Detailed information for compound 141356

Basic information

Technical information
  • Name: Unnamed compound
  • MW: 163.605 | Formula: C5H10ClN3O
  • H donors: 0 H acceptors: 1 LogP: 0.7 Rotable bonds: 4
    Rule of 5 violations (Lipinski): 1
  • SMILES: ClCC/N=N\N(C(=O)C)C
  • InChi: 1S/C5H10ClN3O/c1-5(10)9(2)8-7-4-3-6/h3-4H2,1-2H3/b8-7-
  • InChiKey: QEIMBUYAZCMEGX-FPLPWBNLSA-N  


Substructure search Similarity search

Network

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Synonyms

No synonyms found for this compound

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
Echinococcus granulosus serotonin transporter 0.1992 1 1
Loa Loa (eye worm) animal heme peroxidase 0.0698 0.3022 0.3022
Schistosoma mansoni sodium/chloride dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) blistered cuticle protein 3 0.0698 0.3022 0.3022
Onchocerca volvulus 0.0698 0.3022 0.3022
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Loa Loa (eye worm) norepinephrine transporter 0.1992 1 1
Schistosoma mansoni norepinephrine/norepinephrine transporter 0.1992 1 1
Brugia malayi Animal haem peroxidase family protein 0.0698 0.3022 0.3022
Plasmodium falciparum transporter, putative 0.0338 0.1079 0.5
Chlamydia trachomatis Ssodium-dependent amino acid transporter 0.0338 0.1079 0.5
Brugia malayi hypothetical protein 0.0698 0.3022 0.3022
Toxoplasma gondii Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.5
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Loa Loa (eye worm) solute carrier family 6 member 4 0.1992 1 1
Echinococcus multilocularis tm gpcr rhodopsin gpcr rhodopsin superfamily 0.1251 0.6003 0.6003
Schistosoma mansoni sodium-dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Toxoplasma gondii Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.5
Schistosoma mansoni norepinephrine/norepinephrine transporter 0.0338 0.1079 0.1079
Echinococcus multilocularis peroxidasin 0.0698 0.3022 0.3022
Plasmodium falciparum amino acid transporter, putative 0.0338 0.1079 0.5
Loa Loa (eye worm) hypothetical protein 0.0884 0.4025 0.4025
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Onchocerca volvulus 0.0698 0.3022 0.3022
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Plasmodium vivax amine transporter, putative 0.0338 0.1079 0.5
Brugia malayi Sodium:neurotransmitter symporter family protein 1, putative 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Schistosoma mansoni biogenic amine (octopamine/dopamine) receptor 0.0438 0.1617 0.1617
Brugia malayi Animal haem peroxidase family protein 0.0698 0.3022 0.3022
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Brugia malayi hypothetical protein 0.0338 0.1079 0.1079
Echinococcus multilocularis uncharacterized sodium dependent transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.1992 1 1
Loa Loa (eye worm) hypothetical protein 0.0438 0.1617 0.1617
Brugia malayi Animal haem peroxidase family protein 0.0698 0.3022 0.3022
Brugia malayi Serotonin receptor 0.1974 0.9904 0.9904
Toxoplasma gondii hypothetical protein 0.0338 0.1079 0.5
Onchocerca volvulus Chorion peroxidase homolog 0.0698 0.3022 0.3022
Toxoplasma gondii Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.5
Brugia malayi Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.1079
Brugia malayi Blistered cuticle protein 3 0.0698 0.3022 0.3022
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0438 0.1617 0.1617
Loa Loa (eye worm) Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.1079
Schistosoma mansoni sodium/chloride dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Echinococcus granulosus sodium and chloride dependent glycine 0.0338 0.1079 0.1079
Schistosoma mansoni sodium-dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Onchocerca volvulus Dual oxidase homolog 0.0698 0.3022 0.3022
Onchocerca volvulus Peroxidasin homolog 0.0698 0.3022 0.3022
Schistosoma mansoni sodium-dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Mycobacterium tuberculosis Probable flavin-containing monoamine oxidase AofH (amine oxidase) (MAO) 0.0859 0.3888 0.5
Loa Loa (eye worm) animal heme peroxidase 0.0698 0.3022 0.3022
Echinococcus granulosus peroxidasin 0.0698 0.3022 0.3022
Echinococcus granulosus biogenic amine 5HT receptor 0.0884 0.4025 0.4025
Echinococcus granulosus tm gpcr rhodopsin 0.1251 0.6003 0.6003
Echinococcus multilocularis serotonin transporter 0.1992 1 1
Loa Loa (eye worm) hypothetical protein 0.1992 1 1
Loa Loa (eye worm) hypothetical protein 0.0383 0.1322 0.1322
Schistosoma mansoni sodium/chloride dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Trypanosoma brucei C-8 sterol isomerase, putative 0.075 0.3299 0.5
Echinococcus granulosus sodium:chloride dependent neurotransmitter 0.0338 0.1079 0.1079
Onchocerca volvulus 0.0338 0.1079 0.1079
Onchocerca volvulus Peroxidase homolog 0.0698 0.3022 0.3022
Loa Loa (eye worm) animal heme peroxidase 0.0698 0.3022 0.3022
Toxoplasma gondii hypothetical protein 0.0338 0.1079 0.5
Schistosoma mansoni peroxidasin 0.0698 0.3022 0.3022
Echinococcus multilocularis sodium:chloride dependent neurotransmitter 0.0338 0.1079 0.1079
Brugia malayi Peroxidasin 0.0698 0.3022 0.3022
Schistosoma mansoni sodium/chloride dependent transporter 0.1992 1 1
Loa Loa (eye worm) hypothetical protein 0.075 0.3299 0.3299
Loa Loa (eye worm) hypothetical protein 0.0884 0.4025 0.4025
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Echinococcus multilocularis serotonin receptor 0.0884 0.4025 0.4025
Echinococcus granulosus uncharacterized sodium dependent transporter 0.0338 0.1079 0.1079
Echinococcus multilocularis sodium and chloride dependent glycine 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Brugia malayi ERG2 and Sigma1 receptor like protein 0.075 0.3299 0.3299
Brugia malayi Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.1079
Echinococcus granulosus uncharacterized sodium dependent transporter 0.0338 0.1079 0.1079
Trypanosoma cruzi C-8 sterol isomerase, putative 0.075 0.3299 0.5
Onchocerca volvulus Peroxidasin homolog 0.0698 0.3022 0.3022
Schistosoma mansoni sodium-dependent amino acid transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Onchocerca volvulus 0.0338 0.1079 0.1079
Onchocerca volvulus 0.1992 1 1
Brugia malayi Animal haem peroxidase family protein 0.0698 0.3022 0.3022
Mycobacterium ulcerans flavin-containing monoamine oxidase AofH 0.0924 0.4239 0.5
Echinococcus granulosus sodium and chloride dependent glycine 0.0338 0.1079 0.1079
Onchocerca volvulus 0.0698 0.3022 0.3022
Plasmodium vivax hypothetical protein, conserved 0.0338 0.1079 0.5
Onchocerca volvulus Peroxidase homolog 0.0698 0.3022 0.3022
Loa Loa (eye worm) serotonin transporter b 0.1992 1 1
Echinococcus multilocularis serotonin receptor 0.0884 0.4025 0.4025
Loa Loa (eye worm) hypothetical protein 0.1992 1 1
Echinococcus granulosus hypothetical protein 0.155 0.7618 0.7618
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Loa Loa (eye worm) animal heme peroxidase 0.0698 0.3022 0.3022
Treponema pallidum sodium- and chloride- dependent transporter 0.1992 1 0.5
Brugia malayi Serotonin/octopamine receptor family protein 7 0.0438 0.1617 0.1617
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Echinococcus multilocularis conserved hypothetical protein 0.1412 0.6873 0.6873
Brugia malayi Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Schistosoma mansoni amine GPCR 0.1299 0.6261 0.6261
Echinococcus granulosus sodium dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Schistosoma mansoni sodium/chloride dependent transporter 0.0338 0.1079 0.1079
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079
Loa Loa (eye worm) Sodium:neurotransmitter symporter family protein 0.0338 0.1079 0.1079
Mycobacterium ulcerans flavin-containing monoamine oxidase AofH 0.0924 0.4239 0.5
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Onchocerca volvulus 0.0338 0.1079 0.1079
Echinococcus multilocularis sodium and chloride dependent glycine 0.0338 0.1079 0.1079
Schistosoma mansoni peroxidasin 0.0698 0.3022 0.3022
Loa Loa (eye worm) hypothetical protein 0.0698 0.3022 0.3022
Leishmania major C-8 sterol isomerase-like protein 0.075 0.3299 0.5
Brugia malayi Animal haem peroxidase family protein 0.0698 0.3022 0.3022
Echinococcus multilocularis sodium dependent neurotransmitter transporter 0.0338 0.1079 0.1079
Schistosoma mansoni sodium/chloride dependent transporter 0.0338 0.1079 0.1079
Schistosoma mansoni norepinephrine/norepinephrine transporter 0.0338 0.1079 0.1079
Schistosoma mansoni biogenic amine (5HT) receptor 0.0884 0.4025 0.4025
Loa Loa (eye worm) hypothetical protein 0.0338 0.1079 0.1079

Activities

Activity type Activity value Assay description Source Reference
IC50 (functional) = 8 uM Evaluated for the inhibitory concentration required to cause growth inhibition of LOX melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 8 uM Evaluated for the inhibitory concentration required to cause growth inhibition of LOX melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 12 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A427Mer- cell line of lung using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 12 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A427Mer- cell line of lung using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MCF-7 breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of WiDR breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of SK-MEL-5 melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MCF-7 breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of WiDR breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 15 uM Evaluated for the inhibitory concentration required to cause growth inhibition of SK-MEL-5 melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 17 uM Evaluated for the inhibitory concentration required to cause growth inhibition of RPMI7951 melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 17 uM Evaluated for the inhibitory concentration required to cause growth inhibition of RPMI7951 melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H522 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of U251 cell line of central nervous system (CNS) using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A498Rem- renal cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of OVCAR-4 ovarian cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of TE85Mer+ sarcoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of U251 cell line of central nervous system (CNS) using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A498Rem- renal cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of OVCAR-4 ovarian cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 18 uM Evaluated for the inhibitory concentration required to cause growth inhibition of TE85Mer+ sarcoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 20 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H23 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 20 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A172Mer- cell line of central nervous system (CNS) using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 20 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H23 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 20 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A172Mer- cell line of central nervous system (CNS) using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 24 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MCF-7ADR breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 24 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MCF-7ADR breast cell line using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 25 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MALME-3M melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 25 uM Evaluated for the inhibitory concentration required to cause growth inhibition of OVCAR-3 ovarian cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 25 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MALME-3M melanoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 25 uM Evaluated for the inhibitory concentration required to cause growth inhibition of OVCAR-3 ovarian cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 26 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A549Rem- cell line of lung using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 26 uM Evaluated for the inhibitory concentration required to cause growth inhibition of DOD-1 breast cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 26 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A704Rem- renal cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 26 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A549Rem- cell line of lung using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 26 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A704Rem- renal cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 32 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H322M cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 32 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H322M cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 35 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A673Mer+ sarcoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 35 uM Evaluated for the inhibitory concentration required to cause growth inhibition of A673Mer+ sarcoma cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 42 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H125 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 44 uM Evaluated for the inhibitory concentration required to cause growth inhibition of MAR BEL fibroblasts cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 50 uM Evaluated for the inhibitory concentration required to cause growth inhibition of TE-671 cell line of central nervous system (CNS)using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 50 uM Evaluated for the inhibitory concentration required to cause growth inhibition of TE-671 cell line of central nervous system (CNS)using the MTT Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H358M cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H460 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of CCD-19Lu fibroblasts cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H358M cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of H460 cell line of lung using the Microculture Tetrazolium (MTT) Cytotoxicity Assay ChEMBL. 2391696
IC50 (functional) = 60 uM Evaluated for the inhibitory concentration required to cause growth inhibition of CCD-19Lu fibroblasts cell line using the MTT Cytototoxicity Assay ChEMBL. 2391696
T/C (functional) = 157 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 13.12 mg/kg ChEMBL. 2391696
T/C (functional) = 157 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 13.12 mg/kg ChEMBL. 2391696
T/C (functional) = 217 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 26.25 mg/kg ChEMBL. 2391696
T/C (functional) = 217 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 26.25 mg/kg ChEMBL. 2391696
T/C (functional) = 257 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 52.5 mg/kg ChEMBL. 2391696
T/C (functional) = 257 % Evaluated in vivo for antineoplastic activity against P388 murine leukemia tumor xenograft in nude mice after administering intra peritoneal injection at a dose of 52.5 mg/kg ChEMBL. 2391696

Phenotypes

Whole-cell/tissue/organism interactions

Species name Source Reference Is orphan
Homo sapiens ChEMBL23 2391696

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

No external resources registered for this compound

Bibliographic References

1 literature reference was collected for this gene.

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