SCHEMBL874147

SCHEMBL874147

[c]1ccc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNN4 O15554 3/20 0.43
KIF11 P52732 1/20 0.36
MAPK1 P28482 1/20 0.33
ALDH1A1 P00352 3/20 0.32
TSHR P16473 2/20 0.32
NR3C2 P08235 2/20 0.32
HDAC3 O15379 1/20 0.31
HDAC4 P56524 1/20 0.31
HDAC1 Q13547 1/20 0.31
HDAC7 Q8WUI4 1/20 0.31
HDAC2 Q92769 1/20 0.31
HDAC10 Q969S8 1/20 0.31
HDAC11 Q96DB2 1/20 0.31
HDAC8 Q9BY41 1/20 0.31
HDAC6 Q9UBN7 1/20 0.31
HDAC9 Q9UKV0 1/20 0.31
HDAC5 Q9UQL6 1/20 0.31
TAAR1 Q96RJ0 1/20 0.31
ALOX15 P16050 1/20 0.31
ESR1 P03372 2/20 0.30

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
SCHEMBL11279906 0.84 KCNN4 (0.52) KCNN4KIF11MAPK1ALDH1A1TSHR
SCHEMBL27675660 0.79 KCNN4 (0.40) KCNN4KIF11MAPK1ALDH1A1TSHR
Biphenyl SCHEMBL7519251 0.76 KCNN4 (0.44) KCNN4KIF11MAPK1ALDH1A1TSHR
SCHEMBL23112981 0.74 KCNN4 (0.43) KCNN4KIF11MAPK1ALDH1A1TSHR
SCHEMBL18035826 0.74 ALDH1A1 (0.44) KCNN4KIF11MAPK1ALDH1A1
SCHEMBL7535593 0.74 KCNN4 (0.39) KCNN4KIF11MAPK1ALDH1A1TSHR
SCHEMBL27860651 0.71 KCNN4 (0.44) KCNN4MAPK1ALDH1A1TSHRTAAR1
SCHEMBL654702 0.71 MAPK13 (0.42) KCNN4ALDH1A1HDAC3HDAC4HDAC1
SCHEMBL2164357 0.70 ESR1 (0.54) KCNN4MAPK1ALDH1A1TSHRHDAC3
SCHEMBL294517 0.70 ESR1 (0.54) KCNN4MAPK1ALDH1A1TSHRNR3C2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9714560-B2 Protected scale inhibitors and methods relating thereto HALLIBURTON ENERGY SERVICES, INC. (US) 2017-07-25 US claimed
US-20240228433-A1 COMPOUNDS AND METHODS FOR LIQUID PHASE OLIGONUCLEOTIDE SYNTHESIS HONGENE BIOTECH CORPORATION 2024-07-11 US disclosed
CN-118317970-A Synthesis of 2' acetyl-ester protected nucleosides 兆维生物科技公司 2024-07-09 CN disclosed
WO-2024137756-A1 COMPOUNDS AND METHODS FOR LIQUID PHASE OLIGONUCLEOTIDE SYNTHESIS HONGENE BIOTECH CORPORATION (US) 2024-06-27 WO disclosed
WO-2024118503-A1 FUNCTIONALIZED N-ACETYLGALACTOSAMINE ANALOGS HONGENE BIOTECH CORPORATION (US) 2024-06-06 WO disclosed
US-11993626-B2 Functionalized N-acetylgalactosamine analogs HONGENE BIOTECH CORPORATION (US) 2024-05-28 US disclosed
EP-4355336-A1 PRODRUGS OF DEOXYNUCLEOSIDES FOR TREATMENT OF MITOCHONDRIAL DISEASES CAUSED BY UNBALANCED NUCLEOTIDE POOLS Zogenix, Inc. (US) 2024-04-24 EP disclosed
US-11897914-B2 Synthesis of 2′ protected nucleosides HONGENE BIOTECH CORPORATION (US) 2024-02-13 US disclosed
CN-117500510-A Deoxynucleoside prodrugs for treating mitochondrial diseases caused by unbalanced nucleotide pools 周格尼克斯公司 2024-02-02 CN disclosed
US-20230416295-A1 SYNTHESIS OF 2' PROTECTED NUCLEOSIDES HONGENE BIOTECH CORPORATION 2023-12-28 US disclosed
US-20130109850-A1 MODIFIED 5' DIPHOSPHATE NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM ISIS PHARMACEUTICALS, INC (US) 2013-05-02 US disclosed
US-20130084576-A1 MODIFIED NUCLEOSIDES, ANALOGS THEREOF AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 2013-04-04 US disclosed
WO-2012040523-A2 PHOSPHOHISTIDINE ANALOGS THE ROCKEFELLER UNIVERSITY (US) 2012-03-29 WO disclosed
WO-2011139702-A2 MODIFIED NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 2011-11-10 WO disclosed
WO-2011139695-A2 MODIFIED 5' DIPHOSPHATE NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 2011-11-10 WO disclosed
WO-2011139911-A2 LIPID FORMULATED SINGLE STRANDED RNA ISIS PHARMACEUTICALS, INC. (US) 2011-11-10 WO disclosed
WO-2011139699-A2 5' MODIFIED NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM ISIS PHARMACEUTICALS, INC. (US) 2011-11-10 WO disclosed
CN-1218001-C Yellow toner compound and aqueous ink for ink-jet recording apparatus using the same MITSUI CHEMICALS INC (JP) 2005-09-07 CN disclosed
CN-1322227-A Yellow toner compound and aqueous ink for ink-jet recording apparatus using the same MITSUI CHEMICALS INC (JP) 2001-11-14 CN disclosed
CN-1227555-A Cytokine production inhibitors triazepine compounds, and intermediates thereof JAPAN TOBACCO INC (JP) 1999-09-01 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 (6 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-20240228433-A1 COMPOUNDS AND METHODS FOR LIQUID PHASE OLIGONUCLEOTIDE SYNTHESIS POLR2H, POLRMT, POLR2E KCNN4 4844/4885KIF11 1171/4885MAPK1 3564/4885
US-11993626-B2 Functionalized N-acetylgalactosamine analogs FUT6, CSGALNACT1, GALNT6 KCNN4 4331/4885KIF11 2735/4885MAPK1 4233/4885
US-20130084576-A1 MODIFIED NUCLEOSIDES, ANALOGS THEREOF AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM RNMT, HNRNPM, NOP2 KCNN4 4827/4885KIF11 1696/4885MAPK1 4718/4885
US-20230416295-A1 SYNTHESIS OF 2' PROTECTED NUCLEOSIDES NSUN2, RNMT, RNGTT KCNN4 4022/4885KIF11 3777/4885MAPK1 2950/4885
US-20130109850-A1 MODIFIED 5' DIPHOSPHATE NUCLEOSIDES AND OLIGOMERIC COMPOUNDS PREPARED THEREFROM RNMT, POLRMT, RNGTT KCNN4 4757/4885KIF11 1649/4885MAPK1 4552/4885
US-11897914-B2 Synthesis of 2′ protected nucleosides NSUN2, RNMT, RNGTT KCNN4 4007/4885KIF11 3733/4885MAPK1 2950/4885

“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.