SCHEMBL4279383

SCHEMBL4279383

O=C(c1ccccc1)N1CCc2ccccc2C1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HPGD P15428 11/20 0.73
▸ LMNA P02545 2/20 0.73
▸ ALDH1A1 P00352 7/20 0.70
▸ SMN1; SMN2 Q16637 4/20 0.70
▸ CA1 P00915 1/20 0.68
▸ CA2 P00918 1/20 0.68
▸ CA7 P43166 1/20 0.68
▸ CA9 Q16790 1/20 0.68
▸ CA14 Q9ULX7 1/20 0.68
▸ NAMPT P43490 1/20 0.68
▸ CYP3A4 P08684 2/20 0.67
▸ CYP2C19 P33261 2/20 0.67
▸ CYP2D6 P10635 1/20 0.67
▸ NOTUM Q6P988 1/20 0.64
▸ HTT P42858 3/20 0.62
▸ CYP2C9 P11712 1/20 0.62
▸ MEN1 O00255 2/20 0.62
▸ KMT2A Q03164 2/20 0.62
▸ TP53 P04637 2/20 0.62
▸ MAPT P10636 1/20 0.62

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
SCHEMBL30277860 1.00 HPGD (0.73) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL10414745 0.88 HPGD (0.74) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL14818002 0.87 HPGD (0.66) HPGDLMNAALDH1A1SMN1; SMN2CA1
Hydrochloric Acid SCHEMBL10414730 0.87 HPGD (0.72) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL13211911 0.87 HTT (0.71) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL31396748 0.87 HPGD (0.66) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL12459664 0.87 CA1 (0.70) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL94624 0.87 HPGD (0.66) HPGDLMNAALDH1A1SMN1; SMN2CA1
SCHEMBL4167985 0.87 NAMPT (0.64) HPGDLMNAALDH1A1SMN1; SMN2NAMPT
SCHEMBL16523571 0.84 CA1 (0.61) HPGDLMNAALDH1A1SMN1; SMN2CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7534793-B2 Aminopiperidine quinolines and their azaisosteric analogues with antibacterial activity SMITHKLINE BEECHAM P.L.C. (GB) 2009-05-19 — — US claimed
US-20230145822-A1 SMALL MOLECULES INDUCING THE DEGRADATION OF THE CELLULAR PRION PROTEIN FONDAZIONE TELETHON (IT) 2023-05-11 — — US disclosed
US-20230145822-A1 SMALL MOLECULES INDUCING THE DEGRADATION OF THE CELLULAR PRION PROTEIN FONDAZIONE TELETHON (IT) 2023-05-11 — — US disclosed
WO-2022258986-A1 COMPOUNDS USEFUL IN THE TREATMENT OR PREVENTION OF A PRMT5-MEDIATED DISORDER Argonaut Therapeutics Limited (GB) 2022-12-15 — — WO disclosed
EP-1773786-B1 FIVE-MEMBERED HETEROCYCLES USEFUL AS SERINE PROTEASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2017-04-26 — — EP disclosed
US-9278905-B2 Production method for compound comprising amino group and/or hydroxyl group KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (JP) 2016-03-08 — — US disclosed
US-9278905-B2 Production method for compound comprising amino group and/or hydroxyl group KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (JP) 2016-03-08 — — US disclosed
EP-2867210-A1 A PROCESS FOR THE PREPARATION OF SOLIFENACIN OR A SALT THEREOF Pharmathen S.A. (GR) 2015-05-06 — — EP disclosed
US-20150105559-A1 PRODUCTION METHOD FOR COMPOUND COMPRISING AMINO GROUP AND/OR HYDROXYL GROUP KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (JP) 2015-04-16 — — US disclosed
US-20150105559-A1 PRODUCTION METHOD FOR COMPOUND COMPRISING AMINO GROUP AND/OR HYDROXYL GROUP KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (JP) 2015-04-16 — — US disclosed
EP-2821389-A1 PRODUCTION METHOD FOR COMPOUND COMPRISING AMINO GROUP AND/OR HYDROXYL GROUP Kyushu University, National University Corporation (JP) 2015-01-07 — — EP disclosed
WO-2014005601-A1 A PROCESS FOR THE PREPARATION OF SOLIFENACIN OR A SALT THEREOF PHARMATHEN S.A. (GR) 2014-01-09 — — WO disclosed
US-20090075978-A1 SUBSTITUTED PROPIOLIC ACID AMIDES AND THEIR USE FOR PRODUCING DRUGS GRUNENTHAL GMBH (DE) 2009-03-19 — — US disclosed
WO-2007079957-A1 SUBSTITUTED PROPIOLIC ACID AMIDES AND THEIR USE FOR PRODUCING DRUGS Grünenthal GmbH (DE) 2007-07-19 — — 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 (3 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-20150105559-A1 PRODUCTION METHOD FOR COMPOUND COMPRISING AMINO GROUP AND/OR HYDROXYL GROUP CA7, DAO, CA4 HPGD 264/4885LMNA 2891/4885ALDH1A1 732/4885
US-20090075978-A1 SUBSTITUTED PROPIOLIC ACID AMIDES AND THEIR USE FOR PRODUCING DRUGS PCCA, PPARA, PTGES HPGD 64/4885LMNA 2581/4885ALDH1A1 360/4885
US-20230145822-A1 SMALL MOLECULES INDUCING THE DEGRADATION OF THE CELLULAR PRION PROTEIN PRNP, PPIE, PPIC HPGD 1484/4885LMNA 1493/4885ALDH1A1 4190/4885

“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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