SCHEMBL18955751

SCHEMBL18955751

Oc1ccc2ccccc2c1CN1CCCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 11/20 1.00
KDM4E B2RXH2 11/20 1.00
ALDH1A1 P00352 9/20 1.00
GAA P10253 6/20 1.00
CRHBP P24387 1/20 0.97
CRHR2 Q13324 1/20 0.97
KMT2A Q03164 7/20 0.75
TDP1 Q9NUW8 4/20 0.71
HTT P42858 2/20 0.71
HPGD P15428 2/20 0.71
HSD17B10 Q99714 4/20 0.64
MEN1 O00255 2/20 0.64
CYP1A2 P05177 1/20 0.58
CYP2C9 P11712 1/20 0.58
CYP2C19 P33261 1/20 0.58
MAPK1 P28482 1/20 0.57
ALOX12 P18054 1/20 0.57
ERN1 O75460 1/20 0.55
TAAR1 Q96RJ0 1/20 0.54
GLA P06280 1/20 0.50

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
SCHEMBL29432837 1.00 MAPT (1.00) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL30294879 0.98 CRHBP (1.00) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL13700903 0.98 CRHBP (1.00) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL23802529 0.86 MAPT (0.75) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL30616755 0.86 MAPT (0.75) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL6057649 0.86 KDM4E (1.00) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL31618184 0.84 KDM4E (0.72) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL15347439 0.83 KDM4E (1.00) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL13969347 0.81 KDM4E (0.85) MAPTKDM4EALDH1A1GAACRHBP
SCHEMBL31618209 0.81 KDM4E (0.68) MAPTKDM4EALDH1A1GAACRHBP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117024364-A Pyrazole ionic liquid and method for catalyzing Betti reaction by using pyrazole ionic liquid 山西师范大学 2023-11-10 CN claimed
CN-117024364-A Pyrazole ionic liquid and method for catalyzing Betti reaction by using pyrazole ionic liquid 山西师范大学 2023-11-10 CN disclosed
US-11638706-B2 Methods for treating Huntington's disease PTC THERAPEUTICS, INC. (US) 2023-05-02 US disclosed
EP-3638318-A1 METHODS FOR MODIFYING RNA SPLICING PTC Therapeutics, Inc. (US) 2020-04-22 EP disclosed
WO-2018232039-A1 METHODS FOR MODIFYING RNA SPLICING PTC THERAPEUTICS, INC. (US) 2018-12-20 WO disclosed
EP-3386511-A1 METHODS FOR TREATING HUNTINGTON'S DISEASE PTC Therapeutics, Inc. (US) 2018-10-17 EP disclosed
WO-2017100726-A1 METHODS FOR TREATNG HUNTINGTON'S DISEASE PTC THERAPEUTICS, INC. (US) 2017-06-15 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 (1 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-11638706-B2 Methods for treating Huntington's disease HTT, HYPK, FH MAPT 16/4885KDM4E 3361/4885ALDH1A1 1311/4885

“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.