SCHEMBL178366

SCHEMBL178366

Cc1ccc(C(=O)NCc2ccccc2)cc1

nearest known ligand 0.75

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK14 Q16539 1/20 0.75
POLB P06746 4/20 0.72
MEN1 O00255 2/20 0.72
KMT2A Q03164 2/20 0.72
HDAC6 Q9UBN7 3/20 0.72
HDAC2 Q92769 1/20 0.72
HDAC8 Q9BY41 1/20 0.72
LMNA P02545 3/20 0.71
RAB9A P51151 2/20 0.71
NPC1 O15118 1/20 0.71
SMN1; SMN2 Q16637 1/20 0.69
HPGD P15428 2/20 0.68
ALDH1A1 P00352 3/20 0.67
MAPT P10636 2/20 0.67
KDM4E B2RXH2 2/20 0.67
HTT P42858 1/20 0.67
RECQL P46063 2/20 0.66
BLM P54132 1/20 0.66
MCL1 Q07820 1/20 0.66
TDP1 Q9NUW8 1/20 0.66

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
SCHEMBL9302673 0.93 MAPK14 (0.75) MAPK14POLBMEN1KMT2AHDAC6
SCHEMBL13932522 0.91 ALDH1A1 (0.78) MAPK14POLBMEN1KMT2AHDAC6
SCHEMBL11900090 0.91 HDAC6 (0.85) POLBHDAC6HDAC2HDAC8LMNA
SCHEMBL1927145 0.90 EPHX2 (0.77) MAPK14POLBMEN1KMT2AHDAC6
SCHEMBL457082 0.87 HDAC6 (0.79) HDAC6HDAC2HDAC8LMNARAB9A
SCHEMBL31061058 0.86 MAPK14 (1.00) MAPK14LMNARAB9ANPC1SMN1; SMN2
SCHEMBL16589429 0.86 HDAC6 (0.72) POLBHDAC6HDAC2HDAC8LMNA
SCHEMBL6843720 0.85 HDAC6 (0.77) POLBHDAC6HDAC2HDAC8LMNA
SCHEMBL4747957 0.85 NR1H4 (0.81) POLBKMT2AHDAC6HDAC2HDAC8
SCHEMBL15985750 0.85 MAPK14 (0.65) MAPK14POLBMEN1KMT2AHDAC6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118005468-B Method for synthesizing N-alkylated amide compound by catalyzing alcohols and nitriles with nitrogen-carbon material 常州大学 2026-05-19 CN disclosed
CN-118005468-A Method for synthesizing N-alkylated amide compound by catalyzing alcohols and nitriles with nitrogen-carbon material 常州大学 2024-05-10 CN disclosed
CN-115304506-B Preparation method of secondary amide compound by activating primary amide through boron salt catalysis 中国人民解放军国防科技大学 2023-11-14 CN disclosed
US-20230046065-A1 MERGING C(sp3)-H ACTIVATION WITH DNA-ENCODING THE SCRIPPS RESEARCH INSTITUTE 2023-02-16 US disclosed
WO-2023015236-A2 COMPOSITION AND METHOD FOR TREATMENT OF GRAM NEGATIVE BACTERIAL INFECTION THE RESEARCH FOUNDATION FOR THE STATE UNIVERSITY OF NEW YORK (US) 2023-02-09 WO disclosed
CN-115557849-A Method for synthesizing imide compound under induction of NBS and water by visible light 西南大学 2023-01-03 CN disclosed
CN-115304506-A Preparation method of secondary amide compound by activating primary amide under catalysis of boron salt 中国人民解放军国防科技大学 2022-11-08 CN disclosed
WO-2022224212-A1 GPR35 AGONIST COMPOUNDS HEPTARES THERAPEUTICS LIMITED (GB) 2022-10-27 WO disclosed
US-11471868-B2 Redox dehydration coupling catalysts and methods related thereto EMORY UNIVERSITY (US) 2022-10-18 US disclosed
EP-4067355-A1 SPIRO-CONDENSED PYRROLIDINE DERIVATIVES AS DEUBIQUITYLATING ENZYME (DUB) INHIBITORS Mission Therapeutics Limited (GB) 2022-10-05 EP disclosed
US-20090299098-A1 Catalytic Metathesis of Secondary Amides WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2009-12-03 US disclosed
US-20090186875-A1 Dihydrothienopyrimidines, suitable for the treatment of respiratory, gastrointestinal, inflammatory, nervous system disorders and/or cancer BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2009-07-23 US disclosed
US-20090029990-A1 Dihydropteridinones in the treatment of respiratory diseases MAIER UDO 2009-01-29 US disclosed
US-7432292-B2 Sulfhydantoins as phosphate isosteres VERTEX PHARMACEUTICALS INCORPORATED (US) 2008-10-07 US disclosed
CN-101184758-A Novel compounds GLAXO GROUP LTD (GB) 2008-05-21 CN disclosed
US-7253158-B2 Sulfonamides HOFFMANN-LA ROCHE INC. (US) 2007-08-07 US disclosed
US-20070043055-A1 Dihydropteridinones in the treatment of respiratory diseases BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2007-02-22 US disclosed
US-6958243-B2 Performing a one-pot organic reaction, which includes carbon monoxide (CO) as reactant and does not use of an external gas source, by contacting a non-catalyzing CO releasing compound such as a metal carbonyl with an energy source BIOTAGE AB (SE) 2005-10-25 US disclosed
US-20050221389-A1 Organic reactions with CO generating materials BIOTAGE AB (SE) 2005-10-06 US disclosed
US-20020161266-A1 Performing a one-pot organic reaction, which includes carbon monoxide (CO) as reactant and does not use of an external gas source, by contacting a non-catalyzing CO releasing compound such as a metal carbonyl with an energy source BIOTAGE AB (SE) 2002-10-31 US 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 (7 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-20090186875-A1 Dihydrothienopyrimidines, suitable for the treatment of respiratory, gastrointestinal, inflammatory, nervous system disorders and/or cancer DPYD, DHODH, FH MAPK14 3540/4885POLB 861/4885MEN1 2282/4885
US-20090299098-A1 Catalytic Metathesis of Secondary Amides NAAA, NAT1, NAT10 MAPK14 1283/4885POLB 625/4885MEN1 251/4885
US-20070043055-A1 Dihydropteridinones in the treatment of respiratory diseases QDPR, DHPS, NDUFS6 MAPK14 4305/4885POLB 3804/4885MEN1 1447/4885
US-20050221389-A1 Organic reactions with CO generating materials KIT, NOS1, NOS2 MAPK14 2550/4885POLB 1053/4885MEN1 1563/4885
US-20020161266-A1 Performing a one-pot organic reaction, which includes carbon monoxide (CO) as reactant and does not use of an external gas source, by contacting a non-catalyzing CO releasing compound such as a metal carbonyl with an energy source KIT, CBR1, NOS1 MAPK14 2554/4885POLB 1986/4885MEN1 1233/4885
US-20090029990-A1 Dihydropteridinones in the treatment of respiratory diseases QDPR, DHPS, NDUFS6 MAPK14 4305/4885POLB 3804/4885MEN1 1447/4885
US-11471868-B2 Redox dehydration coupling catalysts and methods related thereto SCLY, TST, SQOR MAPK14 2463/4885POLB 1584/4885MEN1 3987/4885

“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.