SCHEMBL1460113

SCHEMBL1460113

O=CCc1c(F)cccc1Cl

nearest known ligand 0.55

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 2/20 0.55
GAA P10253 1/20 0.52
HTT P42858 3/20 0.49
BACE1 P56817 1/20 0.49
KDM4E B2RXH2 1/20 0.47
KMT2A Q03164 4/20 0.46
SMN1; SMN2 Q16637 3/20 0.46
MEN1 O00255 3/20 0.46
ALDH1A1 P00352 1/20 0.46
MAPT P10636 1/20 0.45
DAO P14920 2/20 0.44
ATM Q13315 2/20 0.44
LMNA P02545 1/20 0.44
CYP2A13 Q16696 1/20 0.44
CNR1 P21554 1/20 0.43
TP53 P04637 1/20 0.43
PKM P14618 1/20 0.43
NPSR1 Q6W5P4 1/20 0.42
TDP1 Q9NUW8 1/20 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
SCHEMBL29569478 1.00 TAAR1 (0.55) TAAR1GAAHTTBACE1KDM4E
SCHEMBL168585 0.85 KMT2A (0.48) TAAR1GAAKMT2ASMN1; SMN2MEN1
SCHEMBL1459660 0.85 ERN1 (0.40) TAAR1GAAHTTBACE1KDM4E
SCHEMBL2200019 0.81 TAAR1 (0.61) TAAR1GAAHTTBACE1KDM4E
SCHEMBL8042811 0.80 TAAR1 (0.55) TAAR1GAAHTTBACE1KDM4E
SCHEMBL27479766 0.77 TAAR1 (0.52) TAAR1GAAHTTBACE1KDM4E
SCHEMBL3040407 0.77 TAAR1 (0.61) TAAR1GAAHTTBACE1KDM4E
SCHEMBL23507137 0.76 P2RX7 (0.40) TAAR1GAAKMT2ASMN1; SMN2MEN1
SCHEMBL5071067 0.76 AKR1B1 (0.44) TAAR1GAAKMT2ASMN1; SMN2MEN1
SCHEMBL5078599 0.76 EED (0.37) TAAR1GAAHTTBACE1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
US-11225655-B2 Bi-functional complexes and methods for making and using such complexes NUEVOLUTION A/S (DK) 2022-01-18 US disclosed
WO-2020146636-A1 COMPOUNDS AND METHODS FOR TREATING OR PREVENTING HEART FAILURE DREXEL UNIVERSITY (US) 2020-07-16 WO disclosed
EP-3540059-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES Nuevolution A/S (DK) 2019-09-18 EP disclosed
EP-2558577-B1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION AS (DK) 2018-12-12 EP disclosed
WO-2016191366-A1 MODULATORS FOR NICOTINIC ACETYLCHOLINE RECEPTOR α2 AND α4 SUBUNITS THE SCRIPPS RESEARCH INSTITUTE (US) 2016-12-01 WO disclosed
EP-1973917-B1 PROTEIN KINASE INHIBITORS ABBVIE INC (US) 2015-06-10 EP disclosed
US-20130281324-A1 BI-FUNCTINAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2013-10-24 US disclosed
WO-2013050270-A1 BENZOXAZINE DERIVATIVES AS CRAC MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2013-04-11 WO disclosed
US-20130023541-A1 VOLTAGE-GATED SODIUM CHANNEL BLOCKERS GLAXO GROUP LIMITED 2013-01-24 US disclosed
US-20070037829-A1 e.g. trans-(4-Phenethyloxy-cyclohexyl)-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-amine; neurodegenerative disorders, analgesic, antidepressant, anxiolytic agent; Parkinson's disease, Alzheimer's disease, epilepsy, ischemic brain injury, stroke; with other active ingredients MERCK & CO., INC. (US) 2007-02-15 US disclosed
EP-1656379-B1 4-CYCLOALKYLAMINOPYRAZOLO PYRIMIDINE NMDA/NR2B ANTAGONISTS MERCK & CO INC (US) 2007-01-10 EP disclosed
CN-1286810-C 2-acyl indol derivatives and their use as anti-tumour agents BAKST HEALTH AG (CH) 2006-11-29 CN disclosed
EP-1656379-A1 4-CYCLOALKYLAMINOPYRAZOLO PYRIMIDINE NMDA/NR2B ANTAGONISTS Merck & Co., Inc. (US) 2006-05-17 EP disclosed
US-20050054658-A1 4-Cycloalkylaminopyrazolo pyrimidine NMDA/NR2B antagonists THOMPSON WAYNE (US) 2005-03-10 US disclosed
WO-2005019221-A1 4-CYCLOALKYLAMINOPYRAZOLO PYRIMIDINE NMDA/NR2B ANTAGONISTS MERCK & CO., INC. (US) 2005-03-03 WO disclosed
CN-1431997-A 2-acylindole derivatives and their use as antitumor agents BAKST HEALTH AG (CH) 2003-07-23 CN disclosed
US-5225602-A Catalytic rearrangement of phenyl-substituted epoxide BASF AKTIENGESELLSCHAFT (DE) 1993-07-06 US disclosed
EP-0228675-B1 NEW PHENYLACETALDEHYDES AND A PROCESS FOR THE PRODUCTION OF PHENYLACETALDEHYDES BASF Aktiengesellschaft (DE) 1990-05-16 EP disclosed
EP-0228675-A2 New phenylacetaldehydes and a process for the production of phenylacetaldehydes BASF Aktiengesellschaft (DE) 1987-07-15 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 (3 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-20130023541-A1 VOLTAGE-GATED SODIUM CHANNEL BLOCKERS KCNB1, KCNB2, SCNN1B TAAR1 2156/4885GAA 2499/4885HTT 1090/4885
US-20070037829-A1 e.g. trans-(4-Phenethyloxy-cyclohexyl)-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)-amine; neurodegenerative disorders, analgesic, antidepressant, anxiolytic agent; Parkinson's disease, Alzheimer's disease, epilepsy, ischemic brain injury, stroke; with other active ingredients GRIN2B, GRIN3A, GRIN2A TAAR1 598/4885GAA 171/4885HTT 114/4885
US-20050054658-A1 4-Cycloalkylaminopyrazolo pyrimidine NMDA/NR2B antagonists GRIN2B, GRIN1, GRIN2A TAAR1 485/4885GAA 1729/4885HTT 860/4885

“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.