Detailed information for compound 277842

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 456.598 | Formula: C25H32N2O4S
  • H donors: 3 H acceptors: 4 LogP: 5.15 Rotable bonds: 12
    Rule of 5 violations (Lipinski): 1
  • SMILES: O=C([C@@H](NC(=O)[C@H](C(C)C)S)Cc1ccc(cc1)c1ccccc1)N[C@H](C(=O)O)C(C)C
  • InChi: 1S/C25H32N2O4S/c1-15(2)21(25(30)31)27-23(28)20(26-24(29)22(32)16(3)4)14-17-10-12-19(13-11-17)18-8-6-5-7-9-18/h5-13,15-16,20-22,32H,14H2,1-4H3,(H,26,29)(H,27,28)(H,30,31)/t20-,21-,22-/m0/s1
  • InChiKey: GZYRWDGMLKVWBN-FKBYEOEOSA-N  

Network

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Synonyms

No synonyms found for this compound

Targets

Known targets for this compound

Species Target name Source Bibliographic reference
Rattus norvegicus Neprilysin Starlite/ChEMBL No references
Homo sapiens angiotensin I converting enzyme 2 Starlite/ChEMBL No references

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Toxoplasma gondii peptidase family M13 protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Schistosoma mansoni family M13 unassigned peptidase (M13 family) Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Brugia malayi Hypothetical zinc metalloproteinase T16A9.4 Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Echinococcus multilocularis endothelin converting enzyme 1 Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Echinococcus granulosus endothelin converting enzyme 1 Get druggable targets OG5_127344 All targets in OG5_127344
Neospora caninum hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Schistosoma japonicum ko:K01415 endothelin-converting enzyme [EC3.4.24.71], putative Get druggable targets OG5_127344 All targets in OG5_127344
Mycobacterium tuberculosis Probable zinc metalloprotease Zmp1 Get druggable targets OG5_127344 All targets in OG5_127344
Mycobacterium leprae probable zinc metalloprotease Get druggable targets OG5_127344 All targets in OG5_127344
Brugia malayi Peptidase family M13 containing protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Mycobacterium ulcerans zinc metalloprotease Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) peptidase family M13 containing protein Get druggable targets OG5_127344 All targets in OG5_127344
Schistosoma japonicum IPR000718,Peptidase M13, neprilysin,domain-containing Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) peptidase family M13 containing protein Get druggable targets OG5_127344 All targets in OG5_127344
Onchocerca volvulus Get druggable targets OG5_127344 All targets in OG5_127344
Loa Loa (eye worm) hypothetical protein Get druggable targets OG5_127344 All targets in OG5_127344

By sequence similarity to non orthologous known druggable targets
Species Potential target Known druggable target Length Alignment span Identity
Onchocerca volvulus Neprilysin   750 aa 682 aa 31.1 %
Onchocerca volvulus Neprilysin   750 aa 713 aa 34.1 %
Schistosoma mansoni family M13 non-peptidase homologue (M13 family) Neprilysin   750 aa 778 aa 20.2 %

Obtained from network model

Ranking Plot


Putative Targets List


Species Potential target Raw Global Species
Echinococcus granulosus endothelin converting enzyme 1 0.0114 0.4078 0.5
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Loa Loa (eye worm) hypothetical protein 0.0114 0.4078 0.2662
Mycobacterium tuberculosis Probable zinc metalloprotease Zmp1 0.0114 0.4078 0.5
Mycobacterium ulcerans zinc metalloprotease 0.0114 0.4078 0.5
Loa Loa (eye worm) angiotensin-converting enzyme family protein 0.0196 1 1
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Toxoplasma gondii peptidase family M13 protein 0.0114 0.4078 0.5
Echinococcus multilocularis endothelin converting enzyme 1 0.0114 0.4078 0.5
Mycobacterium leprae probable zinc metalloprotease 0.0114 0.4078 0.5
Loa Loa (eye worm) hypothetical protein 0.0114 0.4078 0.2662
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Schistosoma mansoni family M13 unassigned peptidase (M13 family) 0.0114 0.4078 1
Loa Loa (eye worm) hypothetical protein 0.0086 0.2073 0.0177
Loa Loa (eye worm) hypothetical protein 0.0114 0.4078 0.2662

Activities

Activity type Activity value Assay description Source Reference
Duration of action (functional) = 70 min Time taken for 50 % or more inhibition of angiotensin-I (AI) induced pressor response in normotensive rats ChEMBL. No reference
IC50 (binding) = 33 nM Inhibition of neutral endopeptidase (NEP) 24.11 ChEMBL. No reference
IC50 (binding) = 33 nM Inhibition of neutral endopeptidase (NEP) 24.11 ChEMBL. No reference
IC50 (binding) = 175 nM Inhibition of angiotensin converting enzyme (ACE) ChEMBL. No reference
IC50 (binding) = 175 nM Inhibition of angiotensin converting enzyme (ACE) ChEMBL. No reference
Inhibition (functional) = 10 mg kg-1 Compound concentration that causes inhibition of angiotensin-I (AI) induced pressor response in normotensive rats after intraarterial injection ChEMBL. No reference

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

No literature references available for this target.

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