SCHEMBL638646

SCHEMBL638646

O=C(c1ccccc1)C1CCCNC1

nearest known ligand 0.64

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SLC6A1 P30531 2/20 0.56
SLC6A11 P48066 1/20 0.56
TSHR P16473 1/20 0.56
LMNA P02545 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
SLC6A13 Q9NSD5 1/20 0.56
KMT2A Q03164 2/20 0.54
KDM4E B2RXH2 1/20 0.50
MAPT P10636 1/20 0.50
ATM Q13315 1/20 0.50
CYP2D6 P10635 1/20 0.50
MCL1 Q07820 1/20 0.44
SRD5A2 P31213 1/20 0.44

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
Hydrochloric Acid SCHEMBL4028302 0.98 SLC6A1 (0.55) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL407286 0.89 KMT2A (0.53) TSHRKMT2ACYP2D6MCL1
Hydrochloric Acid SCHEMBL440964 0.88 KMT2A (0.56) KMT2ACYP2D6MCL1
Tert-Butyl Formate SCHEMBL27689725 0.85 KMT2A (0.42) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
Tert-Butyl Formate SCHEMBL27751802 0.85 KMT2A (0.42) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL2323451 0.83 HSD11B1 (0.49) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL5583005 0.83 KMT2A (0.51) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL4671412 0.83 MGLL (0.49) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL7001156 0.83 KMT2A (0.64) SLC6A1SLC6A11TSHRLMNASMN1; SMN2
SCHEMBL4777663 0.83 MGLL (0.47) SLC6A1SLC6A11TSHRLMNASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112707857-A Method for preparing piperidine compound by hydrogen transfer reduction of pyridine compound 西南石油大学 2021-04-27 CN disclosed
US-20200131125-A1 ARYL-PIPERIDINE DERIVATIVES ARTAX BIOPHARMA INC. 2020-04-30 US disclosed
US-20200131125-A1 ARYL-PIPERIDINE DERIVATIVES ARTAX BIOPHARMA INC. 2020-04-30 US disclosed
WO-2018170078-A1 ARYL-PIPERIDINE DERIVATIVES ARTAX BIOPHARMA, INC. (US) 2018-09-20 WO disclosed
EP-3375778-A1 ARYL-PIPERIDINE DERIVATIVES Artax Biopharma Inc. (US) 2018-09-19 EP disclosed
EP-2909170-A1 SUBSTITUTED CARBAMATE COMPOUNDS AND THEIR USE AS TRANSIENT RECEPTOR POTENTIAL (TRP) CHANNEL ANTAGONISTS F. Hoffmann-La Roche AG (CH) 2015-08-26 EP disclosed
US-20150218141-A1 SUBSTITUTED CARBAMATE COMPOUNDS HOFFMANN-LA ROCHE INC. (US) 2015-08-06 US disclosed
US-8741934-B2 Inhibitors of ion channels PFIZER LIMITED (GB) 2014-06-03 US disclosed
US-8741934-B2 Inhibitors of ion channels PFIZER LIMITED (GB) 2014-06-03 US disclosed
WO-2014060341-A1 SUBSTITUTED CARBAMATE COMPOUNDS AND THEIR USE AS TRANSIENT RECEPTOR POTENTIAL (TRP) CHANNEL ANTAGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2014-04-24 WO disclosed
EP-0983238-A4 PROCESSES AND INTERMEDIATES FOR RESOLVING PIPERIDYL ACETAMIDE STEREOISOMERS CELGENE CORP (US) 2001-08-08 EP disclosed
EP-1082307-A1 PROCESSES AND INTERMEDIATES FOR PREPARING 2-SUBSTITUTED PIPERIDINE STEREOISOMERS CELGENE CORPORATION (US) 2001-03-14 EP disclosed
EP-0983238-A1 PROCESSES AND INTERMEDIATES FOR RESOLVING PIPERIDYL ACETAMIDE STEREOISOMERS CELGENE CORPORATION (US) 2000-03-08 EP disclosed
WO-1999061425-A1 PROCESSES AND INTERMEDIATES FOR PREPARING 2-SUBSTITUTED PIPERIDINE STEREOISOMERS CELGENE CORPORATION (US) 1999-12-02 WO disclosed
US-5965734-A REACTING 2-SUBSTITUTED PYRIDINE WITH HYDROGEN IN THE PRESENCE OF CATALYST AND ALKANOIC ACID, ADDING AKLYL ALKANOATE, AND THEN REACTING WITH AQUEOUS BASE THEN WITH ACID AND RESOLVING AGENT TO FORM ACID SALTS OF 1-ERYTHRO PIPERIDINE STEREOSIOMERS CELGENE CORPORATION (US) 1999-10-12 US disclosed
US-5936091-A Processes and intermediates for resolving piperidyl acetamide stereoisomers CELGENE CORPORATION (US) 1999-08-10 US disclosed
WO-1998052921-A1 PROCESSES AND INTERMEDIATES FOR RESOLVING PIPERIDYL ACETAMIDE STEREOISOMERS CELGENE CORPORATION (US) 1998-11-26 WO disclosed
EP-0028473-A1 Chloro- and alkoxy-substituted-2,4-diaminoquinazolines and pharmaceutical compositions containing them PFIZER INC. (US) 1981-05-13 EP disclosed
US-4101662-A DISUBSTITUTED PIPERIDINES A. H. ROBINS COMPANY, INCORPORATED (US) 1978-07-18 US disclosed
US-3968217-A ANTIDEPRESSANT A. H. ROBINS COMPANY, INCORPORATED (US) 1976-07-06 US 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-20200131125-A1 ARYL-PIPERIDINE DERIVATIVES CD4, CD2, CCR1 SLC6A1 4617/4885SLC6A11 4836/4885TSHR 1207/4885
US-20150218141-A1 SUBSTITUTED CARBAMATE COMPOUNDS TRPA1, TRPV1, TRPV3 SLC6A1 357/4885SLC6A11 529/4885TSHR 1185/4885

“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.