SCHEMBL722344

SCHEMBL722344

C[C@H](NCc1ccc(F)cc1F)C(=O)OP(=O)(Cl)Oc1cccc2ccccc12

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARG P37231 3/20 0.42
MAOB P27338 3/20 0.41
SMN1; SMN2 Q16637 1/20 0.36
MAOA P21397 1/20 0.36
TGM2 P21980 1/20 0.36
KDM4E B2RXH2 2/20 0.36
ALDH1A1 P00352 2/20 0.36
TDP1 Q9NUW8 1/20 0.36
PSMB11 A5LHX3 1/20 0.36
PSMA7 O14818 1/20 0.36
PSMB1 P20618 1/20 0.36
PSMA1 P25786 1/20 0.36
PSMA2 P25787 1/20 0.36
PSMA3 P25788 1/20 0.36
PSMA4 P25789 1/20 0.36
PSMB8 P28062 1/20 0.36
PSMB9 P28065 1/20 0.36
PSMA5 P28066 1/20 0.36
PSMB4 P28070 1/20 0.36
PSMB6 P28072 1/20 0.36

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
SCHEMBL18192797 0.87 PPARG (0.41) PPARGMAOBSMN1; SMN2TGM2MME
SCHEMBL15486994 0.83 ACP3 (0.45) KDM4EALDH1A1TDP1PSMB5KMT2A
SCHEMBL15720879 0.83 ACP3 (0.45) KDM4EALDH1A1TDP1PSMB5KMT2A
SCHEMBL721545 0.78 PPARG (0.40) PPARGMAOBSMN1; SMN2TGM2KMT2A
SCHEMBL721544 0.78 PPARG (0.40) PPARGMAOBSMN1; SMN2TGM2KMT2A
SCHEMBL15720921 0.77 CYP2D6 (0.46) SMN1; SMN2KDM4EALDH1A1TDP1KMT2A
SCHEMBL1028181 0.76 BTN3A1 (0.40) KDM4EALDH1A1KMT2AMEN1BTN3A1
SCHEMBL1786739 0.76 BTN3A1 (0.41) KDM4EALDH1A1KMT2ABTN3A1
SCHEMBL15487036 0.75 ALDH1A1 (0.39) KDM4EALDH1A1KMT2AMEN1BTN3A1
SCHEMBL723909 0.75 PPARG (0.39) PPARGMAOBSMN1; SMN2ALDH1A1SCN9A

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-8759318-B2 Phosphoramidate derivatives of guanosine nucleoside compounds for treatment of viral infections INHIBITEX, INC. (US) 2014-06-24 US disclosed
US-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections UNIVERSITY COLLEGE CARDIFF CONSULTANTS LIMITED (GB) 2012-03-01 US disclosed
EP-2385951-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS University College Cardiff Consultants, Ltd. (GB) 2011-11-16 EP disclosed
US-20110254856-A1 MOBILE TERMINAL AND METHOD OF CONTROLLING OPERATION OF THE MOBILE TERMINAL LG ELECTRONICS INC. (KR) 2011-10-20 US disclosed
WO-2010081082-A2 PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS UNIVERSITY COLLEGE OF CARDIFF CONSULTANTS LIMITED (GB) 2010-07-15 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-20120052046-A1 Phosphoramidate Derivatives of Guanosine Nucleoside Compunds for Treatment of Viral Infections PNP, SAMHD1, MTAP PPARG 1792/4885MAOB 3783/4885SMN1; SMN2 858/4885

“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.