SCHEMBL327233

SCHEMBL327233

c1ccc(C2NCCc3ccccc32)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PRCP P42785 6/20 1.00
GAA P10253 1/20 0.96
RECQL P46063 1/20 0.74
GID4 Q8IVV7 3/20 0.68
KDM1A O60341 1/20 0.62
MEN1 O00255 1/20 0.57
KMT2A Q03164 1/20 0.57
DRD2 P14416 1/20 0.55
DRD1 P21728 1/20 0.55
SLC22A1 O15245 1/20 0.54

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
SCHEMBL29478499 1.00 PRCP (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL30721685 1.00 PRCP (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL325083 1.00 PRCP (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL12046710 1.00 PRCP (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL1668148 1.00 PRCP (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL1694774 0.98 PRCP (0.96) PRCPGAARECQLGID4KDM1A
Hydrochloric Acid SCHEMBL1735508 0.98 GAA (1.00) PRCPGAARECQLGID4KDM1A
SCHEMBL1694744 0.98 PRCP (0.96) PRCPGAARECQLGID4KDM1A
SCHEMBL1694844 0.98 PRCP (0.96) PRCPGAARECQLGID4KDM1A
SCHEMBL19610875 0.98 PRCP (0.96) PRCPGAARECQLGID4KDM1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025111482-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS BEXSON BIOMEDICAL, INC. (US) 2025-05-30 WO claimed
CN-117263929-A Preparation method of circularly polarized light-emitting heat-activating delayed fluorescent material 宁波工程学院 2023-12-22 CN claimed
CN-111574448-B Preparation method of phenyl tetrahydroisoquinoline 广东东阳光药业股份有限公司 2023-10-20 CN claimed
CN-111621805-B Method for preparing 3, 4-dihydroisoquinoline by electrocatalytic selective dehydrogenation 天津大学 2022-02-18 CN claimed
CN-111943134-A Room-temperature dehydrogenation reaction system of photocatalytic organic liquid hydrogen storage material and preparation method and application thereof 中国科学院理化技术研究所 2020-11-17 CN claimed
CN-111925266-A Preparation method of (S) -1-phenyl-1, 2,3, 4-tetrahydroisoquinoline 西华大学 2020-11-13 CN claimed
CN-111621805-A Method for preparing 3, 4-dihydroisoquinoline by electrocatalytic selective dehydrogenation 天津大学 2020-09-04 CN claimed
CN-111574448-A Preparation method of phenyltetrahydroisoquinoline 广东东阳光药业有限公司 2020-08-25 CN claimed
EP-2406257-B1 A NEW METHOD FOR THE PREPARATION OF SOLIFENACIN AND NEW INTERMEDIATE THEREOF MEGAFINE PHARMA P LTD (IN) 2019-08-07 EP claimed
CN-109438348-A The preparation method and preparation method thereof of one kind (S) -1- phenyl -1,2,3,4- tetrahydroisoquinoline 凯瑞斯德生化(苏州)有限公司 2019-03-08 CN claimed
EP-1879867-A2 INTERMEDIATES FOR PREPARING SOLIFENACIN Teva Pharmaceutical Industries Ltd (IL) 2008-01-23 EP claimed
CN-101094672-A 4-phenyl substituted tetrahydroisoquinolines and their use to block reuptake of norepinephrine, dopamine, and 5-hydroxytryptamine AMR TECHNOLOGY INC (US) 2007-12-26 CN claimed
WO-2007076116-A2 INTERMEDIATES FOR PREPARING SOLIFENACIN TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2007-07-05 WO claimed
US-6967199-B2 Substituted diamine derivatives useful as motilin antagonists ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2005-11-22 US claimed
US-20030203906-A1 A phenylamide derivatives for treating gastrointestinal reflux disorders, eating disorder obesity and irritable bowel disorder JOHNSON SIGMONG G (US) 2003-10-30 US claimed
CN-1440390-A Substituted diamine derivatives as motilin antagonists ORTHO MCNEIL PHARM INC (US) 2003-09-03 CN claimed
CN-1413197-A 4-phenyl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine and serotonin ALBANY MOLECULAR RES CO (US) 2003-04-23 CN claimed
EP-1294695-A2 SUBSTITUTED DIAMIDE DERIVATIVES USEFUL AS MOTILIN ANTAGONISTS Ortho-McNeil Pharmaceutical, Inc. (US) 2003-03-26 EP claimed
US-20020013352-A1 For therapy of gastrointestinal reflux disorders, eating disorders leading to obesity and irritable bowel disorder ORTHO-MCNEIL PHARMACEUTICAL, INC. 2002-01-31 US claimed
WO-2001085694-A2 SUBSTITUTED DIAMIDE DERIVATIVES USEFUL AS MOTILIN ANTAGONISTS ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2001-11-15 WO claimed

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-20020013352-A1 For therapy of gastrointestinal reflux disorders, eating disorders leading to obesity and irritable bowel disorder MLNR, GIPR, NPY1R PRCP 1396/4885GAA 447/4885RECQL 376/4885
US-20030203906-A1 A phenylamide derivatives for treating gastrointestinal reflux disorders, eating disorder obesity and irritable bowel disorder MLNR, GIPR, NPY1R PRCP 1213/4885GAA 477/4885RECQL 789/4885

“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.