Detailed information for compound 13746
Basic information
Technical information
- TDR Targets ID: 13746
- Name: 6-(4-phenoxyphenyl)-5H-[1,3]dioxolo[4,5-g]qui nolin-8-one
- MW: 357.359 | Formula: C22H15NO4
-
H donors: 1
H acceptors: 2
LogP: 4.84
Rotable bonds: 3
Rule of 5 violations (Lipinski): 1 - SMILES: Oc1cc(nc2c1cc1OCOc1c2)c1ccc(cc1)Oc1ccccc1
- InChi: 1S/C22H15NO4/c24-20-11-18(23-19-12-22-21(10-17(19)20)25-13-26-22)14-6-8-16(9-7-14)27-15-4-2-1-3-5-15/h1-12H,13H2,(H,23,24)
- InChiKey: RLBXEENBVHIEDK-UHFFFAOYSA-N
Network
Hover on a compound node to display the structore
Synonyms
- 6-[4-(phenoxy)phenyl]-5H-[1,3]dioxolo[4,5-g]quinolin-8-one
- NSC649120
- NCI60_017129
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 |
|---|---|---|---|---|
| Toxoplasma gondii | adenosylhomocysteinase, putative | 0.041 | 0.5227 | 0.5 |
| Trypanosoma brucei | S-adenosylhomocysteine hydrolase, putative | 0.041 | 0.5227 | 0.5 |
| Mycobacterium leprae | putative S-adenosyl-L-homocysteine hydrolase SahH | 0.041 | 0.5227 | 0.5 |
| Entamoeba histolytica | adenosylhomocysteinase, putative | 0.041 | 0.5227 | 0.5 |
| Echinococcus granulosus | p2X purinoceptor 4 | 0.0552 | 1 | 1 |
| Mycobacterium tuberculosis | Probable adenosylhomocysteinase SahH (S-adenosyl-L-homocysteine hydrolase) (adohcyase) | 0.041 | 0.5227 | 0.5 |
| Trypanosoma cruzi | S-adenosylhomocysteine hydrolase, putative | 0.041 | 0.5227 | 0.5 |
| Schistosoma mansoni | adenosylhomocysteinase | 0.041 | 0.5227 | 0.5227 |
| Schistosoma mansoni | P2X receptor subunit | 0.0552 | 1 | 1 |
| Plasmodium falciparum | adenosylhomocysteinase | 0.041 | 0.5227 | 0.5 |
| Trypanosoma cruzi | S-adenosylhomocysteine hydrolase, putative | 0.041 | 0.5227 | 0.5 |
| Echinococcus multilocularis | p2X purinoceptor 4 | 0.0552 | 1 | 1 |
| Loa Loa (eye worm) | adenosylhomocysteinase | 0.041 | 0.5227 | 0.5 |
| Echinococcus granulosus | p2X purinoceptor 4 | 0.0552 | 1 | 1 |
| Plasmodium vivax | adenosylhomocysteinase(S-adenosyl-L-homocystein e hydrolase), putative | 0.041 | 0.5227 | 0.5 |
| Schistosoma mansoni | P2X receptor subunit | 0.0552 | 1 | 1 |
| Schistosoma mansoni | P2X receptor subunit | 0.0552 | 1 | 1 |
| Brugia malayi | Adenosylhomocysteinase | 0.041 | 0.5227 | 0.5 |
| Trichomonas vaginalis | adenosylhomocysteinase, putative | 0.041 | 0.5227 | 0.5 |
| Trichomonas vaginalis | adenosylhomocysteinase, putative | 0.041 | 0.5227 | 0.5 |
| Mycobacterium ulcerans | S-adenosyl-L-homocysteine hydrolase | 0.041 | 0.5227 | 0.5 |
| Toxoplasma gondii | S-Adenosyl homocysteine hydrolase | 0.041 | 0.5227 | 0.5 |
| Echinococcus multilocularis | p2X purinoceptor 4 | 0.0552 | 1 | 1 |
| Schistosoma mansoni | P2X receptor subunit | 0.0552 | 1 | 1 |
| Echinococcus multilocularis | p2X purinoceptor 4 | 0.0552 | 1 | 1 |
| Leishmania major | S-adenosylhomocysteine hydrolase | 0.041 | 0.5227 | 0.5 |
Activities
| Activity type | Activity value | Assay description | Source | Reference |
|---|---|---|---|---|
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of NCI-H226, a non small-cell lung cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of DMS114, a non small-cell lung cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of HCT-116, colon cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of KM20L2, colon cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of OVCAR-3, ovarian cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of RXF-393, renal cancer cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of SK-Mel-5, melanoma cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of SF-268, CNS tumor cell line | ChEMBL. | 8164254 |
| GI50 (functional) | > -4 | In vitro inhibition of tumor cell growth of SF-295, CNS tumor cell line | ChEMBL. | 8164254 |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SN12C Renal cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the NCI-H23 Non-Small Cell Lung cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the UO-31 Renal cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the ACHN Renal cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the HL-60(TB) Leukemia cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SF-539 Central Nervous System cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the MALME-3M Melanoma cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| GI50 (functional) | -4 | PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-5 Melanoma cell line. (Class of assay: confirmatory) | ChEMBL. | No reference |
| IC50 (functional) | > 40 uM | Inhibition of tubulin polymerization | ChEMBL. | 8164254 |
| IC50 (functional) | > 40 uM | Inhibition of tubulin polymerization | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of NCI-H226, a non small-cell lung cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of DMS114, a non small-cell lung cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of HCT-116, colon cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of KM20L2, colon cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of OVCAR-3, ovarian cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of RXF-393, renal cancer cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of SK-Mel-5, melanoma cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of SF-268, CNS tumor cell line | ChEMBL. | 8164254 |
| Log GI50 (functional) | > -4 uM | In vitro inhibition of tumor cell growth of SF-295, CNS tumor cell line | ChEMBL. | 8164254 |
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.
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: CHEMBL14544
- PubChem: 373171
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.