SCHEMBL322128

SCHEMBL322128

C=CCc1ccc2ccc3ncccc3c2n1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.56
CYP3A4 P08684 2/20 0.45
MAPT P10636 4/20 0.44
KDM4E B2RXH2 3/20 0.44
HTR2C P28335 3/20 0.39
HTR2A P28223 2/20 0.39
HTR2B P41595 2/20 0.39
HSP90AA1 P07900 2/20 0.37
HTT P42858 2/20 0.37
HIF1A Q16665 2/20 0.37
MEN1 O00255 1/20 0.37
HSP90AB1 P08238 1/20 0.37
BLM P54132 1/20 0.37
KMT2A Q03164 1/20 0.37
TSHR P16473 2/20 0.36
SMN1; SMN2 Q16637 2/20 0.36
GMNN O75496 1/20 0.36
TP53 P04637 1/20 0.36
MMP2 P08253 1/20 0.36
CYP2D6 P10635 1/20 0.36

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
SCHEMBL253273 0.81 LMNA (0.55) LMNACYP3A4MAPTKDM4EHSP90AA1
SCHEMBL8944459 0.80 LMNA (0.61) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL8944497 0.80 LMNA (0.61) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL28648679 0.80 LMNA (0.61) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL7049964 0.79 LMNA (0.49) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL28653682 0.77 LMNA (0.57) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL28585914 0.77 LMNA (0.57) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL2134705 0.76 LMNA (0.61) LMNACYP3A4MAPTKDM4EHTR2C
SCHEMBL16681812 0.76 CCR1 (0.50) CYP3A4TSHRSMN1; SMN2TP53ALOX15
SCHEMBL3673030 0.76 LMNA (0.56) LMNACYP3A4MAPTKDM4EHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106946878-B Bipolar luminescent material which can be processed by environment-friendly solvent and takes alkyl phenanthroline unit as core, and preparation method and application thereof 华南理工大学 2020-09-22 CN claimed
CN-106946878-A Bipolarity luminescent material using alkyl phenanthroline unit as core of environmentally friendly solvent processing and preparation method and application can be used 华南理工大学 2017-07-14 CN claimed
JP-2299827-A None JP disclosed
US-20240199527-A1 PRODUCTION METHOD OF DIALKYL CARBONATE AND PRODUCTION APPARATUS FOR DIALKYL CARBONATE ASAHI KASEI KABUSHIKI KAISHA (JP) 2024-06-20 US disclosed
EP-4332084-A1 METHOD FOR MANUFACTURING DIALKYL CARBONATE AND DEVICE FOR MANUFACTURING DIALKYL CARBONATE Asahi Kasei Kabushiki Kaisha (JP) 2024-03-06 EP disclosed
WO-2023068288-A1 METHOD FOR PRODUCING DIPHENYL CARBONATE 旭化成株式会社 2023-04-27 WO disclosed
CN-106946878-B Bipolar luminescent material which can be processed by environment-friendly solvent and takes alkyl phenanthroline unit as core, and preparation method and application thereof 华南理工大学 2020-09-22 CN disclosed
CN-106946878-B Bipolar luminescent material which can be processed by environment-friendly solvent and takes alkyl phenanthroline unit as core, and preparation method and application thereof 华南理工大学 2020-09-22 CN disclosed
CN-106946878-B Bipolar luminescent material which can be processed by environment-friendly solvent and takes alkyl phenanthroline unit as core, and preparation method and application thereof 华南理工大学 2020-09-22 CN disclosed
CN-111518232-A Polymer added with heterocyclic compound, composition and application of composition 深圳市康益保健用品有限公司 2020-08-11 CN disclosed
CN-106946878-A Bipolarity luminescent material using alkyl phenanthroline unit as core of environmentally friendly solvent processing and preparation method and application can be used 华南理工大学 2017-07-14 CN disclosed
EP-0889025-B1 PROCESS FOR CONTINUOUSLY PREPARING DIALKYL CARBONATES AND DIOLS ASAHI CHEMICAL IND (JP) 2002-04-03 EP disclosed
CN-1335828-A Process for continuous production of dialkyl carbonate and diol ASAHI CHEMICAL IND (JP) 2002-02-13 CN disclosed
US-6346638-B1 CONTINUOUS MULTISTAGE DISTILLATION OF COLUMNS WITH ESTER INTERCHANGE ASAHI KASEL KABUSHIKI KAISHA (JP) 2002-02-12 US disclosed
EP-1174406-A1 PROCESS FOR CONTINUOUSLY PRODUCING DIALKYL CARBONATE AND DIOL Asahi Kasei Kabushiki Kaisha (JP) 2002-01-23 EP disclosed
CN-1303361-A Process for continuous production of dialkyl carbonate and diol ASAHI CHEMICAL IND (JP) 2001-07-11 CN disclosed
EP-1086940-A1 PROCESS FOR CONTINUOUS PRODUCTION OF DIALKYL CARBONATE AND DIOL Asahi Kasei Kogyo Kabushiki Kaisha (JP) 2001-03-28 EP disclosed
EP-0889025-A1 PROCESS FOR CONTINUOUSLY PREPARING DIALKYL CARBONATES AND DIOLS Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1999-01-07 EP disclosed
US-5847189-A Method for continuously producing a dialkyl carbonate and a diol ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1998-12-08 US disclosed
JP-H02299827-A HEAT EXCHANGER FIN MATERIAL SUMITOMO METAL MINING CO LTD 1990-12-12 JP 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-20240199527-A1 PRODUCTION METHOD OF DIALKYL CARBONATE AND PRODUCTION APPARATUS FOR DIALKYL CARBONATE DCLK3, AGL, DCLK2 LMNA 1537/4885CYP3A4 848/4885MAPT 4395/4885

“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.