
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSC 0.1398 0.4953 0.6337
Mycobacterium tuberculosis Probable polyketide synthase Pks5 0.1276 0.4391 0.5799
Mycobacterium ulcerans polyketide synthase MbtD 0.0405 0.0382 0.0454
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsA 0.1317 0.4577 0.6044
Mycobacterium tuberculosis Polyketide synthase Pks2 0.1276 0.4391 0.5799
Mycobacterium tuberculosis Conserved protein 0.0397 0.0345 0.0455
Chlamydia trachomatis 3-oxoacyl-ACP synthase 0.033 0.004 0.5
Mycobacterium tuberculosis Polyketide synthase Pks13 0.1968 0.7572 1
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsD 0.1317 0.4577 0.6044
Brugia malayi Methyltransferase-like protein 4 0.0397 0.0345 0.0306
Mycobacterium tuberculosis Probable polyketide synthase Pks1 0.0946 0.2871 0.3791
Mycobacterium ulcerans thioesterase TesA 0.1097 0.3567 0.4682
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSE 0.0871 0.2525 0.2941
Loa Loa (eye worm) AMP-binding enzyme family protein 0.123 0.4179 0.4782
Leishmania major hypothetical protein, conserved 0.0397 0.0345 1
Mycobacterium tuberculosis Probable polyketide synthase Pks8 0.1077 0.3473 0.4587
Mycobacterium ulcerans polyketide synthase Pks13 0.1968 0.7572 1
Mycobacterium ulcerans multifunctional mycocerosic acid synthase membrane-associated Mas 0.1398 0.4953 0.6522
Onchocerca volvulus 0.2292 0.9062 0.9285
Mycobacterium ulcerans Type I modular polyketide synthase 0.1317 0.4577 0.6023
Wolbachia endosymbiont of Brugia malayi 3-oxoacyl-ACP synthase 0.033 0.004 0.5
Mycobacterium tuberculosis Probable membrane bound polyketide synthase Pks6 0.1968 0.7572 1
Mycobacterium tuberculosis Probable thioesterase TesA 0.1097 0.3567 0.4711
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsC 0.1317 0.4577 0.6044
Plasmodium vivax 3-oxoacyl-[acyl-carrier-protein] synthase i/ii, putative 0.033 0.004 0.5
Mycobacterium tuberculosis Probable polyketide synthase Pks15 0.0532 0.0969 0.128
Toxoplasma gondii beta-ketoacyl synthase, N-terminal domain-containing protein 0.0854 0.2449 0.4903
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsC 0.1398 0.4953 0.6522
Toxoplasma gondii type I fatty acid synthase, putative 0.0937 0.2831 0.5682
Mycobacterium ulcerans fatty acid synthase Fas 0.0414 0.0423 0.0508
Trichomonas vaginalis conserved hypothetical protein 0.0397 0.0345 0.5
Mycobacterium tuberculosis Probable polyketide synthase Pks7 0.1398 0.4953 0.6541
Trypanosoma cruzi beta-ketoacyl synthase family protein, putative 0.033 0.004 0.5
Toxoplasma gondii AMP-binding enzyme domain-containing protein 0.0665 0.1581 0.3136
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsD 0.1317 0.4577 0.6023
Mycobacterium leprae PROBABLE THIOESTERASE TESA 0.1097 0.3567 0.4398
Mycobacterium tuberculosis Probable fatty acid synthase Fas (fatty acid synthetase) 0.0414 0.0423 0.0558
Mycobacterium tuberculosis Polyketide synthetase MbtC (polyketide synthase) 0.0453 0.0602 0.0795
Mycobacterium leprae Polyketide synthase Pks13 0.1968 0.7572 1
Schistosoma mansoni methyltransferase-related 0.0397 0.0345 1
Onchocerca volvulus Fatty acid synthase homolog 0.2373 0.9438 1
Mycobacterium ulcerans thioesterase 0.1097 0.3567 0.4682
Mycobacterium tuberculosis Phenyloxazoline synthase MbtB (phenyloxazoline synthetase) 0.123 0.4179 0.5519
Loa Loa (eye worm) acyl carrier protein 0.0605 0.1305 0.1462
Mycobacterium tuberculosis Hypothetical protein 0.0397 0.0345 0.0455
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSB 0.1059 0.3393 0.4155
Trypanosoma cruzi beta-ketoacyl synthase family protein, putative 0.033 0.004 0.5
Toxoplasma gondii type I fatty acid synthase, putative 0.1398 0.4953 1
Loa Loa (eye worm) fatty acid synthase 0.1299 0.4496 0.5149
Mycobacterium ulcerans polyketide synthase Pks9 0.0871 0.2525 0.3299
Echinococcus multilocularis 3 oxoacyl (acyl carrier protein) synthase 0.033 0.004 0.5
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsB 0.1059 0.3393 0.4452
Mycobacterium leprae Probable multifunctional mycocerosic acid synthase membrane associated enzyme Mas 0.1398 0.4953 0.6337
Loa Loa (eye worm) hypothetical protein 0.0738 0.1914 0.2164
Mycobacterium tuberculosis Polyketide synthase Pks12 0.1398 0.4953 0.6541
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsE 0.0871 0.2525 0.3299
Giardia lamblia Methyltransferase like 2 0.0397 0.0345 0.5
Mycobacterium tuberculosis Probable polyketide synthase Pks9 0.0749 0.1963 0.2593
Mycobacterium ulcerans polyketide synthase 0.1398 0.4953 0.6522
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSA 0.1317 0.4577 0.581
Brugia malayi Beta-ketoacyl synthase, N-terminal domain containing protein 0.1317 0.4577 0.4555
Loa Loa (eye worm) hypothetical protein 0.2212 0.8695 1
Mycobacterium ulcerans Type I modular polyketide synthase 0.1317 0.4577 0.6023
Mycobacterium tuberculosis Probable multifunctional mycocerosic acid synthase membrane-associated Mas 0.1398 0.4953 0.6541
Mycobacterium tuberculosis Polyketide synthetase MbtD (polyketide synthase) 0.0405 0.0382 0.0505
Echinococcus granulosus 3 oxoacyl acyl carrier protein synthase 0.033 0.004 0.5
Plasmodium falciparum 3-oxoacyl-acyl-carrier protein synthase I/II 0.033 0.004 0.5
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsA 0.1059 0.3393 0.4452
Mycobacterium leprae Probable polyketide synthase Pks1 0.1398 0.4953 0.6337
Brugia malayi AMP-binding enzyme family protein 0.123 0.4179 0.4155
Mycobacterium ulcerans polyketide synthase 0.1317 0.4577 0.6023
Trypanosoma brucei beta-ketoacyl-ACP synthase 0.033 0.004 0.5
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSD 0.1317 0.4577 0.581
Brugia malayi AMP-binding enzyme family protein 0.0405 0.0382 0.0343
Mycobacterium ulcerans Type I modular polyketide synthase 0.1317 0.4577 0.6023

Activities

Activity type Activity value Assay description Source Reference
EC50 (functional) Agonist activity at rat TRPV1 expressed in CHO cells by 45Ca2+ uptake assay ChEMBL. 22227463
Ki (functional) = 367 nM Antagonist activity at rat TRPV1 expressed in CHO cells by 45Ca2+ uptake assay ChEMBL. 22227463
Ki (binding) = 1060 nM Displacement of [3H]RTX from rat TRPV1 expressed in CHO cells ChEMBL. 22227463

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.
 
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External resources for this compound

Bibliographic References

No literature references available for this target.

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