SCHEMBL2093541

SCHEMBL2093541

Fc1ccc(CNc2ccccc2)cc1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNH3 Q9ULD8 2/20 0.64
MEN1 O00255 1/20 0.58
CYP1A2 P05177 1/20 0.58
CYP3A4 P08684 1/20 0.58
CYP2C9 P11712 1/20 0.58
CYP2C19 P33261 1/20 0.58
KMT2A Q03164 1/20 0.58
MAOB P27338 3/20 0.56
NPC1 O15118 1/20 0.56
POLB P06746 1/20 0.56
RAB9A P51151 1/20 0.56
GAA P10253 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55
FFAR1 O14842 1/20 0.55
PTPRF P10586 1/20 0.55
PTPN2 P17706 1/20 0.55
PTPN1 P18031 1/20 0.55
PTPN11 Q06124 1/20 0.55
HTT P42858 1/20 0.53
PLA2G1B P04054 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
Iodide SCHEMBL30486758 0.98 KCNH3 (0.62) KCNH3MEN1CYP1A2CYP3A4CYP2C9
SCHEMBL4241915 0.91 HTT (0.64) KCNH3CYP1A2POLBGAAL3MBTL1
SCHEMBL10055033 0.89 LMNA (0.61) KCNH3MEN1KMT2APOLBGAA
SCHEMBL6419238 0.89 LMNA (0.61) KCNH3MEN1KMT2APOLBGAA
SCHEMBL2065031 0.89 CYP1A2 (0.69) MEN1CYP1A2CYP3A4CYP2C9CYP2C19
SCHEMBL11510992 0.88 FFAR1 (0.63) KCNH3MEN1KMT2AGAAL3MBTL1
Propionic Acid SCHEMBL11468427 0.86 FFAR1 (0.59) KCNH3MEN1CYP1A2CYP3A4CYP2C9
SCHEMBL6692354 0.85 PPARA (0.54) KCNH3MEN1KMT2AMAOB
SCHEMBL22628164 0.84 HTT (0.71) KCNH3MEN1CYP1A2CYP3A4CYP2C9
N-Benzylaniline SCHEMBL7840 0.84 HTT (0.71) KCNH3MEN1CYP1A2CYP3A4CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119701982-A Application of niobium oxide supported copper catalyst in synthesis of secondary amine or derivative thereof from aromatic nitro compound and benzyl alcohol compound 兰州大学 2025-03-28 CN disclosed
CN-112409188-B Method for synthesizing N-alkylamine 南京理工大学 2023-05-05 CN disclosed
CN-112206777-B Preparation method and application of carbonized octahedral material HKUST-1-400 三峡大学 2022-03-18 CN disclosed
CN-109046463-B Bidentate aza-carbene-manganese catalyst, preparation method and alkylation synthesis application thereof 中山大学 2021-05-04 CN disclosed
CN-108380245-B Bidentate phosphorus-aza-carbene p-cymene type ruthenium complex catalyst, preparation method and synthesis application thereof 中山大学 2020-06-09 CN disclosed
EP-3006432-B1 2,3-BUTANEDIAMIDE EPOXIDE COMPOUND AND PREPARATION METHOD AND USE THEREOF INST PHARMACOLOGY & TOXICOLOGY ACAD MILITARY MEDICAL SCIENCES PLA CHINA (CN) 2017-11-15 EP disclosed
US-9630957-B2 2,3-butanediamide epoxide compound and preparation method and use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2017-04-25 US disclosed
US-20160115160-A1 2, 3-Butanediamide Epoxide Compound and Preparation Method and Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2016-04-28 US disclosed
EP-3006432-A1 2,3-BUTANEDIAMIDE EPOXIDE COMPOUND AND PREPARATION METHOD AND USE THEREOF Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2016-04-13 EP disclosed
CN-103004006-B Additive for nonaqueous electrolyte, nonaqueous electrolyte, and electricity storage device SUMITOMO SEIKA CHEMICALS 2014-02-19 CN 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
WO-2006060731-A2 USE OF ATAZANAVIR FOR IMPROVING THE PHARMACOKINETICS OF DRUGS METABOLIZED BY UGT1A1 MERCK & CO., INC. (US) 2006-06-08 WO 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-1089988-A4 FLUOROPHENYL RESIN COMPOUNDS AVENTIS PHARM PROD INC (US) 2005-01-19 EP disclosed
CN-1185259-C Fluorophenyl resin compounds AVENTIES PHARMACEUTICALS INC (US) 2005-01-19 CN disclosed
US-6639023-B1 Such as 4-hydroxy, sulfonic acid or sulfonyl chloride-2,3,5,6-tetrafluorobenzamidomethyl-polystyrene resin; solid phase synthesis AVENTIS PHARMACEUTICALS INC. 2003-10-28 US disclosed
CN-1306524-A Fluorophenyl resin compounds AVENTIES PHARMACEUTICALS INC (US) 2001-08-01 CN disclosed
EP-1089988-A1 FLUOROPHENYL RESIN COMPOUNDS Aventis Pharmaceuticals Products Inc. (US) 2001-04-11 EP disclosed
WO-1999067228-A1 FLUOROPHENYL RESIN COMPOUNDS AVENTIS PHARMACEUTICALS PRODUCTS INC. (US) 1999-12-29 WO disclosed
US-4152452-A N-BENZYLANILINE AND DERIVATIVES WILLIAM H. RORER, INC. (US) 1979-05-01 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 (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-20160115160-A1 2, 3-Butanediamide Epoxide Compound and Preparation Method and Use Thereof ECE2, GNE, EPHX2 KCNH3 1897/4885MEN1 2462/4885CYP1A2 95/4885

“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.