Detailed information for compound 596890
Basic information
Technical information
- TDR Targets ID: 596890
- Name: 2-(4-methoxyphenyl)-1-oxidoindol-1-ium-3-one
- MW: 253.253 | Formula: C15H11NO3
-
H donors: 0
H acceptors: 2
LogP: 2.04
Rotable bonds: 2
Rule of 5 violations (Lipinski): 1 - SMILES: COc1ccc(cc1)C1=[N+]([O-])c2c(C1=O)cccc2
- InChi: 1S/C15H11NO3/c1-19-11-8-6-10(7-9-11)14-15(17)12-4-2-3-5-13(12)16(14)18/h2-9H,1H3
- InChiKey: ZPCJCVQIWZJBSH-UHFFFAOYSA-N
Network
Hover on a compound node to display the structore
Synonyms
- 2-(4-methoxyphenyl)-1-oxido-indol-1-ium-3-one
- 2-(4-methoxyphenyl)-1-oxido-3-indol-1-iumone
- 25410-78-0
- NSC626104
- ZINC01569831
- NSC81014
- 3H-Indol-3-one, 2-(4-methoxyphenyl)-, 1-oxide
- AIDS-067252
- AIDS067252
- STOCK1N-47972
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 |
|---|---|---|---|---|
| Trypanosoma brucei | prostaglandin f synthase | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Mycobacterium tuberculosis | Probable oxidoreductase | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Trichomonas vaginalis | aldo/keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo/keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Leishmania major | prostaglandin f2-alpha synthase/D-arabinose dehydrogenase | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase | 0.00179965 | 1 | 1 |
| Leishmania major | aldo-keto reductase-like protein | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Entamoeba histolytica | aldose reductase, putative | 0.00179965 | 1 | 0.5 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.00179965 | 1 | 0.5 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Loa Loa (eye worm) | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.00179965 | 1 | 0.5 |
| Leishmania major | prostaglandin f synthase, putative | 0.00179965 | 1 | 0.5 |
| Loa Loa (eye worm) | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Loa Loa (eye worm) | hypothetical protein | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Mycobacterium leprae | PROBABLE OXIDOREDUCTASE | 0.00179965 | 1 | 1 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Trypanosoma cruzi | aldo/keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase | 0.00179965 | 1 | 1 |
| Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase | 0.00179965 | 1 | 1 |
| Mycobacterium ulcerans | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Schistosoma mansoni | aldo-keto reductase | 0.00179965 | 1 | 0.5 |
| Leishmania major | aldehyde reductase, putative,oxidoreductase, putative | 0.00179965 | 1 | 0.5 |
| Loa Loa (eye worm) | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Schistosoma mansoni | aldo-keto reductase | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase | 0.00179965 | 1 | 1 |
| Giardia lamblia | Aldose reductase | 0.00179965 | 1 | 0.5 |
| Onchocerca volvulus | 0.00179965 | 1 | 0.5 | |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Echinococcus granulosus | hypothetical protein | 0.00179965 | 1 | 1 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Brugia malayi | oxidoreductase, aldo/keto reductase family protein | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Entamoeba histolytica | aldose reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase | 0.00179965 | 1 | 1 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Echinococcus granulosus | aldo keto reductase | 0.00179965 | 1 | 1 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Entamoeba histolytica | aldose reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Loa Loa (eye worm) | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Trypanosoma brucei | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Loa Loa (eye worm) | oxidoreductase | 0.00179965 | 1 | 0.5 |
| Echinococcus granulosus | aldo keto reductase family 1 member B4 | 0.00179965 | 1 | 1 |
| Trichomonas vaginalis | dihydrodiol dehydrogenase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Toxoplasma gondii | aldose reductase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo/keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
| Echinococcus multilocularis | aldo keto reductase | 0.00179965 | 1 | 1 |
| Echinococcus multilocularis | aldo keto reductase family 1, member B4 | 0.00179965 | 1 | 1 |
| Trypanosoma cruzi | aldo-keto reductase | 0.00179965 | 1 | 0.5 |
| Giardia lamblia | Aldose reductase | 0.00179965 | 1 | 0.5 |
| Schistosoma mansoni | pol-related | 0.00179965 | 1 | 0.5 |
| Trichomonas vaginalis | aldo-keto reductase, putative | 0.00179965 | 1 | 0.5 |
Activities
| Activity type | Activity value | Assay description | Source | Reference |
|---|---|---|---|---|
| Activity (functional) | = 32.4 % | Antimalarial activity against Plasmodium berghei ANKA infected Swiss mice (Mus musculus) assessed as reduction in parasitemia at 30 mg/kg, perorally after 3 days measured on day 4 | ChEMBL. | 20014857 |
| Activity (functional) | = 40.5 % | Antimalarial activity against Plasmodium berghei ANKA infected Swiss mice (Mus musculus) assessed as reduction in parasitemia at 30 mg/kg, intraperitoneally after 3 days measured on day 4 | ChEMBL. | 20014857 |
| CC50 (ADMET) | > 39.5 uM | Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay | ChEMBL. | 20014857 |
| CC50 (ADMET) | = 457 uM | Cytotoxicity against human KB cells after 72 hrs by alamar blue assay | ChEMBL. | 20014857 |
| IC50 (functional) | = 101 nM | Antimalarial activity against drug-sensitive Plasmodium falciparum 3D7 assessed as [3H]hypoxanthine incorporation by scintillation counting | ChEMBL. | 20014857 |
| Inhibition (functional) | = -0.74 % | 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) | = 0.24 % | 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) | = 0.97 % | 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) | = 2 % | GSK_TCMDC: Percent inhibition of human HepG2 cell line. Test compounds present at 10uM. | ChEMBL. | 20485427 |
| Inhibition (functional) | = 61 % | 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) | = 93 % | 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) | = 2.16 | Inhibition Frequency Index (IFI) | GSK. | 20485427 |
| Percent growth inhibition (functional) | = -1 % | Percent inhibition of P. falciparum lactate dehydrogenase activity (at 2 uM) | GSK. | 20485427 |
| Percent growth inhibition (functional) | = 2 % | Percent inhibition of HepG2 growth (at 10 uM) | GSK. | 20485427 |
| Percent growth inhibition (functional) | = 61 % | Percent inhibition of P. falciparum Dd2 growth (at 2 uM) | GSK. | 20485427 |
| Percent growth inhibition (functional) | = 93 % | Percent inhibition of P. falciparum 3D7 growth (at 2 uM) | GSK. | 20485427 |
| Ratio IC50 (functional) | = 1.2 | Resistance index, ratio of IC50 for chloroquine-resistant Plasmodium falciparum K1 to IC50 for drug-sensitive Plasmodium falciparum 3D7 | ChEMBL. | 20014857 |
| Ratio IC50 (functional) | = 1.9 | Resistance index, ratio of IC50 for chloroquine-resistant Plasmodium falciparum FcB1 to IC50 for drug-sensitive Plasmodium falciparum 3D7 | ChEMBL. | 20014857 |
| XC50 (functional) | = 6.11 | XC50 determination of P. falciparum 3D7 growth | GSK. | 20485427 |
| XC50 (functional) | = 0.78336 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
| Species name | Source | Reference | Is orphan |
|---|---|---|---|
| Plasmodium falciparum | ChEMBL23 | 20014857 |
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.
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
- ChEMBL: CHEMBL581422
- Search by GSK
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.