Detailed information for compound 603491

Basic information

Technical information
  • TDR Targets ID: 603491
  • Name: di(phenyl)phosphoryl-(4-nitrophenyl)methanol
  • MW: 353.308 | Formula: C19H16NO4P
  • H donors: 1 H acceptors: 4 LogP: 3.27 Rotable bonds: 5
    Rule of 5 violations (Lipinski): 1
  • SMILES: OC(P(=O)(c1ccccc1)c1ccccc1)c1ccc(cc1)[N+](=O)[O-]
  • InChi: 1S/C19H16NO4P/c21-19(15-11-13-16(14-12-15)20(22)23)25(24,17-7-3-1-4-8-17)18-9-5-2-6-10-18/h1-14,19,21H
  • InChiKey: UELQCFGDYHELTK-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

No curated genes were found associated with this compound

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 ulcerans fatty-acid-CoA ligase 0.0023 0.0329 1
Onchocerca volvulus 0.0049 0.1122 1
Mycobacterium ulcerans hypothetical protein 0.0023 0.0329 1
Plasmodium falciparum ataxin-2 like protein, putative 0.0025 0.0367 1
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3638 1
Mycobacterium tuberculosis Probable fatty-acid-CoA ligase FadD2 (fatty-acid-CoA synthetase) (fatty-acid-CoA synthase) 0.0023 0.0329 1
Loa Loa (eye worm) hypothetical protein 0.0017 0.0145 0.0398
Entamoeba histolytica acyl-coA synthetase, putative 0.0023 0.0329 0.5
Onchocerca volvulus 0.0027 0.0429 0.1266
Brugia malayi RNA recognition motif domain containing protein 0.0129 0.3638 1
Loa Loa (eye worm) intermediate filament tail domain-containing protein 0.0027 0.0429 0.1181
Echinococcus multilocularis tar DNA binding protein 0.0129 0.3638 0.3638
Echinococcus granulosus lamin dm0 0.0027 0.0429 0.0429
Mycobacterium leprae PROBABLE FATTY-ACID-CoA LIGASE FADD2 (FATTY-ACID-CoA SYNTHETASE) (FATTY-ACID-CoA SYNTHASE) 0.0023 0.0329 0.5
Loa Loa (eye worm) hypothetical protein 0.0049 0.1122 0.3084
Trypanosoma brucei PAB1-binding protein , putative 0.0025 0.0367 0.5
Loa Loa (eye worm) RNA binding protein 0.0129 0.3638 1
Loa Loa (eye worm) hypothetical protein 0.0017 0.0145 0.0398
Onchocerca volvulus 0.0027 0.0429 0.1266
Loa Loa (eye worm) hypothetical protein 0.0025 0.0367 0.101
Brugia malayi AMP-binding enzyme family protein 0.0023 0.0329 0.0793
Brugia malayi Intermediate filament tail domain containing protein 0.0027 0.0429 0.1072
Echinococcus granulosus intermediate filament protein 0.0027 0.0429 0.0429
Mycobacterium tuberculosis Fatty-acid-AMP ligase FadD30 (fatty-acid-AMP synthetase) (fatty-acid-AMP synthase) 0.0017 0.0145 0.139
Mycobacterium leprae PROBABLE FATTY-ACID-CoA LIGASE FADD7 (FATTY-ACID-CoA SYNTHETASE) (FATTY-ACID-CoA SYNTHASE) 0.0023 0.0329 0.5
Mycobacterium tuberculosis Probable chain -fatty-acid-CoA ligase FadD13 (fatty-acyl-CoA synthetase) 0.0023 0.0329 1
Echinococcus granulosus tar DNA binding protein 0.0129 0.3638 0.3638
Brugia malayi hypothetical protein 0.0016 0.0095 0.0142
Trypanosoma cruzi PAB1-binding protein , putative 0.0025 0.0367 0.5
Entamoeba histolytica acyl-CoA synthetase, putative 0.0023 0.0329 0.5
Loa Loa (eye worm) hypothetical protein 0.0027 0.0429 0.1181
Echinococcus multilocularis tumor protein p63 0.0332 1 1
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3638 1
Entamoeba histolytica acyl-CoA synthetase, putative 0.0023 0.0329 0.5
Brugia malayi AMP-binding enzyme family protein 0.0023 0.0329 0.0793
Plasmodium falciparum ataxin-2 like protein, putative 0.0025 0.0367 1
Toxoplasma gondii LsmAD domain-containing protein 0.0025 0.0367 0.5
Loa Loa (eye worm) hypothetical protein 0.0017 0.0145 0.0398
Brugia malayi AMP-binding enzyme family protein 0.0023 0.0329 0.0793
Loa Loa (eye worm) cytoplasmic intermediate filament protein 0.0014 0.0044 0.0121
Mycobacterium ulcerans long-chain fatty-acid CoA ligase 0.0023 0.0329 1
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3638 1
Echinococcus multilocularis lamin 0.0027 0.0429 0.0429
Trypanosoma cruzi PAB1-binding protein , putative 0.0025 0.0367 0.5
Mycobacterium ulcerans acyl-CoA synthetase 0.0023 0.0329 1
Leishmania major hypothetical protein, conserved 0.0025 0.0367 1
Mycobacterium ulcerans long-chain-fatty-acid-CoA ligase 0.0023 0.0329 1
Brugia malayi TAR-binding protein 0.0129 0.3638 1
Brugia malayi hypothetical protein 0.0025 0.0367 0.0899
Echinococcus multilocularis musashi 0.0027 0.0429 0.0429
Loa Loa (eye worm) TAR-binding protein 0.0129 0.3638 1
Loa Loa (eye worm) RNA recognition domain-containing protein domain-containing protein 0.0129 0.3638 1
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3638 1
Plasmodium vivax ataxin-2 like protein, putative 0.0025 0.0367 1
Brugia malayi intermediate filament protein 0.0027 0.0429 0.1072
Loa Loa (eye worm) hypothetical protein 0.0017 0.0145 0.0398
Mycobacterium ulcerans acyl-CoA synthetase 0.0023 0.0329 1
Loa Loa (eye worm) hypothetical protein 0.0023 0.0329 0.0905
Mycobacterium ulcerans acyl-CoA synthetase 0.0023 0.0329 1
Schistosoma mansoni cellular tumor antigen P53 0.0049 0.1122 0.2158
Loa Loa (eye worm) hypothetical protein 0.0026 0.0414 0.1139
Loa Loa (eye worm) hypothetical protein 0.0023 0.0329 0.0905
Brugia malayi RNA binding protein 0.0129 0.3638 1
Echinococcus granulosus lamin 0.0027 0.0429 0.0429
Echinococcus multilocularis lamin dm0 0.0027 0.0429 0.0429
Loa Loa (eye worm) hypothetical protein 0.0017 0.0145 0.0398
Chlamydia trachomatis acylglycerophosphoethanolamine acyltransferase 0.0017 0.0145 0.5
Schistosoma mansoni tar DNA-binding protein 0.0129 0.3638 1
Loa Loa (eye worm) intermediate filament protein 0.0027 0.0429 0.1181
Loa Loa (eye worm) hypothetical protein 0.0023 0.0329 0.0905
Mycobacterium ulcerans long-chain-fatty-acid--CoA ligase 0.0023 0.0329 1

Activities

Activity type Activity value Assay description Source Reference
Inhibition (functional) = -0.85 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmPfHT that are glucose transport deficient and complemented with the Plasmodium falciparum hexose transporter. Activity is measured by by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = -0.33 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGLUT1 that are glucose transport deficient and complemented with the human glucose transporter GLUT1. Activity is measured by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = -0.11 % ST_JUDE_LEISH: Cytotoxicity at 2uM final concentration against transgenic Leishmania Mexicana promastigotes LmGT2 that are glucose transport deficient and complemented with the L. Mexicana glucose transporter 2. Activity is measured by by DNA content using SYBR green in vitro ChEMBL. No reference
Inhibition (functional) = 0 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 LDH activity, using an LDH reporter assay. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 1 % GSK_TCMDC: Inhibition of Plasmodium falciparum Dd2 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM ChEMBL. 20485427
Inhibition (functional) = 1 % GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. ChEMBL. 20485427
Inhibition (functional) = 98 % GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole red blood cells, using parasite LDH activity as an index of growth. Test compounds present at 2uM ChEMBL. 20485427
Inhibition frequency index (IFI) (functional) = 0.76 Inhibition Frequency Index (IFI) GSK. 20485427
Percent growth inhibition (functional) = 0 % Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 1 % Percent inhibition of P. falciparum Dd2 growth (at 2 uM) GSK. 20485427
Percent growth inhibition (functional) = 1 % Percent inhibition of HepG2 growth (at 10 uM) GSK. 20485427
Percent growth inhibition (functional) = 98 % Percent inhibition of P. falciparum 3D7 growth (at 2 uM) GSK. 20485427
XC50 (functional) = 6.47 XC50 determination of P. falciparum 3D7 growth GSK. 20485427
XC50 (functional) = 0.34145 uM GSK_TCMDC: Inhibition of Plasmodium falciparum 3D7 in whole erythrocytes, using parasite LDH activity as an index of growth. ChEMBL. 20485427

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

Bibliographic References

1 literature reference was collected for this gene.

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