SCHEMBL4398768

SCHEMBL4398768

CCCCCCOc1ccc(Nc2ccccc2)cc1

nearest known ligand 0.64

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 2/20 0.64
FAAH O00519 8/20 0.61
NR5A1 Q13285 1/20 0.56
NPC1 O15118 1/20 0.55
RAB9A P51151 1/20 0.55
UNG P13051 2/20 0.55
TP53 P04637 1/20 0.54
TSHR P16473 1/20 0.54
HRH2 P25021 1/20 0.54
HRH3 Q9Y5N1 1/20 0.54
PLA2G4B P0C869 1/20 0.53
NAMPT P43490 1/20 0.52

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
SCHEMBL8962153 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL8962099 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL8962156 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL9478885 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL8962108 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL24145746 1.00 LTA4H (0.64) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL30682518 0.95 LTA4H (0.58) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL8962169 0.95 LTA4H (0.63) LTA4HFAAHNPC1RAB9ATSHR
SCHEMBL8962079 0.93 NR5A1 (0.63) LTA4HFAAHNR5A1NPC1RAB9A
SCHEMBL11470886 0.93 NR5A1 (0.63) LTA4HFAAHNR5A1NPC1RAB9A

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
WO-2020021969-A1 COMPOSITION, CURED PRODUCT, OPTICAL FILTER, AND PRODUCTION METHOD FOR CURED PRODUCT 株式会社ADEKA 2020-01-30 WO disclosed
CN-107132730-A Photosensitive resin composition and application thereof 奇美实业股份有限公司 2017-09-05 CN disclosed
CN-104672237-B Based on phenanthroline for electron acceptor organic photosensitive dyestuff and preparation method and application 中国科学院化学研究所 2017-03-01 CN disclosed
CN-104672237-A Organic photosensitive dye based on phenanthroline as electron acceptor as well as preparation method and application of organic photosensitive dye CHINESE ACAD INST CHEMISTRY 2015-06-03 CN disclosed
CN-102898854-B Organic dye taking alkoxy substituted fluorene unit-containing triarylated amine as donor and application thereof in dye-sensitized solar cell CHANGCHUN APPLIED CHEMISTRY 2013-11-27 CN disclosed
CN-102898854-A Organic dye taking alkoxy substituted fluorene unit-containing triarylated amine as donor and application thereof in dye-sensitized solar cell CHANGCHUN APPLIED CHEMISTRY 2013-01-30 CN disclosed
US-20090306376-A1 OPTICAL RECORDING MEDIUM AND COMPOUND USED FOR THE SAME MITSUI CHEMICALS, INC. (JP) 2009-12-10 US disclosed
US-7405030-B2 Imide compound and optical recording media made by using the same MITSUI CHEMICALS, INC. (JP) 2008-07-29 US disclosed
EP-1930339-A2 Imide compound MITSUI CHEMICALS, INC. (JP) 2008-06-11 EP disclosed
US-20070259151-A1 Imide compound and optical recording media made by using the same MITSUI CHEMICALS, INC. (JP) 2007-11-08 US disclosed
US-7259260-B2 Imide compound and optical recording media made by using the same MITSUI CHEMICALS, INC. (JP) 2007-08-21 US disclosed
US-20070054084-A1 Optical recording medium and compound used for the same MITSUI CHEMICALS, INC. (JP) 2007-03-08 US disclosed
US-7166240-B2 Hydrocarbon compounds, materials for organic electroluminescent elements and organic electroluminescent elements MITSUI CHEMICALS, INC. (JP) 2007-01-23 US disclosed
EP-1672626-A1 OPTICAL RECORDING MEDIUM AND COMPOUND USED IN THE OPTICAL RECORDING MEDIUM Mitsui Chemicals, Inc. (JP) 2006-06-21 EP disclosed
US-20050208425-A1 Imide compound and optical recording media made by using the same YAMAMOTO CHEMICALS, INC. (JP) 2005-09-22 US disclosed
US-6929870-B2 Hydrocarbon compounds, materials for organic electroluminescent elements and organic electroluminescent elements MITSUI CHEMICALS, INC. (JP) 2005-08-16 US disclosed
US-20050074631-A1 Hydrocarbon compounds, materials for organic electroluminescent elements and organic electroluminescent elements MITSUI CHEMICALS, INC. (JP) 2005-04-07 US disclosed
EP-1445115-A1 IMIDE COMPOUNDS AND OPTICAL RECORDING MEDIA MADE BY USING THE SAME Mitsui Chemicals, Inc. (JP) 2004-08-11 EP disclosed
US-20030087126-A1 Hydrocarbon compound, material for organic electroluminescent element and organic electroluminescent element IDEMITSU KOSAN CO., LTD. (JP) 2003-05-08 US disclosed
EP-1221434-A1 HYDROCARBON COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT AND ORGANIC ELECTROLUMINESCENT ELEMENT Mitsui Chemicals, Inc. (JP) 2002-07-10 EP 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-20090306376-A1 OPTICAL RECORDING MEDIUM AND COMPOUND USED FOR THE SAME CACNA1B, KCNN4, KCNN2 LTA4H 2574/4885FAAH 1943/4885NR5A1 4308/4885
US-20050208425-A1 Imide compound and optical recording media made by using the same CRY1, MTNR1A, TRPA1 LTA4H 4491/4885FAAH 3493/4885NR5A1 375/4885

“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.