SCHEMBL6825758

SCHEMBL6825758

Cc1ccc(C(N)=O)cc1C(N)=O

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PARP1 P09874 3/20 0.50
▸ TDP1 Q9NUW8 2/20 0.47
▸ SIRT3 Q9NTG7 1/20 0.47
▸ NNMT P40261 2/20 0.46
▸ MAPT P10636 1/20 0.45
▸ LCK P06239 1/20 0.44
▸ ALDH1A1 P00352 2/20 0.43
▸ KDM4E B2RXH2 1/20 0.43
▸ BRD4 O60885 1/20 0.43
▸ BRPF1 P55201 1/20 0.43
▸ SMN1; SMN2 Q16637 1/20 0.43
▸ HSD17B10 Q99714 1/20 0.43
▸ PRSS1 P07477 1/20 0.42
▸ PRSS2 P07478 1/20 0.42
▸ PRSS3 P35030 1/20 0.42
▸ CA1 P00915 1/20 0.42
▸ CA2 P00918 1/20 0.42
▸ PARP10 Q53GL7 1/20 0.42
▸ PARP2 Q9UGN5 1/20 0.42
▸ PARP4 Q9UKK3 1/20 0.42

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
SCHEMBL10261196 0.88 ALDH1A1 (0.47) PARP1TDP1MAPTLCKALDH1A1
SCHEMBL13544664 0.88 PARP1 (0.47) PARP1TDP1SIRT3NNMTMAPT
SCHEMBL13254936 0.88 TDP1 (0.44) TDP1SIRT3NNMTMAPTMAPK1
SCHEMBL2128609 0.84 PARP1 (0.52) PARP1TDP1SIRT3NNMTLCK
SCHEMBL19993588 0.84 PARP1 (0.44) PARP1TDP1SIRT3NNMTMAPT
SCHEMBL29503140 0.82 PRSS1 (0.61) PARP1TDP1MAPTLCKALDH1A1
SCHEMBL1002832 0.82 PRSS1 (0.61) PARP1TDP1MAPTLCKALDH1A1
SCHEMBL7481641 0.81 TDP1 (0.52) PARP1TDP1MAPTALDH1A1KDM4E
SCHEMBL7083041 0.81 NNMT (0.50) PARP1TDP1SIRT3NNMTMAPT
SCHEMBL1003845 0.80 MEN1 (0.53) PARP1TDP1SIRT3MAPTALDH1A1

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8288552-B2 Dihydropyridone amidesas P2X7 modulators ROCHE PALO ALTO LLC (US) 2012-10-16 — — US claimed
US-8835673-B2 Process for preparing isocyanates BASF SE (DE) 2014-09-16 — — US disclosed
WO-2013142266-A1 ESTROGEN RECEPTOR MODULATORS AND USES THEREOF SERAGON PHARMACEUTICALS, INC. (US) 2013-09-26 — — WO disclosed
US-20120253063-A1 PROCESS FOR PREPARING ISOCYANATES BASF SE (DE) 2012-10-04 — — US disclosed
US-6781010-B1 OBTAINED DIRECTLY BY THE SYNTHESIS AND THERMOLYSIS OF THE REACTION PRODUCT OF THE CORRESPONDING FORMAMIDE AND A DIORGANOCARBONATE LYONDELL CHEMICAL COMPANY 2004-08-24 — — US disclosed
WO-2002024634-A2 NON-PHOSGENE ROUTE TO THE MANUFACTURE OF ORGANIC ISOCYANATES ARCO CHEMICAL TECHNOLOGY, L.P. (US) 2002-03-28 — — WO disclosed
US-5686645-A REACTION WITH ALCOHOL TO FORM CARBAMATE, TRANSITION METAL CATALYST ARCO CHEMICAL TECHNOLOGY, L.P. (US) 1997-11-11 — — US disclosed
US-5155267-A Forming unsymmetric carbamates and ureas; reacting primary formamide with dialkyl amine or alcohol ARCO CHEMICAL TECHNOLOGY, L.P. (US) 1992-10-13 — — US disclosed
US-4455309-A MICROBIOCIDES BAYER AKTIENGESELLSCHAFT (DE) 1984-06-19 — — US disclosed
US-4259258-A Preparation of bis-n-chloramides of cycloaliphatic carboxylic acids AKZONA INCORPORATED (US) 1981-03-31 — — US disclosed
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