SCHEMBL2554077

SCHEMBL2554077

CC[C@](O)(c1cccc(O)c1)[C@@H](C)CN(C)C

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.50
CYP2D6 P10635 2/20 0.50
CYP2C19 P33261 1/20 0.50
HSD17B10 Q99714 1/20 0.50
OPRM1 P35372 7/20 0.47
SLC22A1 O15245 1/20 0.47
CYP3A4 P08684 2/20 0.40
MEN1 O00255 1/20 0.39
TTR P02766 1/20 0.39
KMT2A Q03164 1/20 0.39
OPRD1 P41143 6/20 0.37
OPRK1 P41145 5/20 0.37
KCNH2 Q12809 3/20 0.37
HTR2A P28223 2/20 0.37
ADRA1A P35348 2/20 0.37
MRGPRX2 Q96LB1 1/20 0.37
CHRM3 P20309 1/20 0.37
HRH2 P25021 1/20 0.37
LMNA P02545 1/20 0.35
MAPT P10636 1/20 0.35

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
SCHEMBL3899366 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
SCHEMBL354619 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
SCHEMBL3893895 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
SCHEMBL4495715 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
SCHEMBL174568 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
SCHEMBL3908680 1.00 ALDH1A1 (0.50) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
Hydrochloric Acid SCHEMBL7673673 0.99 ALDH1A1 (0.49) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
Hydrochloric Acid SCHEMBL7673668 0.99 ALDH1A1 (0.49) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
Cadaverine Tartrate SCHEMBL2551513 0.90 LMNA (0.45) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1
Cadaverine Tartrate SCHEMBL2551782 0.90 LMNA (0.45) ALDH1A1CYP2D6CYP2C19HSD17B10OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130096347-A1 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2013-04-18 US claimed
EP-2556048-A2 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF Actavis Group PTC EHF (IS) 2013-02-13 EP claimed
WO-2011128784-A2 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2011-10-20 WO claimed
EP-1633697-B1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS GRUENENTHAL GMBH (DE) 2009-03-11 EP claimed
US-7417170-B2 Process for the preparation of substituted 3-aryl-butylamine compounds GRUENENTHAL GMBH (DE) 2008-08-26 US claimed
US-20060194988-A1 Process for the preparation of substitued 3-aryl-butylamine compounds GRUENENTHAL GMBH 2006-08-31 US claimed
EP-1633697-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS Grünenthal GmbH (DE) 2006-03-15 EP claimed
WO-2004108658-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS Grünenthal GmbH (DE) 2004-12-16 WO claimed
WO-2014005546-A1 PREPARATION METHOD OF TAPENTADOL HYDROCHLORIDE AND COMPOUNDS FOR PREPARATION OF TAPENTADOL HYDROCHLORIDE 江苏恩华药业股份有限公司 (CN) 2014-01-09 WO disclosed
US-20130096347-A1 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2013-04-18 US disclosed
US-20130096347-A1 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2013-04-18 US disclosed
US-20130096347-A1 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2013-04-18 US disclosed
EP-2556048-A2 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF Actavis Group PTC EHF (IS) 2013-02-13 EP disclosed
WO-2011128784-A2 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2011-10-20 WO disclosed
WO-2011128784-A2 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF ACTAVIS GROUP PTC EHF (IS) 2011-10-20 WO disclosed
EP-1633697-B1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS GRUENENTHAL GMBH (DE) 2009-03-11 EP disclosed
US-7417170-B2 Process for the preparation of substituted 3-aryl-butylamine compounds GRUENENTHAL GMBH (DE) 2008-08-26 US disclosed
US-20060194988-A1 Process for the preparation of substitued 3-aryl-butylamine compounds GRUENENTHAL GMBH 2006-08-31 US disclosed
EP-1633697-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS Grünenthal GmbH (DE) 2006-03-15 EP disclosed
WO-2004108658-A1 METHOD FOR THE PRODUCTION OF SUBSTITUTED 3-ARYL-BUTYL AMINE COMPOUNDS Grünenthal GmbH (DE) 2004-12-16 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 (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-20060194988-A1 Process for the preparation of substitued 3-aryl-butylamine compounds BRD3, TYR, BBOX1 ALDH1A1 543/4885CYP2D6 134/4885CYP2C19 467/4885
US-20130096347-A1 NOVEL PROCESS FOR PREPARING HIGHLY PURE TAPENTADOL OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF TPMT, OPRD1, COMT ALDH1A1 681/4885CYP2D6 94/4885CYP2C19 202/4885

“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.