SCHEMBL7108246

SCHEMBL7108246

O=C(NC(=O)c1c(F)cccc1F)Nc1ccc(OC(F)(F)C(F)F)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 5/20 0.53
KMT2A Q03164 5/20 0.53
MAPT P10636 3/20 0.53
USP2 O75604 1/20 0.53
ALOX15 P16050 1/20 0.53
TDP1 Q9NUW8 2/20 0.50
TRPV1 Q8NER1 1/20 0.50
EPHX2 P34913 2/20 0.49
ATM Q13315 1/20 0.48
NPC1 O15118 4/20 0.46
RAB9A P51151 3/20 0.46
PKM P14618 1/20 0.46
KDM4E B2RXH2 2/20 0.46
ALDH1A1 P00352 1/20 0.46
MAPK1 P28482 1/20 0.46
SMN1; SMN2 Q16637 2/20 0.45
HTT P42858 2/20 0.45
LMNA P02545 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
TLR8 Q9NR97 4/20 0.43

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
SCHEMBL10707659 0.96 MEN1 (0.50) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL11026869 0.91 MEN1 (0.53) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL10871199 0.91 MEN1 (0.64) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL10795425 0.90 TDP1 (0.51) MEN1KMT2AMAPTUSP2ALOX15
Diftrifmeouron SCHEMBL7104017 0.90 EPHX2 (0.63) MEN1KMT2AMAPTTDP1TRPV1
SCHEMBL9651342 0.89 MEN1 (0.48) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL11552769 0.88 TRPV1 (0.48) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL9635433 0.87 MEN1 (0.52) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL10786095 0.87 MEN1 (0.43) MEN1KMT2AMAPTUSP2ALOX15
SCHEMBL9651658 0.87 MEN1 (0.47) MEN1KMT2AMAPTUSP2ALOX15

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-RE32418-E INSECTICIDES THE DOW CHEMICAL COMPANY (US) 1987-05-12 US claimed
US-4170657-A INSECTICIDES THE DOW CHEMICAL COMPANY (US) 1979-10-09 US claimed
US-4089975-A DIPHENYL ACYLUREA DERIVATIVE THE DOW CHEMICAL COMPANY (US) 1978-05-16 US claimed
EP-0917822-B1 Method to control animal ecto-parasites SUMITOMO CHEMICAL CO (JP) 2003-10-08 EP disclosed
US-6333355-B2 1-(2,6-DIFLUOROBENZOYL)-3-(2-FLUORO-4-(1,1,2,3,3,3 -HEXAFLUOROP ROPOXY)PHENYL)UREA; FLEAS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-12-25 US disclosed
US-20010044470-A1 METHOD TO CONTROL ANIMAL ECTO-PARASITES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-11-22 US disclosed
EP-0917822-A1 Method to control animal ecto-parasites SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1999-05-26 EP disclosed
US-4431667-A Imino ethers useful for controlling insect and arachnoid pests THE UPJOHN COMPANY (US) 1984-02-14 US disclosed
US-4089975-A DIPHENYL ACYLUREA DERIVATIVE THE DOW CHEMICAL COMPANY (US) 1978-05-16 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 (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-20010044470-A1 METHOD TO CONTROL ANIMAL ECTO-PARASITES ENPP3, ENPP1, TUBA3C MEN1 3311/4885KMT2A 1802/4885MAPT 4466/4885

“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.