SCHEMBL292030

SCHEMBL292030

O=C1[CH]c2ccccc2C1=O

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 6/20 0.70
MEN1 O00255 4/20 0.70
KMT2A Q03164 4/20 0.70
PTPRC P08575 4/20 0.70
MAPT P10636 4/20 0.70
IDO1 P14902 4/20 0.70
KDM4E B2RXH2 3/20 0.70
LMNA P02545 3/20 0.70
ALDH1A1 P00352 3/20 0.70
HPGD P15428 3/20 0.70
BCHE P06276 2/20 0.70
POLB P06746 2/20 0.70
THRB P10828 2/20 0.70
CES1 P23141 2/20 0.70
RECQL P46063 2/20 0.70
PTPN22 Q9Y2R2 2/20 0.70
PKM P14618 2/20 0.70
ALOX15 P16050 1/20 0.70
ACHE P22303 1/20 0.70
HSD17B10 Q99714 1/20 0.70

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
1,2-Naphthoquinone SCHEMBL15167712 0.82 PTPRC (1.00) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL173316 0.82 PTPRC (1.00) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL29363665 0.82 PTPRC (1.00) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL30715501 0.80 PTPRC (0.95) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL30697786 0.80 PTPRC (0.95) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL9245768 0.78 PTPRC (0.91) PTPN1MEN1KMT2APTPRCMAPT
9,10-Phenanthrenequinone SCHEMBL19809110 0.77 PTPRC (0.87) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL7746067 0.77 PTPRC (0.87) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL28601611 0.77 PTPRC (0.87) PTPN1MEN1KMT2APTPRCMAPT
1,2-Naphthoquinone SCHEMBL20212026 0.75 PTPRC (0.83) PTPN1MEN1KMT2APTPRCMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110053981-A1 Methods and Compositions Using Cholinesterase Inhibitors EISAI R&D MANAGEMENT CO., LTD. (JP) 2011-03-03 US claimed
EP-2140868-A1 Use of a cholinesterase inhibitor for the treatment of dementia and cognitive impairments associated with or caused by chemotherapy Eisai R&D Management Co., Ltd. (JP) 2010-01-06 EP claimed
EP-2138177-A1 Use of a cholinesterase inhibitor for the treatment of dementia and cognitive impairments Eisai R&D Management Co., Ltd. (JP) 2009-12-30 EP claimed
EP-2133078-A1 Use of a cholinesterase inhibitor for the treatment of dementia and cognitive impairments Eisai R&D Management Co., Ltd. (JP) 2009-12-16 EP claimed
EP-2130538-A1 Use of a cholinesterase inhibitor for the delaying the onset of Alzheimer's disease Eisai R&D Management Co., Ltd. (JP) 2009-12-09 EP claimed
US-20080312189-A1 Cadasil Treatment with Cholinesterase Inhibitors EISAI CO., LTD. (JP) 2008-12-18 US claimed
EP-1729761-A4 CADASIL TREATMENT WITH CHOLINESTERASE INHIBITORS EISAI CO LTD (JP) 2008-09-03 EP claimed
US-20080045500-A1 Nerve Regeneration Stimulator EISAI R&D MANAGEMENT CO., LTD. (JP) 2008-02-21 US claimed
EP-1779867-A1 NERVE REVENERATION PROMOTER Eisai R&D Management Co., Ltd. (JP) 2007-05-02 EP claimed
EP-1764101-A1 Use of a cholinesterase inhibitor for the treatment of dementia and cognitive impairments Eisai R&D Management Co., Ltd. (JP) 2007-03-21 EP claimed
US-20020052373-A1 Combination treatment for dementia or cognitive deficits associated with alzheimer's disease and parkinson's disease ZORN STEVIN H (US) 2002-05-02 US claimed
EP-1201268-A2 Combinations of D4 dopamine receptor antagonists with acetylcholine esterase inhibitors Pfizer Products Inc. (US) 2002-05-02 EP claimed
CN-1328451-A Medicine for improving excretion capacity of bladder TAKEDA CHEMICAL INDUSTRIES LTD (JP) 2001-12-26 CN claimed
WO-2001066114-A1 NOVEL METHODS USING CHOLINESTERASE INHIBITORS EISAI CO., LTD. (JP) 2001-09-13 WO claimed
EP-1118322-A1 DRUGS FOR IMPROVING VESICAL EXCRETORY STRENGTH Takeda Chemical Industries, Ltd. (JP) 2001-07-25 EP claimed
EP-1116716-A1 Piperidine and piperazine compounds for use in the treatment of Alzheimer Eisai Co., Ltd. (JP) 2001-07-18 EP claimed
EP-0742207-A1 2-(Indan-1-one-2-yl-alkyl)-1-phenylalkyl-piperidines and processes for their preparation Eisai Co., Ltd. (JP) 1996-11-13 EP claimed
EP-0673927-A1 4-[2-indanyl-1-one]alkylpiperidines as anticholinergic agents Eisai Co., Ltd. (JP) 1995-09-27 EP claimed
US-5100901-A Treatment of Alzheimer*s disease EISAI CO., LTD. (JP) 1992-03-31 US claimed
EP-0296560-A2 1,4-Substituted piperidines as acetylcholinesterase inhibitors and their use for the treatment of Alzheimer's disease Eisai Co., Ltd. (JP) 1988-12-28 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 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-20020052373-A1 Combination treatment for dementia or cognitive deficits associated with alzheimer's disease and parkinson's disease ACHE, BCHE, CHRM4 PTPN1 4423/4885MEN1 3739/4885KMT2A 2509/4885
US-20080045500-A1 Nerve Regeneration Stimulator ACHE, NGF, GAP43 PTPN1 3825/4885MEN1 3831/4885KMT2A 3031/4885
US-20080312189-A1 Cadasil Treatment with Cholinesterase Inhibitors NOTCH3, NOTCH2, NOTCH4 PTPN1 4612/4885MEN1 927/4885KMT2A 140/4885
US-20110053981-A1 Methods and Compositions Using Cholinesterase Inhibitors PSEN1, BACE1, PSENEN PTPN1 3986/4885MEN1 571/4885KMT2A 1022/4885

“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.