SCHEMBL6582240

SCHEMBL6582240

CC(C)(C)OC(=O)NC1CCN(CC2CCNCC2)CC1

nearest known ligand 0.53

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 8/20 0.53
KCNA3 P22001 1/20 0.49
CTSK P43235 2/20 0.47
JAK2 O60674 2/20 0.44
JAK1 P23458 2/20 0.44
DRD3 P35462 1/20 0.41
BTK Q06187 1/20 0.41
CA1 P00915 1/20 0.41
CA2 P00918 1/20 0.41
CYP2C9 P11712 1/20 0.40
HSD11B1 P28845 1/20 0.40
CCR5 P51681 1/20 0.40
EPHX1 P07099 2/20 0.39

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
SCHEMBL2483799 0.90 DRD2 (0.61) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL27225010 0.90 DRD2 (0.58) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL1604214 0.86 DRD2 (0.55) DRD2KCNA3CTSKBTKCA1
SCHEMBL8187882 0.86 DRD2 (0.55) DRD2KCNA3CTSKBTKCA1
SCHEMBL30399978 0.83 DRD2 (0.55) DRD2JAK2JAK1
SCHEMBL3489007 0.83 DRD2 (0.55) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL12501447 0.82 DRD2 (0.62) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL14651348 0.82 DRD2 (0.62) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL14760990 0.82 DRD2 (0.51) DRD2KCNA3CTSKJAK2JAK1
SCHEMBL6584897 0.82 DRD2 (0.51) DRD2KCNA3CTSKJAK2JAK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4709720-A1 INHIBITORS AND DEGRADERS OF PIP4K PROTEIN Larkspur Biosciences, Inc. (US) 2026-03-18 EP disclosed
WO-2024233846-A1 INHIBITORS AND DEGRADERS OF PIP4K PROTEIN LARKSPUR BIOSCIENCES, INC. (US) 2024-11-14 WO disclosed
US-11833208-B2 PLK1 selective degradation inducing compound UPPTHERA, INC. (KR) 2023-12-05 US disclosed
US-11833208-B2 PLK1 selective degradation inducing compound UPPTHERA, INC. (KR) 2023-12-05 US disclosed
US-11833208-B2 PLK1 selective degradation inducing compound UPPTHERA, INC. (KR) 2023-12-05 US disclosed
US-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND UPPTHERA (KR) 2023-11-23 US disclosed
US-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND UPPTHERA (KR) 2023-11-23 US disclosed
US-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND UPPTHERA (KR) 2023-11-23 US disclosed
US-20230104076-A1 PLK1 Selective Degradation Inducing Compound UPPTHERA INC. (KR) 2023-04-06 US disclosed
CN-1653063-A (S)-4-amino-5-chloro-2-methoxy-N-[1-[1-(2-tetrahydrofurylcarbonyl)-4-piperidinylmethyl]-4-piperidinyl]benzamide, and method for producing the same, pharmaceutical composition containing the same and i DAINIPPON PHARMACEUTICAL CO (JP) 2005-08-10 CN disclosed
EP-1076055-B1 1- (1-SUBSTITUTED-4-PIPERIDINYL)METHYL]-4-PIPERIDINE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, MEDICINAL COMPOSITIONS CONTAINING THE SAME AND INTERMEDIATES OF THESE COMPOUNDS DAINIPPON PHARMACEUTICAL CO (JP) 2004-11-24 EP disclosed
EP-1362857-B1 (S)-4-amino-5-chloro-2-methoxy-N-[1-[1-(2-tetrahydrofuryl-carbonyl)-4-piperidinylmethyl]-4-piperidinyl]benzamide for treating gastrointestinal motility disorders DAINIPPON PHARMACEUTICAL CO (JP) 2004-08-11 EP disclosed
US-6696468-B2 GASTROINTESTINAL MOTILITY ENHANCER OR PROKINETIC AGENT; AFFINITY FOR 5-HT4 RECEPTOR; REDUCED SIDE EFFECTS TO HEART OR CENTRAL NERVOUS SYSTEM DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 2004-02-24 US disclosed
WO-2003097638-A1 (S)-4-AMINO-5-CHLORO-2-METHOXY-N-[1-[1-(2-TETRAHYDROFURYLCARBONYL)-4-PIPERIDINYLMETHYL]-4-PIPERIDINYL]BENZAMIDE, PROCESS FOR THE PREPARATION THEREOF, PHARMACEUTICAL COMPOSITION CONTAINING THE SAME, AND INTERMEDIATE THEREFOR DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 2003-11-27 WO disclosed
US-20030216433-A1 (S)-4-amino-5-chloro-2-methoxy-N-[1-[1-(2-tetrahydrofuryl-carbonyl)-4-piperidinylmethyl]-4-piperidinyl]benzamide, process for the preparation thereof, pharmaceutical composition containing the same, and intermediate therefor DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 2003-11-20 US disclosed
EP-1362857-A1 (S)-4-amino-5-chloro-2-methoxy-n-[1-[1-(2-tetrahydrofuryl-carbonyl)-4-piperidinymethyl]-4-piperidinyl]benzamide for treating gastrointestinal motility disorders Dainippon Pharmaceutical Co., Ltd. (JP) 2003-11-19 EP disclosed
US-6294555-B1 SEROTONIN HT3 RECEPTOR ANTAGONIST FOR GASTROINTESTINAL DISORDERS DAINIPPON PHARMACEUTICAL CO., LTD. (JP) 2001-09-25 US disclosed
EP-1076055-A1 1- (1-SUBSTITUTED-4-PIPERIDINYL)METHYL]-4-PIPERIDINE DERIVATIVES, PROCESS FOR PRODUCING THE SAME, MEDICINAL COMPOSITIONS CONTAINING THE SAME AND INTERMEDIATES OF THESE COMPOUNDS Dainippon Pharmaceutical Co., Ltd. (JP) 2001-02-14 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-20230372498-A1 PLK1 SELECTIVE DEGRADATION INDUCING COMPOUND PLK1, BUB1B, BUB1 DRD2 3885/4885KCNA3 3663/4885CTSK 1058/4885
US-20230104076-A1 PLK1 Selective Degradation Inducing Compound PLK1, BUB1B, BUB1 DRD2 3885/4885KCNA3 3663/4885CTSK 1058/4885
US-11833208-B2 PLK1 selective degradation inducing compound PLK1, BUB1B, BUB1 DRD2 3885/4885KCNA3 3663/4885CTSK 1058/4885
US-20030216433-A1 (S)-4-amino-5-chloro-2-methoxy-N-[1-[1-(2-tetrahydrofuryl-carbonyl)-4-piperidinylmethyl]-4-piperidinyl]benzamide, process for the preparation thereof, pharmaceutical composition containing the same, and intermediate therefor GIPR, MLNR, HTR5A DRD2 12/4885KCNA3 889/4885CTSK 3621/4885

“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.