SCHEMBL186752

SCHEMBL186752

O=C1C(N2CCOCC2)=CCCN1c1ccccc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 1/20 0.51
▸ MAPT P10636 4/20 0.47
▸ SMN1; SMN2 Q16637 2/20 0.47
▸ RAD51 Q06609 1/20 0.47
▸ MEN1 O00255 4/20 0.43
▸ KMT2A Q03164 4/20 0.43
▸ NPC1 O15118 3/20 0.43
▸ RAB9A P51151 3/20 0.43
▸ ATM Q13315 2/20 0.43
▸ APAF1 O14727 1/20 0.43
▸ TDP2 O95551 1/20 0.43
▸ NSD2 O96028 1/20 0.43
▸ GALK1 P51570 1/20 0.43
▸ BLM P54132 1/20 0.43
▸ HKDC1 Q2TB90 1/20 0.43
▸ NOD2 Q9HC29 1/20 0.43
▸ ATG4B Q9Y4P1 1/20 0.43
▸ ALDH1A1 P00352 3/20 0.43
▸ CYP2C9 P11712 2/20 0.42
▸ AKR1C3 P42330 2/20 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
SCHEMBL15731795 0.87 PIK3R1 (0.39) LMNAMAPTSMN1; SMN2RAD51MEN1
SCHEMBL17576245 0.85 AKR1C3 (0.44) MAPTSMN1; SMN2MEN1KMT2ANPC1
SCHEMBL20050092 0.85 ALDH1A1 (0.42) LMNAMAPTSMN1; SMN2MEN1KMT2A
SCHEMBL1919863 0.85 AKR1C3 (0.44) MAPTSMN1; SMN2RAD51MEN1KMT2A
SCHEMBL6330031 0.85 KMT2A (0.49) LMNAMAPTSMN1; SMN2RAD51MEN1
SCHEMBL29483984 0.85 RAD51 (0.51) MAPTSMN1; SMN2RAD51MEN1KMT2A
SCHEMBL8014932 0.85 MAPT (0.40) LMNAMAPTSMN1; SMN2RAD51MEN1
SCHEMBL20694863 0.84 GSK3B (0.39) RAD51
SCHEMBL18028120 0.84 ALDH1A1 (0.42) MAPTSMN1; SMN2RAD51MEN1KMT2A
SCHEMBL18058760 0.84 PTGS2 (0.41) MAPTSMN1; SMN2MEN1KMT2ATDP1

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
CN-119241539-A Pyrazolo piperidine (ketone) -containing derivative, and preparation method and application thereof 沈阳药科大学 2025-01-03 — — CN disclosed
WO-2017187245-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF APIXABAN OPTIMUS DRUGS (P) LIMITED (IN) 2017-11-02 — — WO disclosed
EP-2310389-B1 HETEROCYCLES AS PROTEIN KINASE INHIBITORS AMGEN INC (US) 2012-01-04 — — EP disclosed
US-20110118285-A1 HETEROCYCLES AS PROTEIN KINASE INHIBITORS AMGEN INC. 2011-05-19 — — US disclosed
EP-2310389-A1 HETEROCYCLES AS PROTEIN KINASE INHIBITORS Amgen Inc. (US) 2011-04-20 — — EP disclosed
WO-2009143477-A1 HETEROCYCLES AS PROTEIN KINASE INHIBITORS AMGEN INC. (US) 2009-11-26 — — WO disclosed
EP-1467984-A4 SYNTHESIS OF 4,5-DIHYDRO-PYRAZOLO (3,4-C) PYRID-2-ONES BRISTOL MYERS SQUIBB CO (US) 2005-12-07 — — EP disclosed
CN-1639147-A Synthesis of 4, 5-dihydro-pyrazolo [3, 4-c ] pyridin-2-ones BRISTOL MYERS SQUIBB CO (US) 2005-07-13 — — CN disclosed
EP-1467984-A2 SYNTHESIS OF 4,5-DIHYDRO-PYRAZOLO (3,4-C) PYRID-2-ONES Bristol-Myers Squibb Company (US) 2004-10-20 — — EP disclosed
WO-2003049681-A2 SYNTHESIS OF 4,5-DIHYDRO-PYRAZOLO [3,4-C] PYRID-2-ONES BRISTOL-MYERS SQUIBB COMPANY (US) 2003-06-19 — — 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-20110118285-A1 HETEROCYCLES AS PROTEIN KINASE INHIBITORS HGF, HGFAC, MET LMNA 4022/4885MAPT 2627/4885SMN1; SMN2 2802/4885

“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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