Detailed information for compound 1643892

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 402.487 | Formula: C22H27O3PS
  • H donors: 0 H acceptors: 1 LogP: 5.47 Rotable bonds: 8
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCOP(=O)(C(c1sc2c(c1C)cccc2)Cc1cccc(c1)C)OCC
  • InChi: 1S/C22H27O3PS/c1-5-24-26(23,25-6-2)20(15-18-11-9-10-16(3)14-18)22-17(4)19-12-7-8-13-21(19)27-22/h7-14,20H,5-6,15H2,1-4H3
  • InChiKey: IOLMGELFICNBDC-UHFFFAOYSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Canis familiaris Transient receptor potential M8 protein 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
Species Potential target Known druggable target Length Alignment span Identity
Echinococcus multilocularis transient receptor potential cation channel Transient receptor potential M8 protein   1104 aa 1108 aa 25.5 %
Schistosoma mansoni transient receptor potential cation channel subfamily m member Transient receptor potential M8 protein   1104 aa 1075 aa 25.3 %
Echinococcus granulosus transient receptor potential cation channel Transient receptor potential M8 protein   1104 aa 1114 aa 24.9 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Brugia malayi Beta-ketoacyl synthase, N-terminal domain containing protein 0.0053 0.4361 0.4361
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsA 0.0042 0.3131 0.4188
Mycobacterium ulcerans thioesterase 0.0044 0.3311 0.443
Mycobacterium ulcerans fatty acid synthase Fas 0.0017 0.0042 0.0056
Mycobacterium tuberculosis Probable polyketide synthase Pks9 0.003 0.1644 0.2199
Mycobacterium ulcerans polyketide synthase Pks9 0.0035 0.2228 0.2981
Mycobacterium tuberculosis Probable polyketide synthase Pks15 0.0021 0.061 0.0817
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSB 0.0042 0.3131 0.4155
Onchocerca volvulus Fatty acid synthase homolog 0.0095 0.9416 1
Mycobacterium ulcerans Type I modular polyketide synthase 0.0053 0.4361 0.5834
Mycobacterium tuberculosis Probable polyketide synthase Pks7 0.0056 0.4752 0.6357
Mycobacterium tuberculosis Probable polyketide synthase Pks8 0.0043 0.3214 0.4299
Mycobacterium tuberculosis Phenyloxazoline synthase MbtB (phenyloxazoline synthetase) 0.0049 0.3948 0.528
Mycobacterium ulcerans thioesterase TesA 0.0044 0.3311 0.443
Mycobacterium tuberculosis Probable polyketide synthase Pks1 0.0038 0.2588 0.3461
Toxoplasma gondii beta-ketoacyl synthase, N-terminal domain-containing protein 0.0034 0.2149 0.2574
Mycobacterium leprae Polyketide synthase Pks13 0.0079 0.7476 1
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsB 0.0042 0.3131 0.4188
Mycobacterium tuberculosis Polyketide synthase Pks12 0.0056 0.4752 0.6357
Mycobacterium tuberculosis Polyketide synthase Pks13 0.0079 0.7476 1
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsC 0.0056 0.4752 0.6357
Loa Loa (eye worm) AMP-binding enzyme family protein 0.0049 0.3948 0.3889
Mycobacterium tuberculosis Polyketide synthase Pks2 0.0051 0.4168 0.5576
Mycobacterium tuberculosis Probable membrane bound polyketide synthase Pks6 0.0079 0.7476 1
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsE 0.0035 0.2228 0.2981
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSC 0.0056 0.4752 0.6337
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsA 0.0053 0.4361 0.5834
Mycobacterium tuberculosis Probable polyketide synthase Pks5 0.0051 0.4168 0.5576
Mycobacterium ulcerans polyketide synthase 0.0053 0.4361 0.5834
Toxoplasma gondii type I fatty acid synthase, putative 0.0056 0.4752 1
Loa Loa (eye worm) fatty acid synthase 0.0052 0.4277 0.4318
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSD 0.0053 0.4361 0.581
Mycobacterium tuberculosis Probable multifunctional mycocerosic acid synthase membrane-associated Mas 0.0056 0.4752 0.6357
Mycobacterium tuberculosis Probable thioesterase TesA 0.0044 0.3311 0.443
Toxoplasma gondii type I fatty acid synthase, putative 0.0038 0.2547 0.3708
Onchocerca volvulus 0.0092 0.9025 0.9285
Mycobacterium tuberculosis Polyketide synthetase MbtC (polyketide synthase) 0.0018 0.0229 0.0306
Mycobacterium ulcerans polyketide synthase 0.0056 0.4752 0.6357
Mycobacterium ulcerans Type I modular polyketide synthase 0.0053 0.4361 0.5834
Mycobacterium leprae PROBABLE THIOESTERASE TESA 0.0044 0.3311 0.4398
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSA 0.0053 0.4361 0.581
Mycobacterium ulcerans phenolpthiocerol synthesis type-I polyketide synthase PpsD 0.0053 0.4361 0.5834
Mycobacterium leprae PHENOLPTHIOCEROL SYNTHESIS TYPE-I POLYKETIDE SYNTHASE PPSE 0.0035 0.2228 0.2941
Mycobacterium leprae Probable polyketide synthase Pks1 0.0056 0.4752 0.6337
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsD 0.0053 0.4361 0.5834
Loa Loa (eye worm) hypothetical protein 0.003 0.1592 0.0823
Mycobacterium ulcerans multifunctional mycocerosic acid synthase membrane-associated Mas 0.0056 0.4752 0.6357
Loa Loa (eye worm) hypothetical protein 0.0089 0.8643 1
Mycobacterium tuberculosis Phenolpthiocerol synthesis type-I polyketide synthase PpsC 0.0053 0.4361 0.5834
Mycobacterium tuberculosis Probable fatty acid synthase Fas (fatty acid synthetase) 0.0017 0.0042 0.0056
Mycobacterium leprae Probable multifunctional mycocerosic acid synthase membrane associated enzyme Mas 0.0056 0.4752 0.6337
Mycobacterium ulcerans Type I modular polyketide synthase 0.0053 0.4361 0.5834
Brugia malayi AMP-binding enzyme family protein 0.0049 0.3948 0.3948
Mycobacterium ulcerans polyketide synthase Pks13 0.0079 0.7476 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 0.065 uM Antagonist activity at dog TRPM8 expressed in HEK293 cells assessed as inhibition of icilin-induced increase in intracellular Ca2+ level measured every 5 mins by FLIPR assay ChEMBL. 22421018
Inhibition (functional) Antagonist activity at human TRPV1 expressed in HEK293 cells assessed as inhibition of capsaicin-induced increase in intracellular Ca2+ release at 10 uM measured for 5 mins by FLIPR assay ChEMBL. 22421018

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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