Detailed information for compound 73638

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 473.567 | Formula: C27H31N5O3
  • H donors: 1 H acceptors: 5 LogP: 4.67 Rotable bonds: 9
    Rule of 5 violations (Lipinski): 1
  • SMILES: CCOC(=O)/C=C/1\CC(C)(CCC)CC(=O)N1Cc1ccc(cc1)c1ccccc1c1nn[nH]n1
  • InChi: 1S/C27H31N5O3/c1-4-14-27(3)16-21(15-25(34)35-5-2)32(24(33)17-27)18-19-10-12-20(13-11-19)22-8-6-7-9-23(22)26-28-30-31-29-26/h6-13,15H,4-5,14,16-18H2,1-3H3,(H,28,29,30,31)/b21-15+
  • InChiKey: VDMSVIJAKNJILQ-RCCKNPSSSA-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
Homo sapiens angiotensin II receptor, type 2 Starlite/ChEMBL No references
Bos taurus Angiotensin II type 1a (AT-1a) receptor Starlite/ChEMBL No references
Homo sapiens angiotensin II receptor, type 1 No 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 granulosus neuropeptide receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 319 aa 24.1 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 350 aa 23.1 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 399 aa 25.1 %
Echinococcus multilocularis G-protein coupled receptor, putative Angiotensin II type 1a (AT-1a) receptor   359 aa 308 aa 22.7 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 313 aa 24.6 %
Brugia malayi ORL1-like opioid receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 314 aa 20.4 %
Brugia malayi GnHR receptor homolog Angiotensin II type 1a (AT-1a) receptor   359 aa 366 aa 20.8 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 317 aa 20.5 %
Echinococcus multilocularis tm gpcr rhodopsin gpcr rhodopsin superfamily Angiotensin II type 1a (AT-1a) receptor   359 aa 315 aa 21.0 %
Schistosoma mansoni peptide (allatostatin)-like receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 314 aa 26.4 %
Schistosoma mansoni opsin-like receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 299 aa 25.8 %
Echinococcus granulosus tm gpcr rhodopsin Angiotensin II type 1a (AT-1a) receptor   359 aa 315 aa 21.0 %
Schistosoma japonicum ko:K04134 cholinergic receptor, invertebrate, putative Angiotensin II type 1a (AT-1a) receptor   359 aa 325 aa 21.8 %
Echinococcus granulosus thyrotropin releasing hormone receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 329 aa 23.1 %
Loa Loa (eye worm) hypothetical protein Angiotensin II type 1a (AT-1a) receptor   359 aa 329 aa 22.2 %
Schistosoma japonicum ko:K04209 neuropeptide Y receptor, invertebrate, putative Angiotensin II type 1a (AT-1a) receptor   359 aa 324 aa 24.1 %
Echinococcus granulosus pyroglutamylated rfamide peptide receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 403 aa 18.9 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 292 aa 25.7 %
Schistosoma mansoni adenoreceptor Angiotensin II type 1a (AT-1a) receptor   359 aa 338 aa 23.4 %
Loa Loa (eye worm) hypothetical protein Angiotensin II type 1a (AT-1a) receptor   359 aa 300 aa 28.0 %
Echinococcus multilocularis pyroglutamylated rfamide peptide receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 381 aa 19.7 %
Echinococcus granulosus allatostatin A receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 350 aa 26.6 %
Loa Loa (eye worm) neuropeptide F receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 360 aa 22.2 %
Echinococcus multilocularis neuropeptide receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 319 aa 24.5 %
Schistosoma japonicum Rhodopsin, putative Angiotensin II type 1a (AT-1a) receptor   359 aa 355 aa 23.9 %
Schistosoma mansoni biogenic amine (octopamine/dopamine) receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 362 aa 24.3 %
Echinococcus granulosus pyroglutamylated rfamide peptide receptor angiotensin II receptor, type 2 363 aa 398 aa 18.3 %
Echinococcus multilocularis allatostatin A receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 350 aa 26.6 %
Schistosoma japonicum ko:K04135 adrenergic receptor, alpha 1a, putative Angiotensin II type 1a (AT-1a) receptor   359 aa 346 aa 24.9 %
Echinococcus multilocularis thyrotropin releasing hormone receptor Angiotensin II type 1a (AT-1a) receptor   359 aa 329 aa 22.8 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 349 aa 25.5 %
Echinococcus granulosus pyroglutamylated rfamide peptide receptor angiotensin II receptor, type 1 359 aa 403 aa 19.1 %
Onchocerca volvulus E3 ubiquitin-protein ligase rpm-1 homolog Angiotensin II type 1a (AT-1a) receptor   359 aa 339 aa 21.2 %
Onchocerca volvulus Angiotensin II type 1a (AT-1a) receptor   359 aa 303 aa 25.4 %
Obtained from network model

Ranking Plot

Putative Targets List

Species Potential target Raw Global Species
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Loa Loa (eye worm) hypothetical protein 0.0186 0.2561 0.2555
Echinococcus multilocularis fucosidase, alpha L 1, tissue 0.0463 0.8046 1
Mycobacterium ulcerans alpha-L-fucosidase 0.0463 0.8046 0.5
Onchocerca volvulus Glucosylceramidase homolog 0.0166 0.2154 0.5
Trichomonas vaginalis alpha-L-fucosidase, putative 0.0123 0.1306 0.2362
Loa Loa (eye worm) hypothetical protein 0.008 0.0465 0.0458
Loa Loa (eye worm) alpha-L-fucosidase 0.028 0.4419 0.4415
Toxoplasma gondii melibiase subfamily protein 0.008 0.0465 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Schistosoma mansoni alpha-l-fucosidase 0.028 0.4419 1
Echinococcus granulosus fucosidase alpha L 1 tissue 0.0463 0.8046 1
Echinococcus granulosus beta galactosidase 0.0186 0.2561 0.2765
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Trichomonas vaginalis alpha-L-fucosidase, putative 0.0123 0.1306 0.2362
Trichomonas vaginalis glucosylceramidase, putative 0.0174 0.2331 0.5237
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Brugia malayi O-Glycosyl hydrolase family 30 protein 0.0252 0.3873 0.8763
Entamoeba histolytica beta-galactosidase, putative 0.011 0.1054 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Trichomonas vaginalis conserved hypothetical protein 0.0163 0.21 0.4591
Trichomonas vaginalis beta-galactosidase, putative 0.0163 0.21 0.4591
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Brugia malayi Alpha-L-fucosidase family protein 0.028 0.4419 1
Echinococcus multilocularis beta galactosidase 0.0186 0.2561 0.2765
Trichomonas vaginalis glycoside hydrolases, putative 0.0142 0.1687 0.343
Brugia malayi Melibiase family protein 0.008 0.0465 0.1037
Trichomonas vaginalis beta-glucosidase, putative 0.0142 0.1687 0.343
Trichomonas vaginalis glucosylceramidase, putative 0.0174 0.2331 0.5237
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Trichomonas vaginalis glucosylceramidase, putative 0.0252 0.3873 0.9567
Loa Loa (eye worm) O-glycosyl hydrolase family 30 protein 0.0252 0.3873 0.3869
Trichomonas vaginalis glycoside hydrolase, putative 0.026 0.4028 1
Schistosoma mansoni beta-galactosidase 0.0186 0.2561 0.53
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Plasmodium vivax hypothetical protein, conserved 0.0057 0 0.5
Trichomonas vaginalis glucosylceramidase, putative 0.0166 0.2154 0.4741
Plasmodium falciparum conserved Plasmodium protein, unknown function 0.0057 0 0.5
Schistosoma mansoni hypothetical protein 0.0154 0.1935 0.3717

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 120 nM Ability of the compound to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes ChEMBL. No reference
IC50 (binding) = 120 nM Ability of the compound to displace [125I]- labelled [Sar1,Ileu8] from angiotensin II receptor of bovine adrenal cortex membranes ChEMBL. No reference
Kd (functional) = 7.5 Inhibition of angiotensin II induced contraction in thoracic aortic rings from New Zealand rabbits ChEMBL. No reference
pA2 (functional) = 7.5 Inhibition of angiotensin II induced contraction in thoracic aortic rings from New Zealand rabbits 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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