SCHEMBL513878

SCHEMBL513878

COC(=O)Nc1ccccc1Cl

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 4/20 0.58
KMT2A Q03164 4/20 0.58
ALDH1A1 P00352 3/20 0.57
KDM4E B2RXH2 2/20 0.57
HTT P42858 1/20 0.57
CYP1A2 P05177 2/20 0.56
HPGD P15428 2/20 0.56
CYP2C19 P33261 1/20 0.56
NPC1 O15118 4/20 0.54
RAB9A P51151 3/20 0.54
POLB P06746 2/20 0.54
LMNA P02545 1/20 0.54
PDE4D Q08499 1/20 0.54
ATM Q13315 2/20 0.53
CASP3 P42574 1/20 0.53
SENP8 Q96LD8 1/20 0.53
SENP7 Q9BQF6 1/20 0.53
SENP6 Q9GZR1 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.52
PDK1 Q15118 1/20 0.51

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
SCHEMBL11659356 0.85 HPGD (0.64) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL9819481 0.85 KMT2A (0.62) MEN1KMT2AALDH1A1KDM4EHPGD
SCHEMBL3793403 0.83 NLRP3 (0.53) MEN1KMT2AALDH1A1KDM4EHPGD
SCHEMBL2091197 0.83 ALDH1A1 (0.73) ALDH1A1KDM4EHTTHPGDPOLB
SCHEMBL513877 0.82 MEN1 (0.57) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL3790475 0.82 PDK1 (0.54) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL2093882 0.82 RAF1 (0.53) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL514178 0.82 MEN1 (0.53) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL30207788 0.82 PDK1 (0.54) MEN1KMT2AALDH1A1KDM4EHTT
SCHEMBL1189632 0.82 ALDH1A1 (0.77) MEN1KMT2AALDH1A1CYP1A2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4699994-A METHYLATING N-PHENYL CARBAMIC ACID ESTER NIPPON KOKAN KABUSHIKI KAISHA (JP) 1987-10-13 US claimed
CN-115850119-A Synthetic method of 2-chloro aromatic amine compound 南昌大学 2023-03-28 CN disclosed
EP-3508473-B1 METHOD FOR PRODUCING CARBAMIC ACID ESTER AIST (JP) 2021-05-26 EP disclosed
US-10752579-B2 Production method of carbamic acid ester NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2020-08-25 US disclosed
CN-107434774-B Method for synthesizing diphenylmethane dicarbamic acid ester from phenyl carbamate 中国石油化工股份有限公司 2020-06-02 CN disclosed
EP-3508473-A1 METHOD FOR PRODUCING CARBAMIC ACID ESTER National Institute of Advanced Industrial Science and Technology (JP) 2019-07-10 EP disclosed
US-20190185420-A1 PRODUCTION METHOD OF CARBAMIC ACID ESTER NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2019-06-20 US disclosed
US-20170355997-A1 METHODS AND COMPOSITIONS FOR TREATING OR PREVENTING PRURITIS NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-12-14 US disclosed
US-9771592-B2 Methods and compositions for treating or preventing pruritis THE JOHNS HOPKINS UNIVERSITY (US) 2017-09-26 US disclosed
WO-2014184070-A1 MIXTURES OF HALOALKYLSULFONANILIDE DERIVATIVES AND HERBICIDES SYNGENTA LIMITED (GB) 2014-11-20 WO disclosed
EP-1914221-A1 PROCESS FOR PRODUCING BIARYL COMPOUND Sumitomo Chemical Company, Limited (JP) 2008-04-23 EP disclosed
US-20080027095-A1 Use Of 3-Substituted-2-(Diphenylmethy)-1-Azabicyclo[2.2.2]Octanes For Treating Mrg-X1 Receptor Mediated Diseases MERCK SHARP & DOHME CORP. 2008-01-31 US disclosed
EP-1678185-A1 2,3-DIHYDRO-6-NITROIMIDAZO [2,1-B] OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-07-12 EP disclosed
US-20050143454-A1 4-Alkyl-2-haloaniline derivative and process and process for producing the same MEIJI SEIKA PHARMA CO., LTD. (JP) 2005-06-30 US disclosed
WO-2005042542-A1 2,3-DIHYDRO-6-NITROIMIDAZO (2,1-B) OXAZOLE COMPOUNDS FOR THE TREATMENT OF TUBERCULOSIS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-05-12 WO disclosed
EP-1506954-A1 4-ALKYL-2-HALOANILINE DERIVATIVE AND PROCESS FOR PRODUCING THE SAME MEIJI SEIKA KAISHA LTD. (JP) 2005-02-16 EP disclosed
US-4699994-A METHYLATING N-PHENYL CARBAMIC ACID ESTER NIPPON KOKAN KABUSHIKI KAISHA (JP) 1987-10-13 US disclosed
EP-0216273-A2 Method of manufacturing diphenylmethane dicarbamic acid esters NIPPON KOKAN KABUSHIKI KAISHA (JP) 1987-04-01 EP disclosed
EP-0032733-B1 PROCESS FOR PREPARING POLYMETHYLENE POLYPHENYL POLYCARBAMATES MITSUI TOATSU CHEMICALS, Inc. (JP) 1984-06-13 EP disclosed
EP-0032733-A1 Process for preparing polymethylene polyphenyl polycarbamates MITSUI TOATSU CHEMICALS, Inc. (JP) 1981-07-29 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 (5 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-20170355997-A1 METHODS AND COMPOSITIONS FOR TREATING OR PREVENTING PRURITIS ITCH, CCL11, CPA3 MEN1 4289/4885KMT2A 4208/4885ALDH1A1 2589/4885
US-20080027095-A1 Use Of 3-Substituted-2-(Diphenylmethy)-1-Azabicyclo[2.2.2]Octanes For Treating Mrg-X1 Receptor Mediated Diseases MRGPRX1, MRGPRX2, MRGPRX4 MEN1 2460/4885KMT2A 940/4885ALDH1A1 2071/4885
US-20050143454-A1 4-Alkyl-2-haloaniline derivative and process and process for producing the same NAT1, CYP4X1, HAX1 MEN1 1499/4885KMT2A 279/4885ALDH1A1 441/4885
US-20190185420-A1 PRODUCTION METHOD OF CARBAMIC ACID ESTER CA2, CA7, CA4 MEN1 2437/4885KMT2A 243/4885ALDH1A1 3215/4885
US-10752579-B2 Production method of carbamic acid ester CA2, CA7, CA4 MEN1 2437/4885KMT2A 243/4885ALDH1A1 3215/4885

“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.