SCHEMBL1200149

SCHEMBL1200149

CNC(=O)CC(=O)c1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 8/20 0.67
▸ MEN1 O00255 6/20 0.67
▸ CYP3A4 P08684 2/20 0.67
▸ HPGD P15428 2/20 0.67
▸ MAPK1 P28482 2/20 0.67
▸ KDM4E B2RXH2 1/20 0.67
▸ MAPT P10636 1/20 0.67
▸ ALOX15 P16050 1/20 0.67
▸ CES1 P23141 1/20 0.67
▸ SMN1; SMN2 Q16637 1/20 0.67
▸ TDP1 Q9NUW8 1/20 0.67
▸ ATM Q13315 1/20 0.59
▸ RAB9A P51151 7/20 0.59
▸ NPC1 O15118 6/20 0.59
▸ PTPN1 P18031 2/20 0.57
▸ ERCC5 P28715 1/20 0.57
▸ FEN1 P39748 1/20 0.57
▸ ALDH1A1 P00352 3/20 0.53
▸ HIF1A Q16665 2/20 0.53
▸ PLOD2 O00469 1/20 0.53

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
SCHEMBL7163238 0.83 NR4A2 (0.61) KMT2AMEN1CYP3A4HPGDMAPK1
Dibenzoylmethane SCHEMBL10356288 0.81 MEN1 (1.00) KMT2AMEN1CYP3A4HPGDMAPK1
Dibenzoylmethane SCHEMBL1704711 0.81 MEN1 (1.00) KMT2AMEN1CYP3A4HPGDMAPK1
Dibenzoylmethane SCHEMBL39582 0.81 MEN1 (1.00) KMT2AMEN1CYP3A4HPGDMAPK1
SCHEMBL1201297 0.81 KMT2A (0.62) KMT2AMEN1HPGDKDM4EMAPT
SCHEMBL11004539 0.79 ERCC5 (0.58) KMT2AMEN1KDM4EMAPTCES1
SCHEMBL10606188 0.79 KMT2A (0.61) KMT2AMEN1CYP3A4HPGDMAPK1
SCHEMBL6568801 0.79 KMT2A (0.61) KMT2AMEN1CYP3A4HPGDMAPK1
SCHEMBL5931323 0.79 KMT2A (0.61) KMT2AMEN1CYP3A4HPGDMAPK1
SCHEMBL5160670 0.79 PLOD2 (0.60) KMT2AMEN1CYP3A4HPGDKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114057666-B Synthesis method of 4, 5-disubstituted-2-aminothiazole compound 沈阳药科大学 2023-02-07 — — CN disclosed
CN-114057666-A Synthesis method of 4, 5-disubstituted-2-aminothiazole compound 沈阳药科大学 2022-02-18 — — CN disclosed
US-10322112-B2 Compound combinations for attenuation of bacterial virulence WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2019-06-18 — — US disclosed
US-20190119201-A1 Inhibitors of Quorum Sensing Receptor LasR WISCONSIN ALUMNI RESEARCH FOUNDATION 2019-04-25 — — US disclosed
US-20170231962-A1 Compound Combinations for Attenuation of Bacterial Virulence NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-08-17 — — US disclosed
US-20170231962-A1 Compound Combinations for Attenuation of Bacterial Virulence NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2017-08-17 — — US disclosed
CN-102321066-B Method for producing aryl-aminopropanols SALTIGO GMBH 2014-07-23 — — CN disclosed
CN-1445224-B Process for preparing arylaminopropanols SALTIGO GMBH 2012-07-11 — — CN disclosed
CN-102321066-A The method for preparing the arylamino propyl alcohol SALTIGO GMBH 2012-01-18 — — CN disclosed
US-7893281-B2 Process for preparing arylaminopropanols LANXESS DEUTSCHLAND GMBH (DE) 2011-02-22 — — US disclosed
US-7169938-B2 Process for preparing arylaminopropanols LANXESS DEUTSCHLAND GMBH (DE) 2007-01-30 — — US disclosed
US-20030225153-A1 Process for preparing arylaminopropanols LANXESS DEUTSCHLAND GMBH (DE) 2003-12-04 — — US disclosed
CN-1445224-A Process for preparing arylaminopropanols BAYER AG (DE) 2003-10-01 — — CN disclosed
EP-1346977-A1 Method for producing aryl-aminopropanols Bayer Aktiengesellschaft (DE) 2003-09-24 — — EP disclosed
EP-0114059-B1 METHOD OF PREPARING A POLYAMIDE ACID COMPOSITION FOR PREPARING POLYIMIDE KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1989-06-14 — — EP disclosed
EP-0083690-B1 POLYAMIDE ACID COMPOSITION FOR PREPARING POLYIMIDE AND PROCESS FOR PREPARING POLYIMIDE FROM THE SAME KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1986-03-12 — — EP disclosed
US-4515915-A Polyamide acid composition for preparing polyimide KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1985-05-07 — — US disclosed
EP-0114059-A2 Method of preparing a polyamide acid composition for preparing polyimide KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1984-07-25 — — EP disclosed
US-4454276-A POT LIFE EXTENDING AGENT Kanegafuchi Chkagaku Kogyo Kabushiki Kaisha (JP) 1984-06-12 — — US disclosed
EP-0083690-A1 Polyamide acid composition for preparing polyimide and process for preparing polyimide from the same KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1983-07-20 — — 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 (4 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-20170231962-A1 Compound Combinations for Attenuation of Bacterial Virulence PNISR, PGLS, QRFPR KMT2A 3286/4885MEN1 3990/4885CYP3A4 4776/4885
US-20030225153-A1 Process for preparing arylaminopropanols AHR, CYP1A1, CYP1A2 KMT2A 746/4885MEN1 3279/4885CYP3A4 8/4885
US-10322112-B2 Compound combinations for attenuation of bacterial virulence PNISR, BLVRB, PGLS KMT2A 3318/4885MEN1 4469/4885CYP3A4 4682/4885
US-20190119201-A1 Inhibitors of Quorum Sensing Receptor LasR FFAR1, CYSLTR1, LPAR1 KMT2A 3939/4885MEN1 4652/4885CYP3A4 3438/4885

“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.

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