SCHEMBL16807276

SCHEMBL16807276

Cc1cccc(C(C(=O)c2ccc(Cl)cc2)c2ccccc2)c1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.54
TDP1 Q9NUW8 1/20 0.54
MAOA P21397 1/20 0.46
MAOB P27338 1/20 0.46
KCNK3 O14649 1/20 0.45
ACP3 P15309 1/20 0.44
MDM2 Q00987 1/20 0.44
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
POLB P06746 1/20 0.43
CES2 O00748 2/20 0.42
CES1 P23141 2/20 0.42
KDM4E B2RXH2 3/20 0.41
ALDH1A1 P00352 2/20 0.41
NTSR1 P30989 1/20 0.41
LMNA P02545 1/20 0.41
HTT P42858 1/20 0.41
MCL1 Q07820 1/20 0.41

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
SCHEMBL16807280 0.90 L3MBTL1 (0.56) L3MBTL1TDP1MDM2MEN1KMT2A
SCHEMBL16807284 0.89 L3MBTL1 (0.69) L3MBTL1TDP1KCNK3ACP3MEN1
SCHEMBL16807274 0.86 L3MBTL1 (0.59) L3MBTL1TDP1NPC1RAB9AMEN1
SCHEMBL16807273 0.85 L3MBTL1 (0.62) L3MBTL1TDP1ACP3MEN1KMT2A
SCHEMBL16781984 0.84 L3MBTL1 (0.70) L3MBTL1TDP1MEN1KMT2APOLB
SCHEMBL16781983 0.84 L3MBTL1 (0.56) L3MBTL1TDP1MDM2MEN1KMT2A
SCHEMBL16781985 0.82 TDP1 (0.54) L3MBTL1TDP1MDM2NPC1RAB9A
SCHEMBL16807282 0.82 TDP1 (0.50) L3MBTL1TDP1MDM2NPC1RAB9A
SCHEMBL16781981 0.79 CES2 (0.51) L3MBTL1TDP1ACP3MDM2MEN1
SCHEMBL7589819 0.79 L3MBTL1 (0.73) L3MBTL1TDP1MAOBMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9656947-B2 Process for creating carbon-carbon bonds using carbonyl compounds CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S) (FR) 2017-05-23 US disclosed
US-9656947-B2 Process for creating carbon-carbon bonds using carbonyl compounds CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S) (FR) 2017-05-23 US disclosed
EP-2858966-B1 PROCESS FOR CREATING CARBON-CARBON BONDS USING CARBONYL COMPOUNDS CENTRE NAT RECH SCIENT (FR) 2016-08-10 EP disclosed
US-20150166464-A1 PROCESS FOR CREATING CARBON-CARBON BONDS USING CARBONYL COMPOUNDS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N. R.S.) (FR) 2015-06-18 US disclosed
US-20150166464-A1 PROCESS FOR CREATING CARBON-CARBON BONDS USING CARBONYL COMPOUNDS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N. R.S.) (FR) 2015-06-18 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-20150166464-A1 PROCESS FOR CREATING CARBON-CARBON BONDS USING CARBONYL COMPOUNDS CBR3, CBR1, CYP4F3 L3MBTL1 4386/4885TDP1 4876/4885MAOA 276/4885

“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.