SCHEMBL7311628

SCHEMBL7311628

C1=C(Oc2ccccc2)CCCC1

nearest known ligand 0.44

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 5/20 0.44
TSHR P16473 1/20 0.44
NR1H2 P55055 1/20 0.35
BAX Q07812 1/20 0.35
MAOA P21397 1/20 0.35
TDP1 Q9NUW8 1/20 0.35
HTR1A P08908 1/20 0.34
SLC6A2 P23975 1/20 0.34
SLC6A4 P31645 1/20 0.34
SLC6A3 Q01959 1/20 0.34
CXCR3 P49682 1/20 0.33
BCHE P06276 1/20 0.33
ACHE P22303 1/20 0.33
NISCH Q9Y2I1 1/20 0.33
KDM1A O60341 1/20 0.32
MAOB P27338 1/20 0.32

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
SCHEMBL10942010 0.94 LTA4H (0.46) LTA4HTSHRNR1H2BAXMAOA
SCHEMBL11776519 0.85 HRH1 (0.37) LTA4HTSHRHTR1ASLC6A2SLC6A4
SCHEMBL1134992 0.82 KDM1A (0.36) KDM1A
Phenol SCHEMBL9511612 0.82 CA12 (0.44) LTA4HTSHRNR1H2BAXTDP1
SCHEMBL14918384 0.80
SCHEMBL10876875 0.79 KDM1A (0.34) KDM1A
SCHEMBL10876868 0.79 KDM1A (0.34) KDM1A
SCHEMBL10876862 0.79 KDM1A (0.34) KDM1A
SCHEMBL677021 0.79
SCHEMBL9049936 0.78 PARP15 (0.47) TSHRTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0559656-A1 PROCESS FOR PREPARING MULTICYCLIC OXY-CONTAINING RING COMPONENTS RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC. (US) 1993-09-15 EP claimed
WO-1992009592-A1 PROCESS FOR PREPARING MULTICYCLIC OXY-CONTAINING RING COMPONENTS RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC. (US) 1992-06-11 WO claimed
US-20230090784-A1 Photoredox Catalysts And Methods Of Using Such Catalysts UNIV COLORADO STATE RES FOUND (US) 2023-03-23 US disclosed
CN-115485067-A Benzoperylene imide photoredox catalysts and methods of using such catalysts 科罗拉多州立大学研究基金会 2022-12-16 CN disclosed
EP-4087679-A2 BENZOPERYLENE IMIDE PHOTOREDOX CATALYSTS AND METHODS OF USING SUCH CATALYSTS Colorado State University Research Foundation (US) 2022-11-16 EP disclosed
WO-2021142444-A2 PHOTOREDOX CATALYSTS AND METHODS OF USING SUCH CATALYSTS COLORADO STATE UNIVERSITY RESEARCH FOUNDATION (US) 2021-07-15 WO disclosed
US-10766851-B1 Method to convert lignin 4-O-5 diaryl ethers and their model compounds into organic chemicals THE ROYAL INSTITUTION FOR THE ADVANCEMENT OF LEARNING / MCGILL UNIVERSITY (CA) 2020-09-08 US disclosed
US-8551686-B2 Antireflective composition for photoresists AZ ELECTRONIC MATERIALS USA CORP. (US) 2013-10-08 US disclosed
US-5466838-A Catalytic reaction of olefin with oxygen in the presence of aldehyde SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1995-11-14 US disclosed
EP-0540009-B1 Process for producing epoxides SUMITOMO CHEMICAL CO (JP) 1995-08-30 EP disclosed
US-5367087-A Process for producing epoxide SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1994-11-22 US disclosed
EP-0540009-A1 Process for producing epoxides SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-05-05 EP disclosed
EP-0494140-A4 DIBENZOFURANCARBOXAMIDES 1992-09-02 EP disclosed
EP-0494140-A1 DIBENZOFURANCARBOXAMIDES RORER INTERNATIONAL (HOLDINGS), INC. (US) 1992-07-15 EP disclosed
WO-1992009592-A1 PROCESS FOR PREPARING MULTICYCLIC OXY-CONTAINING RING COMPONENTS RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC. (US) 1992-06-11 WO disclosed
WO-1992009284-A1 2,6-METHANO-2H-1-BENZOXOCINCARBOXAMIDES AS 5-HT3-ANTAGONISTS RHONE-POULENC RORER INTERNATIONAL (HOLDINGS), INC. (US) 1992-06-11 WO disclosed
US-4959485-A 5-HT3 ANTAGONISTS RORER PHARMACEUTICAL CORPORATION (US) 1990-09-25 US disclosed
WO-1989010364-A1 DIBENZOFURANCARBOXAMIDES RORER INTERNATIONAL (OVERSEAS) INC. (US) 1989-11-02 WO disclosed
EP-0339950-A2 Dibenzofurancarboxamides, their use as pharmaceutical agents, a composition containing the same, and a process for the preparation thereof RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC. (US) 1989-11-02 EP disclosed
US-4863921-A Dibenzofurancarboxamides and their pharmaceutical compositions and methods RORER PHARMACEUTICAL CORPORATION (US) 1989-09-05 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-10766851-B1 Method to convert lignin 4-O-5 diaryl ethers and their model compounds into organic chemicals PPOX, DAO, PAH LTA4H 738/4885TSHR 4656/4885NR1H2 1666/4885
US-20230090784-A1 Photoredox Catalysts And Methods Of Using Such Catalysts PPOX, PAH, AHR LTA4H 1501/4885TSHR 4697/4885NR1H2 2361/4885

“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.