SCHEMBL2556486

SCHEMBL2556486

COC(=O)Cc1cc([N+](=O)[O-])ccc1F

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.48
ALDH1A1 P00352 6/20 0.48
POLB P06746 1/20 0.47
GAA P10253 3/20 0.47
THRB P10828 2/20 0.47
HTT P42858 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
HIF1A Q16665 1/20 0.46
PDGFRB P09619 1/20 0.46
FGFR1 P11362 1/20 0.46
PDGFRA P16234 1/20 0.46
FLT1 P17948 1/20 0.46
FGFR3 P22607 1/20 0.46
KDR P35968 1/20 0.46
GLA P06280 1/20 0.45
MEN1 O00255 2/20 0.45
KMT2A Q03164 2/20 0.45
MAPT P10636 3/20 0.43
CYP1A2 P05177 1/20 0.43
PTGS2 P35354 1/20 0.43

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
SCHEMBL30664602 1.00 LMNA (0.48) LMNAALDH1A1POLBGAATHRB
SCHEMBL6597479 0.88 CYP1A2 (0.47) LMNAALDH1A1POLBGAATHRB
SCHEMBL22165300 0.86 MEN1 (0.49) LMNAALDH1A1POLBGAATHRB
SCHEMBL17827840 0.85 ALDH1A1 (0.47) LMNAALDH1A1POLBGAATHRB
SCHEMBL502591 0.84 PDGFRB (0.53) LMNAALDH1A1POLBHTTL3MBTL1
SCHEMBL1441025 0.83 ALDH1A1 (0.50) LMNAALDH1A1POLBGAATHRB
SCHEMBL14439930 0.82 POLB (0.50) LMNAALDH1A1POLBTHRBPDGFRB
SCHEMBL1817138 0.82 POLB (0.47) LMNAALDH1A1POLBGAAHTT
SCHEMBL9156278 0.82 ALDH1A1 (0.58) LMNAALDH1A1GAATHRBHTT
SCHEMBL31444647 0.82 LMNA (0.51) LMNAALDH1A1POLBGAATHRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3573972-B1 RORGAMMA MODULATORS AND USES THEREOF GENFIT (FR) 2026-01-14 EP disclosed
US-20250340560-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2025-11-06 US disclosed
US-20250340556-A1 PYRIMIDOPYRIMIDONE COMPOUNDS AND METHODS OF USE THEREOF SOLTEGO INC (US) 2025-11-06 US disclosed
EP-4526307-A1 PYRIMIDOPYRIMIDONE COMPOUNDS AND METHODS OF USE THEREOF Soltego, Inc. (US) 2025-03-26 EP disclosed
US-20240254128-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2024-08-01 US disclosed
US-20230399312-A1 SUBSTITUTED PYRIMIDINES AND METHODS OF USE THERAVANCE BIOPHARMA R&D IP LLC (US) 2023-12-14 US disclosed
US-20230399312-A1 SUBSTITUTED PYRIMIDINES AND METHODS OF USE THERAVANCE BIOPHARMA R&D IP LLC (US) 2023-12-14 US disclosed
WO-2023225097-A1 PYRIMIDOPYRIMIDONE COMPOUNDS AND METHODS OF USE THEREOF SOLTEGO, INC. (US) 2023-11-23 WO disclosed
US-11673879-B2 Substituted pyrimidines and methods of use THERAVANCE BIOPHARMA R&D IP, LLC (US) 2023-06-13 US disclosed
US-11673879-B2 Substituted pyrimidines and methods of use THERAVANCE BIOPHARMA R&D IP, LLC (US) 2023-06-13 US disclosed
US-20160083392-A1 Fused heterocyclic compounds as protein kinase inhibitors BEIGENE, LTD. (KY) 2016-03-24 US disclosed
US-20160083392-A1 Fused heterocyclic compounds as protein kinase inhibitors BEIGENE, LTD. (KY) 2016-03-24 US disclosed
EP-2989106-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS Beigene, Ltd. (KY) 2016-03-02 EP disclosed
US-20150259354-A1 Fused heterocyclic compounds as protein kinase inhibitors BEIGENE, LTD. (KY) 2015-09-17 US disclosed
US-20150259354-A1 Fused heterocyclic compounds as protein kinase inhibitors BEIGENE, LTD. (KY) 2015-09-17 US disclosed
US-20150259354-A1 Fused heterocyclic compounds as protein kinase inhibitors BEIGENE, LTD. (KY) 2015-09-17 US disclosed
US-20140336252-A1 NOVEL COMPOUND AS KCNQ POTASSIUM CHANNEL AGONIST, PREPARATION METHOD THEREFOR AND USE THEREOF SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2014-11-13 US disclosed
WO-2014173289-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS BEIGENE, LTD. (KY) 2014-10-30 WO disclosed
WO-2014173289-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS BEIGENE, LTD. (KY) 2014-10-30 WO disclosed
WO-2011130741-A1 COMPOUNDS FOR TREATING NEURODEGENERATIVE DISEASES ARRAY BIOPHARMA INC. (US) 2011-10-20 WO 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 (8 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-20250340556-A1 PYRIMIDOPYRIMIDONE COMPOUNDS AND METHODS OF USE THEREOF SIK2, SIK1, SIK3 LMNA 3188/4885ALDH1A1 2257/4885POLB 1297/4885
US-20240254128-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BTK, LCK, SYK LMNA 4691/4885ALDH1A1 3106/4885POLB 2407/4885
US-20150259354-A1 Fused heterocyclic compounds as protein kinase inhibitors BTK, WEE1, LYN LMNA 4466/4885ALDH1A1 3907/4885POLB 4332/4885
US-11673879-B2 Substituted pyrimidines and methods of use ALK, TYMP, ENTPD5 LMNA 2098/4885ALDH1A1 2596/4885POLB 651/4885
US-20160083392-A1 Fused heterocyclic compounds as protein kinase inhibitors BTK, WEE1, LYN LMNA 4466/4885ALDH1A1 3907/4885POLB 4332/4885
US-20140336252-A1 NOVEL COMPOUND AS KCNQ POTASSIUM CHANNEL AGONIST, PREPARATION METHOD THEREFOR AND USE THEREOF KCNQ1, KCNQ4, KCNQ5 LMNA 1631/4885ALDH1A1 1888/4885POLB 2976/4885
US-20230399312-A1 SUBSTITUTED PYRIMIDINES AND METHODS OF USE ALK, TYMP, ENTPD5 LMNA 2098/4885ALDH1A1 2596/4885POLB 651/4885
US-20250340560-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BTK, LCK, SYK LMNA 4691/4885ALDH1A1 3106/4885POLB 2407/4885

“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.