SCHEMBL9402885

SCHEMBL9402885

CONC(=O)c1ccc(OC)cc1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 5/20 0.71
CA2 P00918 5/20 0.71
PLK1 P53350 1/20 0.68
NPC1 O15118 5/20 0.63
RAB9A P51151 5/20 0.63
TP53 P04637 2/20 0.63
SMN1; SMN2 Q16637 2/20 0.63
ALOX15 P16050 1/20 0.63
PARP1 P09874 1/20 0.61
PARP10 Q53GL7 1/20 0.61
PARP2 Q9UGN5 1/20 0.61
PARP4 Q9UKK3 1/20 0.61
LMNA P02545 2/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
F10 P00742 2/20 0.59
CES2 O00748 1/20 0.59
CES1 P23141 1/20 0.59
ALDH1A1 P00352 2/20 0.59
MEN1 O00255 1/20 0.58
CYP1A2 P05177 1/20 0.58

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
SCHEMBL14490986 0.89 RAB9A (0.83) NPC1RAB9ATP53SMN1; SMN2ALOX15
SCHEMBL13900091 0.85 CA1 (0.62) CA1CA2PLK1NPC1RAB9A
SCHEMBL407188 0.83 CA1 (1.00) CA1CA2PLK1NPC1RAB9A
SCHEMBL11705060 0.83 MAPT (0.79) CA1CA2PLK1NPC1RAB9A
SCHEMBL8717056 0.83 PLK1 (0.80) CA1CA2PLK1NPC1RAB9A
SCHEMBL13604055 0.82 CA1 (0.66) CA1CA2PLK1NPC1RAB9A
SCHEMBL13250861 0.82 CA1 (0.50) CA1CA2PLK1NPC1RAB9A
Hydrochloric Acid SCHEMBL4259929 0.82 CA1 (0.96) CA1CA2PLK1NPC1RAB9A
SCHEMBL28796093 0.81 CA1 (0.62) CA1CA2PLK1NPC1RAB9A
SCHEMBL28590876 0.81 PLK1 (0.69) PLK1NPC1RAB9ATP53SMN1; SMN2

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113735756-B Method for synthesizing chiral 3, 3-disubstituted isoindolinone compound by rhodium catalysis 陕西师范大学 2024-04-26 CN disclosed
CN-116574056-A Preparation method of fluoroisoquinolone compound 五邑大学 2023-08-11 CN disclosed
CN-113292477-B Method for synthesizing isoindole-1-ketone compound through iridium-catalyzed hydrocarbon activation reaction 四川大学 2023-06-02 CN disclosed
CN-113149868-B Method for synthesizing axichiral diene compound by trivalent rhodium catalysis 陕西师范大学 2023-05-23 CN disclosed
CN-115433222-A Preparation method and application of 2- (gem-difluoropropylene) benzamide compound 五邑大学 2022-12-06 CN disclosed
CN-113735756-A Method for synthesizing chiral 3, 3-disubstituted isoindolinone compound by rhodium catalysis 陕西师范大学 2021-12-03 CN disclosed
CN-113149868-A Method for synthesizing axial chiral allene compound by using trivalent rhodium as catalyst 陕西师范大学 2021-07-23 CN disclosed
CN-107082761-B Phenanthridinone or benzophenanthridinone derivative and synthesis method thereof 上海大学 2020-04-03 CN disclosed
US-8574463-B2 Metal complex dye, photoelectric conversion element and dye-sensitized solar cell FUJIFILM CORPORATION (JP) 2013-11-05 US disclosed
US-20130087203-A1 METAL COMPLEX DYE, PHOTOELECTRIC CONVERSION ELEMENT AND DYE-SENSITIZED SOLAR CELL FUJIFILM CORPORATION (JP) 2013-04-11 US disclosed
EP-1049117-B1 Ruthenium complex dye FUJIFILM CORP (JP) 2011-11-02 EP disclosed
EP-2280404-A2 Metal complex dye for a photoelectrochemical cell FUJIFILM Corporation (JP) 2011-02-02 EP disclosed
EP-1666551-B1 Ink for ink jet-recording curable through irradiation and method for preparing lithographic printing plates using the same FUJIFILM CORP (JP) 2010-02-17 EP disclosed
US-7648997-B2 Immunomodulators for inducing cytokine biosynthesis, for treatment of diseases including viral and neoplastic diseases; 1-[3-(Aminooxy)propyl]-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine; N-[3-(4-Amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)propoxy]cyclopropanecarboxamide COLEY PHARMACEUTICAL GROUP, INC. (US) 2010-01-19 US disclosed
US-7648997-B2 Immunomodulators for inducing cytokine biosynthesis, for treatment of diseases including viral and neoplastic diseases; 1-[3-(Aminooxy)propyl]-2-propyl-1H-imidazo[4,5-c]quinolin-4-amine; N-[3-(4-Amino-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)propoxy]cyclopropanecarboxamide COLEY PHARMACEUTICAL GROUP, INC. (US) 2010-01-19 US disclosed
US-7635181-B2 Ink for ink jet-recording curable through irradiation with a radioactive ray and method for preparing lithographic printing plates using the same FUJIFILM CORPORATION (JP) 2009-12-22 US disclosed
US-7635181-B2 Ink for ink jet-recording curable through irradiation with a radioactive ray and method for preparing lithographic printing plates using the same FUJIFILM CORPORATION (JP) 2009-12-22 US disclosed
US-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines COLEY PHARMACEUTICAL GROUP, INC. (US) 2008-05-15 US disclosed
US-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines COLEY PHARMACEUTICAL GROUP, INC. (US) 2008-05-15 US disclosed
US-5319123-A Reacting an N-alkoxyamide with an acyl halide in the presence of a hindered base SANDOZ LTD. (CH) 1994-06-07 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-20080114019-A1 Hydroxylamine Substituted Imidazoquinolines IFNG, IRF3, IL2 CA1 3424/4885CA2 4114/4885PLK1 3475/4885
US-20130087203-A1 METAL COMPLEX DYE, PHOTOELECTRIC CONVERSION ELEMENT AND DYE-SENSITIZED SOLAR CELL L1CAM, LSG1, CRY1 CA1 376/4885CA2 142/4885PLK1 2163/4885

“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.