Detailed information for compound 1776695

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 600.447 | Formula: C29H27Cl2N3O7
  • H donors: 3 H acceptors: 4 LogP: 4.97 Rotable bonds: 12
    Rule of 5 violations (Lipinski): 2
  • SMILES: COc1cccc(c1C1=NOC(C1)(C)C(=O)N[C@H](C(=O)O)Cc1ccc(cc1)NC(=O)c1c(Cl)cccc1Cl)OC
  • InChi: 1S/C29H27Cl2N3O7/c1-29(15-21(34-41-29)25-22(39-2)8-5-9-23(25)40-3)28(38)33-20(27(36)37)14-16-10-12-17(13-11-16)32-26(35)24-18(30)6-4-7-19(24)31/h4-13,20H,14-15H2,1-3H3,(H,32,35)(H,33,38)(H,36,37)/t20-,29?/m0/s1
  • InChiKey: WCFJGBKSAFVGBA-OORIHMLWSA-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 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12) Starlite/ChEMBL References

Predicted pathogen targets for this compound

By orthology
Species Potential target Known druggable target/s Ortholog Group
Echinococcus multilocularis integrin beta 2 Get druggable targets OG5_127959 All targets in OG5_127959
Schistosoma mansoni integrin beta subunit Get druggable targets OG5_127959 All targets in OG5_127959
Loa Loa (eye worm) integrin beta-2 Get druggable targets OG5_127959 All targets in OG5_127959
Schistosoma japonicum Integrin beta-3 precursor, putative Get druggable targets OG5_127959 All targets in OG5_127959
Schistosoma japonicum Integrin beta-PS precursor, putative Get druggable targets OG5_127959 All targets in OG5_127959
Echinococcus granulosus integrin beta 2 Get druggable targets OG5_127959 All targets in OG5_127959
Schistosoma japonicum ko:K06464 integrin beta 2, putative Get druggable targets OG5_127959 All targets in OG5_127959
Brugia malayi Integrin beta pat-3 precursor Get druggable targets OG5_127959 All targets in OG5_127959
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
Entamoeba histolytica phosphoglycerate mutase family protein, putative 0.0849 0.5151 0.5
Mycobacterium ulcerans hypothetical protein 0.0849 0.5151 0.5
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.1439 1 1
Loa Loa (eye worm) hypothetical protein 0.0825 0.4952 0.4212
Leishmania major 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.1415 0.98 0.9706
Loa Loa (eye worm) hypothetical protein 0.1415 0.98 0.9771
Trypanosoma brucei 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.1439 1 1
Echinococcus multilocularis 6 phosphofructo 2 kinase:fructose 2 0.1439 1 1
Loa Loa (eye worm) hypothetical protein 0.1439 1 1
Trypanosoma cruzi 6-phosphofructo-2-kinase 1 0.1415 0.98 0.9706
Onchocerca volvulus 0.1439 1 0.5
Trypanosoma brucei 6-phosphofructo-2-kinase 2 0.1415 0.98 0.9706
Brugia malayi Integrin beta pat-3 precursor 0.0378 0.1278 0.5
Leishmania major 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.1439 1 1
Mycobacterium ulcerans fructose-2,6-bisphosphatase GpmB 0.0849 0.5151 0.5
Schistosoma mansoni 6-phosphofructokinase 0.1439 1 1
Giardia lamblia Hypothetical protein 0.0849 0.5151 0.5
Giardia lamblia Hypothetical protein 0.0849 0.5151 0.5
Trypanosoma cruzi 6-phosphofructo-2-kinase 1 0.1415 0.98 0.9706
Trypanosoma cruzi 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase, putative 0.1439 1 1

Activities

Activity type Activity value Assay description Source Reference
IC50 (binding) = 3.5 uM Antagonist activity at VLA-4 receptor in human U937 cells assessed as inhibition of VCAM-1 binding by MTT assay ChEMBL. 23312947

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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