SCHEMBL4354387

SCHEMBL4354387

C#Cc1ccccc1C(=O)c1ccc(-c2ccc(F)cc2)cc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CDC25B P30305 1/20 0.47
ATM Q13315 1/20 0.47
BCL2L1 Q07817 1/20 0.44
BAD Q92934 1/20 0.44
HPGD P15428 3/20 0.42
SMN1; SMN2 Q16637 3/20 0.42
MEN1 O00255 3/20 0.42
KMT2A Q03164 3/20 0.42
HTT P42858 2/20 0.42
NPSR1 Q6W5P4 2/20 0.42
NPC1 O15118 2/20 0.42
MAPT P10636 2/20 0.42
ALOX12 P18054 1/20 0.42
CHRNA7 P36544 2/20 0.40
HSD11B1 P28845 2/20 0.40
LMNA P02545 3/20 0.40
USP2 O75604 1/20 0.40
ALDH1A1 P00352 1/20 0.40
POLB P06746 1/20 0.40
ALPG P10696 1/20 0.40

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
SCHEMBL1746496 1.00 CDC25B (0.47) CDC25BATMBCL2L1BADHPGD
SCHEMBL3611155 0.95 SMN1; SMN2 (0.45) CDC25BATMHPGDSMN1; SMN2MEN1
SCHEMBL4305925 0.87 ATM (0.53) CDC25BATMMEN1KMT2ANPSR1
SCHEMBL4358130 0.86 MAPT (0.56) CDC25BATMBCL2L1HPGDMEN1
SCHEMBL4354384 0.84 CDC25B (0.51) CDC25BATMBCL2L1BADMEN1
SCHEMBL1637254 0.81 AKR1C3 (0.55) CDC25BATMMEN1KMT2ANPSR1
SCHEMBL13444936 0.79 AKR1C3 (0.59) HPGDSMN1; SMN2MEN1KMT2ANPSR1
SCHEMBL15660414 0.78 SLC6A4 (0.49) CDC25BATMBCL2L1BADHPGD
SCHEMBL7557424 0.77 NPC1 (0.41) CDC25BHPGDSMN1; SMN2NPC1MAPT
SCHEMBL1754308 0.77 AKR1C3 (0.58) CDC25BATMHPGDSMN1; SMN2MEN1

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-8952200-B2 Liquid crystal oligomer, synthesis composition, preparation method thereof, and liquid crystal material BOE TECHNOLOGY GROUP CO., LTD. (CN) 2015-02-10 US disclosed
US-20120264980-A1 LIQUID CRYSTAL OLIGOMER, SYNTHESIS COMPOSITION, PREPARATION METHOD THEREOF, AND LIQUID CRYSTAL MATERIAL BEIJING BOE DISPLAY TECHNOLOGY CO., LTD (CN) 2012-10-18 US disclosed
EP-1457511-B1 CROSSLINKABLE AROMATIC RESINS HAVING PROTONIC ACID GROUPS AND ION CONDUCTIVE POLYMER MEMBRANES BINDERS AND FUEL CELLS MADE BY USING THE SAME MITSUI CHEMICALS INC (JP) 2009-07-15 EP disclosed
US-20040191602-A1 Crosslinkable aromatic resin having protonic acid group, and ion conductive polymer membrane, binder and fuel cell using the resin MITSUI CHEMICALS, INC. (JP) 2004-09-30 US disclosed
EP-1457511-A1 CROSSLINKABLE AROMATIC RESINS HAVING PROTONIC ACID GROUPS AND ION CONDUCTIVE POLYMER MEMBRANES BINDERS AND FUEL CELLS MADE BY USING THE SAME Mitsui Chemicals, Inc. (JP) 2004-09-15 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 (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-20120264980-A1 LIQUID CRYSTAL OLIGOMER, SYNTHESIS COMPOSITION, PREPARATION METHOD THEREOF, AND LIQUID CRYSTAL MATERIAL RNMT, DNMT3A, DNMT1 CDC25B 1975/4885ATM 1208/4885BCL2L1 1122/4885

“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.