Detailed information for compound 1651385

Basic information

Technical information
  • TDR Targets ID: 1651385
  • Name: 4,5-dimethylcyclohex-4-ene-1,1,2,2-tetracarbo nitrile
  • MW: 210.235 | Formula: C12H10N4
  • H donors: 0 H acceptors: 4 LogP: 0.21 Rotable bonds: 0
    Rule of 5 violations (Lipinski): 1
  • SMILES: N#CC1(C#N)CC(=C(CC1(C#N)C#N)C)C
  • InChi: 1S/C12H10N4/c1-9-3-11(5-13,6-14)12(7-15,8-16)4-10(9)2/h3-4H2,1-2H3
  • InChiKey: CKESBCLFVFLERD-UHFFFAOYSA-N  

Network

Hover on a compound node to display the structore

Synonyms

  • 69155-29-9
  • 1,1,2,2-CYCLOHEX-4-ENETETRACARBONITRILE, 4,5-DIMETHYL-
  • 1,2-Dimethyl-4,4,5,5-cyclohex-1-enetetracarbonitrile
  • 4,5-Dimethyl-1,1,2,2-cyclohex-4-enetetracarbonitrile
  • 4-09-00-03795 (Beilstein Handbook Reference)
  • BRN 2618867
  • NCI60_020833
  • 4,5-Dimethyl-4-cyclohexene-1,1,2,2-tetracarbonitrile
  • AIDS-142169
  • AIDS142169
  • NSC659167

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
Plasmodium falciparum chromatin assembly factor 1 protein WD40 domain, putative 0.0025 0 0.5
Onchocerca volvulus 0.0237 0.1801 0.5
Loa Loa (eye worm) WD domain-containing protein 0.0293 0.2273 0.2248
Brugia malayi SET domain containing protein 0.0484 0.3899 1
Plasmodium falciparum chromatin assembly factor 1 subunit, putative 0.0025 0 0.5
Echinococcus granulosus polycomb protein EED 0.0293 0.2273 0.2273
Echinococcus multilocularis histone lysine N methyltransferase E(z) 0.0484 0.3899 0.3899
Echinococcus granulosus histone lysine N methyltransferase Ez 0.0484 0.3899 0.3899
Echinococcus multilocularis polycomb protein suz12 A 0.1003 0.8299 0.8299
Toxoplasma gondii RbAp48 0.0025 0 0.5
Schistosoma mansoni ae-1 binding protein aebp2 0.1204 1 1
Schistosoma mansoni enhancer of zeste ezh 0.0484 0.3899 0.3899
Plasmodium vivax chromatin assembly factor 1 P55 subunit, putative 0.0025 0 0.5
Toxoplasma gondii WD domain, G-beta repeat-containing protein 0.0025 0 0.5
Toxoplasma gondii RbAp46 0.0025 0 0.5
Entamoeba histolytica WD domain containing protein 0.0025 0 0.5
Schistosoma mansoni hypothetical protein 0.1003 0.8299 0.8299
Brugia malayi WD domain containing protein 0.0293 0.2273 0.2248
Echinococcus multilocularis Zinc finger protein jing protein 0.1204 1 1
Leishmania major hypothetical protein, conserved 0.0025 0 0.5
Plasmodium vivax chromatin assembly factor 1 protein WD40 domain, putative 0.0025 0 0.5
Giardia lamblia Histone acetyltransferase type B subunit 2 0.0025 0 0.5
Echinococcus multilocularis polycomb protein EED 0.0293 0.2273 0.2273
Schistosoma mansoni embryonic ectoderm development protein 0.0293 0.2273 0.2273
Loa Loa (eye worm) SET domain-containing protein 0.0484 0.3899 1
Plasmodium vivax chromatin assembly factor 1 P55 subunit, putative 0.0025 0 0.5
Echinococcus granulosus polycomb protein suz12 A 0.1003 0.8299 0.8299
Plasmodium falciparum chromatin assembly factor 1 P55 subunit, putative 0.0025 0 0.5

Activities

Activity type Activity value Assay description Source Reference
GI50 (functional) -5.834 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the HL-60(TB) Leukemia cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.484 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the HOP-92 Non-Small Cell Lung cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.36 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the NCI-H23 Non-Small Cell Lung cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.321 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the MDA-N Breast cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.208 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SK-MEL-5 Melanoma cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.056 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the ACHN Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5.04 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SN12C Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the UO-31 Renal cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the DU-145 Prostate cell line. (Class of assay: confirmatory) ChEMBL. No reference
GI50 (functional) -5 PUBCHEM_BIOASSAY: NCI human tumor cell line growth inhibition assay. Data for the SF-539 Central Nervous System cell line. (Class of assay: confirmatory) 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.

If you have references for this compound, please enter them in a user comment (below) or Contact us.