SCHEMBL611657

SCHEMBL611657

O=C(Nc1ccc(Cl)cc1)c1ccc(Cl)cc1

nearest known ligand 0.76

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 3/20 0.76
RAB9A P51151 3/20 0.76
SMN1; SMN2 Q16637 1/20 0.76
KMT2A Q03164 4/20 0.75
NT5E P21589 1/20 0.75
MAPK1 P28482 1/20 0.75
KCNQ3 O43525 1/20 0.68
KCNQ2 O43526 1/20 0.68
KCNE1 P15382 1/20 0.68
KCNQ1 P51787 1/20 0.68
LMNA P02545 2/20 0.67
NAMPT P43490 1/20 0.67
MEN1 O00255 3/20 0.66
TDP1 Q9NUW8 2/20 0.66
PRMT1 Q99873 1/20 0.65
MAPT P10636 1/20 0.65
HSD17B10 Q99714 1/20 0.65
PTGS2 P35354 1/20 0.64
POLB P06746 1/20 0.63
PKM P14618 1/20 0.63

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
SCHEMBL10939703 1.00 NPC1 (0.76) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL9767723 1.00 NPC1 (0.76) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL674167 0.92 HDAC8 (0.69) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL27918627 0.92 NPC1 (0.67) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL6556039 0.92 NPC1 (0.67) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL2409003 0.92 NPC1 (0.67) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL6710662 0.92 MITF (0.68) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL493839 0.90 RAB9A (0.81) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL3823913 0.90 PTPN1 (0.73) NPC1RAB9ASMN1; SMN2KMT2ANT5E
SCHEMBL21698103 0.90 NPC1 (0.70) NPC1RAB9ASMN1; SMN2KMT2ANT5E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118420484-B Method for preparing amide compounds 四川大学 2024-08-30 CN disclosed
CN-118420484-A Method for preparing amide compounds 四川大学 2024-08-02 CN disclosed
CN-115304507-A Synthesis method of N-substituted aryl formamide 兰州石化职业技术大学 2022-11-08 CN disclosed
US-20220162224-A1 P38ALPHA MITOGEN-ACTIVATED PROTEIN KINASE INHIBITORS GEN1E LIFESCIENCES INC. 2022-05-26 US disclosed
EP-2206547-B1 NITROGEN-CONTAINING AROMATIC COMPOUNDS AND PROCESSES FOR THE PRODUCTION OF THE SAME, POLYMERS AND PROTON CONDUCTIVE MEMBRANES OF THESE COMPOUNDS JSR CORP (JP) 2016-03-16 EP disclosed
US-20140154610-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND USES THEREOF JSR CORPORATION (JP) 2014-06-05 US disclosed
EP-2738194-A1 AROMATIC COPOLYMER HAVING PROTON CONDUCTIVE GROUP AND APPLICATION THEREOF JSR Corporation (JP) 2014-06-04 EP disclosed
EP-1906473-B1 ELECTRODE PASTE FOR USE IN SOLID POLYMER FUEL CELL JSR CORP (JP) 2014-02-12 EP disclosed
US-8399148-B2 Varnish for a solid polymer fuel cell JSR CORPORATION (JP) 2013-03-19 US disclosed
EP-1947717-B1 ELECTRODE CATALYST LAYER JSR CORP (JP) 2013-02-13 EP disclosed
US-20030173547-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR CORPORATION (JP) 2003-09-18 US disclosed
EP-1329444-A1 Halogenated aromatic compound, (co)polymer thereof, and proton-conductive membrane comprising same JSR Corporation (JP) 2003-07-23 EP disclosed
US-20020177656-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR CORPORATION (JP) 2002-11-28 US disclosed
US-20020172850-A1 Polymer electrolyte membrane and solid polymer electrolyte fuel cell using same HONDA GIKEN KOGYO KABUSHIKI KAISHA, JSR CORPORATION 2002-11-21 US disclosed
EP-1245554-A1 Monomer containing electron-withdrawing group and electron-donative group, and copolymer and proton-conductive membrane comprising same JSR Corporation (JP) 2002-10-02 EP disclosed
WO-1996010560-A1 BENZAMIDE SEMICARBAZONE DERIVATIVES AND THEIR USE AS PESTICIDES NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 1996-04-11 WO disclosed
US-4499167-A Photoconductive compositions comprising an organic photoconductor and an amide compound and electro-photographic light-sensitive materials using the compositions FUJI PHOTO FILM CO., LTD. (JP) 1985-02-12 US disclosed
EP-0051828-B1 N-BENZOYL-ALPHA-ANILINO ALKANE CARBOXYLIC ACIDS, SALTS AND ESTERS THEREOF, PROCESS FOR PRODUCING THE SAME AND PHARMACEUTICAL PREPARATIONS CONTAINING THE SAME A. Nattermann & Cie. GmbH (DE) 1984-03-14 EP disclosed
US-4386031-A ANTICOAGULANTS; ANTIALLERGENS; ANTINFLAM-MATORY AND ANTILIPEMIC AGENTS; ANTIHISTAMINES; CARDIOVASCULAR DISORDERS A. NATTERMANN & CIE GMBH (DE) 1983-05-31 US disclosed
EP-0051828-A1 N-benzoyl-alpha-anilino alkane carboxylic acids, salts and esters thereof, process for producing the same and pharmaceutical preparations containing the same A. Nattermann & Cie. GmbH (DE) 1982-05-19 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 (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-20220162224-A1 P38ALPHA MITOGEN-ACTIVATED PROTEIN KINASE INHIBITORS MAPKAPK2, MAPK1, MAPK8 NPC1 2511/4885RAB9A 2172/4885SMN1; SMN2 2453/4885

“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.