SCHEMBL42351

SCHEMBL42351

Nc1nc2[nH]c(-c3cccs3)nc2c(=O)[nH]1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOS1 P29475 1/20 0.55
KDM4E B2RXH2 5/20 0.49
HPGD P15428 4/20 0.49
PKM P14618 1/20 0.49
ERCC1 P07992 5/20 0.48
FEN1 P39748 5/20 0.48
ERCC4 Q92889 5/20 0.48
ALDH1A1 P00352 4/20 0.47
GAA P10253 3/20 0.47
GLA P06280 3/20 0.47
MAPT P10636 2/20 0.47
LMNA P02545 2/20 0.47
MEN1 O00255 1/20 0.47
MAPK1 P28482 1/20 0.47
HTT P42858 1/20 0.47
KMT2A Q03164 1/20 0.47
ADORA3 P0DMS8 2/20 0.46
MGAM O43451 1/20 0.46
SI P14410 1/20 0.46
MGAM2 Q2M2H8 1/20 0.46

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL38655985 0.78 DHFR (0.51) KDM4EHPGDPKMERCC1FEN1
SCHEMBL17060210 0.76 FGFR1 (0.59) NOS1KDM4EHPGDALDH1A1GLA
SCHEMBL26968497 0.75 ADORA3 (0.62) KDM4EHPGDPKMERCC1FEN1
SCHEMBL41999 0.74 ADORA3 (0.49) NOS1KDM4EHPGDPKMERCC1
Hydrochloric Acid SCHEMBL1895412 0.72 ADORA3 (0.48) NOS1KDM4EHPGDPKMERCC1
8-Aminoguanine SCHEMBL21760 0.70 KDM4E (0.60) KDM4EPKMALDH1A1GLAMAPT
SCHEMBL26968368 0.70 ADORA3 (0.48) KDM4EHPGDPKMERCC1FEN1
SCHEMBL26968714 0.69 KDM4E (0.47) KDM4EHPGDPKMERCC1FEN1
SCHEMBL29108569 0.68 ADORA3 (0.43) KDM4EHPGDPKMERCC1FEN1
SCHEMBL9253425 0.68 ADORA2B (0.59) KDM4EHPGDPKMERCC1FEN1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 1889 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117778530-A Method for adding preset joint to 5' end of single-stranded DNA 清华大学 2024-03-29 CN claimed
US-11939582-B2 Antisense oligonucleotides targeting SCN2A for the treatment of SCN1A encephalopathies ROGCON, INC. (US) 2024-03-26 US claimed
EP-4330397-A1 ANTISENSE-OLIGONUCLEOTIDES FOR PREVENTION OF KIDNEY DYSFUNCTION PROMOTED BY ENDOTHELIAL DYSFUNCTION BY EPHRIN-B2 SUPPRESSION Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2024-03-06 EP claimed
WO-2023196944-A2 OLIGONUCLEOTIDE INTERFERENCE TREATMENTS OF PROSTATE CANCER THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA (US) 2023-10-12 WO claimed
WO-2023192885-A2 METHODS OF USING OLIGOMERIC COMPOUNDS TO TREAT SCN2A-RELATED DISORDERS PRAXIS PRECISION MEDICINES, INC. (US) 2023-10-05 WO claimed
WO-2023150716-A2 METHODS FOR THE TREATMENT OF SCN2A-RELATED DISORDERS PRAXIS PRECISION MEDICINES, INC. (US) 2023-08-10 WO claimed
WO-2022263569-A1 ANTISENSE-OLIGONUCLEOTIDES FOR PREVENTION OF KIDNEY DYSFUNCTION PROMOTED BY ENDOTHELIAL DYSFUNCTION BY EPHRIN-B2 SUPPRESSION MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2022-12-22 WO claimed
EP-4105328-A1 ANTISENSE-OLIGONUCLEOTIDES FOR PREVENTION OF KIDNEY DYSFUNCTION PROMOTED BY ENDOTHELIAL DYSFUNCTION BY EPHRIN-B2 SUPPRESSION Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2022-12-21 EP claimed
US-20220143071-A1 ANTISENSE-OLIGONUCLEOTIDES AS INHIBITORS OF TGF-R SIGNALING Neurovision Pharma GmbH (DE) 2022-05-12 US claimed
US-11186849-B2 Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-11-30 US claimed
US-20090275133-A1 ANTISENSE MODULATION OF C-REACTIVE PROTEIN EXPRESSION ISIS PHARMACEUTICALS, INC. (US) 2009-11-05 US claimed
US-7223849-B1 Oligonucleotides from the untranslated regions of housekeeping genes and methods of using same to modulate cell growth GENESENSE TECHNOLOGIES INC. (CA) 2007-05-29 US claimed
US-7087580-B2 Neuropilin antisense oligonucleotide sequences and methods of using same to modulate cell growth GENESENSE TECHNOLOGIES, INC. (CA) 2006-08-08 US claimed
US-7067497-B2 Modulation of telomere length by oligonucleotides having a G-core sequence ISIS PHARMACEUTICALS, INC. (US) 2006-06-27 US claimed
US-20060024727-A1 Antisense modulation of C-reactive protein expression ISIS PHARMACEUTICALS, INC. (US) 2006-02-02 US claimed
EP-1153128-B1 ANTITUMOR ANTISENSE SEQUENCES DIRECTED AGAINST R1 AND R2 COMPONENTS OF RIBONUCLEOTIDE REDUCTASE GENESENSE TECHNOLOGIES INC (CA) 2005-11-09 EP claimed
EP-0917569-B1 ANTITUMOR ANTISENSE SEQUENCES DIRECTED AGAINST R1 AND R2 COMPONENTS OF RIBONUCLEOTIDE REDUCTASE GENESENSE TECHNOLOGIES INC (CA) 2005-11-09 EP claimed
US-20040049022-A1 Composition & methods for treatment and screening NYCE JONATHAN W (US) 2004-03-11 US claimed
WO-2004011613-A2 COMPOSITION & METHODS FOR TREATMENT AND SCREENING EPIGENESIS PHARMACEUTICALS, INC. (US) 2004-02-05 WO claimed
US-6566514-B1 Antisense oligonucleotides for use in the treatment of tumors GENESENSE TECHNOLOGIES INC. (CA) 2003-05-20 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220143071-A1 ANTISENSE-OLIGONUCLEOTIDES AS INHIBITORS OF TGF-R SIGNALING TGFBR1, TGFBR2, TGFB1 NOS1 2262/4885KDM4E 4454/4885HPGD 4222/4885
US-11939582-B2 Antisense oligonucleotides targeting SCN2A for the treatment of SCN1A encephalopathies SCN1A, SCN2A, SCN1B NOS1 3239/4885KDM4E 2558/4885HPGD 4689/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.