SCHEMBL5035207

SCHEMBL5035207

N#Cc1ccccc1CC=O

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 1/20 0.42
ALDH1A1 P00352 5/20 0.41
SMN1; SMN2 Q16637 4/20 0.41
MAPT P10636 2/20 0.41
TSHR P16473 1/20 0.40
CNR2 P34972 1/20 0.38
FFAR1 O14842 1/20 0.38
CTSB P07858 1/20 0.38
CA1 P00915 1/20 0.37
CA2 P00918 1/20 0.37
NPSR1 Q6W5P4 2/20 0.37
GALR3 O60755 1/20 0.37
RAB9A P51151 1/20 0.37
NOX4 Q9NPH5 1/20 0.37
LMNA P02545 1/20 0.37
PKM P14618 1/20 0.37
HPGD P15428 1/20 0.37
MAPK1 P28482 1/20 0.37
HTT P42858 1/20 0.37
GPR55 Q9Y2T6 1/20 0.37

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
SCHEMBL4549081 0.81 NOTUM (0.34) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL20243770 0.80 CYP19A1 (0.40) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL30669699 0.80 CYP19A1 (0.40) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL28879999 0.79 CYP19A1 (0.42) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL2162474 0.79 GABRA1 (0.42) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL23599602 0.79 CYP1A1 (0.30)
SCHEMBL2372208 0.79 TSHR (0.45) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL2724407 0.79 CYP19A1 (0.48) CYP19A1ALDH1A1SMN1; SMN2MAPTCA1
SCHEMBL25620334 0.78 CYP19A1 (0.41) CYP19A1ALDH1A1SMN1; SMN2MAPTTSHR
SCHEMBL7461135 0.77 TDP1 (0.38) ALDH1A1SMN1; SMN2TSHRCA2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111936144-B JAK inhibitors 廖细斌 2023-12-22 CN claimed
EP-3143055-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP Bridgestone Corporation (JP) 2017-03-22 EP claimed
WO-2015175280-A2 POLYMERS FUNCTIONALIZED WITH PROTECTED OXIME COMPOUNDS CONTAINING A CYANO GROUP BRIDGESTONE CORPORATION (JP) 2015-11-19 WO claimed
WO-2025085560-A1 LYSINE ACETYLTRANSFERASE INHIBITORS Kronos Bio, Inc. (US) 2025-04-24 WO disclosed
CN-111936144-B JAK inhibitors 廖细斌 2023-12-22 CN disclosed
CN-114213410-B Synthesis method of aromatic ring [ a ] carbazole compound and aromatic ring [ g ] pyridine indole compound 湖南师范大学 2023-03-14 CN disclosed
CN-114956933-A Marker containing isotope oxygen atom and preparation method and application thereof 清华大学 2022-08-30 CN disclosed
CN-110325531-B Benzenesulfonamides and their use as therapeutic agents 泽农医药公司 2022-05-27 CN disclosed
CN-114213410-A Synthesis method of aromatic ring [ a ] carbazole compound and aromatic ring [ g ] pyridine indole compound 湖南师范大学 2022-03-22 CN disclosed
US-11174268-B2 Benzenesulfonamide compouds and their use as therapeutic agents XENON PHARMACEUTICALS INC. (CA) 2021-11-16 US disclosed
US-11174268-B2 Benzenesulfonamide compouds and their use as therapeutic agents XENON PHARMACEUTICALS INC. (CA) 2021-11-16 US disclosed
EP-1940856-A1 NOVEL UROKINASE INHIBITORS Universiteit Antwerpen (BE) 2008-07-09 EP disclosed
WO-2007045496-A1 NOVEL UROKINASE INHIBITORS UNIVERSITEIT ANTWERPEN (BE) 2007-04-26 WO disclosed
US-6956046-B2 4-hydroxypiperidine derivatives having analgesic activity MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2005-10-18 US disclosed
US-20040176410-A1 4-hydroxpiperdine derivative with analgetic activity MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2004-09-09 US disclosed
EP-1391452-A1 4-HYDROXPIPERIDINE DERIVATIVE WITH ANALGETIC ACTIVITY MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2004-02-25 EP disclosed
EP-1346994-A1 CHOLESTEROL BIOSYNTHESIS INHIBITORS CONTAINING AS THE ACTIVE INGREDIENT TRICYCLIC SPIRO COMPOUNDS MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2003-09-24 EP disclosed
US-4876266-A DOPAMINE-B-HYDROXYLASE INHIBITORS SMITHKLINE BECKMAN CORPORATION (US) 1989-10-24 US disclosed
EP-0329900-A1 Substituted 1-aralkyl imidazoline-2-thiols SMITHKLINE BEECHAM CORPORATION (US) 1989-08-30 EP disclosed
WO-1989006126-A1 1-ARALKYL-2-MERCAPTOIMIDAZOLINES AS DOPAMINE-beta-HYDROXYLASE INHIBITORS SMITHKLINE BECKMAN CORPORATION (US) 1989-07-13 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 (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-20040176410-A1 4-hydroxpiperdine derivative with analgetic activity HNMT, HDAC1, HDAC3 CYP19A1 1180/4885ALDH1A1 416/4885SMN1; SMN2 485/4885
US-11174268-B2 Benzenesulfonamide compouds and their use as therapeutic agents KCND2, SCN1A, CACNA1D CYP19A1 2954/4885ALDH1A1 2649/4885SMN1; SMN2 467/4885

“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.