SCHEMBL720708

SCHEMBL720708

CC(C)C(NP(=O)(Cl)Oc1cccc2cccnc12)C(=O)O

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 5/20 0.45
LMNA P02545 4/20 0.45
SMN1; SMN2 Q16637 3/20 0.45
RAB9A P51151 3/20 0.45
NPC1 O15118 2/20 0.45
MAPT P10636 5/20 0.44
HSP90AA1 P07900 1/20 0.44
HDAC6 Q9UBN7 2/20 0.43
METAP2 P50579 1/20 0.43
METAP1 P53582 1/20 0.43
POLB P06746 2/20 0.43
GAA P10253 1/20 0.41
ALDH1A1 P00352 5/20 0.41
MEN1 O00255 4/20 0.41
KMT2A Q03164 4/20 0.41
KDM4E B2RXH2 3/20 0.41
RXFP1 Q9HBX9 1/20 0.40
BLM P54132 1/20 0.40
HTT P42858 1/20 0.40
NPSR1 Q6W5P4 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
SCHEMBL1744358 0.85 MAPT (0.42) L3MBTL1LMNASMN1; SMN2RAB9ANPC1
SCHEMBL10208274 0.85 MAPT (0.42) L3MBTL1LMNASMN1; SMN2RAB9ANPC1
SCHEMBL722154 0.83 NR3C1 (0.41) L3MBTL1LMNASMN1; SMN2MAPTPOLB
SCHEMBL721569 0.81 CASP3 (0.43) LMNASMN1; SMN2GAAALDH1A1KMT2A
SCHEMBL722003 0.78 ALDH1A1 (0.48) SMN1; SMN2RAB9ANPC1MAPTPOLB
SCHEMBL31355239 0.73 MMP9 (0.45) L3MBTL1LMNASMN1; SMN2GAAMEN1
SCHEMBL722399 0.73 KDM4E (0.50) L3MBTL1LMNASMN1; SMN2RAB9ANPC1
SCHEMBL1043186 0.71 POLB (0.61) L3MBTL1LMNASMN1; SMN2RAB9ANPC1
SCHEMBL30013579 0.71 POLB (0.61) L3MBTL1LMNASMN1; SMN2RAB9ANPC1
SCHEMBL721386 0.71 TACR3 (0.42) LMNASMN1; SMN2GAAALDH1A1MEN1

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 L3MBTL1 2151/4885LMNA 2094/4885SMN1; 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.