SCHEMBL723660

SCHEMBL723660

CC(NP(=O)(Cl)Oc1cccc2ncccc12)C(=O)OC1CCOCC1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CASP1 P29466 1/20 0.37
CASP3 P42574 1/20 0.37
CASP7 P55210 1/20 0.37
CASP8 Q14790 1/20 0.37
HCRTR1 O43613 1/20 0.36
HCRTR2 O43614 1/20 0.36
KAT2B Q92831 1/20 0.35
BAZ2B Q9UIF8 1/20 0.35
GRM4 Q14833 3/20 0.35
ALDH1A1 P00352 1/20 0.35
SYK P43405 2/20 0.34
NR3C1 P04150 1/20 0.34
GRM5 P41594 1/20 0.34
AR P10275 1/20 0.34
LRRK2 Q5S007 1/20 0.34
P2RX7 Q99572 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.33
HSD17B10 Q99714 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
SCN9A Q15858 1/20 0.33

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
SCHEMBL723661 1.00 CASP1 (0.37) CASP1CASP3CASP7CASP8HCRTR1
SCHEMBL722758 0.85 KAT2B (0.41) CASP1CASP3CASP7CASP8KAT2B
SCHEMBL722759 0.85 KAT2B (0.41) CASP1CASP3CASP7CASP8KAT2B
SCHEMBL720299 0.82 ALDH1A1 (0.41) GRM4ALDH1A1GRM5SMN1; SMN2
SCHEMBL720300 0.82 ALDH1A1 (0.41) GRM4ALDH1A1GRM5SMN1; SMN2
SCHEMBL720108 0.81 MEN1 (0.40) ALDH1A1NR3C1SMN1; SMN2HSD17B10L3MBTL1
SCHEMBL10208208 0.80 NR3C1 (0.39) CASP1CASP3CASP7CASP8ALDH1A1
SCHEMBL719856 0.76 MEN1 (0.40) ALDH1A1SMN1; SMN2HSD17B10L3MBTL1
SCHEMBL719855 0.76 MEN1 (0.40) ALDH1A1SMN1; SMN2HSD17B10L3MBTL1
SCHEMBL722779 0.76 KAT2B (0.39) CASP1CASP3CASP7CASP8KAT2B

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 CASP1 3066/4885CASP3 2736/4885CASP7 2293/4885

“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.