SCHEMBL48235

SCHEMBL48235

CCc1ccc(C(=O)c2cc(Br)ccc2Cl)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.52
HTT P42858 2/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
ALDH1A1 P00352 4/20 0.50
CCR9 P51686 1/20 0.49
RAB9A P51151 1/20 0.49
GAA P10253 3/20 0.47
HPGD P15428 5/20 0.46
CNR1 P21554 1/20 0.46
CNR2 P34972 1/20 0.46
THRB P10828 1/20 0.45
CYP1A2 P05177 1/20 0.45
CYP4F2 P78329 1/20 0.44
CYP4A11 Q02928 1/20 0.44
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
KDM4E B2RXH2 2/20 0.44
LMNA P02545 1/20 0.44
POLB P06746 1/20 0.44
ALOX12 P18054 1/20 0.44

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
SCHEMBL499583 0.86 ALDH1A1 (0.47) MAPTSMN1; SMN2ALDH1A1GAAHPGD
SCHEMBL6442541 0.85 ALDH1A1 (0.46) MAPTSMN1; SMN2ALDH1A1GAAHPGD
SCHEMBL9063310 0.84 GAA (0.59) MAPTHTTSMN1; SMN2ALDH1A1RAB9A
SCHEMBL499767 0.83 MAPT (0.67) MAPTHTTALDH1A1RAB9AGAA
SCHEMBL13979890 0.82 GAA (0.47) MAPTHTTSMN1; SMN2ALDH1A1RAB9A
SCHEMBL12290954 0.82 MAPT (0.52) MAPTHTTSMN1; SMN2ALDH1A1CCR9
SCHEMBL4844927 0.82 MAPT (0.70) MAPTHTTSMN1; SMN2ALDH1A1CCR9
SCHEMBL29809563 0.81 KDM4E (0.65) MAPTHTTSMN1; SMN2ALDH1A1GAA
SCHEMBL17019 0.81 KDM4E (0.65) MAPTHTTSMN1; SMN2ALDH1A1GAA
SCHEMBL499641 0.81 ALDH1A1 (0.43) MAPTHTTSMN1; SMN2ALDH1A1GAA

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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2230907-B1 BENZYLPHENYL CYCLOHEXANE DERIVATIVES AND METHODS OF USE THERACOS INC (US) 2018-05-09 EP disclosed
EP-2230907-B1 BENZYLPHENYL CYCLOHEXANE DERIVATIVES AND METHODS OF USE THERACOS INC (US) 2018-05-09 EP disclosed
US-8129434-B2 Benzylphenyl cyclohexane derivatives and methods of use THERACOS, INC. (US) 2012-03-06 US disclosed
US-8129434-B2 Benzylphenyl cyclohexane derivatives and methods of use THERACOS, INC. (US) 2012-03-06 US disclosed
US-8129434-B2 Benzylphenyl cyclohexane derivatives and methods of use THERACOS, INC. (US) 2012-03-06 US disclosed
EP-2230907-A1 BENZYLPHENYL CYCLOHEXANE DERIVATIVES AND METHODS OF USE Theracos, Inc. (US) 2010-09-29 EP disclosed
EP-2147008-A2 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME Bristol-Myers Squibb Company (US) 2010-01-27 EP disclosed
US-7589193-B2 C-aryl glucoside SGLT2 inhibitors and method BRISTOL-MYERS SQUIBB COMPANY (US) 2009-09-15 US disclosed
US-7589193-B2 C-aryl glucoside SGLT2 inhibitors and method BRISTOL-MYERS SQUIBB COMPANY (US) 2009-09-15 US disclosed
US-7589193-B2 C-aryl glucoside SGLT2 inhibitors and method BRISTOL-MYERS SQUIBB COMPANY (US) 2009-09-15 US disclosed
EP-1791852-B1 C-ARYL GLUCOSIDE SGLT2 INHIBITORS AND METHOD FOR THEIR PRODUCTION BRISTOL MYERS SQUIBB CO (US) 2008-12-31 EP disclosed
EP-1791852-B1 C-ARYL GLUCOSIDE SGLT2 INHIBITORS AND METHOD FOR THEIR PRODUCTION BRISTOL MYERS SQUIBB CO (US) 2008-12-31 EP disclosed
WO-2008144346-A2 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR THEIR PREPARATION BRISTOL-MYERS SQUIBB COMPANY (US) 2008-11-27 WO disclosed
WO-2008144346-A2 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR THEIR PREPARATION BRISTOL-MYERS SQUIBB COMPANY (US) 2008-11-27 WO disclosed
US-20080287529-A1 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME BRISTOL-MYERS SQUIBB COMPANY 2008-11-20 US disclosed
US-20080287529-A1 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME BRISTOL-MYERS SQUIBB COMPANY 2008-11-20 US disclosed
US-20080287529-A1 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME BRISTOL-MYERS SQUIBB COMPANY 2008-11-20 US disclosed
EP-1791852-A2 C-ARYL GLUCOSIDE SGLT2 INHIBITORS AND METHOD FOR THEIR PRODUCTION Brystol-Myers Squibb Company (US) 2007-06-06 EP disclosed
WO-2006034489-A2 C-ARYL GLUCOSIDE SGLT2 INHIBITORS AND METHOD FOR THEIR PRODUCTION BRISTOL-MYERS SQUIBB COMPANY (US) 2006-03-30 WO disclosed
US-20060063722-A1 C-aryl glucoside SGLT2 inhibitors and method BRISTOL-MYERS SQUIBB COMPANY 2006-03-23 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 (2 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-20080287529-A1 CRYSTAL STRUCTURES OF SGLT2 INHIBITORS AND PROCESSES FOR PREPARING SAME SLC5A2, SLC5A1, SLC2A1 MAPT 862/4885HTT 887/4885SMN1; SMN2 3001/4885
US-20060063722-A1 C-aryl glucoside SGLT2 inhibitors and method SLC5A2, SLC5A1, GCG MAPT 1260/4885HTT 1943/4885SMN1; SMN2 4490/4885

“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.