SCHEMBL6476026

SCHEMBL6476026

O=C(Cl)c1cccc(OCc2ccccc2)c1OCc1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SGMS2 Q8NHU3 3/20 0.52
PTGER1 P34995 1/20 0.51
NPC1 O15118 2/20 0.50
HTT P42858 1/20 0.50
FABP3 P05413 2/20 0.49
FABP4 P15090 2/20 0.49
FABP5 Q01469 2/20 0.49
GLRA1 P23415 1/20 0.49
GAA P10253 1/20 0.49
L3MBTL1 Q9Y468 3/20 0.49
MAPT P10636 2/20 0.49
TDP1 Q9NUW8 2/20 0.49
MAPK1 P28482 1/20 0.49
MEN1 O00255 3/20 0.47
KMT2A Q03164 3/20 0.47
FAAH O00519 1/20 0.47
CNR1 P21554 1/20 0.47
CNR2 P34972 1/20 0.47
LMNA P02545 1/20 0.47
ALDH1A1 P00352 1/20 0.47

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
SCHEMBL6775743 0.90 SCN9A (0.57) NPC1GLRA1L3MBTL1MEN1KMT2A
SCHEMBL514323 0.88 L3MBTL1 (0.50) SGMS2PTGER1NPC1GLRA1L3MBTL1
SCHEMBL1305739 0.87 PTGER1 (0.61) SGMS2PTGER1NPC1HTTFABP3
SCHEMBL341109 0.87 SGMS2 (0.62) SGMS2PTGER1NPC1HTTGAA
SCHEMBL16789583 0.85 GLRA1 (0.55) SGMS2GLRA1L3MBTL1MAPTTDP1
SCHEMBL7689222 0.84 SGMS2 (0.52) SGMS2PTGER1NPC1HTTGAA
SCHEMBL7689226 0.84 PARP1 (0.61) SGMS2PTGER1NPC1HTTGAA
SCHEMBL28181099 0.84 CHRM4 (0.53) SGMS2PTGER1NPC1HTTGAA
SCHEMBL8489879 0.84 MAPT (0.57) SGMS2PTGER1NPC1HTTGAA
SCHEMBL20456203 0.84 RXRA (0.42) SGMS2PTGER1NPC1HTTGLRA1

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-4290532-A2 SEPARATION OF METAL IONS BY LIQUID-LIQUID EXTRACTION The Regents of the University of California (US) 2023-12-13 EP disclosed
EP-3520117-B1 SEPARATION OF METAL IONS BY LIQUID-LIQUID EXTRACTION UNIV CALIFORNIA (US) 2023-11-08 EP disclosed
US-11235076-B2 Chelating platform for delivery of radionuclides FRED HUTCHINSON CANCER RESEARCH CENTER (US) 2022-02-01 US disclosed
US-11149046-B2 Antibacterial sideromycins Hsiri Therapeutics, Inc. (US) 2021-10-19 US disclosed
US-20210009510-A1 CHELATING MOLECULES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2021-01-14 US disclosed
US-20190287691-A1 SEPARATION OF METAL IONS BY LIQUID-LIQUID EXTRACTION THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2019-09-19 US disclosed
US-20190184041-A1 CHELATING PLATFORM FOR DELIVERY OF RADIONUCLIDES FRED HUTCHINSON CANCER RESEARCH CENTER (US) 2019-06-20 US disclosed
US-20190153010-A1 ANTIBACTERIAL SIDEROMYCINS Hsiri Therapeutics, LLC 2019-05-23 US disclosed
WO-2018063638-A1 CHELATING MOLECULES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2018-04-05 WO disclosed
WO-2018044812-A2 CHELATING PLATFORM FOR DELIVERY OF RADIONUCLIDES FRED HUTCHINSON CANCER RESEARCH CENTER (US) 2018-03-08 WO disclosed
EP-1077931-B1 BENZAMIDE DERIVATIVES FOR THE TREATMENT OF DISEASES MEDIATED BY CYTOKINES ASTRAZENECA AB (SE) 2004-11-17 EP disclosed
US-20030212068-A1 Benzamide derivatives for the treatment of diseases mediated by cytokines ASTRAZENECA AB 2003-11-13 US disclosed
US-6579872-B1 Such as TNF, in particular of TNF alpha, and various interleukins, in particular IL-1; N-(5-(4-(3-hydroxypropoxy)benzamido)-2-methylphenyl)-3,4-dimethoxybenzamide ASTRAZENECA AB (SE) 2003-06-17 US disclosed
US-6380181-B1 AMINO ACID RESIDUES IN THE 3-AND/OR 4-POSITION FUNCTION AS SIDEROPHORES AND/OR AS BIOLOGICAL CHELATING AGENTS FOR IRON IN GRAM-NEGATIVE BACTERIA GRUENENTHAL GMBH (DE) 2002-04-30 US disclosed
EP-0907633-B1 NEW SYNTHETIC CATECHOL DERIVATIVES, METHOD FOR PRODUCTION AND USE THEREOF GRUENENTHAL GMBH (DE) 2001-08-22 EP disclosed
EP-1077931-A1 BENZAMIDE DERIVATIVES FOR THE TREATMENT OF DISEASES MEDIATED BY CYTOKINES AstraZeneca AB (SE) 2001-02-28 EP disclosed
WO-1999059959-A1 BENZAMIDE DERIVATIVES FOR THE TREATMENT OF DISEASES MEDIATED BY CYTOKINES ASTRAZENECA AB (SE) 1999-11-25 WO disclosed
EP-0241915-B1 METHOD FOR DETERMINING CHOLINESTERASE ACTIVITY NITTO BOSEKI CO., LTD. (JP) 1992-07-08 EP disclosed
US-4861713-A Novel method for determining cholinesterase activity NITTO BOSEKI CO., LTD. (JP) 1989-08-29 US disclosed
EP-0241915-A1 Method for determining cholinesterase activity NITTO BOSEKI CO., LTD. (JP) 1987-10-21 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 (7 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-20190184041-A1 CHELATING PLATFORM FOR DELIVERY OF RADIONUCLIDES SLC40A1, TFRC, SLC39A14 SGMS2 2311/4885PTGER1 3714/4885NPC1 664/4885
US-20030212068-A1 Benzamide derivatives for the treatment of diseases mediated by cytokines IL2, IL6, IL6ST SGMS2 1584/4885PTGER1 592/4885NPC1 1549/4885
US-20190287691-A1 SEPARATION OF METAL IONS BY LIQUID-LIQUID EXTRACTION SLC39A14, SLC39A11, SLC39A7 SGMS2 3817/4885PTGER1 4828/4885NPC1 2967/4885
US-11235076-B2 Chelating platform for delivery of radionuclides SLC40A1, TFRC, SLC39A14 SGMS2 2311/4885PTGER1 3714/4885NPC1 664/4885
US-20210009510-A1 CHELATING MOLECULES SLC39A3, SLC30A6, SLC30A7 SGMS2 678/4885PTGER1 4404/4885NPC1 1603/4885
US-11149046-B2 Antibacterial sideromycins SLC40A1, SFXN1, SLC39A14 SGMS2 737/4885PTGER1 4537/4885NPC1 2148/4885
US-20190153010-A1 ANTIBACTERIAL SIDEROMYCINS SLC40A1, SFXN1, SLC39A14 SGMS2 737/4885PTGER1 4537/4885NPC1 2148/4885

“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.