SCHEMBL592872

SCHEMBL592872

Cc1cc(C)cc(-c2cc(C)c(C)cc2C(=O)O)c1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.46
RXRA P19793 1/20 0.46
RXRB P28702 1/20 0.46
TPMT P51580 1/20 0.45
MCL1 Q07820 3/20 0.41
HSD17B10 Q99714 2/20 0.40
GAA P10253 1/20 0.40
HPGD P15428 1/20 0.40
ALDH1A1 P00352 2/20 0.40
CNR2 P34972 1/20 0.40
FTO Q9C0B1 1/20 0.39
CSNK2A1 P68400 1/20 0.38
PTGS2 P35354 1/20 0.38
NOTUM Q6P988 1/20 0.38
TTR P02766 1/20 0.38
MEN1 O00255 1/20 0.37
KMT2A Q03164 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
IP6K1 Q92551 1/20 0.36
IP6K3 Q96PC2 1/20 0.36

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
SCHEMBL29898488 0.90 RXRA (0.50) KDM4ERXRARXRBTPMTMCL1
SCHEMBL6802081 0.82 MCL1 (0.53) KDM4EMCL1HSD17B10GAAHPGD
SCHEMBL6500060 0.80 ALDH1A1 (0.51) MCL1ALDH1A1
SCHEMBL11491969 0.78 HDAC7 (0.51) KDM4ERXRARXRBTPMTMCL1
SCHEMBL24183987 0.78 MCL1 (0.61) KDM4ERXRARXRBMCL1HSD17B10
SCHEMBL29004334 0.76 RXRA (0.59) KDM4ERXRARXRBTPMTHSD17B10
SCHEMBL6497788 0.76 BCL2L1 (0.46) KDM4ERXRARXRBMCL1HSD17B10
SCHEMBL6497146 0.76 NPC1 (0.53) KDM4EMCL1HSD17B10HPGDALDH1A1
SCHEMBL30442476 0.75 KDM4E (0.54) KDM4ETPMTMCL1HSD17B10GAA
SCHEMBL235710 0.75 KDM4E (0.54) KDM4ETPMTMCL1HSD17B10GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8114993-B2 Use of aryl chlorides in palladium-catalyzed C-H bond functionalization THE UNIVERSITY OF HOUSTON SYSTEM (US) 2012-02-14 US disclosed
US-8114993-B2 Use of aryl chlorides in palladium-catalyzed C-H bond functionalization THE UNIVERSITY OF HOUSTON SYSTEM (US) 2012-02-14 US disclosed
US-8114993-B2 Use of aryl chlorides in palladium-catalyzed C-H bond functionalization THE UNIVERSITY OF HOUSTON SYSTEM (US) 2012-02-14 US disclosed
US-20090012293-A1 USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION THE UNIVERSITY OF HOUSTON SYSTEM (US) 2009-01-08 US disclosed
US-20090012293-A1 USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION THE UNIVERSITY OF HOUSTON SYSTEM (US) 2009-01-08 US disclosed
US-20090012293-A1 USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION THE UNIVERSITY OF HOUSTON SYSTEM (US) 2009-01-08 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-20090012293-A1 USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION DBH, DDT, CYCS KDM4E 2925/4885RXRA 2443/4885RXRB 1866/4885

“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.