SCHEMBL6551622

SCHEMBL6551622

CCCC(Br)c1ccccn1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNA5 P22460 5/20 0.51
KCNH2 Q12809 5/20 0.51
CYP2D6 P10635 3/20 0.49
KCNE1 P15382 1/20 0.49
TSHR P16473 2/20 0.46
SLC6A2 P23975 6/20 0.44
SLC6A4 P31645 6/20 0.44
CHRM2 P08172 6/20 0.44
SCN1A P35498 3/20 0.44
SCN2A Q99250 3/20 0.44
SCN3A Q9NY46 3/20 0.44
ALDH1A1 P00352 1/20 0.42
CYP1A2 P05177 1/20 0.42
SLC6A3 Q01959 5/20 0.42
CHRM1 P11229 5/20 0.42
HRH1 P35367 4/20 0.42
HRH3 Q9Y5N1 4/20 0.42
ADRA2B P18089 3/20 0.42
HTR2A P28223 3/20 0.42
DRD1 P21728 2/20 0.42

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
SCHEMBL28254705 0.89 KCNA5 (0.49) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL29031285 0.87 KCNA5 (0.47) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL28347623 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL21405673 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL28260638 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL28669183 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL29145046 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
Bromide SCHEMBL9168336 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
SCHEMBL28130837 0.86 KCNA5 (0.46) KCNA5KCNH2CYP2D6KCNE1TSHR
Water SCHEMBL28366590 0.84 KCNA5 (0.45) KCNA5KCNH2CYP2D6KCNE1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260078091-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2026-03-19 US disclosed
US-20240300892-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2024-09-12 US disclosed
EP-3483143-B1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC (US) 2023-10-18 EP disclosed
EP-3483143-B1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC (US) 2023-10-18 EP disclosed
EP-4092012-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2022-11-23 EP disclosed
EP-4092012-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2022-11-23 EP disclosed
US-20220169611-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2022-06-02 US disclosed
US-20220169611-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2022-06-02 US disclosed
US-20210179560-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2021-06-17 US disclosed
US-20210179560-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer AMGEN INC (US) 2021-06-17 US disclosed
US-20110319378-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2011-12-29 US disclosed
WO-2011153509-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2011-12-08 WO disclosed
WO-2011153509-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER AMGEN INC. (US) 2011-12-08 WO disclosed
EP-1044991-B1 Process of preparing curable compositions and compositions therefrom ROHM & HAAS (US) 2004-02-11 EP disclosed
US-6645562-B2 Drying a coating of a liquid addition oligomer having pendant functional groups; modifying by curing and crosslinking with an unsaturated compound having a reactive group using a free radical catalyst; films, adhesives, coatings, paints and inks GREENBLATT GARY DAVID (US) 2003-11-11 US disclosed
US-20030069363-A1 Method of preparing a curable coating and curing thereof GREENBLATT GARY DAVID (US) 2003-04-10 US disclosed
US-20020137857-A1 Forming an oligomer containing reactive functional groups,and reacting a modifier that also contains reactive function groups with the oligomer ROHM AND HAAS COMPANY 2002-09-26 US disclosed
US-6433098-B1 CROSSLINKING; PHOTOPOLYMERIZATION ROHM AND HAAS COMPANY 2002-08-13 US disclosed
EP-1044991-A1 Process of preparing curable compositions and compositions therefrom ROHM AND HAAS COMPANY (US) 2000-10-18 EP disclosed
CN-1270186-A Method for preparing curable composition and composition therefrom ROHM & HAAS (US) 2000-10-18 CN 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 (5 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-20240300892-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer MDM2, TP53, CDKN1A KCNA5 4353/4885KCNH2 4697/4885CYP2D6 2390/4885
US-20110319378-A1 PIPERIDINONE DERIVATIVES AS MDM2 INHIBITORS FOR THE TREATMENT OF CANCER MDM2, TP53, CDKN1A KCNA5 4353/4885KCNH2 4697/4885CYP2D6 2390/4885
US-20260078091-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer TP53, HIF1AN, MDM2 KCNA5 3702/4885KCNH2 4455/4885CYP2D6 3100/4885
US-20220169611-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer MDM2, TP53, CDKN1A KCNA5 4353/4885KCNH2 4697/4885CYP2D6 2390/4885
US-20210179560-A1 Piperidinone Derivatives as MDM2 Inhibitors for the Treatment of Cancer MDM2, TP53, CDKN1A KCNA5 4353/4885KCNH2 4697/4885CYP2D6 2390/4885

“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.