SCHEMBL10273422

SCHEMBL10273422

CCn1ccc([N+](=O)[O-])c1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.41
MEN1 O00255 3/20 0.41
CYP1A2 P05177 2/20 0.41
POLB P06746 2/20 0.41
ATM Q13315 1/20 0.41
MAPT P10636 3/20 0.40
ACHE P22303 1/20 0.39
HSD17B10 Q99714 1/20 0.39
HIF1A Q16665 1/20 0.39
LMNA P02545 2/20 0.38
ALDH1A1 P00352 3/20 0.37
HPGD P15428 1/20 0.37
GSK3A P49840 1/20 0.37
GSK3B P49841 1/20 0.37
HTT P42858 1/20 0.37
CYP19A1 P11511 1/20 0.37
CA12 O43570 1/20 0.36
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
CA3 P07451 1/20 0.36

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
SCHEMBL2187545 0.80 TSHR (0.41) KMT2AMEN1CYP1A2POLBATM
SCHEMBL2185729 0.80 KMT2A (0.45) KMT2AMEN1CYP1A2POLBATM
SCHEMBL3263969 0.77 APOBEC3G (0.40) KMT2AMEN1CYP1A2POLBATM
SCHEMBL1095240 0.77 HIF1A (0.38) KMT2AMEN1CYP1A2POLBATM
SCHEMBL1126194 0.77 KDM4E (0.44) KMT2AMEN1CYP1A2POLBATM
SCHEMBL30211545 0.74 CA12 (0.46) KMT2AMEN1CYP1A2POLBATM
SCHEMBL27809179 0.74 MEN1 (0.51) KMT2AMEN1CYP1A2POLBATM
SCHEMBL10910583 0.73 CA12 (0.39) KMT2AMEN1CYP1A2POLBATM
SCHEMBL10911319 0.73 KMT2A (0.36) KMT2AMEN1CYP1A2POLBATM
SCHEMBL1354417 0.72

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110168103-A Reduce the method that primer dimer forms and improves amplification efficiency SEEGENE株式会社 2019-08-23 CN claimed
CN-106399484-A Double bubble shape fluorescence probe, applications thereof, and kit 中国人民解放军第三军医大学第附属医院 2017-02-15 CN claimed
CN-105274096-A Bridge type fluorescent probe with bridge type sequence zone doping into mismatched bases and application and method UNIV PLA 3RD MILITARY MEDICAL 2016-01-27 CN claimed
CN-101189336-B Processes using dual specificity oligonucleotide and dual specificity oligonucleotide SEEGENE INC 2012-10-24 CN claimed
CN-110168103-A Reduce the method that primer dimer forms and improves amplification efficiency SEEGENE株式会社 2019-08-23 CN disclosed
CN-106399484-A Double bubble shape fluorescence probe, applications thereof, and kit 中国人民解放军第三军医大学第附属医院 2017-02-15 CN disclosed
CN-105274096-A Bridge type fluorescent probe with bridge type sequence zone doping into mismatched bases and application and method UNIV PLA 3RD MILITARY MEDICAL 2016-01-27 CN disclosed
CN-102782150-B Target detection of target hybrid and detection primer SEEGENE INC 2015-04-01 CN disclosed
CN-103228797-A Detection of target nucleic acid sequences using dual-abeled immobilized probes on solid phase SEEGENE INC 2013-07-31 CN disclosed
CN-1578841-B Annealing control primer and use of the same VISION GENE CO LTD 2013-03-27 CN disclosed
CN-102782150-A THD primer target detection SEEGENE INC 2012-11-14 CN disclosed
CN-102770556-A Targeted probes and uses thereof SEEGENE INC 2012-11-07 CN disclosed
US-7723509-B2 Conjugated lipophilic group with a modified nucleotide is used to target disease gene, cells, tissue, for drug delivery to target tumor cells; ribose sugar of nucleotide is replaced with a cyclic carrier which has at least one attached phosphate or phosphorothioate group; biodrugs ALNYLAM PHARMACEUTICALS (US) 2010-05-25 US disclosed
US-20100076056-A1 MODIFIED iRNA AGENTS ALNYLAM PHARMACEUTICALS, INC. (US) 2010-03-25 US disclosed
US-7595306-B2 Method of treating neurodegenerative disease NATIONAL INSTITUTE OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2009-09-29 US disclosed
WO-2008113456-A1 TETRAHYDROQUINOLINE DERIVATIVES AND USE OF SAME FOR TREATING CANCER MERCK PATENT GMBH (DE) 2008-09-25 WO disclosed
US-20070179100-A1 Protected monomers ALNYLAM PHARMACEUTICALS, INC. 2007-08-02 US disclosed
US-20070161591-A1 Methods and compositions for treating neurological disease UNIVERSITY OF MASSACHUSETTS (US) 2007-07-12 US disclosed
US-20070161595-A1 Method of treating neurodegenerative disease MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2007-07-12 US disclosed
CN-1578841-A Annealing control primer and use of the same VISION GENE CO LTD (KR) 2005-02-09 CN disclosed

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

For each of this compound's patents that has machine-readable text (4 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-20070161591-A1 Methods and compositions for treating neurological disease SMN1; SMN2, CLN6, INA KMT2A 1675/4885MEN1 1598/4885CYP1A2 4804/4885
US-20070161595-A1 Method of treating neurodegenerative disease SNCA, PARK7, NLN KMT2A 1350/4885MEN1 4796/4885CYP1A2 4840/4885
US-20100076056-A1 MODIFIED iRNA AGENTS LDLR, RNASE1, SARNP KMT2A 2199/4885MEN1 1035/4885CYP1A2 4515/4885
US-20070179100-A1 Protected monomers PCNA, POLN, PARP1 KMT2A 1569/4885MEN1 939/4885CYP1A2 2684/4885

“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.