SCHEMBL2985624

SCHEMBL2985624

O=C(O)C1(Nc2ccccc2)CCN(Cc2ccccc2)CC1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPFFR1 Q9GZQ6 5/20 0.62
NPFFR2 Q9Y5X5 5/20 0.62
OPRK1 P41145 2/20 0.62
OPRM1 P35372 1/20 0.62
OPRD1 P41143 1/20 0.62
FAAH O00519 2/20 0.57
CYP2D6 P10635 2/20 0.56
ALDH1A1 P00352 1/20 0.56
KDM4E B2RXH2 2/20 0.55
MAPT P10636 2/20 0.55
OPRL1 P41146 1/20 0.51
CHRM2 P08172 1/20 0.51
CHRM3 P20309 1/20 0.51
NPC1 O15118 1/20 0.51
TSHR P16473 1/20 0.51
RAB9A P51151 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51
CYP3A4 P08684 1/20 0.50
HSD17B10 Q99714 1/20 0.50
POLB P06746 1/20 0.50

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 SCHEMBL11455282 0.99 NPFFR1 (0.61) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL6045494 0.99 NPFFR1 (0.61) NPFFR1NPFFR2OPRK1OPRM1OPRD1
Hydrochloric Acid SCHEMBL5240984 0.99 NPFFR1 (0.61) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL11567112 0.91 FAAH (0.55) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL11566176 0.91 FAAH (0.55) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL2996293 0.89 CYP2D6 (0.68) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL3169662 0.87 NPFFR1 (0.58) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL11568366 0.87 CYP2D6 (0.58) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL7830278 0.87 ALDH1A1 (0.63) NPFFR1NPFFR2OPRK1OPRM1OPRD1
SCHEMBL3171094 0.86 NPFFR1 (0.60) NPFFR1NPFFR2OPRK1OPRM1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102442937-B Method for preparing 1-benzyl-4-aniline piperidine-4-carboxylic acid SICHUAN SAINANDE TECHNOLOGY CO LTD 2013-11-13 CN claimed
CN-102442937-A Method for preparing 1-benzyl-4-anilinopiperidine-4-carboxylic acid SICHUAN SAINANDE TECHNOLOGY CO LTD 2012-05-09 CN claimed
EP-0433048-A1 Preparation of substituted alkali metal piperidine-4-carboxylates GLAXO WELLCOME INC. (US) 1991-06-19 EP claimed
JP-7165713-A None JP disclosed
WO-2022267798-A1 μ/δ OPIOID RECEPTOR DUAL AGONIST AND MEDICAL USE THEREOF 中国人民解放军军事科学院军事医学研究院 2022-12-29 WO disclosed
WO-2022267798-A1 μ/δ OPIOID RECEPTOR DUAL AGONIST AND MEDICAL USE THEREOF 中国人民解放军军事科学院军事医学研究院 2022-12-29 WO disclosed
EP-3643704-B1 NEW INTERMEDIATES FOR THE PREPARATION OF REMIFENTANIL HYDROCHLORIDE HAMELN PHARMA GMBH (DE) 2020-12-16 EP disclosed
US-10844014-B2 Intermediates for the preparation of remifentanil hydrochloride HAMELN PHARMA GMBH (DE) 2020-11-24 US disclosed
US-20200131127-A1 INTERMEDIATES FOR THE PREPARATION OF REMIFENTANIL HYDROCHLORIDE HAMELN PHARMA PLUS GMBH (DE) 2020-04-30 US disclosed
EP-3643704-A1 NEW INTERMEDIATES FOR THE PREPARATION OF REMIFENTANIL HYDROCHLORIDE hameln pharma plus gmbh (DE) 2020-04-29 EP disclosed
EP-3199523-A1 THE NEW PROCESS FOR PRODUCING N-PHENYL-N-(4-PIPERIDINYL) AMIDE DERIVATIVES SUCH AS REMIFENTANIL AND CARFENTANIL Bioka s. r.o. (SK) 2017-08-02 EP disclosed
US-7208604-B2 Methods for the synthesis of alfentanil, sufentanil, and remifentanil MALLINCKRODT INC. (US) 2007-04-24 US disclosed
US-20070054911-A1 Muscarinic modulators VERTEX PHARMACEUTICALS INCORPORATED 2007-03-08 US disclosed
US-20070054911-A1 Muscarinic modulators VERTEX PHARMACEUTICALS INCORPORATED 2007-03-08 US disclosed
US-20070054911-A1 Muscarinic modulators VERTEX PHARMACEUTICALS INCORPORATED 2007-03-08 US disclosed
US-20060252797-A1 Receptor regulator TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2006-11-09 US disclosed
WO-2006105035-A2 MUSCARINIC MODULATORS VERTEX PHARMACEUTICALS INCORPORATED (US) 2006-10-05 WO disclosed
EP-1559428-A1 RECEPTOR REGULATOR Takeda Pharmaceutical Company Limited (JP) 2005-08-03 EP disclosed
JP-H07165713-A CHEMICAL PROCESS GLAXO GROUP LTD 1995-06-27 JP disclosed
EP-0433048-A1 Preparation of substituted alkali metal piperidine-4-carboxylates GLAXO WELLCOME INC. (US) 1991-06-19 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 (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-20070054911-A1 Muscarinic modulators CHRM3, CHRM5, CHRM4 NPFFR1 591/4885NPFFR2 571/4885OPRK1 118/4885
US-20060252797-A1 Receptor regulator NMUR1, NMUR2, NMBR NPFFR1 39/4885NPFFR2 80/4885OPRK1 146/4885
US-10844014-B2 Intermediates for the preparation of remifentanil hydrochloride OPRK1, OPRM1, OPRD1 NPFFR1 1217/4885NPFFR2 969/4885OPRK1 1/4885
US-20200131127-A1 INTERMEDIATES FOR THE PREPARATION OF REMIFENTANIL HYDROCHLORIDE OPRK1, OPRM1, OPRD1 NPFFR1 1217/4885NPFFR2 969/4885OPRK1 1/4885

“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.