SCHEMBL6402665

SCHEMBL6402665

CCCc1ccc(-c2cc(F)c(CC=C(F)F)c(F)c2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RARB P10826 5/20 0.41
RARA P10276 1/20 0.41
RARG P13631 1/20 0.41
MCL1 Q07820 1/20 0.38
KIF11 P52732 1/20 0.38
NPC1 O15118 3/20 0.35
RAB9A P51151 3/20 0.35
TP53 P04637 1/20 0.35
PKM P14618 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
HSD17B10 Q99714 1/20 0.35
LPL P06858 1/20 0.34
LIPG Q9Y5X9 1/20 0.34
CHKA P35790 1/20 0.34
THRB P10828 2/20 0.33
ALOX5 P09917 1/20 0.33
MAOB P27338 1/20 0.33
MAPT P10636 1/20 0.33
GFER P55789 1/20 0.33
CNR1 P21554 1/20 0.33

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
SCHEMBL502961 0.91 RARB (0.40) RARBRARARARGMCL1KIF11
SCHEMBL503184 0.84 RARB (0.43) RARBRARARARGMCL1KIF11
SCHEMBL16039309 0.83 RARB (0.46) RARBRARARARGMCL1KIF11
SCHEMBL9625064 0.82 MCL1 (0.41) RARBRARAMCL1NPC1RAB9A
SCHEMBL6409307 0.82 RARB (0.43) RARBRARARARGMCL1KIF11
SCHEMBL10030218 0.81 RARB (0.50) RARBRARARARGTP53HSD17B10
SCHEMBL12656525 0.78 RARB (0.43) RARBRARARARGMCL1NPC1
SCHEMBL15868561 0.76 RARB (0.44) RARBRARARARGMCL1KIF11
SCHEMBL16038459 0.76 MCL1 (0.49) RARBRARARARGMCL1NPC1
SCHEMBL9624346 0.76 MCL1 (0.41) RARBRARAMCL1NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6864397-B2 Difluoromethyl ether derivative and process for producing the same CHISSO CORPORATION (JP) 2005-03-08 US disclosed
US-6827876-B2 Using alpha, alpha -difluorocyclohexylidene derivative as starting material to obtain difluoromethyl ether derivative CHISSO CORPORATION (JP) 2004-12-07 US disclosed
US-20040016906-A1 Difluoromethyl ether derivative and process for producing the same JNC CORPORATION (JP) 2004-01-29 US disclosed
US-20040004207-A1 Difluoromethyl ether derivative and process for producing the same JNC CORPORATION (JP) 2004-01-08 US disclosed
US-6605747-B2 Reacting the starting material, an alpha , alpha -difluorocyclohexylidene derivative with a halogen to produce an intermediate, reacting the intermediate with a phenol compound in presence of a base CHISSO CORPORATION (JP) 2003-08-12 US disclosed
US-20020120168-A1 Difluoromethyl ether derivative and process for producing the same JNC PETROCHEMICAL CORPORATION (JP) 2002-08-29 US disclosed
EP-1182186-A2 Difluoromethyl ether derivative and process for producing the same CHISSO CORPORATION (JP) 2002-02-27 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 (3 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-20040004207-A1 Difluoromethyl ether derivative and process for producing the same RCC1, PYM1, SCFD1 RARB 3277/4885RARA 2698/4885RARG 3554/4885
US-20040016906-A1 Difluoromethyl ether derivative and process for producing the same RCC1, SCFD1, AFF1 RARB 3298/4885RARA 2721/4885RARG 3614/4885
US-20020120168-A1 Difluoromethyl ether derivative and process for producing the same LEF1, AFF1, RCC1 RARB 2584/4885RARA 2060/4885RARG 2720/4885

“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.