SCHEMBL3076978

SCHEMBL3076978

CC(C)(CN)Nc1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 2/20 0.48
NPSR1 Q6W5P4 1/20 0.42
CYP2D6 P10635 3/20 0.41
CYP1A2 P05177 2/20 0.41
CYP3A4 P08684 2/20 0.41
PRMT1 Q99873 1/20 0.41
TDP1 Q9NUW8 4/20 0.40
LMNA P02545 2/20 0.40
TSHR P16473 2/20 0.40
PTGS2 P35354 2/20 0.40
IDO1 P14902 2/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
SLC6A2 P23975 2/20 0.38
ALDH1A1 P00352 3/20 0.38
HSD17B10 Q99714 2/20 0.38
CTSD P07339 1/20 0.38
ALOX15 P16050 1/20 0.36
ALOX12 P18054 1/20 0.36
PTGS1 P23219 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
SCHEMBL583081 0.81 CCNE2 (0.44) NPSR1CYP2D6TDP1LMNATSHR
SCHEMBL1162021 0.79 NPSR1 (0.62) NPSR1CYP2D6CYP1A2CYP3A4TDP1
Hydrochloric Acid SCHEMBL17710397 0.79 CCNE2 (0.42) NPSR1CYP2D6TDP1LMNATSHR
SCHEMBL4551365 0.79 POLB (0.48) NPSR1CYP2D6TDP1LMNATSHR
SCHEMBL11691246 0.79 NPSR1 (0.41) NPSR1CYP2D6TDP1LMNATSHR
SCHEMBL1453847 0.77 GAA (0.43) NPSR1CYP2D6TDP1LMNATSHR
SCHEMBL3162604 0.77 KIF11 (0.43) CYP1A2CYP3A4LMNATSHRCYP2C19
SCHEMBL5699071 0.75 PDK1 (0.44) NPSR1CYP2D6CYP1A2CYP3A4TDP1
SCHEMBL8433637 0.74 TDP1 (0.39) TAAR1NPSR1CYP2D6CYP1A2CYP3A4
SCHEMBL23957785 0.74 TAAR1 (0.42) TAAR1NPSR1CYP2D6CYP3A4LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101273016-B Antibacterial quinoline derivatives JANSSEN PHARMACEUTICA NV 2013-01-02 CN claimed
CN-101273016-A Antibacterial quinoline derivatives JANSSEN PHARMACEUTICA NV (BE) 2008-09-24 CN claimed
CN-1665807-B Physiologically active substance MICROBIOPHARM JAPAN CO LTD 2013-09-11 CN disclosed
CN-101273016-B Antibacterial quinoline derivatives JANSSEN PHARMACEUTICA NV 2013-01-02 CN disclosed
US-8268827-B2 Pyridazinone derivatives as PARP inhibitors ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI SPA. (IT) 2012-09-18 US disclosed
US-20100261709-A1 PYRIDAZINONE DERIVATIVES AS PARP INHIBITORS MSD ITALIA S.R.L. (IT) 2010-10-14 US disclosed
EP-2220073-A1 PYRIDAZINONE DERIVATIVES AS PARP INHIBITORS Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. (IT) 2010-08-25 EP disclosed
CN-101730693-A Process for producing macrolide compound and production intermediate thereof EISAI R&D MAN CO LTD 2010-06-09 CN disclosed
CN-1671856-B Novel physiologically active substances EISAI R&D MAN CO LTD 2010-05-12 CN disclosed
CN-101663296-A 12-membered ring macrolactam derivatives EISAI R&D MAN CO LTD 2010-03-03 CN disclosed
WO-2009063244-A1 PYRIDAZINONE DERIVATIVES AS PARP INHIBITORS ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI S.P.A. (IT) 2009-05-22 WO disclosed
CN-1671856-A Novel physiologically active substances MERCIAN CORP (JP) 2005-09-21 CN disclosed
CN-1665807-A Novel physiolgically active substances MERCIAN CORP (JP) 2005-09-07 CN disclosed
EP-0266558-A2 5-Alkylbenzimidazoles, process for their preparation and medicaments containing them Roche Diagnostics GmbH (DE) 1988-05-11 EP disclosed
EP-0114374-B1 SUBSTITUTED 4-AMINOMETHYLENE CHROMANS OR CHROMENES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN MEDICINES BAYER AG (DE) 1986-07-23 EP disclosed
US-4563458-A CIRCULATORY SYSTEM DISORDERS BAYER AKTIENGESELLSCHAFT (DE) 1986-01-07 US disclosed
EP-0114374-A1 Substituted 4-aminomethylene chromans or chromenes, process for their preparation and their use in medicines BAYER AG (DE) 1984-08-01 EP disclosed
EP-0020401-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF 1,4-DIAZA-2-CYCLOALKANONE AND SUBSTITUTED DERIVATIVES THEREOF. GOODRICH CO B F (US) 1981-01-07 EP disclosed
EP-0020401-A4 IMPROVED PROCESS FOR THE SYNTHESIS OF 1,4-DIAZA-2-CYCLOALKANONE AND SUBSTITUTED DERIVATIVES THEREOF. GOODRICH CO B F (US) 1980-08-11 EP disclosed
WO-1980000702-A1 IMPROVED PROCESS FOR THE SYNTHESIS OF 1,4-DIAZA-2-CYCLOALKANONE AND SUBSTITUTED DERIVATIVES THEREOF GOODRICH CO B F (US) 1980-04-17 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 (1 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-20100261709-A1 PYRIDAZINONE DERIVATIVES AS PARP INHIBITORS PARP1, PARP2, PARP3 TAAR1 4229/4885NPSR1 4377/4885CYP2D6 2258/4885

“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.