SCHEMBL880264

SCHEMBL880264

O=C1CC(c2cccc(Cl)c2)c2ccccc2N1

nearest known ligand 0.67

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.67
KMT2A Q03164 3/20 0.47
MEN1 O00255 2/20 0.47
NPC1 O15118 2/20 0.47
TDP1 Q9NUW8 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
RAB9A P51151 1/20 0.47
TP53 P04637 2/20 0.46
PKM P14618 1/20 0.46
GAA P10253 2/20 0.46
MAPT P10636 1/20 0.46
ALDH1A1 P00352 1/20 0.46
HTR2A P28223 2/20 0.44
HTR2C P28335 2/20 0.44
HTR2B P41595 2/20 0.44
HRH3 Q9Y5N1 2/20 0.44
SLC6A3 Q01959 1/20 0.44

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
SCHEMBL30005837 1.00 LMNA (0.67) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL8920256 0.86 LMNA (0.54) LMNATP53GAAMAPTSLC6A3
SCHEMBL10280718 0.85 LMNA (0.63) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL13522407 0.85 LMNA (0.66) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL880483 0.84 LMNA (0.62) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL880444 0.84 TP53 (0.59) LMNAKMT2AMEN1TP53MAPT
SCHEMBL880376 0.83 ALDH1A1 (0.58) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL7156373 0.83 ALDH1A1 (0.58) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL12698414 0.83 ALDH1A1 (0.58) LMNAKMT2AMEN1NPC1TDP1
SCHEMBL10280290 0.82 LMNA (0.70) LMNAKMT2AMEN1NPC1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113072490-B High-efficiency synthesis method of tipifarnib quinolinone intermediate 中国海洋大学 2022-08-16 CN claimed
CN-113072490-A High-efficiency synthesis method of tipifarnib quinolinone intermediate 中国海洋大学 2021-07-06 CN claimed
CN-113072490-B High-efficiency synthesis method of tipifarnib quinolinone intermediate 中国海洋大学 2022-08-16 CN disclosed
CN-113072490-A High-efficiency synthesis method of tipifarnib quinolinone intermediate 中国海洋大学 2021-07-06 CN disclosed
US-20130289022-A1 TETRAMERIC ALPHA-SYNUCLEIN AND USE THEREOF BRANDEIS UNIVERSITY (US) 2013-10-31 US disclosed
US-8440705-B2 2,3,4,7,8,9-hexahydro-1H-cyclopenta[h]quinolin-2-one or 2,3,4,6,7,8-hexahydro-1H-cyclopenta[g]quinolin-2-one; Alzheimer's disease WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2013-05-14 US disclosed
EP-2433634-A2 Compounds, compositions and methods of inhibiting a-synuclein toxicity The Whitehead Institute for Biomedical Research (US) 2012-03-28 EP disclosed
US-20110294794-A1 TREATMENT OF PROTEINOPATHIES USING A FARNESYL TRANSFERASE INHIBITOR LINK MEDICINE CORPORATION (US) 2011-12-01 US disclosed
EP-2358370-A2 TREATMENT OF PROTEINOPATHIES USING A FARNESYL TRANSFERASE INHIBITOR Link Medicine Corporation (US) 2011-08-24 EP disclosed
US-20110060005-A1 TREATMENT OF MITOCHONDRIAL DISORDERS USING A FARNESYL TRANSFERASE INHIBITOR LINK MEDICINE CORPORATION (US) 2011-03-10 US disclosed
US-20100331363-A1 TREATMENT OF MITOCHONDRIAL DISORDERS USING A FARNESYL TRANSFERASE INHIBITOR LINK MEDICINE CORPORATION (US) 2010-12-30 US disclosed
WO-2002024683-A1 FARNESYL TRANSFERASE INHIBITING 6-[(SUBSTITUTED PHENYL)METHYL]-QUINOLINE AND QUINAZOLINE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 2002-03-28 WO disclosed
EP-1162201-A2 Farnesyl protein transferase inhibiting (imidazol-5-yl)methyl-2-quinolinone derivatives JANSSEN PHARMACEUTICA N.V. (BE) 2001-12-12 EP disclosed
US-6169096-B1 FOR INHIBITING TUMOR GROWTH IN A MAMMAL JANSSEN PHARMACAEUTIC N.V. (BE) 2001-01-02 US disclosed
EP-0988038-A1 (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES AS INHIBITORS OF SMOOTH MUSCLE CELL PROLIFERATION JANSSEN PHARMACEUTICA N.V. (BE) 2000-03-29 EP disclosed
US-6037350-A USEFUL AS ANTICANCER AGENTS FOR TUMORS JANSSEN PHARMACEUTICA, N.V. (BE) 2000-03-14 US disclosed
CN-1203598-A Farnesyl protein transferase inhibiting (imidazol-5-yl) methyl-2-quinolinone derivatives JANSSEN PHARMACEUTICA NV (BE) 1998-12-30 CN disclosed
WO-1998055124-A1 (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES AS INHIBITORS OF SMOOTH MUSCLE CELL PROLIFERATION JANSSEN PHARMACEUTICA N.V. (BE) 1998-12-10 WO disclosed
EP-0865440-A1 FARNESYL PROTEIN TRANSFERASE INHIBITING (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1998-09-23 EP disclosed
WO-1997021701-A1 FARNESYL PROTEIN TRANSFERASE INHIBITING (IMIDAZOL-5-YL)METHYL-2-QUINOLINONE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1997-06-19 WO 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 (3 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-20110060005-A1 TREATMENT OF MITOCHONDRIAL DISORDERS USING A FARNESYL TRANSFERASE INHIBITOR NLN, FNTA, ACAT1 LMNA 1392/4885KMT2A 1658/4885MEN1 1419/4885
US-20100331363-A1 TREATMENT OF MITOCHONDRIAL DISORDERS USING A FARNESYL TRANSFERASE INHIBITOR NLN, ACAT1, FH LMNA 1206/4885KMT2A 2316/4885MEN1 1484/4885
US-20110294794-A1 TREATMENT OF PROTEINOPATHIES USING A FARNESYL TRANSFERASE INHIBITOR FNTA, FNTB, BDNF LMNA 2407/4885KMT2A 1852/4885MEN1 599/4885

“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.