SCHEMBL2673535

SCHEMBL2673535

CCc1cc(-c2coc(CN3CCCC3)c2)c(C)[nH]c1=O

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KDM4E B2RXH2 10/20 0.37
▸ ALDH1A1 P00352 9/20 0.37
▸ KMT2A Q03164 7/20 0.37
▸ MEN1 O00255 6/20 0.37
▸ POLB P06746 6/20 0.37
▸ L3MBTL1 Q9Y468 5/20 0.37
▸ RECQL P46063 4/20 0.37
▸ BLM P54132 4/20 0.37
▸ TDP1 Q9NUW8 4/20 0.37
▸ MAPT P10636 3/20 0.37
▸ USP2 O75604 3/20 0.37
▸ THRB P10828 1/20 0.37
▸ APEX1 P27695 1/20 0.37
▸ ALOX15 P16050 3/20 0.36
▸ HSD17B10 Q99714 6/20 0.35
▸ GAA P10253 3/20 0.35
▸ HPGD P15428 2/20 0.35
▸ S1PR1 P21453 1/20 0.35
▸ GLA P06280 2/20 0.34
▸ CASP1 P29466 1/20 0.34

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
SCHEMBL6372024 0.80 ALDH1A1 (0.41) KDM4EALDH1A1KMT2AMEN1POLB
SCHEMBL2674025 0.77 KDM5B (0.42) KDM4EALDH1A1KMT2AMEN1TDP1
SCHEMBL6372062 0.75 CCNC (0.39) KDM4EALDH1A1KMT2AMEN1POLB
SCHEMBL6371157 0.74 KDM4E (0.40) KDM4EALDH1A1KMT2AMEN1POLB
Hydrochloric Acid SCHEMBL2674323 0.74 CDC7 (0.38) KDM4EALDH1A1KMT2AMEN1POLB
Hydrochloric Acid SCHEMBL2674615 0.73 KDM4E (0.39) KDM4EALDH1A1KMT2AMEN1POLB
SCHEMBL2674592 0.73 S1PR1 (0.35) KDM4EALDH1A1BLMGAAHPGD
SCHEMBL6370969 0.72 TNKS (0.53) KDM4EALDH1A1HSD17B10
Hydrochloric Acid SCHEMBL2673942 0.71 TNKS (0.52) KDM4EALDH1A1HSD17B10
SCHEMBL6371216 0.71 HTT (0.41) KDM4EALDH1A1KMT2AMEN1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1732896-B1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMA INC (US) 2012-12-12 — — EP claimed
US-20120202795-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMACEUTICALS INC. (US) 2012-08-09 — — US claimed
US-20070032489-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMACEUTICALS INC. (US) 2007-02-08 — — US claimed
EP-1732896-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) Aventis Pharmaceuticals Inc. (US) 2006-12-20 — — EP claimed
WO-2005097750-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMACEUTICALS INC. (US) 2005-10-20 — — WO claimed
US-11130843-B2 Methods of manufacture of polyetherimides SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2021-09-28 — — US disclosed
US-10457778-B2 Methods of manufacture of polyetherimides SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2019-10-29 — — US disclosed
US-20180258225-A1 METHODS OF MANUFACTURE OF POLYETHERIMIDES SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2018-09-13 — — US disclosed
US-20170029567-A1 METHODS OF MANUFACTURE OF POLYETHERIMIDES SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2017-02-02 — — US disclosed
EP-1732896-B1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMA INC (US) 2012-12-12 — — EP disclosed
EP-1732896-B1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMA INC (US) 2012-12-12 — — EP disclosed
US-20120202795-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) AVENTIS PHARMACEUTICALS INC. (US) 2012-08-09 — — US disclosed
US-6590108-B1 Transimidation of bis(imide) in presence of phthalic anhydride having substituent selected from group consisting of nitro, bromo, fluoro and chloro, to yield dianhydride GENERAL ELECTRIC COMPANY 2003-07-08 — — US disclosed
WO-2003050165-A1 METHODS FOR THE PREPARATION OF POLY(ETHERIMIDES)S GENERAL ELECTRIC COMPANY (US) 2003-06-19 — — WO disclosed
US-6498224-B1 SOLUTION POLYMERIZATION OF A DIANHYDRIDE AND A DIAMINE WHICH ELIMINATES THE NITRATION STEP; HIGH HEAT ENGINEERING PLASTICS GENERAL ELECTRIC COMPANY 2002-12-24 — — US disclosed
US-6096900-A Solventless preparation of phthalimides GENERAL ELECTRIC COMPANY (US) 2000-08-01 — — US disclosed
US-6066743-A Solventless preparation of phthalimides GENERAL ELECTRIC COMPANY (US) 2000-05-23 — — US disclosed
EP-0330220-B1 Process for the preparation and recovery of oxydiphthalic anhydrides OCCIDENTAL CHEM CO (US) 1994-06-01 — — EP disclosed
US-5206391-A Reacting BR2 with halohydrophthalic anhydride, reacting HBR with CL2 to regenerate bromine OCCIDENTAL CHEMICAL CORPORATION (US) 1993-04-27 — — US disclosed
EP-0330220-A2 Process for the preparation and recovery of oxydiphthalic anhydrides OCCIDENTAL CHEMICAL CORPORATION (US) 1989-08-30 — — EP 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 (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-20120202795-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) PARP1, PARP2, PARP3 KDM4E 1262/4885ALDH1A1 280/4885KMT2A 1291/4885
US-20070032489-A1 SUBSTITUTED PYRIDONES AS INHIBITORS OF POLY(ADP-RIBOSE) POLYMERASE (PARP) PARP1, PARP2, PARP3 KDM4E 1262/4885ALDH1A1 280/4885KMT2A 1291/4885

“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.

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