SCHEMBL4174589

SCHEMBL4174589

CCN(C)c1ccccc1O

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.39
MAPT P10636 2/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
KDM4E B2RXH2 1/20 0.39
NPC1 O15118 1/20 0.39
CA12 O43570 1/20 0.39
GMNN O75496 1/20 0.39
EGFR P00533 1/20 0.39
CA2 P00918 1/20 0.39
LMNA P02545 1/20 0.39
FYN P06241 1/20 0.39
POLB P06746 1/20 0.39
CA3 P07451 1/20 0.39
CYP3A4 P08684 1/20 0.39
MMP9 P14780 1/20 0.39
HPGD P15428 1/20 0.39
ALOX15 P16050 1/20 0.39
NFKB1 P19838 1/20 0.39
CA4 P22748 1/20 0.39
APEX1 P27695 1/20 0.39

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
SCHEMBL6821782 1.00 ALDH1A1 (0.39) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
Bromide SCHEMBL15398508 0.98 TSHR (0.38) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
SCHEMBL31718392 0.83 SIGMAR1 (0.37) ALDH1A1MAPTSMN1; SMN2KDM4ELMNA
SCHEMBL6880337 0.83 HTR1A (0.47) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
SCHEMBL6880115 0.79 HTR1A (0.41) ALDH1A1MAPTKDM4ELMNATDP1
SCHEMBL10333062 0.79 ALDH1A1 (0.42) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
SCHEMBL387883 0.79 ALDH1A1 (0.42) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
SCHEMBL5164785 0.78 HSD17B10 (0.42) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1
SCHEMBL4630050 0.78 ALDH1A1 (0.41) ALDH1A1MAPTNPC1RAB9ATSHR
SCHEMBL2204568 0.77 LMNA (0.39) ALDH1A1MAPTSMN1; SMN2KDM4ENPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1304486-C Phthalocyanine compound, process for producing the same, and optical recording medium containing the same MITSUI CHEMICALS INC (JP) 2007-03-14 CN claimed
CN-1170812-C Method for synthesizing diphenyl-keto-acid derivative 上海麦普化工有限公司 2004-10-13 CN claimed
CN-1354168-A Method for synthesizing diphenyl-keto-acid derivative SHANGHAI MAIPU CHEMICAL INDUST (CN) 2002-06-19 CN claimed
US-20210078989-A1 HETEROCYCLIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME CHANGCHUN HYPERIONS TECHNOLOGY CO., LTD (CN) 2021-03-18 US disclosed
CN-105264021-B Hydrophobic inorganic particles, resin composition for heat dissipation member, electronic component device, and method for producing hydrophobic inorganic particles 住友电木株式会社 2018-04-10 CN disclosed
CN-105246983-B Hydrophobic inorganic particles, resin composition for heat-dissipating member, and electronic component device 住友电木株式会社 2017-10-24 CN disclosed
EP-2656410-B1 ORGANIC ELECTROLUMINESCENT DEVICE MERCK PATENT GMBH (DE) 2017-07-05 EP disclosed
WO-2012084115-A1 ORGANIC ELECTROLUMINESCENT DEVICE MERCK PATENT GMBH (DE) 2012-06-28 WO disclosed
US-20090181413-A1 SIMULTANEOUS AND DIFFERENTIAL QUANTIFICATION OF TWO TARGET ANALYTES IN BIOLOGICAL SAMPLE DENKA SEIKEN CO., LTD. 2009-07-16 US disclosed
EP-1930443-A1 METHOD FOR SELECTIVE, SIMULTANEOUS QUANTIFICATION OF TWO SUBSTANCES IN BIOLOGICAL SAMPLE DENKA SEIKEN Co., Ltd. (JP) 2008-06-11 EP disclosed
US-7332261-B2 Phthalocyanine compound, process for preparing the same, and optical recording medium containing the same CIBA SPECIALTY CHEMICALS CORPORATION (US) 2008-02-19 US disclosed
CN-1170812-C Method for synthesizing diphenyl-keto-acid derivative 上海麦普化工有限公司 2004-10-13 CN disclosed
US-6498245-B2 A CARRIER WHICH COMPRISES A BASE MATERIAL AND A COMPOUND HAVING ONE OR MORE ALKYLATING GROUPS AND THE NUCLEIC ACIDS ARE IMMOBILIZED IN MULTI DOT LIKE AREAS ON CARRIER THROUGH INTERMEDIARY OF ALKYLATING GROUPS NISSHINBO INDUSTRIES, INC. (JP) 2002-12-24 US disclosed
CN-1354168-A Method for synthesizing diphenyl-keto-acid derivative SHANGHAI MAIPU CHEMICAL INDUST (CN) 2002-06-19 CN disclosed
US-20010003649-A1 Nucleic acid-immobilized substrate NISSHINBO INDUSTRIES, INC. (JP) 2001-06-14 US disclosed
EP-1104687-A2 Nucleic acid-immobilized substrate NISSHINBO INDUSTRIES, INC. (JP) 2001-06-06 EP disclosed
EP-0114374-B1 SUBSTITUTED 4-AMINOMETHYLENE CHROMANS OR CHROMENES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN MEDICINES BAYER AG (DE) 1986-07-23 EP disclosed
EP-0114374-A1 Substituted 4-aminomethylene chromans or chromenes, process for their preparation and their use in medicines BAYER AG (DE) 1984-08-01 EP disclosed
US-4381265-A Aromatic nitrile-containing compounds useful as dyestuff intermediates MILLIKEN RESEARCH CORPORATION (US) 1983-04-26 US disclosed
US-4330476-A CONDENSATION OF AROMATIC ALDEHYDE WITH AROMATIC AMINE FOLLOWED BY OXIDATION BAYER AKTIENGESELLSCHAFT (DE) 1982-05-18 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 (2 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-20010003649-A1 Nucleic acid-immobilized substrate DNMT1, DNMT3A, DNMT3L ALDH1A1 1236/4885MAPT 3705/4885SMN1; SMN2 1167/4885
US-20210078989-A1 HETEROCYCLIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME SOX18, TYR, L1CAM ALDH1A1 1610/4885MAPT 985/4885SMN1; SMN2 2991/4885

“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.