SCHEMBL1307659

SCHEMBL1307659

COc1ccc(-c2ccco2)cc1C(O)c1ccccc1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 5/20 0.42
KMT2A Q03164 5/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
ERN1 O75460 1/20 0.42
TP53 P04637 1/20 0.42
NFKB1 P19838 1/20 0.42
MAPK1 P28482 1/20 0.42
NFKB2 Q00653 1/20 0.42
RELA Q04206 1/20 0.42
CNR2 P34972 1/20 0.42
HPGD P15428 2/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41
MAPT P10636 1/20 0.41
TSHR P16473 1/20 0.41
HSD17B10 Q99714 1/20 0.41
ADORA2A P29274 2/20 0.40
PIK3R1 P27986 1/20 0.40
PIK3CA P42336 1/20 0.40
TACR1 P25103 1/20 0.39

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
SCHEMBL1309639 0.82 MEN1 (0.43) MEN1KMT2ASMN1; SMN2ERN1TP53
SCHEMBL1308701 0.77 TUBB4A (0.37) MEN1KMT2ASMN1; SMN2ERN1TP53
SCHEMBL11634342 0.75 MEN1 (0.66) MEN1KMT2ASMN1; SMN2ERN1TP53
SCHEMBL30943709 0.74 ADRA2A (0.57) MEN1KMT2AMAPK1CNR2TSHR
SCHEMBL22910008 0.74 CNR2 (0.47) MEN1KMT2ACNR2ALDH1A1MAPT
SCHEMBL8806213 0.74 ADRA2A (0.57) MEN1KMT2AMAPK1CNR2TSHR
SCHEMBL477540 0.73 IDO1 (0.55) MEN1KMT2ASMN1; SMN2TP53CNR2
SCHEMBL30986735 0.73 IDO1 (0.55) MEN1KMT2ASMN1; SMN2TP53CNR2
SCHEMBL3862578 0.73 IDO1 (0.55) MEN1KMT2ASMN1; SMN2TP53CNR2
SCHEMBL30273872 0.73 IDO1 (0.55) MEN1KMT2ASMN1; SMN2TP53CNR2

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
EP-2066632-B1 BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE CHONG KUN DANG PHARM CORP (KR) 2013-09-04 EP disclosed
US-8053439-B2 Benzophenone derivatives useful for inhibiting formation of microtubule CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2011-11-08 US disclosed
US-20090275575-A1 BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2009-11-05 US disclosed
EP-2066632-A1 BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE Chong Kun Dang Pharmaceutical Corp. (KR) 2009-06-10 EP disclosed
WO-2008038955-A1 BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2008-04-03 WO 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-20090275575-A1 BENZOPHENONE DERIVATIVES USEFUL FOR INHIBITING FORMATION OF MICROTUBULE TUBB1, TUBA1C, TUBB6 MEN1 3206/4885KMT2A 3246/4885SMN1; SMN2 1781/4885

“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.