Detailed information for compound 303004

Basic information

Technical information
  • TDR Targets ID: 303004
  • Name: 6-methylfuro[2,3-h]chromen-2-one
  • MW: 200.19 | Formula: C12H8O3
  • H donors: 0 H acceptors: 1 LogP: 2.68 Rotable bonds: 0
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=c1ccc2c(o1)c1ccoc1c(c2)C
  • InChi: 1S/C12H8O3/c1-7-6-8-2-3-10(13)15-12(8)9-4-5-14-11(7)9/h2-6H,1H3
  • InChiKey: PFVGXOYZQOJGGR-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

  • 6-methyl-2-furo[2,3-h][1]benzopyranone
  • 6-methylangelicin
  • 6-methyl-2-furo[2,3-h]chromenone
  • 90370-14-2
  • 2H-Furo(2,3-h)-1-benzopyran-2-one, 6-methyl-

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 carboxylesterase LipQ 0.0317 0 0.5
Mycobacterium ulcerans esterase/lipase 0.0317 0 0.5
Mycobacterium tuberculosis Probable lipase LipH 0.0317 0 0.5
Mycobacterium ulcerans lipase LipI 0.0317 0 0.5
Toxoplasma gondii alpha/beta hydrolase fold domain-containing protein 0.0317 0 0.5
Treponema pallidum N-acetylphosphinothricin-tripetide-deacetylase 0.0317 0 0.5
Trichomonas vaginalis Esterase, putative 0.0317 0 0.5
Mycobacterium ulcerans lipase/esterase LipN 0.0317 0 0.5
Mycobacterium ulcerans esterase LipW 0.0317 0 0.5
Mycobacterium tuberculosis Probable lipase/esterase LipN 0.0317 0 0.5
Loa Loa (eye worm) hypothetical protein 1.869 1 1
Leishmania major ecotin, putative 0.0317 0 0.5
Schistosoma mansoni hormone-sensitive lipase (S09 family) 1.869 1 1
Trypanosoma cruzi Isoprenylcysteine alpha-carbonyl methylesterase, putative 0.0317 0 0.5
Trypanosoma brucei Isoprenylcysteine alpha-carbonyl methylesterase, putative 0.0317 0 0.5
Schistosoma mansoni hormone-sensitive lipase (S09 family) 1.869 1 1
Brugia malayi aryl-acylamidase 0.0317 0 0.5
Onchocerca volvulus 0.0317 0 0.5
Mycobacterium tuberculosis Probable esterase LipO 0.0317 0 0.5
Mycobacterium tuberculosis Probable acetyl-hydrolase/esterase LipR 0.0317 0 0.5
Mycobacterium ulcerans lipase LipU 0.0317 0 0.5
Mycobacterium ulcerans esterase LipC 0.0317 0 0.5
Mycobacterium tuberculosis Probable esterase LipM 0.0317 0 0.5
Mycobacterium ulcerans hypothetical protein 0.0317 0 0.5
Trypanosoma cruzi Alpha/beta hydrolase domain-containing protein 0.0317 0 0.5
Mycobacterium ulcerans lipase LipH 0.0317 0 0.5
Trichomonas vaginalis conserved hypothetical protein 0.0317 0 0.5
Mycobacterium ulcerans lipase LipU 0.0317 0 0.5
Mycobacterium ulcerans acetyl hydrolase MbtJ 0.0317 0 0.5
Schistosoma mansoni hormone-sensitive lipase (S09 family) 1.869 1 1
Echinococcus multilocularis hormone sensitive lipase 1.869 1 0.5
Mycobacterium tuberculosis Possible lipase LipU 0.0317 0 0.5
Toxoplasma gondii alpha/beta hydrolase fold domain-containing protein 0.0317 0 0.5
Trypanosoma cruzi Isoprenylcysteine alpha-carbonyl methylesterase, putative 0.0317 0 0.5
Mycobacterium leprae Possible lipase LipU 0.0317 0 0.5
Mycobacterium tuberculosis Probable esterase LipC 0.0317 0 0.5
Trichomonas vaginalis Esterase, putative 0.0317 0 0.5
Trichomonas vaginalis Esterase, putative 0.0317 0 0.5
Leishmania major hypothetical protein, conserved 0.0317 0 0.5
Mycobacterium ulcerans esterase LipO 0.0317 0 0.5
Mycobacterium tuberculosis Possible esterase LipW 0.0317 0 0.5
Mycobacterium ulcerans membrane-bound esterase LipM 0.0317 0 0.5
Mycobacterium tuberculosis Probable esterase/lipase LipF 0.0317 0 0.5
Mycobacterium tuberculosis Putative acetyl hydrolase MbtJ 0.0317 0 0.5
Mycobacterium tuberculosis Probable carboxylesterase LipQ 0.0317 0 0.5
Trypanosoma cruzi serine peptidase, Clan SC, Family S9D 0.0317 0 0.5
Mycobacterium tuberculosis Probable non lipolytic carboxylesterase NlhH 0.0317 0 0.5

Activities

Activity type Activity value Assay description Source Reference
Activity (binding) = 0.048 Compound was evaluated for the frequency of the binding site that is the number of molecules bound to every nucleotide (1/n) ChEMBL. 6540313
Activity (binding) = 20.83 Compound was evaluated for the binding parameter by determining the number of nucleotides occluded by a bound angelicin (n) ChEMBL. 6540313
ID50 (functional) = 2.63e-17 quanta Compound was evaluated for 50% inhibition of DNA synthesis in Ehrlisch ascites tumor cells by irradiation (365 nM) at 1.9 x 10e -5M incubated with [3H]-thymidine at 37 degree C (p 0.05) ChEMBL. 6540313
ID50 (functional) = 2.63e-17 quanta Compound was evaluated for 50% inhibition of DNA synthesis in Ehrlisch ascites tumor cells by irradiation (365 nM) at 1.9 x 10e -5M incubated with [3H]-thymidine at 37 degree C (p 0.05) ChEMBL. 6540313
K (binding) = 925 Compound was evaluated for the association constant to an isolated site of DNA ChEMBL. 6540313
Rate constant (binding) = 0.036 min-1 Compound was evaluated for the binding parameter by determining rate constant ChEMBL. 6540313

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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