SCHEMBL7795645

SCHEMBL7795645

O=[P](c1cccc(C(F)(F)F)c1)c1cccc(C(F)(F)F)c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 1/20 0.48
TSHR P16473 2/20 0.48
MAPK1 P28482 1/20 0.48
MGLL Q99685 1/20 0.44
MAPT P10636 2/20 0.43
ALDH1A1 P00352 1/20 0.42
P2RX1 P51575 1/20 0.42
LMNA P02545 1/20 0.42
ACP3 P15309 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
MMP1 P03956 1/20 0.42
MMP2 P08253 1/20 0.42
MMP9 P14780 1/20 0.42
MMP8 P22894 1/20 0.42
MMP13 P45452 1/20 0.42
TAAR1 Q96RJ0 1/20 0.41
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41
SRD5A2 P31213 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
SCHEMBL7167520 0.82 TSHR (0.52) CES2TSHRMAPK1MGLLMAPT
SCHEMBL2153943 0.78 HDAC8 (0.47) ALDH1A1P2RX1RAB9A
SCHEMBL10705760 0.78 TSHR (0.48) CES2TSHRMAPK1MGLLMAPT
SCHEMBL3025058 0.78 CES2 (0.48) CES2TSHRMAPK1MGLLMAPT
SCHEMBL7798387 0.77 CES2 (0.46) CES2TSHRMAPTALDH1A1P2RX1
SCHEMBL29149633 0.76 TSHR (0.52) TSHRMAPK1MAPTALDH1A1LMNA
SCHEMBL62723 0.75 TSHR (0.67) CES2TSHRMAPK1MGLLMAPT
SCHEMBL2154620 0.74 HDAC8 (0.43) MAPK1MAPTALDH1A1KMT2AHTT
Benzene SCHEMBL8568955 0.73 TSHR (0.67) CES2TSHRMAPK1MGLLMAPT
SCHEMBL30553105 0.73 TSHR (0.64) CES2TSHRMAPK1MGLLMAPT

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-8722912-B2 Metal complex compound and process for producing amides utilizing the metal complex compound NATIONAL UNIVERSITY CORPORATION OKAYAMA UNIVERSITY (JP) 2014-05-13 US disclosed
US-20130131366-A1 Metal Complex Compound and Process for Producing Amides Utilizing the Metal Complex Compound NATIONAL UNIVERSITY CORPORATION OKAYAMA UNIVERSITY (JP) 2013-05-23 US disclosed
EP-0731105-B1 Optically active tertiary phosphine compounds, transition metal complexes comprising the same as ligands and process for preparing optically active organic silicon compounds using said transition metal complexes SUMITOMO CHEMICAL CO (JP) 2001-12-05 EP disclosed
US-5621129-A Optically active tertiary phosphine compound, transition metal complex comprising the same as ligand and process for preparing optically active organic silicon compound using said transition metal complex SUMITOMO CHEMICAL CO., LTD. (JP) 1997-04-15 US disclosed
EP-0731105-A1 Optically active tertiary phosphine compounds, transition metal complexes comprising the same as ligands and process for preparing optically active organic silicon compounds using said transition metal complexes SUMITOMO CHEMICAL COMPANY LIMITED (JP) 1996-09-11 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-20130131366-A1 Metal Complex Compound and Process for Producing Amides Utilizing the Metal Complex Compound AP2M1, ASH2L, AP2A1 CES2 3764/4885TSHR 1738/4885MAPK1 1811/4885

“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.