Piperidine

Piperidine

SCHEMBL2675445

C1CCNCC1.O=C(Cl)Cl

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.60
SMN1; SMN2 Q16637 2/20 0.41
CXCR4 P61073 1/20 0.41
CA2 P00918 2/20 0.40
CHKA P35790 1/20 0.40
EPHX1 P07099 2/20 0.36
SLC6A1 P30531 2/20 0.33
TSHR P16473 2/20 0.33
SLC6A11 P48066 1/20 0.33
GABRP O00591 1/20 0.33
GABRD O14764 1/20 0.33
GABRA1 P14867 1/20 0.33
GABRB1 P18505 1/20 0.33
GABRG2 P18507 1/20 0.33
GABRB3 P28472 1/20 0.33
GABRA5 P31644 1/20 0.33
GABRA3 P34903 1/20 0.33
GABRA2 P47869 1/20 0.33
GABRB2 P47870 1/20 0.33
GABRA4 P48169 1/20 0.33

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
Azepane SCHEMBL27420992 1.00 ALDH1A1 (0.60) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Pyrrolidine SCHEMBL1202575 0.97
Azetidine SCHEMBL17460271 0.89
Piperidine SCHEMBL4603677 0.88 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Azepane SCHEMBL9671876 0.88 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Pyrrolidine SCHEMBL3402069 0.84
Azepane SCHEMBL714889 0.83 ALDH1A1 (0.64) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Piperidine SCHEMBL720107 0.83 ALDH1A1 (0.64) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Piperidine SCHEMBL4577836 0.83 ALDH1A1 (0.64) ALDH1A1SMN1; SMN2CXCR4CA2CHKA
Piperazine SCHEMBL3987157 0.82 HIF1A (0.50) ALDH1A1SMN1; SMN2CXCR4CA2CHKA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117164596-A Coumarin compound and preparation method and application thereof 新疆农业大学 2023-12-05 CN disclosed
US-9981972-B2 N-hydroxy bicyclic hydantoin carbamates as tools for identification of serine hydrolase targets ABIDE THERAPEUTICS, INC. (US) 2018-05-29 US disclosed
US-20170183353-A1 N-HYDROXY BICYCLIC HYDANTOIN CARBAMATES AS TOOLS FOR INDETIFICATION OF SERINE HYDROLASE TARGETS H. LUNDBECK A/S (DK) 2017-06-29 US disclosed
WO-2015179563-A2 N-HYDROXY BICYCLIC HYDANTOIN CARBAMATES AS TOOLS FOR IDENTIFICATION OF SERINE HYDROLASE TARGETS ABIDE THERAPEUTICS, INC. (US) 2015-11-26 WO disclosed
US-8173648-B2 1,2,3,4-tetrahydroisoquinoline derivatives, preparation process therefor and pharmaceutical composition containing the same NATIONAL DEFENSE MEDICAL CENTER (TW) 2012-05-08 US disclosed
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same NATIONAL DEFENSE MEDICAL CENTER (TW) 2010-01-21 US disclosed
CN-101547926-A 4, 5, 6, 7-tetrahydro-thieno [3, 2-c] pyridine derivatives as H3 modulators HOFFMANN LA ROCHE (CH) 2009-09-30 CN disclosed
CN-101541810-A 4,5,6, 7-tetrahydro-thieno [2, 3-c ] pyridines as H3 modulators HOFFMANN LA ROCHE (CH) 2009-09-23 CN disclosed
CN-100486973-C Novel benzodioxoles HOFFMANN LA ROCHE (CH) 2009-05-13 CN disclosed
US-7354922-B2 Bridged ring NK1 antagonists SCHERING CORPORATION (US) 2008-04-08 US disclosed
US-20030236267-A1 Benzimidazole derivatives MSD K.K. (JP) 2003-12-25 US disclosed
WO-2002085866-A1 NOVEL COMPOUNDS ASTRAZENECA AB (SE) 2002-10-31 WO disclosed
US-5869480-A ALLEVIATING MEMORY DYSFUNCTION CHARACTERIZED BY CHOLINERGIC DEFICIT HOECHST MARION ROUSSEL INC. (US) 1999-02-09 US disclosed
US-5866565-A ALZHEIMER'S DISORDERS HOECHST MARION ROUSSEL INC. (US) 1999-02-02 US disclosed
US-5821239-A USEFUL FOR TREATING ALZHEIMER'S DISEASE CAUSED BY CHOLINERGIC DEFICIT FROMMER LAWRENCE & HUAG LLP (US) 1998-10-13 US disclosed
EP-0477903-B1 Substituted-4-amino-3-pyridinols, a process for their preparation and their use as medicaments HOECHST ROUSSEL PHARMA (US) 1996-04-03 EP disclosed
EP-0477903-A2 Substituted-4-amino-3-pyridinols, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1992-04-01 EP disclosed
EP-0147909-B1 ARYLOXY-N-(AMINOALKYL)-1-PYRROLIDINE AND PIPERIDINE CARBOXAMIDES AND CARBOTHIOAMIDES HAVING ANTIARRHYTHMIC ACTIVITY A.H. ROBINS COMPANY, INCORPORATED (US) 1989-12-06 EP disclosed
US-4547514-A Aryloxy-N-(aminoalkyl)-1-pyrrolidine and piperidine carboxamides and carbothioamides having antiarrhythmic activity A. H. ROBINS COMPANY, INCORPORATED (US) 1985-10-15 US disclosed
EP-0147909-A1 Aryloxy-N-(aminoalkyl)-1-pyrrolidine and piperidine carboxamides and carbothioamides having antiarrhythmic activity A.H. ROBINS COMPANY, INCORPORATED (US) 1985-07-10 EP 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-20030236267-A1 Benzimidazole derivatives OPRL1, GPR119, NPBWR1 ALDH1A1 1636/4885SMN1; SMN2 2200/4885CXCR4 568/4885
US-20100016309-A1 1,2,3,4-Tetrahydroisoquinoline Derivatives, Preparation Process therefor and Pharmaceutical Composition Containing the Same APP, BACE1, PSEN1 ALDH1A1 881/4885SMN1; SMN2 2712/4885CXCR4 1097/4885
US-20170183353-A1 N-HYDROXY BICYCLIC HYDANTOIN CARBAMATES AS TOOLS FOR INDETIFICATION OF SERINE HYDROLASE TARGETS HPN, BCHE, PRSS1 ALDH1A1 1289/4885SMN1; SMN2 3880/4885CXCR4 3243/4885

“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.