SCHEMBL1532841

SCHEMBL1532841

O=C(O)c1ccc(OCC2CCCCC2)cc1

nearest known ligand 0.74

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 7/20 0.74
PARP15 Q460N3 6/20 0.74
PARP2 Q9UGN5 2/20 0.67
NR1H4 Q96RI1 1/20 0.54
FFAR1 O14842 1/20 0.54
KMT2A Q03164 2/20 0.50
MEN1 O00255 1/20 0.50
PKM P14618 1/20 0.50
MAP4K4 O95819 1/20 0.50
FNTA P49354 1/20 0.49
FNTB P49356 1/20 0.49
ALDH1A1 P00352 1/20 0.49
LMNA P02545 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
CCNA2 P20248 1/20 0.48
CDK2 P24941 1/20 0.48
CCNA1 P78396 1/20 0.48

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
SCHEMBL12420700 1.00 PARP10 (0.74) PARP10PARP15PARP2NR1H4FFAR1
SCHEMBL1532862 1.00 PARP10 (0.74) PARP10PARP15PARP2NR1H4FFAR1
SCHEMBL12420703 0.98 PARP10 (0.73) PARP10PARP15PARP2NR1H4FFAR1
SCHEMBL2885506 0.95 PARP10 (0.73) PARP10PARP15PARP2NR1H4FFAR1
SCHEMBL416244 0.91 PARP15 (0.72) PARP10PARP15PARP2NR1H4PKM
SCHEMBL6958286 0.85 PARP10 (0.72) PARP10PARP15PARP2FFAR1KMT2A
SCHEMBL8016856 0.84 PARP15 (0.62) PARP10PARP15PARP2NR1H4PKM
SCHEMBL10932224 0.84 PARP10 (0.70) PARP10PARP15PARP2FFAR1ALDH1A1
SCHEMBL12420708 0.84 PARP15 (0.58) PARP10PARP15PARP2NR1H4KMT2A
SCHEMBL4688420 0.84 TDP1 (0.60) PARP10PARP15PARP2NR1H4PKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111995567-B Formamide pyridone iron chelator derivative with potential multi-target anti-AD activity and preparation method and application thereof 浙江工业大学 2022-11-25 CN disclosed
CN-111995567-A Formamide pyridone iron chelator derivative with potential multi-target anti-AD activity and preparation method and application thereof 浙江工业大学 2020-11-27 CN disclosed
EP-2129218-B1 COMPOUNDS HAVING A CYCLIC MOIETY AND COMPOSITIONS FOR DELIVERING ACTIVE AGENTS EMISPHERE TECH INC (US) 2016-10-19 EP disclosed
EP-2607362-B1 Piperidine and piperazine carboxylates as FAAH inhibitors ASTELLAS PHARMA INC (JP) 2014-12-31 EP disclosed
EP-1849773-B1 Piperazine derivatives for the treatment of urinary incontinence and pain ASTELLAS PHARMA INC (JP) 2013-10-16 EP disclosed
EP-2607362-A1 Piperidine and piperazine carboxylates as FAAH inhibitors Astellas Pharma Inc. (JP) 2013-06-26 EP disclosed
US-8383852-B2 Compounds having a cyclic moiety and compositions for delivering active agents EMISPHERE TECHNOLOGIES, INC. (US) 2013-02-26 US disclosed
US-8383852-B2 Compounds having a cyclic moiety and compositions for delivering active agents EMISPHERE TECHNOLOGIES, INC. (US) 2013-02-26 US disclosed
US-20110172230-A1 UREA COMPOUND OR SALT THEREOF ASTELLAS PHARMA INC. (JP) 2011-07-14 US disclosed
US-20110172230-A1 UREA COMPOUND OR SALT THEREOF ASTELLAS PHARMA INC. (JP) 2011-07-14 US disclosed
EP-1828177-A2 NOVEL MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY (US) 2007-09-05 EP disclosed
WO-2006066173-A2 NOVEL MCH RECEPTOR ANTAGONISTS ELI LILLY AND COMPANY (US) 2006-06-22 WO disclosed
EP-0777471-B1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING & MFG (US) 2002-11-27 EP disclosed
EP-0927035-A4 THROMBIN INHIBITORS MERCK & CO INC (US) 2002-11-13 EP disclosed
EP-0927035-A1 THROMBIN INHIBITORS Merck & Co., Inc. (US) 1999-07-07 EP disclosed
US-5872138-A INHIBITING LOSS OF BLOOD PLATELETS, INHIBITING FORMATION OF BLOOD PLATELET AGGREGATES, INHIBITING FORMATION OF FIBRIN, INHIBITING THROMBUS FORMATION, AND INHIBITING EMBOLUS FORMATION IN A MAMMAL MERCK & CO., INC. (US) 1999-02-16 US disclosed
WO-1998010763-A1 THROMBIN INHIBITORS MERCK & CO., INC. (US) 1998-03-19 WO disclosed
EP-0777471-A1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-06-11 EP disclosed
US-5612377-A OXYUREA DERIVATIVE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-03-18 US disclosed
WO-1996003983-A1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1996-02-15 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-20110172230-A1 UREA COMPOUND OR SALT THEREOF FAAH, FAAH2, UTS2R PARP10 2889/4885PARP15 2099/4885PARP2 2872/4885

“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.